Operator's Manual

Manufacturer: EU Authorized Representative:

Alcon Laboratories, Inc. Alcon Laboratories (U.K.) Ltd.
6201 South Freeway Boundary Way, Hemel Hempstead

Fort Worth, Texas 76134-2099

U.S.A. Hertfordshire,
United Kingdom HP2 7UD

Produced By:
Alcon Laboratories, Inc.
15800 Alton Parkway
Irvine, California 92618-3818
U.S.A.

Telephone: 949/753-1393 Directive 93/42/EEC

800/832-7827
FAX: 949/753-6614

8065751606 T, CATALOG NUMBER

905-2100-006 C, TEXT ONLY © 2009-2010 Alcon, Inc.

For Reference Only

 Infniti® Vision System Operator's Manual
8065751606

MANUAL REVISION RECORD

DATE REVISION ECN NUMBER AND DESCRIPTION

July 2009 N 20091225 - Initial release of operator's manual with catalog number
8065751606, and 905-2100-006 text (applies toInfniti® Vision System
consoles with software version 2.04). This manual includes theOzil®
® ®
IP feature, and the 23 gaugeInfniti UltraVit probe.
September 2009 R 20091528 - Add note on text cover sheet to inspect per generic QIP manual.

April 2010 T 20100589 - Regulatory updates for hazardous substance

considerations, new safety warnings, coagulation specications
expanded, tables 1-1 to 1-5 updated by one digit. Pages affected are: i,
ii, vii, 1.3, 1.4, 1.5, 1.6, 1.12, 1.15, 1.16, 1.18, 7.1-7.4.

END USER LICENSE AGREEMENT:

This product contains software licensed from Microsoft Corporation.

* Registered in the U.S. Patent & Trademark Ofce.

** Mackool is a trademark of Richard J. Mackool, M.D.
SmartPhaco is a registered trademark of Micro Medical Devices, Inc.
SmartPhaco is licensed from Micro Medical Devices, Inc.
Cycoloy and Lexan are registered trademarks of Sabic Innovative Plastics IP

ii 8065751606
For Reference Only
 TABLE OF CONTENTS

SECTION ONE - GENERAL INFORMATION PAGE #

Introduction.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .1.1
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1.2
Warnings and Cautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1.7
Product Service.. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. .. 1.16
Limited Warranty .. .. .. .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .1.17

SECTION TWO - DESCRIPTION PAGE #

Introduction.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.1
INFINITI® VISION SYSTEM CONSOLE AND ACCESSORIES
Console ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... ... .2.2
RearPanel... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.5
Footswitch .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.7
Remote Control . .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .2.14
Handpieces,Tips,a ndI nfusionS leeves. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.19
Fluidic Management System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.29
Inniti® AquaLase® B alanced Salt Solution Bottle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.30
Consumable Pak Congurations ..... ..... ..... ..... ..... ..... ..... ..... ..... ..... 2.31
Inniti® VideOverlayS ystem. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.34
INFINITI® VISION SYSTEM OPERATOR INTERFACE
Front Display Panel and Touch Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.38
Setup Screen and its Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.39
Doctor Name .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.40
Handpiece Type.. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .2.40
TipType ... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.41
Procedure Type .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .2.41
Cataract Grade .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .2.41
Irrigation Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.42
Metrics Display. .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .2.43
Footswitch Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.45
CustomB utton .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.47
Setup Status Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.62
Setup Steps .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.63
Surgery Screen and its Functions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.65
Main Window .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.65
Surgery Control Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.66
Fluidics Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.67
Surgery Controls .. .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .2.67
Adjust Button and Information Bar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.69
Surgery Controls Window with I/A Steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.70
Surgery Controls Window with Vitrectomy Steps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.70
Surgery Controls Window with Coagulation Steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.70
Surgery Menu .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.71
Setup Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.72
8065751606 iii
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 Procedural Step Buttons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.72
Stationary Step Buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.72
SurgeryM odes.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.73
Ultrasound (U/S) Mode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.73
NeoSoniX®M ode of Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.77
OZil® M ode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.81
OZil® I PFeature .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.86
AquaLase® L iquefaction Mode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.88
Irrigation/Aspiration Mode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.90
Fill Mode of Operation for Irrigation/Aspiration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.91
Coagulation (Coag) Mode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.92

Anterior Vitrectomy Mode ofOperation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.94

SECTION THREE - OPERATING INSTRUCTIONS PAGE #

Introduction.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .3.1
Power Up Sequence .. .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. 3.1
InitialS ystemS etup .. .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. 3.2
Standard Phacoemulsication Setup.. ..... ..... ..... ..... ..... ..... ..... ..... ..... ... 3.3
Standard AquaLase® S ystem Setup.. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. 3.8
Irrigation/AspirationH andpieceS etup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3.12
Anterior Vitrectomy Probe Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3.13
Coagulation Handpiece Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3.15

SECTION FOUR - CARE AND MAINTENANCE PAGE #

Introduction.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .4.1
Upon Completion of the Day's Surgical Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4.2
Care and Cleaning.. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. 4.4
SterilizationI nstructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4.5
Fuse Replacement.. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. 4.6

SECTION FIVE - TROUBLESHOOTING PAGE #

Introduction.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .5.1
Problem Conditions .. .. .. . .. .. . .. .. .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. 5.4
Advisories.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5.8
Warnings.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5.10
Faults.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .5.10

SECTION SIX - ACCESSORIES AND PARTS PAGE #

Catalog Numbers and Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6.2

SECTION SEVEN - INDEX PAGE #

Alphabetical Listing of Topics .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7.1

iv 8065751606
For Reference Only
 LIST OF FIGURES

FIGURE# TITLE PAGE #

Figure 1-1 The Inniti® Vision System .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1.1
Figure 1-2 Icons Used With the Inniti® Vision System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1.19
Figure 1-3 Labeling on Inniti® V ision System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1.20
Figure 1-4 Coagulation Power Outputs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1.21

Figure 2-1 The Console . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.2

Figure 2-2 The Front Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.3
Figure 2-3 The Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.5
Figure 2-4 The Right Side Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.6
Figure 2-5 The Accurus®/Legacy® and Inniti® F ootswitches . . . . . . . . . . . . . . . . . . . . . . . . . . .2.7
Figure 2-6 Footswitch Cable Routing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.8
Figure 2-7 Diagram of Footpedal Positions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.9
Figure 2-8 Footswitches Used with the Inniti® V ision System . . . . . . . . . . . . . . . . . . . . . . . .2.11
Figure 2-9 The Remote Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.14
Figure 2-10 The Remote Control Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.15
Figure 2-11 Proper Orientation of Two Halves of Remote Control . . . . . . . . . . . . . . . . . . . . . .2.17
Figure 2-12 The Remote Control Settings Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.18
Figure 2-13 OZil® Torsional Handpiece . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.19
Figure 2-14 Inniti® NeoSoniX® H andpiece . .. .. . .. .. . .. .. .. .. . .. .. . .. .. .. .. . .. .. . .2.19
Figure 2-15 Inniti® U ltrasonic (U/S) Handpiece . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.19
Figure 2-16 TurboSonics® Tips ... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.21
Figure 2-17 AquaLase® Liquefaction Handpiece . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.22
Figure 2-18 Inniti® U /S HP with Infusion Sleeve and BSI . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.22
Figure 2-19 Ultraow™* IT Handpiece and Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.25
Figure 2-20 Ultraow™* IT HP with infusion sleeve, reusable I/A tip, and tip adapter . . . . . .2.25
Figure 2-21 Ultraow™* O-ring tool with large and small O-rings . . . . . . . . . . . . . . . . . . . . . .2.25
Figure 2-22 Ultraow™* SP Handpiece.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.25
Figure 2-23 Inniti® Vitrectomy Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.26
Figure 2-24 Single use bipolar brush . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.28
Figure 2-25 The Inniti® Ultrasound Fluidic Management System (FMS) . . . . . . . . . . . . . . . .2.29
Figure 2-26 The AquaLase®/Balanced Salt Solution Bottle . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.30
Figure 2-27 VideOverlay Front Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.34
Figure 2-28 VideOverlay Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.35
Figure 2-29 Wall Outlet Adapters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.36
Figure 2-30 Standard VideOverlay Connection Diagram. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.36
Figure 2-31 High Denition VideOverlay Connection Diagram .. .. .. .. .. .. .. .. .. .. .. .. .2.37
Figure 2-32 The Inniti® Vision System Front Display Panel and Touch Screen . . . . . . . . . . . .2.38
Figure 2-33 Navigating the Inniti® V ision System User Screens . . . . . . . . . . . . . . . . . . . . . . .2.38
Figure 2-34 Functional Areas of the Setup Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.39
Figure 2-35 Bottle Height Measurement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.42
Figure 2-36 Metrics Dialog Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.44
Figure 2-37 Footswitch Buttons Dialogs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.45
Figure 2-38 Footswitch Treadle Dialogs .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.45
Figure 2-39 Setup Screen with Custom Drop List Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.47
Figure 2-40 Doctor Settings Dialog Screen - General Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.48

8065751606 v
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FIGURE# TITLE PAGE #
Figure 2-41 OZil® T orsional Function Before Phaco . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.49
Figure 2-42 Doctor Settings Dialog Screen - Steps Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.51
Figure 2-43 Doctor Settings Dialog Screen - Defaults Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.52
Figure 2-44 Doctor Settings Dialog Screen - Advanced Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.52
Figure 2-45 Copy/Delete Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.54
Figure 2-46 Copy/Delete Dialog with Enabled and Disabled Tips . . . . . . . . . . . . . . . . . . . . . . .2.56
Figure 2-47 System Settings Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.58
Figure 2-47 IV Pole Extender Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.59
Figure 2-48 Sound Settings Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.60
Figure 2-50 AquaLase® O cclusion Settings Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.60
Figure 2-51 About Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.61
Figure 2-52 Functional Area of the Setup Status Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.62
Figure 2-53 Functional Areas of the Setup Steps Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.63
Figure 2-54 Functional Areas of the Inniti® V ision System Surgery Screen . . . . . . . . . . . . . . .2.65
Figure 2-55 Surgery Control Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.66
Figure 2-56 Lower and Upper Limits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.69
Figure 2-57 Surgery Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.71
Figure 2-58 U/S Footpedal Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.73
Figure 2-59 The Ultrasound Continuous Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.74
Figure 2-60 The Ultrasound Pulse Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.74
Figure 2-61 The Ultrasound Burst Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.75
Figure 2-62 The U/S Custom Pulse Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.76
Figure 2-63 NeoSoniX® F ootpedal Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.77
Figure 2-64 The NeoSoniX® Continuous Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.78
Figure 2-65 The NeoSoniX® Pulse Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.79
Figure 2-66 The NeoSoniX® Burst Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.79
Figure 2-67 The NeoSoniX® C ustom Pulse Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.80
Figure 2-68 OZil® Footpedal Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.81
Figure 2-69 The OZil® Continuous Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.82
Figure 2-70 The OZil® P ulse Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.83
Figure 2-71 Phaco Duty Cycle (% Time On) Not Adjustable . . . . . . . . . . . . . . . . . . . . . . . . . . .2.83
Figure 2-72 The OZil® B urst Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.84
Figure 2-73 The OZil® Custom Pulse Surgery Screen .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.85
Figure 2-74 Surgery Screen with OZil®I P Enabled. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.86
Figure 2-75 OZil®I PDialog.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.86
Figure 2-76 OZil®I PDialog.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2.87
Figure 2-77 The AquaLase® Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.89
Figure 2-78 AquaLase® F ootpedal Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.89
Figure 2-79 The Irrigation/Aspiration Surgery Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.90
Figure 2-80 Irrigation/Aspiration Footpedal Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.90
Figure 2-81 The Coagulation Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.92
Figure 2-82 Coagulation Footpedal Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.92
Figure 2-83 Anterior Vitrectomy Footpedal Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.94
Figure 2-84 Anterior Vitrectomy Screen with Vit Probes in Drop Down List . . . . . . . . . . . . . 2.94
Figure 2-85 Anterior Vitrectomy Surgery Screen Using 20 Gauge Inniti® Vitrectomy Probe . 2.95
Figure 2-86 Anterior Vitrectomy Surgery Screen Using 23 Gauge Inniti® UltraVit® Pr obe . . 2.95
Figure 2-87 Vitrectomy Setup Screen..... ..... ..... ..... ..... ..... ..... ..... ..... 2.96

vi 8065751606
For Reference Only
FIGURE# TITLE PAGE #
Figure 3-1 U/S Tip/Wrench Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.5
Figure 3-2 Mackool**Tips .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .3.5
Figure 3-3 Protective Cap Removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3.6
Figure 3-4 Preparing Test Chamber and Placing Handpiece in Pouch . . . . . . . . . . . . . . . . . . . .3.6

Figure 4-1 Footswitch Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4.3

Figure 5-1 Advisories Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5.1

Figure 5-2 Warnings Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5.2
Figure 5-3 Faults Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5.2
Figure 5-4 Troubleshooting Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5.3

LIST OF TABLES
TABLE# TITLE PAGE #

Table 1-1 Information on Location of Hazardous Substances in Inniti® Vision System . . . . .1.4
Table 1-2 Guidance and Manufacturer's Declaration - Electromagnetic Emissions . . . . . . . . .1.4
Table 1-3 Guidance and Manufacturer's Declaration - Electromagnetic Immunity . . . . . . . . .1.5
Table 1-4 Recommended Separation Distances Between Portable and Mobile
RF Communications Equipment and the Inniti® Vision System . . . . . . . . . . . . . . .1.6
Table 1-5 Specications ..... ..... ..... ..... ..... ..... ..... ..... ..... ..... .... 1.18
Table 1-6 Abbreviations Used with the Inniti® Vision System . . . . . . . . . . . . . . . . . . . . . . .1.18

Table 2-1 Table of Footpedal Positions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.9

Table 2-2 Programming the Footswitch Treadle. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.45
Table 2-3 Parameters in Surgery Controls Area . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.67

Table 5-1 Problem Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5.4

Table 5-2 Error Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5.8

8065751606 vii
For Reference Only
 PREFACE

This operator's manual is your written guide to theInniti® Vision System and considers all options
available to the customer; therefore, when reading this manual, ignore the options which do not
apply to your specic unit.

Please read the entire manual carefully before operating the instrument. Recommended settings are
given only as guidelines, and are not meant to restrict the surgeon; however, before trying other
settings, the surgeon and support personnel should be experienced with the system and familiar with
the new settings.

NOTE: If an inconsistency exists between the instructions in the operator's manual and the
Directions For Use (DFU) supplied with a cons umable pak or accessory, follow the DFU.

Equipment improvement is an on-going process and, as such, changes may be made to the
equipment after this manual is printed.

Pay close attention to Warnings, Cautions, and Notes in this manual. A WARNING! statement is
written to protect individuals from bodily harm. A Caution statement, with the CAUTION heading
centered above the text, is written to protect the instrument from damage. A NOTE: is written to
bring attention to highlighted information.

If you have questions, or want additional information, please contact your local Alcon representative
or the Alcon Technical Services Department at:

Alcon Laboratories, Inc.

15800 Alton Parkway
Irvine, California 92618
(949) 753-1393
FAX (949) 753-6614

CAUTION: U.S. Federal Law restricts this device to sale by or on the order of a physician.

viii LAST PAGE OF THIS SECTION 8065751606

For Reference Only
 SECTION ONE
GENERAL INFORMATION

INTRODUCTION

Alcon’s Inniti® Vision System is an ophthalmic surgical instrument designed to be reliable,

safe, and easy to operate. The Inniti® Vision System provides four modes for cataract
lens extraction using AquaLase®, OZil® torsional, NeoSoniX®, and high performance U/S
handpieces. This instrument has been developed to be user friendly, combining hardware
that is easy to install and maintain
along with software that increases
the effectivity of the user.

The Infiniti ® Vision System is

intended for use in small incision
cataract lens extraction surgical
procedures. This system allows the
surgeon to emulsify and aspirate
the lens in the eye, while replacing
aspirated uid and lens material
with balanced salt solution. This
process maintains a stable (inated)
eye chamber volume. Using system
controls the surgeon regulates the
amount of power applied to the
handpiece tip, the rate of aspiration,
vacuum, and the ow of BSS® or
BSS®Plus irrigation solution. The
system controls include a footswitch
to enable the surgeon to control
irrigation ow, aspiration rate, phaco
power, vitrectomy cut rate, and
coagulation power.

Figure 1-1 The Infniti® Vision System

8065751606 1.1
For Reference Only
GENERAL INFORMATION

The Inniti® Vision System is designed for use in anterior segment procedures that
require simultaneous cataract lens extraction, irrigation, and aspiration, as well as
associated procedures such as vitrectomy and coagulation. It was developed with a dual
purpose: to make it simple to operate, and to allow the surgeon tremendous versatility
and control. The system is designed to allow the surgeon to customize the treatment of
every patient.

Following are key features of the Inniti® Vision System:

• Customized cataract handpiece

- OZil® torsional lens removal options:
with ultrasonic torsional oscillations which can be
used exclusively or alternated with traditional phaco.
- AquaLase® liquefaction device handpiece, technology, and accessories.
- Inniti® NeoSoniX® handpiece combining the features of a phaco handpiece with
sonic oscillations.
- High performance Inniti® U/S handpiece: 40 kHz, piezoelectric, slim,
lightweight, autoclavable.
• Advanced uidics with quick, smooth control of peristaltic aspiration.
• Fully programmable, multi-microprocessor control.
• Modularized uidic connections achieved with the disposable Fluidic
Management System (FMS).
• Emulation of venturi-like uidic performance.
• Ability to drive a high performance Inniti® vitrectomy guillotine cutter.
• Bipolar coagulation capability.
• Several traditional modalities of ultrasonic power control including continuous,
pulsed, and “burst” application of ultrasonic power, as well as duty cycle
management.
• Automated IV pole, controlled via the front panel, footswitch, or remote control.
• Linear footswitch control of ultrasonic power in U/S steps (sophisticated control
loop offers low-end control).
• Linear footswitch control of aspiration ow rate (AFR) in I/A, VIT, and lens
removal modes.
• Linear footswitch control of vacuum in I/A, VIT, and lens removal modes.
• On-demand continuous irrigation.
• Programmable, pressurized reux via the footswitch.
• Ability to set vacuum levels and aspiration ow rates to desired levels in phaco,
I/A, and VIT steps.
• Ability to switch between surgical steps using touch screen, remote, or footpedal.
• Emission of variable tones for conrmation of system operational status.
• Voice conrmation during surgical step or mode changes.
• Flat screen, active matrix color LCD with touch screen display that is tiltable and
rotatable.
• High-tech graphical user interface.
• Multi-channel wireless remote control.

1.2 8065751606
For Reference Only
 Abbreviation Descriptions

Many of the abbreviations used in this manual and on the Inniti® Vision System are
described in Table 1-5. Icons are identied in Figure 1-2.

Accessory Equipment

Accessory equipment connected to or used with this equipment must be certied

according to the respective IEC Standard (e.g., IEC 950 for data processing
equipment, and IEC 60601-1 for medical equipment). Furthermore, all congurations
shall comply with System Standard IEC 60601-1-1. Anyone connecting additional

equipment
by Alcon isorresponsible
otherwise causing a different
for continued system conguration
compliance than provided
to the requirements of System
Standard IEC 60601-1-1. If in doubt, consult the Technical Services department or
your local Alcon representative.

Follow local governing ordinances and recycling plans regarding disposal or

recycling of device components and packaging.

User Information – Environmental Considerations

The equipment that you have purchased requires the use of natural resources for its
production and operation. This equipment may also contain hazardous substances which
could have potential effect on the environment and human health if disposed of improperly.

In order to avoid the entry of any such substances into our environment, and to pro-
mote natural resource conservation, please install, maintain, and operate the equip-
ment in accordance with the instructions. Information on the location of hazardous
substances, resource consumption and emissions of the equipment can be found
throughout this Operator's Manual. Please use the appropriate take-back systems.
Such take-back systems reuse or recycle many of the materials in your end-of-life
equipment in a benecial way. Please contact your local Alcon ofce for assistance in
take-back options through Alcon or other providers.

The crossed-bin symbol located on this equipment reminds you to use take-back sys-
tems, while also emphasizing the requirement to collect waste equipment separately,
and not dispose of it as unsorted municipal waste. The Pb notation, if present, indi-
cates that the labeled device contains greater than 0.004% lead.

Pb If you need more information on the collection, reuse or recycle systems available to
you, please contact your local or regional waste administration, or contact your local
Alcon ofce for more information.

8065751606 1.3
For Reference Only
Table 1-1 Information on the Location of Hazardous Substances in the Infniti® Vision System - The
Infniti® Vision System contains hazardous substances which could have potenti al effect
on the environment and human health if disposed of improperly.

Material Location Hazardous Substances Contained

Printed Circuit Board Assembly Lead, Polybrominated Biphenyls (PBB)
Other Electrical / Electronic Device Lead, Polybrominated Biphenyls (PBB)
Cable Assembly Lead
Power Supply Lead, Polybrominated Biphenyls (PBB)
Host PC Module Lead, Polybrominated Biphenyls (PBB)
Liquid Crystal Display Lead
Battery Lead, Lithium, Zn/MnO
2
IV Pole Assembly Lead, Polybrominated Biphenyls (PBB)
Remote Control Lead
Fluidics Assembly Lead
Pneumatic Assembly Lead

Universal Precautions
Universal precautions shall be observed by all people who come in contact with the
instrument and/or accessories to help prevent their exposure to blood-borne pathogens and/or
other potentially infectious materials. In any circumstance, wherein the exact status of blood
or body uids/tissues encountered are unknown, it shall be uniformly considered potentially
infectious and handled in accordance with OSHA or your own national guidelines.

EMC Statement
It is important to install and use the equipment in accordance with the instructions in order
to prevent harmful interference with other devices in the vicinity. If this equipment causes
harmful interference to other devices (determined by turning the equipment off and on), the
user is encouraged to try to correct the interference by one or more of the following measures:
• Reorient or relocate the other device(s).
• Increase the distance between the equipment.
• Connect this equipment into an outlet on a circuit different from that to which the
other device(s) is connected.
• Consult the manufacturer or your Alcon eld service engineer for help.

Table 1-2 Guidance and Manufacturer's Declaration - Electromagnetic Emissions - The Infniti®
Vision System is intended for use in the electromagnetic environment specied below. The
customer or the user of the Infniti® Vision System should assure that it is used in such an
environment.
Emissions Test Compliance Electromagnetic Environment-Guidance

RF emissions Group 1 The Infniti® Vision Vision System uses RF energy only for its internal
CISPR 11 function. Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.

RF emissions Class A Based on extensive eld experience the Infniti® Vision System is suitable
CISPR 11 for use in all establishments including domestic and those directly
connected
to the public low voltage power supply network that supplies buildings
Harmonic emissions Class A used for domestic purposes.
IEC 61000-3-2
The EMC Statement provides guidance on steps to take in case of
Voltage uctuations/ Complies electromagnetic interference.
Flicker emissions
IEC 61000-3-3

1.4 8065751606
For Reference Only
Table 1-3 Guidance and Manufacturer's Declaration - Electromagnetic Immunity - The Infniti® Vision
System is intended for use in the electromagnetic environment specied below. The
customer or the user of the Infniti® Vision System should assure that it is used in such an
environment.
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment-Guidance

Electrostatic • ±6 kV contact • ±6 kV contact Floors should be wood, concrete, or ceramic tile. Do

discharge (ESD) • ±8 kV air • ±8 kV air not use around oors that are covered with synthetic
IEC 61000-4-2 material to avoid system stoppage due to ESD.
Electrical fast • ±2 kV for power • ±2 kV for power Mains power quality should be that of a typical
transient/burst supply lines supply lines commercial or hospital environment. To avoid pre-
IEC 61000-4-4 • ±1 kV for input/ • ±1 kV for input/ mature shutdown due to fast transients avoid powering
output lines output lines the Infniti® Vision System on the same branch
circuit with sources that can generate fast transients
(inductive switching; e.g., high current motors).
Surge • ±1 kV differential • ±1 kV differential Mains power quality should be that of a typical
IEC 61000-4-5 mode mode commercial or hospital environment.
• ±2 kV common • ±2 kV common
mode mode
Voltage dips, short • <5% UT (>95% dip in • <5% UT (>95% dip in Mains power quality should be that of a typical
interruptions, and UT) for 0.5 cycle UT) for 0.5 cycle commercial or hospital environment. If the use of the
voltage variations • 40% UT (60% dip in • 40% UT (60% dip in Infniti® Vision System requires continued operation
on power supply UT) for 5 cycles UT) for 5 cycles during power mains interruptions, it is recommended
input lines • 70% UT (30% dip in • 70% UT (30% dip in that the Infniti® Vision System be powered from an
IEC 61000-4-11 UT) for 25 cycles UT) for 25 cycles uninterruptible power supply or a battery.
• <5% UT (>95% dip in • <5% UT (>95% dip in
UT) for 5 sec UT) for 5 sec

Power frequency 3 A/m 3 A/m Power frequency magnetic elds should be at

(50/60 Hz) levels characteristic of a typical location in a typical
magnetic eld commercial or hospital environment.
IEC 61000-4-8

Portable and mobile RF communications equipment

should be used no closer to any part of the Infniti®
Conducted RF 3 Vrms 3 Vrms Vision System, including cables, than the recommended
IEC 61000-4-6 150 kHz to 80 MHz separation todistance calculated from the equation
applicable the frequency to the transmitter.
Recommended separation distance:
d = 1.2√P
d = 1.2√P 80 MHz to 800 MHz
Radiated RF 3 V/m 3V/m d = 2.3√P 800 MHz to 2.5 GHz
IEC 61000-4-3 80 MHz to 2.5 GHz
where P is the maximum output power rating to the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in meters (m).
Field strength from fixed RF transmitters, as
determined by an electromagnetic site surveya,
should be less than the compliance level in each
frequency rangeb.
Interference may occur in the vicinity of
equipment marked with following symbol.

Note: U T is the a.c. mains voltage prior to application of the test level.
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reection from
structures, objects, and people.
a
Field strengths from xed transmitters, such as base stations for radio (cellular/cordless) and land mobile radios, amateur radio, AM and
FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To access the electromagnetic environment due
to xed RF transmitters, an electromagnetic site survey should be considered. If the measured eld strength in the location in which the
(equipment or system) is used exceeds the applicable RF compliance level above, the (equipment or system) should be observed to
verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating
the Infniti® Vision System.
b
Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3 V/m.

8065751606 1.5
For Reference Only
Table 1-4 Recommended Separation Distances Between Portable and Mobile RF Communications
Equipment and the Infniti® Vision System - The Infniti® Vision System is intended for use in an
electromagnetic environment in which radiated RF disturbances are controlled. The customer
or the user of the Infniti® Vision System can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and the Infniti® Vision System as recommended below, according to the maximum
output power of the communications equipment.

Separation distance according to frequency of transmitter

Rated maximum output (m)
power of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
(W) d = 1.2√P d = 1.2√P d = 2.3√P

0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73

1 1.2 1.2 2.3

10 3.8 3.8 7.3

100 12 12 23

For transmitters rates at a maximum output power not listed above, the recommended separation distance d in meters (m) can
be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
Note 1 - At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2 - These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reection from
structures, objects, and people.

1.6 8065751606
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WARNINGS AND CAUTIONS

Most of these warnings are stated elsewhere in this manual; however, for easy reference
they are repeated in greater detail here. If additional information is required, please
contact your local Alcon service representative, or the Technical Services Department.

There are no user serviceable components inside the Infniti® Vision System console or
footswitch. Refer all service issues to your factory-trained Alcon service engineer.

WARNINGS!
The Infniti® Vision System battery can only be serviced by a factory-trained Alcon
service engineer. Access by untrained personnel can lead to injury.
Good clinical practice dictates testing for adequate irrigation, aspiration ow, reux,
and operation as applicable for each handpiece prior to entering eye.
Ensure that the tubings are not occluded during any phase of operation.
Do not exceed maximum capacity of drain bag (500 ml). Excessive pressure can
result from exceeding drain bag maximum capacity and potentially result in a haz-
ardous condition for the patient.
Inadvertent actuation of Prime or Tune while a handpiece is in the eye can create a
hazardous condition that may result in patient injury.
Inadvertent pressing of Standby switch when system is active will cause unit to
shut down.
If the handpiece test chamber is collapsed after tuning, there is a potential of low
irrigation ow through the handpiece and may result in a uidic imbalance. This, in
turn, may cause a shallowing or collapsing of the anterior chamber.
Avoid setting the patient above the FMS. Operating with the patient above the FMS will result
in a lower irrigation pressure than indicated on the display, and possible underventing.

If the Infniti® Vision System is used at the 220V - 240V range in the United States or
Canada, it should be used on a center-tapped, 240V single phase circuit.
Keep clear of the IV pole when it is in motion to prevent skin, hair, and/or clothing
from being trapped in the IV pole mechanism. The IV pole moves during power on/
off, priming, and bottle height adjustment.
Keep clear of display base when raising display from stored position to prevent skin,
hair, and /or clothing from being trapped at the base.
A qualied technician must perform a visual inspection of the following components
every twelve months:
• Warning Labels (see section one of this manual)
• Power Cord
• Fuses
In case of a deciency, do not use the system; call Alcon Technical Services.
A qualied technician must check ground continuity for leakage current every
twelve months to ensure
EN60601-1/IEC601-1). they
Values arebe
must within the applicable
recorded, and if theystandards (forapplicable
are above the example:
standards, or 50% above initial measurement, do not use the system; call Alcon
Technical Services.

8065751606 1.7
For Reference Only
 WARNINGS!

Use of accessories and cables other than those provided may result in increased
emissions or decreased immunity of the system. Portable and mobile RF
communications equipment can affect this medical electrical equipment.

Handpiece Care

The Inniti® AquaLase®, OZil® torsional, NeoSoniX®, and high performance U/S
handpieces are surgical instruments and must be handled with care. The handpiece tip
should not touch any solid object while in operation. Immediately following surgery
the handpiece must be thoroughly cleaned. Be sure handpiece connector is completely
dry before connecting it to console. For cleaning and sterilization procedures, see the
Directions for Use (DFU) supplied with the handpiece.

WARNING!
If in the medical opinion of the physician a patient with a prion related disease
undergoes a high risk procedure, the instrument should be destroyed or be
processed according to local requirements.

The Inniti® NeoSoniX®, OZil® torsional, and U/S handpieces must be at room
temperature just before use. Allow the handpiece to air cool for at least 15 minutes
after autoclaving; never immerse the handpiece in liquid when hot.

CAUTIONS
Never ultrasonically clean the Infniti® AquaLase®, OZil® torsional, NeoSoniX®, or

U/S handpieces; irreparable damage may result.

Prior to sterilization, the Infniti® AquaLase®, OZil® torsional, NeoSoniX®, and
U/S handpieces should always have the connector end cap secured and placed in
the sterilization tray. This will prevent damage to the connectors and ha ndpieces
during handling, and especially during autoclaving.

Do not operate OZil® torsional, NeoSoniX®, or U/S handpieces unless the tip is
immersed in BSS® sterile irrigating solution or distilled water or is in su rgical
use. Irreparable damage to the handpiece and tip can result if run dry.

Ensure that test chamber is lled with BSS® sterile irrigating solution before
tuning OZil® torsional, NeoSoniX®, or U/S handpieces. Tuning a handpiece dry
may result in premature tip failure and breakage.

Quenching a hot handpiece in water can cause damage and will void warranty.

Be sure handpiece is completely dry before connecting it to console. Damage to

handpiece and console may result if plugged in when wet.

1.8 8065751606
For Reference Only
 WARNINGS!

Use of the OZil® torsional, Infniti® NeoSoniX ®, U/S, or AquaLase® handpiece in the
absence of irrigation ow and/or in the presence of reduced or lost aspiration ow
can cause excessive heating and potential thermal injury to adjacent eye tissues.

Appropriate use of Infniti® Vision System parameters and accessories is important

for successful procedures. Use of low vacuum limits, low ow rates, low bottle
heights, high power settings, extended power usage, power usage during occlusion
conditions (beeping tones), failure to sufciently aspirate viscoelastic prior to using
power, excessively tight incisions, and combinations of the above actions may
result in signicant temperature increases at incision site and inside the eye, and
lead to severe thermal eye tissue damage.

Use of an ultrasonic handpiece other than the OZil® torsional, Infniti® NeoSoniX ®,
or U/S handpiece, or use of a handpiece repaired without Alcon authorization, is
not permitted, and may result in patient injury, including potential shock hazard to
patient and/or operator.

The U/S tips supplied in the Infniti® Vision System pak are only to be used on the
OZil® torsional, Infniti® NeoSoniX ®, or U/S handpieces. Each U/S tip is intended to
be used only once per case, and then disposed of according to local governing
ordinances.

Use 0.9 mm U/S tips exclusiv ely with 0.9 mm infusion sleeves. U se 1.1 mm U/S a nd
1.1 mm liquefaction tips exclusively with 1.1 mm infusion sleeves. Mismatching U/S
tips and infusion sleeves may create potentially hazardous uidic imbalances.

Directing energy toward non-lens material may cause tissue damage.

IV Pole and Extender

WARNINGS!

Once the IV pole extender is installed, the upper hook is to be used. Do not change
bottle height by manually hanging the bottle on the lower hook. Manually lowering the
IV bottle to the lower hook will introduce an error in the displayed height indication and
negatively impact the performance of the Infusion Pressure Drop detection feature,
causing false indications at low bottle levels.

Empirical numbers for bottle heights are not a replacement for competent surgical
technique. The surgeon should visually and physically monitor intraocular pressure.

8065751606 1.9
For Reference Only
 Ultraow™* (I/A) Handpiece

Prior to each procedure inspect the two O-rings where the tip screws onto the
Ultraow™* handpiece. If damaged or missing, replace the o-rings. If in doubt,
contact Alcon's Technical Services Department.

WARNINGS!
Use of non-Alcon surgical reusable or disposable I/A handpieces that do not meet
Alcon surgical specications, or use of an Alcon handpiece not specied for use
with the Infniti® Vision System, may result in a uidic imbalance. This, in turn, may
cause a shallowing or collapsing of the anterior chamber.

Exceeding
cause the recommended
anterior level of
chamber shallowing 100 mmHg
and/or with a 0.5
incarceration ormm or larger
tearing of theI/A tip may
posterior
capsule.

I/A tips are not to be used with NeoSoniX®, OZil® torsional, or U/S handpieces.

Recommended Vacuum Range for I/A Tips

It is important that only the proper size I/A tip be used when operating with maximum
vacuum. Only 0.2 mm or 0.3 mm I/A tips should be used with vacuum limits above
100 mmHg.

I/A adjustable vacuum range is 0-650+.

Handpiece Tips
Ensure that handpiece tip is fully tightened to the handpiece. If not securely attached,
an error may be generated and/or inadequate tuning will occur. Ensure that the tip is
not too tight so that it can be removed after use.

Use of a tool other than tip wrenches supplied by Alcon may cause damage to the tip
and/or handpiece.

WARNING!
Poor clinical performance will result if tip is not secured tightly to the handpiece.

During any ultrasonic procedure, metal particles may result from inadvertent
touching of the ultrasonic tip with a second instrument. Another potential source
of metal particles resulting from any ultrasonic handpiece may be the result of
ultrasonic energy causing micro abrasion of the ultrasonic tip.

Check for the

tips. Never presence
attempt and correct
to remove position
the tubing. Useofofthe
polymer tubing on the Mackool**
the Mackool** tips without polymer
tubing may result in a hazardous condition for the patient.

1.10 8065751606
For Reference Only
 Infniti® Vitrectomy Probe

The Infniti® vitrectomy probe, a guillotine vitreous cutter, is intended for single use only.

WARNINGS!
Do not test or operate vitrectomy probes unless tip of probe is immersed in
BSS ® sterile irrigating solution or distilled water or is in surgical use. Irreparable
damage to the handpiece and tip can result if run dry.

After lling and testing, and before surgical use, verify that the probe i s prop -
erly actuating and aspirating. This may require lowering cut rate to achieve
good visualization. The port should always remain in open position in footpedal
position 1. If cutting port is partially closed while in position 1, replace the probe.
Prior to entry into the eye, and with tip of probe in sterile irrigating solution,
the surgeon should step on the footpedal for visual verication that the probe
is cutting; alternatively, press the Test button on the Vitrectomy Setup Screen: if
the cutter is observed to not fully close, or does not move when the probe is
actuated, replace the probe.
• If cutting port is parti ally closed while idle, replace the probe.
• If air bubbles are observed in the aspiration line or exiting the probe tip during
priming, replace the probe.
• If a reduction of cutting capability or vacuum is observed during the surgical
procedure, stop immediately and replace the probe.

Aspiration/Vacuum Adjustments

Adjusting aspiration rates or vacuum limits above the preset values may result in
aspiration levels (volumes) exceeding irrigation inow.

Dynamic Rise values of 1, 2, 3, or 4 will achieve vacuum in shorter periods of time.

Care must be taken not to engage non-lens material.

WARNING!
Adjusting aspiration rates or vacuum limits above the preset values, or lowering
the IV pole below the preset values, may cause chamber shallowing or collapse
which may result in patient injury.

Presurgical Check -out Tests

Presurgical check-out tests must be performed as outlined in the Operating Instructions

section. If an error message or advisory message is displayed on the front panel, refer to
the Troubleshooting section of this manual. If the problem persists, DO NOT PROCEED.

WARNINGS!
When lling handpiece test chamber, if stream of uid is weak or absent, good
uidics response will be jeopardized. Good clinical practice dictates the testing for
adequate irrigation and aspiration ow prior to entering the eye.

Ensure that tubings are not occluded or pinched during any phase of operation.

8065751606 1.11
For Reference Only
 Footswitch

Never pick up or move the footswitch by the cable. Dropping or kicking the
footswitch can cause irreparable damage.

If required, the footswitch may be wiped with alcohol, mild soap and water, or any
germicidal solution that is compatible with the plastic parts.

WARNING!
Route the footswitch cable properly to avoid tripping.

CAUTION
Do not clean the footswitch using solvents, abrasives, or any cleaner that is not
compatible with plastic parts made of GE Cycoloy CU 6800 and LEXAN 920A.
Damage may result.

High Altitudes

Vitrectomy cutting performance may vary at high altitudes. Consult Alcon Technical
Service for additional information.

Occlusion Tones

Two different occlusion tones (intermittent beeping tones during occlusion) indicate
that the vacuum is near or at its preset limit, and aspiration ow is reduced or
stopped to avoid exceeding the limit. The rst type, the I/A occlusion tone, sounds
when occlusion occurs during aspiration only (in the absence of ultrasonic power
or AquaLase® system magnitude). The I/A occlusion tone is a lower, intermittent
single beep. The second type of occlusion tone, the phaco occlusion tone, is a higher,
intermittent double beep, and sounds when occlusion occurs during application of
ultrasonic power or AquaLase® system magnitude.

The I/A occlusion and phaco occlusion tones indicate that the vacuum has reached its
maximum allowed preset value. The I/A occlusion tone can be turned off, while the
phaco occlusion tone cannot be turned off.

WARNINGS!
The phaco occlusion bell indicates no aspiration ow. Use of high U/S settings
and/or prolonged use may lead to thermal injury.

Use of the NeoSoniX®, OZil® torsional, U/S, or AquaLase® handpiece in the absence
of irrigation ow and/or in the presence of reduced or lost aspiration ow can cause
excessive heating and potential thermal injury to adjacent eye tissues.

Vacuum Tone

A vacuum tone is provided. The pitch will vary relative to the amount of vacuum. A
high vacuum can indicate that little to no ow is occuring. This tone can be reduced
in volume, but not turned off.

1.12 8065751606
For Reference Only
 WARNINGS!
A moderate to high vacuum tone may indicate little to no ow is occuring. Use of
the NeoSoniX®, OZil® torsional, U/S, or AquaLase® handpiece in the absence of
irrigation ow and/or in the presence of reduced or lost aspiration ow can cause
excessive heating and potential thermal injury to adjacent eye tissues.

Do not exceed maximum capacity of drain bag (500 ml). Excessive pressure can
result from exceeding drain bag maximum capacity and potentially result in a
hazardous condition for the patient.

Coagulation Function

Listed below are general precautions to be followed when using the Coagulation function:

• To ensure safe operation of the coagulation function, only approved cables

and accessories must be used (See your Alcon representative). Coagulation
performance can be guaranteed only when using Alcon components or Alcon-
endorsed components.
• To reduce the risk of accidental burns, caution should always be taken when
operating high-frequency surgical equipment.
• Interference produced by the operation of high-frequency surgical equipment may
adversely inuence the operation of other electronic equipment.
• Accessories should be checked regularly; electrode cables should particularly be
checked for possible damage to the insulation.
• Operation of the coagulation step is limited to extraocular uses only.
• The lowest power level in coagulation step should always be selected for the
intended purpose.
• Skin-to-skin contact (for example between the arms and body of the patient)
should be avoided, for example by insertion of dry gauze.
• When HF (high frequency) surgical equipment and physiological monitoring
equipment are used simultaneously on the same patient, any monitoring electrodes
should be placed as far as possible from the surgical electrodes. Needle monitoring
electrodes are not recommended.
• In all cases, monitoring systems incorporating high frequency current-limiting
devices are recommended.
• The cables to the surgical electrodes should be positioned in such a way that
contact with the patient or other leads is avoided.
• Temporarily unused active electrodes should be stored so that they are isolated
from the patient.
• The use of ammable anaesthetics or oxidizing gases such as nitrous oxide (N 2O)
and oxygen should be avoided if a surgical procedure is carried out in the region of
the thorax or the head, unless these agents are sucked away.

Non-ammable
• • Flammable agents
agents usedshould be usedorfor
for cleaning cleaning andordisinfection
disinfecting, as solventswherever possible.
of adhesives,
should be allowed to evaporate before the application of HF surgery. Some
materials, for example cotton, wool and gauze, when saturated with oxygen may
be ignited by sparks produced in normal use of the HF surgical equipment.
• Accessories should have a rated voltage equal to or greater than the maximum
coagulation output voltage.
8065751606 1.13
For Reference Only
 Coagulation Function (from prior page)

WARNINGS!
Do not use the coagulation function on patients with pacemakers or implanted
debrillatory devices. If electrosurgery is used on patients with implanted cardiac
pacemakers or debrillatory devices or pacemaker electrodes, be aware that
irreparable damage to the pacemaker or debrillatory device and its function
may occur and lead to ventricular brillation. Please check with the pacemaker
or debrillatory device manufacturers for their recommendations.

Failure of the HF surgical equipment (coagulation circuitry) could result in an

unintended increase of output power.

CAUTION
The Infniti® Vision System is not protected against the effects of debr illator
discharge.

Cautery, Diathermy, Coagulation Denition

The Inniti® Vision System uses the word “Coagulation” in place of Cautery or
Diathermy, based on the following denition:

Coagulation - Isolated, bipolar, high frequency current supplied to conductors (e.g.

forceps). Current passes between these electrodes, halting bleeding. (Abbreviated
“Coag” in some of the text of this operator’s manual.)

Infniti® VideOverlay System (IVO)

WARNINGS!
Do not remove VideOverlay cover; there are no user-serviceable parts inside.
Refer servicing to qualied service personnel.

Do not simultaneously touch the VideOverlay enclosure and the patient.

CAUTIONS
• Do not use multiple portable socket outlets with this system.
• Use only the Alcon-supplied serial cable to connect the Infniti® Vision System
to the IVO.

1.14 8065751606
For Reference Only
 Consumable Paks

Consumable items used with the Inniti® Vision System during surgery are designed
to be used once and then discarded, unless labeled otherwise.

All Inniti® paks contain Directions for Use (DFU). It is important to read and under-
stand the DFU’s prior to use.

NOTE: If an inconsistency exists between the instructions in the operator’s

manual and the Directions For Use (DFU) supplied with a consumable pak o r
accessory, follow the DFU

WARNINGS!

Mismatch of consumable components and use of settings not specially adjusted for
a particular combination of consumable components may create a patient hazard.

Do not use paks that have exceeded the expiration date.

Sterile disposable medical devices should not be reused! These components have
been designed for one time use only; do not reuse.

Potential risk from reuse or reprocessing the following products labeled for single
use include:
• Bipolar Coagulation Instruments- Thermal injury or electrical shock caused by
a damaged bipolar instrument, and foreign particle introduction into the eye.
• Fluid Management Components- Fluid path leaks or obstruction resulting in
reduced uidics performance, and foreign particle introduction into the eye.
• Phacoemulsifcation Tips- Reduced tip cutting performance, presence of tip
burrs, uid path obstruction, and foreign particle introduction into the eye.
• Vitreous Cutting Instruments- Reduced vitreous cutting performance, uid path
obstruction, and foreign particle introduction into the eye.

The equipment used in conjunction with the Alcon disposables constitutes a com-
plete surgical system. Use of disposables other than Alcon disposables may affect
system performance and create potential hazards, and if it is determined to have
contributed to the malfunction of the equipment under contract, could result in the
voidance of the contract and/or invoicing at prevailing hourly rates.

In all cases, the instrument setup instructions contained in the manual should be
thoroughly understood prior to using any of the pak congurations.

Read all package label material printed on the consumable paks prior to their use.

8065751606 1.15
For Reference Only
 Miscellaneous
CAUTIONS

• Do not use the Inniti® Vision System near ammable anesthetics.

• Avoid spilling BSS® solution, or moisture of any kind, around the electrical
handpiece connectors.
• Do not push or pull the unit by the display, the tray, or the IV pole. Handles located
at the rear and sides of the unit are provided for moving the instrument. The unit
should be pulled and not pushed, especially over elevator and door thresholds.
• Do not place more than a 20 lb. load on tray support.
• The USB connector ( ) and Infniti®port ( ) located on the rear panel are
for use by Alcon trained personnel only. Failure to comply will void warranty.

WARNINGS!

Tray support must be set in its stored position when moving instrument.

Route the footswitch cable, power cord and any other cables connected to the Infniti®
Vision System to avoid tripping.

PRODUCT SERVICE

For product service, please contact Alcon’s Technical Services Department at the
number provided below.

Operators experiencing problems with the system should refer to the Operating
Instructions and Troubleshooting sections of this manual. A problem which persists
should be referred to the Alcon Technical Services Department or your local
authorized service representative.

For optimum performance, it is the user’s responsibility to schedule preventive

maintenance service on the system and its accessories a minimum of one time per
year. Additional preventive maintenance may be required based upon system use.
Alcon’s Field Service Engineers are trained and equipped to provide the highest
quality of workmanship.

Safety performance should be veried by the user (e.g., qualied service personnel) at
least twice a year. Ground resistance, leakage current, and dielectric withstand voltage
must be checked to appropriate national standard.

To avoid unnecessary shipping, please contact your Alcon Technical Services

Department prior to return of any system or accessories. If return of the equipment is

deemed
shippingnecessary, a Return Material Authorization will be issued with appropriate
instructions.

Alcon Technical Services Department

15800 Alton Parkway
Irvine, California 92618-3818
(800) 832-7827, or (949) 753-1393

1.16 8065751606
For Reference Only
LIMITED WARRANTY

Alcon will repair or replace at its option, any system or accompanying accessories
found to be defective in material and/or workmanship for a period of one (1) year
from the date of initial installation. This warranty applies to the srcinal purchaser
of the system, when said system is properly installed, maintained, and operated in
accordance with published instructions.

Alcon shall not be obligated to provide services under this warranty for damage to
or destruction of systems covered where such damage or destruction is a result of
or caused by re or explosion of any srcin, riot, civil commotion, aircraft, war, or

any Act of God including, but not limited to lightning, windstorm, hail, ood or an
earthquake.

This warranty does not cover damage resulting from service repair or other alteration
by any person other than an Alcon-authorized service person, and any warranties
provided by Alcon with respect to this equipment shall become void and of no further
force and effect if this equipment is serviced by anyone other than Alcon-authorized
service personnel. In particular, Alcon shall have no obligation to replace, repair or
credit customer’s account for the cost of the equipment, which has been subject to
service or other alteration by persons other than Alcon-authorized service personnel.

The express warranty above is the sole warranty obligation of Alcon, and the
remedy provided above is in lieu of any and all other remedies. There are no other
agreements, guarantees, or warranties – oral or written, expressed or implied –
including , without limitation, warranties of merchantability or tness for a particular
purpose. Alcon shall have no liability whatsoever for any incidental or consequential
damages arising out of any defect, improper use, or unauthorized service or repair.

WARNING!
The consumable products used in conjunction with Alcon instrument products
constitute a complete surgical system. Use of consumable products and
handpieces other than those manufactured by Alcon may affect system
performance and create potential hazards. If it is determined that consumable
products or handpieces not manufactured by Alcon have contributed to the
malfunction of the equipment during warranty period, service will be provided
at prevailing hourly rates.

8065751606 1.17
For Reference Only
 CONSOLE PERFORMANCE SPECIFICATIONS

DIMENSIONS Height: 160 cm (63 inches) PHACOEMULSIFICATION

Submodes: Continuous, Pulse, Burst
Width: 58.5 cm (23 inches)
Tip Stroke @ 100%: 88.9 ±27.0 um (.0035 ±.0005 in.)
Depth: 76 cm (30 inches) ResonantFrequency: 38.0 ±1.9 KHz
Pulse Rate Range: 0-100 pps
WEIGHT Unpacked: 107 kg (235 pounds) Burst Length: 5 to 500 mS
Packed: 150 kg (330 pounds)
OZil® TORSIONAL HANDPIECE
Longitudinal Frequency: 44.0 ±2.0 KHz
ENVIRONMENTAL Torsional
Frequency: 32.0 ±2.0 KHz
LIMITATIONS Operating Non-Operating Pulse Rate Range: 1-100 pps
Burst Length: 20 to 500 mS
Altitude: 2438 meters 12,191 meters
AquaLase® LIQUEFACTION DEVICE
(8,000 feet) (40,000 feet)
Pulse Rate Range: 10-75 pps
Burst Time On: 7-100 %
Temperature: 10° C to 35° C -40° C to 60° C
(50° F to 95° F) (-40° F to 140° F) ANTERIOR VITRECTOMY
Submodes: Cut I/A, I/A Cut
20 ga Infniti®Vit Probe: 10 to 800 cpm
Relative 10% to 95% 10% to 95%
23 ga Infniti® UltraVit® Probe: 10 to 2500 cpm
Humidity: without without
condensation condensation COAGULATION
10 Watts max., 75 ohm load
ELECTRICAL REQUIREMENTS 100 - 120 VAC, 50/60 Hz 76 Vpp @ 1.5 MHz ±5%, 75 ohm load
220 - 240 VAC, 50/60 Hz 117 Vpp @ 1.5 MHz ±5%, no load (100% setting)

COAGULATION ACCESSORIES
REMOTE CONTROL Method: Infrared Single Use Bipolar Cables: 846 Vpp
Channels: 4 Reusable Bipolar Cables: 1200 Vpp
Batteries: AAA (3) All Brushes: 1410 Vpp
All Forceps: 1110 Vpp
MAXIMUM INPUT CURRENT: 6A
VACUUM @ SEA LEVEL
PROTECTION AGAINST ELECTRIC SHOCK: Class I Phacoemulsication: 0 to 650 mmHg
CLASSIFICATION OF ALL APPLIED PARTS: Type BF Vitrectomy: 0 to 650 mmHg
DATA CARD: MMC (MultiMedia Card), or SD (Secure D igital) 32 Mb min. Irrigation/Aspiration: 0 to 650 mmHg

POWER IV POLE
Height Range: 13 to 110 cm
With Alcon IV Pole Extender 45 to 142 cm

Table 1-5 SPECIFICATIONS - This table is a quick reference point to identify basic system specications,
system requirements, and performance gures.

Abbreviation Description Abbreviation Description

A Amperes IPX8 International protection code - solid
AC Alternating Current objects X (not specied), water 8
AqL AquaLase® (continuous immersion)
Asp Aspiration IRR Irrigation
BF Body Floating IT Interchangeable Tip
C Centigrade IVO Infniti® VideOverlay
cc/min Cubic centimeters per minute MMC MultiMedia Card
Coag Coagulation mmHg Millimeters of Mercury
CPM Cuts Per Minute PEL Patient Eye Level
DFU Directions for Use PPS Pulses Per Second
ESD Electro Static Discharge RCAT Remote Control Aseptic Transfer
F Fahrenheit SP Single-Piece
FMS Fluidic Management System UL Underwriters Laboratories
FTSW Footswitch U/S Ultrasonic
HIS High Infusion Sleeve USB Universal Serial Bus
HP Handpiece V Volts
Hz Hertz Vac Vacuum
I/A Irrigation/Aspiration Vit Vitrectomy
IEC International Electrotechnical Commission

Table 1-6 ABBREVIATIONS USED WITH THE INFINITI® VISION SYSTEM

1.18 8065751606
For Reference Only
 Type BF equipment, providing both the REF Catalog Number
attributes of basic insulation and "floated"
isolation.
SN Serial Number

Date of Manufacture
Dangerous Voltage

Manufacturer

CAUTION: Consult accompanying documents

Eject FMS

U/S Handpiece
Equipotential ground connection Cable Connector

AC Voltage AquaLase® Handpiece

Cable Connector

Power stand-by state Vitrectomy Probe

for a part of equipment Tubing Connector

Bottle Receptacle for

ON (POWER) AquaLase®/BSS® Solution

Coagulation
OFF (POWER) Cable Connector

Footswitch USB Connector

Serial Connector
Fuse Size and Rating
T6.3A/250
Infiniti® Port

Use appropriate take-back system

(see Environmental Considerations in this manual) ESD Sensitive Connector
Pb notation, if present, indicates lead
content greater than 0.004%.
Pb NRTL TUV Mark - With respect to
electrical shock, fire and mechanical
hazards only in accordance with
UL 60601-1, CSA 22.2 601-1,
IEC 60601-1-2, and IEC 60601-2-2

Figure 1-2 ICONS USED WITH THEINFINITI® VISION SYSTEM -Icons identifying modes, functions, etc.,
that are used with the Infniti® Vision System are identied in this chart.

8065751606 1.19
For Reference Only
 DANGER: RISK OF EXPLOSION IF USED IN THE PRESENCE OF
FLAMMABLEANESTHETICS. 100-120V 50/60 Hz 6A
UL60601-1 CSA C22.2 NO. 601.1
RISQUE D'EXPLOSION. NE PAS EMPLOYER EN
DANGER: PRESENCE D'ANESTHESIQUES INFLAMMABLES.
220-240V 50/60 Hz 6A
CAUTION: GROUNDING REALIABILITY CAN ONLY BE ACHIEVED
WHEN EQUIPMENT IS CONNECTED TO AN EQUIVALENT
RECEPTACLE MARKED HOSPITAL GRADE.

CAUTION: RISK OF BURNS AND FIRE - DO NOT USE NEAR

CONDUCTIVE MATERIALS. RENEW ELECTRODE
CABLES UPON EVIDENCE OD DETERIORATION.

WARNING:THE PNEUMATIC SYSTEM CONTAINS A PRESSURE

VESSEL WITH THE FOLLOWING RATINGS:
PS = 4.1 BAR, Tmax= 10° C, V=0.3L.

ALCO N LA BORAT ORIE S, IN C.

6201 SOUTH FREEWAY
FORT WORTH, TX 76134-2099 USA
MADE IN USA

*Reg. U.S. Pat & TM. O ff.

© 2005, 2007,2009 Alcon Inc.

210-2137-003 REV B

WARNING: FOR CONTINUED

PROTECTION AGAINST RISK OF FIRE,
REPLACE ONLY WITH SAME TYPE
T6.3A/250 AND RATING OF FUSE.

Figure 1-3 LABELING ON INFINITI ® VISION SYSTEM - Labels used on the Infniti ® Vision System are
illustrated here. The labels on this page are intended for reference only.

1.20 8065751606
For Reference Only
 10

8 100% Set Power

75% Set Power
7 50% Set Power

) 25% Set Power

W 6
(
R
E 5
W
O 4
P

0
10 50 75 200 500 1000
LOAD (OHMS)
COAGULATION POWER GRAPH

10

)
6
(W
R
E
W
O 4
P

0
0 10 20 30 40 50 60 70 80 90 100
SETTING (%)
POWER ACROSS 75 OHM LOAD

40

) 35
(V
E
G 30
A
T
L 25
O
V
K 20
A
E
P 15

10

0
0 10 20 30 40 50 60 70 80 90 100
SETTING (%)
VOLTAGE (PEAK) ACROSS 75 OHM LOAD

Figure 1-4 COAGULATIO N POWER OUTPUTS - Set coagulation power at the intended output control
setting in the intended operating mode in reference to gures above.

8065751606 1.21
For Reference Only
 THIS PAGE INTENTIONALLY BLANK

1.22 LAST PAGE OF THIS SECTION 8065751606

For Reference Only
 SECTION TWO
DESCRIPTION

INTRODUCTION

Alcon’s Inniti® Vision System is a multi microprocessor-controlled ophthalmic

surgical instrument with associated memory and input/output (I/O) circuitry. The
system communicates to the user via its Front Panel display, with voice conrmations,
and with tones. An automatic self-test is initiated each time system power is turned
on.

This test performs a variety of functions including the following:

• Tests the Central Processing Unit (CPU)

• Tests the RAM and ROM memory, and the I/O circuits
• Initializes the system

When the system successfully completes the self-test, it automatically goes into the
Setup mode. If the system fails the self-test, an error message is displayed.

This section of the manual is broken into two major parts. The rst part describes the
console and its accessories. All the parts of the system will be described, including the
display panel, IV pole, connectors, uidic interface, footswitch, remote control, and
VideOverlay system. The second part of this section describes the operator interface.
This is where the display screens for system setup, surgery, programming, and dialogs
are shown.

8065751606 2.1
For Reference Only
 INFINITI® VISION SYSTEM CONSOLE AND ACCESSORIES

CONSOLE

Fluidics Module

The uidics module is located at the top of the front panel. The module allows fast
and easy insertion of the Fluidic Management System (FMS), and because the module
contains all the connections required, surgery can be started without delay.

IV Pole with Bottle Hanger

Front Display Panel and
Touch Screen

Front Connector Panel

Fluidic Management System (FMS)

inserted into Fluidic Module

Instrument Tray

Accessory Drawers

Footswitch Drawer

Caster Wheels (4)

Footswitch

Figure 2-1 The Console - The console contains all the controls, connectors, and
communication devices required by the surgeon to perform cataract lens extraction
surgery.

2.2 8065751606
For Reference Only
 Front Display Panel an d Touch Screen
The front display panel tilts and rotates, allowing easy maneuverability during setup
and surgery. For storage and transport the front panel folds down. The front display
is the user's main source of system control, allowing ngertip command of system
functions.

Front Connector Panel

The connector panel is located to the right of the uidics module. It provides two
self-locking U/S handpiece connectors, oneAquaLase® handpiece connector, two
connectors for bipolar coagulation handpieces, anAquaLase®/balanced salt solution
bottle receptacle, and two luer lock pneumatic connectors for an anterior vitrectomy

probe. Symbols near the connectors facilitate handpiece identication.

Coagulation Cable
Connectors (2)

AquaLase® Handpiece Connector

® ®
OZil Torsional, NeoSoniX ,
and U/S Handpiece Connectors (2) AquaLase®/BSS® Bottle Receptacle

Dual Vitrectomy
Handpiece Connectors

Figure 2-2 The Front Connector Panel - The front connector panel allow quick and
easy connection of handpieces and consumables.

8065751606 2.3
For Reference Only
 Footswitch Drawer
The footswitch drawer is at the bottom of the front panel. When not in use, this
drawer is used to store and protect the footswitch. The enhancedInniti® footswitch,
identied by its ribbed rubber footpedal surface and two small holes in its heel,
requires that a plastic insert be placed in the bottom of the drawer. This allows easy
insertion and removal of the enhanced footswitch. If theAccurus®/Legacy® footswitch
is used, remove plastic insert from bottom of drawer.

Two footswitch cable connectors are located behind this drawer. The left connector
is for the Inniti® and enhanced Inniti® footswitch; the right forAccurus®/Legacy®
footswitch. The footswitch cord is also stored in, and exits from, the drawer.

Instrument Tray
Provides a movable instrument tray within the sterile eld. There is a curved metal
rod on the tray arm that allows for creation of a sterile pouch when used with sterile
tray support cover. The tray is capable of accommodating a variety of positions in the
operating room environment: right, left, front and rear of the surgeon as well as the
front of the bed. The tray is height adjustable.

IV Pole with Bottle Hanger

A bottle of BSS® or BSS Plus® irrigating uid is hung from the hook on top of this
pole. The IV pole is used to raise and lower the bottle height, causing irrigation
pressure to increase or decrease.

Accessory Drawers
Two drawers allow storage of miscellaneous accessories.

Caster Wheels
Four large caster wheels support the Inniti® Vision System. The wheels rotate 360º
for ease of system mobility, and two wheels have a locking lever to secure the system
in place. The wheels should always be locked when the unit is in use, and unlocked
when being moved.

Handles
Handles are located on the sides and back of the instrument, and should always be
used to move the unit. For greater safety and control, the unit should be pulled, not
pushed.
CAUTION
The system must be moved carefully, otherwise the system could tip over and
become damaged. Do not push or pull the unit by the display, the tray, or the IV
pole. Handles located at the rear and sides of the unit are provided for moving the
instrument. The unit should be pulled and not pushed, especially over elevator and
door thresholds.

2.4 8065751606
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REAR PANEL

Power Module
The power module contains an AC power connector, AC power switch, and a fuse
drawer. The power module is located at the bottom of the rear panel. A standby power
switch is located at the top of the rear panel.
• AC Power Connector - Power cord from AC power outlet connects here. A
hospital grade power cord must be used.
• Main Power Switch - Connects AC power to power supply.
• Fuse Drawer - Holds fuse. Refer to label on back of system to identify size and type.

Equipotential Ground Connector

For Service personnel use.
Cord Wrap
Used to store the power supply cord. Located on the right side of the rear panel.

Connectors and CD/DVD Drive

This module, located in the middle of the rear panel, contains various connectors
and outlets used for electrical interconnections. A CD/DVD drive, located next to the
connectors, is used for software upgrades to the system.
• USB Connector - Not used.
• 10101Serial Connector - Used for VideOverlay.

• Inniti® Port - Not used.

CAUTION
The USBconnector ( ) and Infnti®port ( ) located on the rear panel are
for use by Alcon trained personnel only. Failure to comply will void warranty.

Connectors and CD/DVD Drive Cord Wrap

Equipotential Ground Connector

Fuse Drawer, Main Power Switch,

and AC Power Connector

Figure 2-3 The Rear Panel - The rear panel contains the power module, electrical con-
nectors, CD/DVD drive, cord wrap, and standby power switch (shown on next page).

8065751606 2.5
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 Data Card Slot
A data card (e.g., Multi Media Card (MMC)) can be inserted into this data card slot
when the user wants to back up or restore system settings. This is done by using the
Copy/Delete option from theCustom drop list. The Copy/Delete dialog allows the
user to copy data from theInniti® Vision System to a data card (backup), or copy
data from a data card to theInniti® Vision System (restore).

Standby Power Switch

This pushbutton switch is used to turn secondary power ON and OFF. If system
freezes and is unresponsive to operator commands, press Standby switch for ve
seconds to shut down system, then re-boot.

WARNING!
Inadvertent pressing of Standby switch when system is active will cause unit to shut down.

Audio Speaker (2)

Standby Power Switch

Multi Media Card in

Data Card Slot

Figure 2-4 The Right Side Panel - The right side panel contains the data card slot and
one-of-two audio speakers. The left side panel has the other speaker and two accessory
drawers.

Audio Speaker
The audio speakers are located on each side of the console. These speakers produce
voice conrmations, in conjunction with multiple tones, to allow the Inniti® Vision
System to communicate with the user. Audible tones are generated to indicate a
change in the operating mode and to alert the operator of certain conditions such as
an occluded line. Additionally, a varied pitch tone is generated to audibly indicate
vacuum levels; the pitch increases as the vacuum level increases. Speaker volumes
are adjustable via theCustom menus.

2.6 8065751606
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FOOTSWITCH

The Inniti® Vision System can utilize two different Alcon footswitches. TheInniti®
footswitch has a footpedal, on/off toe switches (horizontal and vertical), and on/off
footpedal swivel switches. TheAccurus®/Legacy® footswitch contains heel switches
rather than a swivel footpedal.

The footswitch icon button on the display screen is a graphical representation of the
footswitch connected. When connected, the icon's footpedal position (0, 1, 2, or 3)
is displayed in the center of the icon, and a triangular arrow appears next to the icon
each time a switch is activated. If a footswitch is not connected, no footpedal position

is displayed in the icon.

Several functions within the system's operating modes are controlled by the surgeon
using the footswitch. The footpedal enables the surgeon to control irrigation ow,
aspiration rate; OZil®, NeoSoniX®, or U/S system power;AquaLase® system energy,
vitrectomy cutting, and coagulation power. The switches are used to turn functions
on/off, to adjust function settings, and to progress through surgical steps.

The footswitch actions are shown in Figure 2-8. Footpedal positions are shown in
Figure 2-7, and footpedal positions/functions in each mode of operation are listed in
Table 2-1. To program the footswitch, see theCustom feature later on in this section
of the operator's manual.

CAUTION
Never pick up or move the footswitch by the cable. Dropping or kicking the footswitch
can cause irrepara ble damage.

® ® ®

Figure 2-5 The Accurus /Legacy and Infniti Footswitches

8065751606 2.7
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 Plugging in the Footswitch
The footswitch plugs into one-of-two connectors behind the footswitch drawer.
One connector is for theInniti® footswitch; the other is for theAccurus®/Legacy®
footswitch. To plug in the footswitch follow the directions below.

1. Open the footswitch drawer.

2. Simultaneously press a metal drawer extension latch on each of two hinges to
release the drawer and allow access to the footswitch cable connectors.
3. Grasping the footswitch cable connector, plug the cable into one of the two
connectors. The red dot on the cable connector must be in alignment with the red
dot on the console connector, and when the connector is in the correct position it

will slide in smoothly.

NOTE: Only one footswitch connector is intended to b e used at a time. If both
connectors are used at the same time, only the Infniti® footswitch connector is
functional.

4. A cable restraint is located on the back of the drawer. Loosen the two screws
securing the cable restraint and place the cable through its center. Replace the
cable restraint over the cable and secure it with the two screws. Ensure that a
slight amount of excess cable exists between the connector and the restraint.
5. Loop the cable through the slot in the back of the drawer, then route it through the
left or right slot of the cable management system in the front of the drawer. There
are high and low slots on each side of the drawer.
6. Shut the footswitch drawer.

footswitch cable connectors (2)

cable restraint

footswitch cable management system

footswitch drawer

drawer extension latch

Figure 2-6 Footswitch Cable Routing

2.8 8065751606
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 Footpedal Control
Depending on the surgery step, the user may have the option to select linear or
xed footpedal control of a surgical parameter (i.e., aspiration, vacuum, power,
coagulation). With linear footpedal control, the angle of depression within the pedal
range is directly proportional to the parameter output. The parameter output is 0
POSITION 0
resting position
POSITION 1
detent 1
DAL
TPE POSITION 2
FOO detent 2
POSITION 3
full footpedal depression

FOOTSWITCH ASSEMBLY

Figure 2-7 Diagram of Footpedal Positions

Footpedal Control of Surgical Functions

Position Position Position Position

Mode 0 1 2 3

Phaco Resting Irrigation Irrigation/Aspiration Irrigation/Aspiration

• Phaco Power
or • NeoSonix Amplitude
NeoSonix® • Torsional Amplitude
• AquaLase Magnitude
or
OZil® Continuous Irrigation Irrigation/Aspiration Irrigation/Aspiration
• Phaco Power
or • NeoSonix Amplitude
AquaLase® • Torsional Amplitude
• AquaLase Magnitude

I/AResting Irrigation Irrigation/Aspiration

Continuous Irrigation Irrigation/Aspiration

Resting Irrigation Irrigation/Aspiration Irrigation/Aspiration

Vit Cutting
I/A Cut
Continuous Irrigation Irrigation/Aspiration Irrigation/Aspiration
Cutting

Resting Irrigation Irrigation/Cutting Irrigation/Cutting

Vit Aspiration
Cut I/A
Continuous Irrigation Irrigation/Cutting Irrigation/Cutting
Aspiration

Coag Resting Coagulation Power

Table 2-1 Table of Footpedal Positions - The footpedal is used by the surgeon to control
several surgical functions. This table shows the functions controlled, dependent on mode
of operation and type of irrigation selected. As the footpedal is depressed it travels from
the resting position into its active positions.

8065751606 2.9
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 at the very start of the treadle range, and the parameter output is equal to the limit
value specied at the end of the treadle range. With xed footpedal control, the
parameter output is xed at its limit value throughout the treadle range. Footpedal
detents identify the transition from one footpedal position to another, and are felt by
the operator when slightly more pressure is required to press the footpedal from one
position into the next. Detents can also be accompanied by vibration if programmed
to do so.

The footswitch's Buttons and Treadle adjustments are programmable and are available
by pressing the Footswitch Button in the Main Window. The Footswitch Button is
described later in this section of the manual.

Switch Control
The footswitch has six switches that can be programmed to control various surgical
functions. The Inniti® footswitch has left and right toe switches that operate
horizontally and vertically, and footpedal switches that activate when the pedal is
shifted left or right. The Accurus® /Legacy® footswitch has left and right toe switches
that operate horizontally and vertically, and heel switches that activate when pressed
down.

Switch functions are programmable by pressing the footswitch icon and making
selections on the display. The left horizonal switch is the only switch with a factory
default action: Reux. The other ve switches are listed as None, their functions are
mutually exclusive, and must be programmed by the user. When a switch is given
a function already designated to another switch, the other switch is given a None
designation. Choices are Cont. Irr., Reux, Irr. Up, Irr. Down, Step+, Step-, Step+/-,
Grade+, Grade-, Grade+/-, Vit Cutter, Video Overlay, and None.

If the footpedal is not depressed, any switch may be engaged; however, the assigned
switches are mutually exclusive and cannot be engaged until all other assigned
switches are disengaged. If the footpedal is depressed, depending on the mode of
operation, certain switches may or may not be allowed to engage. Furthermore, even
if a switch is permitted to be engaged with the treadle depressed, some functions are
not available when the treadle is depressed, and the command will not be performed.

2.10 8065751606
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 Pressing this button allows the operator Footpedal swiveled left and right
to adjust the toe switch for a narrow (3), toggles switches. The Accurus®
medium (2), or wide (1) foot. footswitch utilizes heel switches
for the same functions.
The footswitch's removeable cable
plugs into this end. The footpedal
Left toe switch is pressed tension knob and carrying handle
left for one function, and are also on this end.
down for another.

Right toe switch is pressed right for

one function, and down for another.
12 3

32
1

Pressing this button allows the operator

to adjust the heel rest forward or backward
for a short (S), medium (M), or long (L) foot
size. It can also be adjusted to attain a
different balance and feel.

Tension Adjustment Knob

Footpedal

Left Horizontal/Vertical Switch Right Horizontal/Vertical Switch

Left Heel Switch Right Heel Switch

Figure 2-8 Footswitches Used with the Infniti® Vision System - Shown at the top is the
Infniti® footswitch with its switch actions identied. Shown below is the
Accurus®/Legacy® footswitch.

8065751606 2.11
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 The following sections indicate whether each switch function is permitted with the
treadle depressed. If it is permitted, and the user intends to control that function when
the treadle is depressed, the function must be assigned to a switch that is permitted to
be engaged with the treadle depressed.

• Continuous Irrigation On/Off

When a switch assigned to Continuous Irrigation On/Off is toggled, the continuous
irrigation status immediately activates/deactivates. Continuous irrigation toggling
is available when the footpedal is in any position, but is not available in a
Coagulation step.

• Reux
The default reux pressure is equal to the current bottle height pressure. The reux
pressure can be increased using the Reux Offset control in the Custom/Doctor menu.

In all cases, reux is not available when the footpedal is depressed, and is not
available in a Coagulation step.

• Irrigation Up, Irrigation Down

A switch may be assigned as irrigation up or irrigation down. When the switch is
pressed and immediately released, the IV pole position will increment up or down.
If the switch is pressed and held for more than 1/2 second, the IV pole will move
continuously up or down until the switch is released. Control of this irrigation
function is available in all steps but coagulation, and in all footpedal positions.

• Step Advance, Step Back, Step Advance/Back

A switch may be assigned as step advance (Step +), step back (Step -), or step
advance/back (Step +/-).The Setup, Coagulation, and Anterior Vitrectomy steps are
excluded from this stepping sequence.

If step advance or step back is assigned, when the switch is pressed, the next or
previous step to the current step is selected in the surgery menu. If step advance/back
is assigned to a switch, then step advance will be activated if the switch is pressed for
less than 1/2 second. If the switch is pressed for more than 1/2 second, then the step
back function will be activated.

2.12 8065751606
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 • Cataract Grade Increase, Decrease, Increase/Decrease
A switch may be assigned as cataract grade increase (Grade +), cataract grade
decrease (Grade -), or cataract grade increase/decrease (Grade +/-). Footswitch
control of the cataract grade is only available in phaco andAquaLase® steps, and is
available whether or not the footswitch treadle is depressed.

If cataract grade increase or cataract grade decrease is assigned, when the switch is
pressed, the next or previous cataract grade to the current cataract grade is selected. If
cataract grade increase/decrease is assigned to a switch, then cataract grade increase
will be activated if the switch is pressed for less than 200 milliseconds. If the switch
is pressed for more than 200 milliseconds, then the cataract grade decrease function

will be activated.
If the highest cataract grade is currently selected, and cataract grade increase is
selected, the lowest cataract grade will be selected. Similarly, if the lowest cataract
grade is currently selected and cataract grade decrease is selected, the highest cataract
grade will be selected.

When a new cataract grade is selected, surgical parameters will be updated with those
specied for the new cataract grade.

• Vit Cutter On/Off

A switch may be assigned to enable and disable the Vit Cutter (the left horizontal
switch is an exception). The Vit Cutter function is available only in the Vit step; at
all other times the designated button does nothing. The Vit Cutter is automatically
enabled when the Vit step is selected. When the Vit Cutter is disabled, the I/A
functionality in footpedal positions 2 and 3 is unchanged, but the Vit Cutter does not
cut. The Vit Cutter switch may be pressed in footpedal positions 1, 2, or 3, and the
function takes effect immediately. When the current step is Vit, and the Vit Cutter is
disabled, the message “Vit Cutter Disabled” is displayed in the Surgery Screen.

• VideOverlay On/Off
When a switch assigned to VideOverlay On/Off is toggled, the video overlay output
(including Alcon logo) is toggled on/off on the video display. Control of this function
is available in any footpedal position when it is assigned to a switch in which
activation is permitted with the pedal depressed.

8065751606 2.13
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REMOTE CONTROL

The remote control for the Inniti® system is wireless and can be used in one of two
ways. It can be laid in its tray assembly receptacle and operated under the sterile tray
support cover supplied in the disposable pak; this offers the Scrub Nurse or Sterile
Assistant access to the controls from the sterile eld. Alternatively, the Circulating
Nurse can operate the remote control in a non-sterile manner. Programmability and
custom user setup features are functions which are not accessible from the remote
control.

CAUTION
Do not sterilize the remote control as it will damage the unit.

Figure 2-9 The Remote Control - The remote control ts securely in its tray assembly
receptacle and allows rotation in any orientation. The sterile tray suppo rt
cover is then draped over the remote and tray.

2.14 8065751606
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 Remote Control Keys and Buttons
The following describes the remote control keys and buttons. The following
sections will describe the function of each, and indicate when they are valid. When
a remote control key or button is pressed, a valid or invalid key tone is generated as
appropriate.

The remote control is divided into three sections from top to bottom. Each section
of the remote approximately corresponds to its associated section of the Inniti®
Vision System display screen. The three sections of the display screen are 1) the setup
status/surgery control window, 2) the main window, and 3) the setup steps/surgery
menu. The Adjust button and items in the Adjust bar are not accessible with the

remote.
• Irrigation Control Up/Down Keys
The Irrigation Control up/down keys on the remote function as they do on the
touchscreen. Each individual press raises the IV pole 1 cmH2O up or down. To move
rapidly up or down, a key is pressed and held until the desired height is reached. The
irrigation control keys are only valid in the Setup and Surgery screens, and are not
valid when any dialog is displayed.

Irrigation Control
up / down keys

TOP

Parameter Selection button

Cataract Grade key

Parameter Value Adjustment

up / down keys

Backlight button (2)

Forward / Back
arrow keys

Enter key

BOTTOM

Figure 2-10 The Remote Control Keys

8065751606 2.15
For Reference Only
 • Cataract Grade Key
The Cataract Grade key is only valid in the setup screen and during lens removal
surgery steps, and is not valid when any dialog is displayed. Each time this key is
pressed it cycles the cataract grade upward until it reaches 4, and then begins again at
grade 1. The Default Grade can be programmed in the Custom/Doctor/General menu.

The rst press of the Cataract Grade key, or the rst press after ve seconds have
elapsed from the last press, simply invokes the voice conrmation of the currently
selected grade. Each subsequent press of the key within ve seconds selects the next
cataract grade, with voice conrmation of the grade.

• Parameter Selection
The Parameter Button
Selection button is used to select parameters for adjustment, and to
select Coag and Vit steps. The current selection is indicated with a yellow border.
With this button the user can navigate up, down, left, and right to select the desired
parameter. This button is valid when the footpedal and/or a footswitch button is up or
depressed, but is invalid when a dialog is displayed.

• Parameter Value Adjustment Up/Down Keys

The Parameter Value Adjustment up/down keys affect settings in the Surgery Control
Window that have adjustment arrows (i.e., power, vacuum, aspiration) and the
linear/xed toggle buttons. When a surgical parameter is selected via the Parameter
Selection button, a yellow border indicates that the item is selected; the Parameter
Value Adjustment up/down keys can then be used to adjust its value.

If a linear/xed toggle button is selected, either of the parameter value adjustment

up/down keys can be pressed to toggle the value between linear and xed.

• Forward/Back Arrow Keys

The Forward/Back Arrow keys are used to move left and right through the Setup Step
buttons and the Surgery Menu steps. In the Surgery screens, when a step is selected
using the Forward key or Back key on the remote, the step is immediately selected.
The Forward key and Back key do not wrap around.

If Coagulation or Anterior Vitrectomy is the current step, a Forward/Back key will

select the next or previous step relative to the last non-coagulation and non-anterior
vitrectomy step selected. Additionally, if the Back key scrolls all the way to the left,
the system will select the Setup button; the Enter key must be pressed to invoke the
Setup Screen.

In the Setup Screen, when a Forward/Back key is used to move to a Setup Step
button, the button will be highlighted, but the Enter key must be pressed to activate

2.16 8065751606
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 the button. If the Forward key is pressed during the draw uid portion of the priming
sequence, the system will skip to the vacuum check.

The Forward key and Back key can also be used in an information dialog to select a
button (e.g., OK, Cancel, Save, etc.).

• Enter Key
The Enter key is only valid to do the following: 1) select the Coag or Ant Vit step after
it has been selected with the Parameter Selection button, 2) go to the Setup Screen
when the Setup button has been selected with the Back key, 3) invoke a setup function
(e.g. prime FMS, ll, test handpiece.) when the function has been selected in the Setup

screen with the Forward/Back key, 4) invoke the highlighted button in dialogs, 5) toggle
between Irrigation/Continuous Irrigation when the Irrigation Controls window is
selected with the Parameter Selection button, and 6) select and Reset Metrics to zero
when the Metrics window is selected with the Parameter Selection button.

Remote Control Batteries

When batteries in the remote control are low, the status message “Remote Battery Low”
will appear below the irrigation controls each time a remote key is pressed. The message
will disappear after new batteries are installed and a remote control key is pressed. After
changing batteries, select remote control channel as instucted on next page.

A battery holder inside the remote holds three (3) AAA (LR3) batteries. To replace
batteries, loosen two captive screws on the rear cover with a standard slotted
screwdriver and remove cover. Replace old batteries and replace cover (correct
battery positions are identied inside each battery slot). When closing cover it is
important that rubber buttons slide into slots in other half of remote without binding
(see Figure 2-11).To check correct installation of batteries, press a Backlight button
on the side of the remote and verify that the remote control buttons illuminate, then
turn off after a few seconds. If illuminated buttons don't turn off, rubber buttons are
not properly inserted into slots, so you must repeat procedure. Dispose of batteries
following local governing ordinances and recycling plans.

Rubber Buttons(2)
must enter slots
without binding

Figure 2-11 Proper Orientation of Two Halves of Remote Control

8065751606 2.17
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 Select Remote Control Channel
The remote control can be congured to operate on one-of-four channels. This feature
allows four remote controls to independently control fourInniti® Vision Systems
operating in the same room or area. Remote controls are factory preset to channel
A. For proper remote operation, theInniti® Vision System must be set to the same
channel as the remote.

The Custom/System Settings window allows the selection of four remote receive codes:
A, B, C, & D. This selection must correspond to the channel selection on the remote
control. Set the remote channel as instructed below.

To select a remote channel on the Inniti® Vision System:

1. Press the Custom key to activate its drop-down menu.
2. Press the System key to bring up the System Settings window.
3. Press the Remote Channelbutton to bring up the Remote Control Settings
dialog (see Figure 2-12).
4. Hold the remote control in front of the Inniti® display screen and simultaneously
press its parameter value adjustment up/down keys (labeled 1 & 2 on the screen).
Simultaneously release the buttons.
5. Press the parameter selection button corresponding to the new channel (labeled A
at 9:00, B at 12:00, C at 3:00, and D at 6:00 on the screen).
6. Press the Enter button on the remote (see Figure 2-10), then press Save on the screen.

No additional steps are needed once the remote channel is set, and only one remote
channel is stored per unit.

NOTE: If necessary to distinguish between remote controls, identify the remote

controls and the units with unique labels.

CAUTION
Do not sterilize the remote control as it will damage the unit.

Figure 2-12 The Remote Control Settings Dialog

2.18 8065751606
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HANDPIECES, TIPS, AND INFUSION SLEEVES

Different handpieces, tips, and infusion sleeves are required for different procedural
steps and/or functions. A full selection of handpieces, along with tip styles and sizes
are available. Please contact your Alcon representative for information regarding the
appropriate handpieces, tips, and infusion sleeves for your specic technique and needs.

Following is a general description of the various handpieces, tips, and infusion

sleeves used to perform lens removal procedures.

Phaco Ultrasound Handpieces

Alcon's phaco
functions handpieces
of the integrate
lens extraction stepirrigation,
enable theaspiration
surgeon and emulsication. maintain
to simultaneously The threeor
inate the anterior chamber, emulsify the lens, and aspirate the lens material from the
eye.

a sonic
ltr
U sc
illation
O

und
aso
Ultr

Figure 2-13 OZil® Torsional Handpiece

sci
llatio
O
n

d
s oun
Ultra

Figure 2-14 Infniti® NeoSoniX® Handpiece

nd
ou
ras
Ult

Figure 2-15 Infniti® Ultrasonic (U/S) Handpiece

8065751606 2.19
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 These handpieces require no disassembly other than removal of the disposable tubing,
the ultrasonic tip, and the infusion sleeve with bubble suppression insert.

®
• OZil Torsional Handpiece - TheOZil® torsional handpiece integrates all
functions of the ultrasonic handpiece, and in addition provides ultrasonic
oscillations. This handpiece uses many of the same tips as the U/S handpiece; for
best performance of OZil® torsional handpiece, use tips recommended by your
Alcon representative.

• Inniti® Ultrasonic (U/S) Handpiece - This handpiece is used for ultrasonic

applications on the Inniti® Vision System with 1.1 mmTurboSonics® tips or 0.9
®
ABS®
mm TurboSonics tips, including ared and/or tips.
® ® ®
• Inniti NeoSoniX Handpiece - The NeoSoniX handpiece integrates all
functions of the ultrasonic handpiece, and in addition provides sonic oscillations.
This handpiece uses the same tips as the U/S handpiece.

CAUTIONS

Do not test or operate U/S, OZil® torsional, or NeoSoniX® handpieces unless the tip
is immersed in BSS® sterile irrigating solution or distilled water or is in surgical
use. Irreparable damage to the handpiece and tip can result if run dry.

Ensure that test chamber is lled with BSS® sterile irrigating solution before tuning
U/S, OZil® torsional, or NeoSoniX® handpieces. Tuning a handpiece dry may result
in premature tip failure and breakage.

WARNINGS!

Use of an ultrasonic handpiece other than the OZil ® torsional, NeoSoniX ®, or U/S,
or use of a handpiece repaired without Alcon authorization, is not permitted, and
may result in patient injury, including potential shock hazard to patient and/or
operator.

Use of the OZil ® torsional, NeoSoniX ®, U/S, or AquaLase ® handpiece in the absence
of irrigation ow and/or in the presence of reduced or lost aspiration ow can cause
excessive heating and potential thermal injury to adjacent eye tissues.

2.20 8065751606
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 TurboSonics® Family of Tips
U/S tips are made of medical grade titanium alloy, and are attached to an Ozil®
torsional, U/S, or NeoSoniX® handpiece to deliver mechanical energy to the lens,
assisting in its removal by aspiration. Depending on the needs and technique preferred
by the surgeon, various styles of tips and tip bevels are available (see Figure 2-16).
Various U/S tip styles are color coded.

Each doctor selects the Ozil®, U/S, and NeoSoniX® tips offered at the top of the
surgery screen for his selected handpiece. The tips offered for each doctor are enabled
or disabled from the Custom Copy/Delete feature.

• 1.1 mm U/S Tips - The standard ultrasonic tips are the srcinal 1.1 mm
TurboSonics® tips. They are designed for use only with 1.1 mm infusion sleeves.
• 0.9 mm U/S Tips - The 0.9 mm ultrasonic tips are designed to allow entry through
a smaller incision. They are designed for use only with 0.9 mm infusion sleeves.
• Mackool** U/S Tips - The Mackool** ultrasonic tips contain a polymer tubing
over the main part of the tip shaft. This necessary part of theMackool** tip
provides additional thermal and uidic advantages.
• Aspiration Bypass System - TheABS® tip contains a small hole in the distal
portion of the tip’s wall. This helps to maintain ow through the system even
during occlusion of the tip’s main port.

WARNINGS!
Use 0.9 mm tips with 0.9 mm infusion sleeves. Use 1.1 mm tips with 1.1 mm
infusion sleeves. Mismatch of consumable components and use of settings not
specially adjusted for a particular combination of consumable components may
create a patient hazard.

Read all package label material printed on the consumable paks prior to their use.

Standard U/S Tip- The 1.1 mm TurboSonics® tip Kelman® Tip - The Kelman® tip has a bent shaft
with the round shaft is the srcinal, classical U/S which generates transverse ultrasound motion, in addition
tip shape. The 0.9 mm has a smaller diameter shaft. to the conventional longitudinal motion, to enhance cutting
efficiency. In addition, the bend allows better visibility
during the surgical procedure.

small hole small hole

The Aspiration Bypass System - The ABS® tip contains Flared ABS® Tip - The flared tip has a larger proximal
a small hole in the distal portion of the tip's wall. port, providing increased holding force. They narrow in the
middle of the shaft, thus allowing smaller incisions and
improving occlusion breaks by reducing outflow from the
small hole anterior chamber, following occlusion breaks. Flared tips
also have the Aspiration Bypass System feature, to further
enhance performance.

Tapered Tip- The tapered ABS® tip is a combination polymer tubing

ABS®
of theand
inner 0.9 mm
outertipdiameters
and the flared
is equivalenttip.
to The shaft
straight tips,
while the distal end is comparable to flared tips. The
tapered ABS® tip has the improved holding force of a Mackool** Series U/S Tip- The Mackool**
flared tip, and the same aspiration flow characteristics ultrasonic tip contains a polymer tubing over the
as a straight tip. main part of the tip shaft.

Figure 2-16 TurboSonics® Tips - Shown here are samples of U/S tips used with the OZil® torsional,
U/S, and NeoSoniX® handpieces.

8065751606 2.21
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 AquaLase® Liquefaction Handpiece
The AquaLase® handpiece utilizes warmed high energy rapid pulses of uid to
perform liquefaction on the lens, while at the same time irrigating the anterior
chamber and aspirating the lens material from the eye.

Each doctor selects the AquaLase® tips offered at the top of the surgery screen for his
selected handpiece. The tips offered for each doctor are enabled or disabled from the
Custom Copy/Delete feature.

• 1.1 mm Liquefaction Tip - Standard tip used with 1.1 mm infusion sleeves.
• 1.1 MI Liquefaction Tip - Micro Incision tip used with 1.1 mm infusion sleeves
for small incision surgery.

Figure 2-17 AquaLase® Liquefaction Handpiece

MicroSmooth® Infusion Sleeves

Infusion sleeves cover the tip of the handpiece to provide irrigation to the anterior
chamber of the eye during surgery (see Figure 2-18). Infusion sleeves are used with
the Inniti® U/S, Ozil® torsional, NeoSoniX®, and AquaLase® handpieces, and with
some Ultraow™* I/A handpieces. Infusion sleeves used withInniti® U/S, Ozil®
torsional, and NeoSoniX® handpieces require a BSI (bubble suppression insert).
Infusion sleeves must be correctly matched to the specic tip type (see the following
descriptions). Inniti® paks contain only MicroSmooth® infusion sleeves.

INFUSION SLEEVE BUBBLE SUPPRESSION INSERT (BSI)

Figure 2-18 Infniti® U/S Handpiece shown with Infusion Sleeve and Bubble Suppression Insert

2.22 8065751606
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 Depending on the needs and technique preferred by the surgeon, various styles of
infusion sleeves are available.

• Standard MicroSmooth® Infusion Sleeves - These are the srcinal infusion sleeves.
Standard infusion sleeves are available in 1.1 mm (blue), to be used with 1.1 mm
tips; and 0.9 mm (purple), to be used with 0.9 mm tips.

• MicroSmooth® High Infusion Sleeves - High infusion sleeves (HIS) have a larger
shaft diameter than srcinal infusion sleeves. The larger shaft diameter of the
high infusion sleeves is compatible with a larger incision. Reduced resistance
to irrigation ow resulting from this larger shaft diameter creates a more stable
anterior chamber. High infusion sleeves are available in semi-transparent blue, to
be used with 1.1 mm tips; and semi-transparent purple, to be used with 0.9 mm
tips.

• MicroSmooth® Ultra Infusion Sleeves - Ultra infusion sleeves have a smaller shaft
diameter than srcinal infusion sleeves. The smaller shaft diameter of the Ultra
infusion sleeves is compatible with a smaller incision. Ultra infusion sleeves are
available in 1.1 mm (green), to be used with 1.1 mm tips; and 0.9 mm (rose), to be
used with 0.9 mm tips.

WARNINGS!

Use 0.9 mm U/S tips exclusiv ely with 0.9 mm infusion sleeves. U se 1.1 mm U/S a nd
1.1 mm liquefaction tips exclusively with 1.1 mm infusion sleeves. Mismatching U/S
tips and infusion sleeves may create potentially hazardous uidic imbalances.

Mismatch of consumable components and use of settings not specially adjusted for a
particular combination of consumable components may create a patient hazard.
Read all package labelling on the consumable paks prior to their use.

8065751606 2.23
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 Ultraow™* Handpieces and Tips
The Ultraow™* handpiece is used in I/A mode to maintain chamber pressure with
irrigation while removing cortical material via aspiration. (See Figure 2-20 and note
the band markings on the tips that identify size of tip aperture.) Some congurations
of the Ultraow™* IT and SP handpieces also use infusion sleeves. The following
Ultraow™* I/A handpieces and tips are available:

• Ultraow™* IT Handpiece and Interchangeable Tips - The Ultraow™* IT consists

of a handpiece body that accepts interchangeable tips. These tips do not require an
adapter or infusion sleeve as they contain a built-in metal infusion sleeve.

• Ultraow™*® I/A Handpiece and Threaded Tip Adapter - Reusable I/A tips with
TurboSonics silicone infusion sleeves can be used with theUltraow™* I/A
handpiece with threaded tip adapter.

• Ultraow™* SP I/A Handpiece (Single-Piece with xed tips) - The Ultraow™*

SP consists of a single-piece handpiece with aspiration tip and a built-in metal
infusion sleeve. Various tip congurations are available.

WARNINGS!

Use of non-Alcon surgical reusable or disposable I/A handpiece s that do not meet
Alcon surgical specications, or use of an Alcon handpiece not specied for use
with the Infniti ® Vision System, may result in a uidic imbalance. This, in turn,
may cause a shallowing or collapsing of the anterior chamber.

Exceeding the recommended level of 100 mmHg with a 0.5 mm or larger I/A tip
may cause anterior chamber shallowing and/or incarceration or tearing of the
posterior capsule.

I/A tips are not to be used with U/S, NeoSoniX ®, or OZil® torsional handpieces.

2.24 8065751606
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 Tip120° 90 Tip ° 45 Tip ° CurvedTip

O-Rings

Straight Tip

Figure 2-19 ULTRAFLOW ™* I/A

with the Ultraow ™*HANDPIECE AND TIPS - A wide variety of tips are available for use
I/A handpiece.

0.2 mm I/A Tip 0.5 mm I/ATip

O-Rings

0.3 mm I/ATip Threaded Tip Adapter

Figure 2-20 ULTRAFLOW™* I/A HANDPIECE AND ACCESSORIES - Shown here is the Ultraow™* I/A
handpiece with infusion sleeve, reusable I/A tip, and threaded tip adapter.

O-Ring Extractor

Large O-Rings

Small O-Rings

Figure 2-21 O-RING REPLACEMENT TOOL - This is the Ultraow™* O-ring replacement tool with
large and small O-rings.

Figure 2-22 ULTRAFLOW™* SP I/A HANDPIECE - Shown here is the Ultraow™* single piece I/A
handpiece with .3 mm 45° tip.

8065751606 2.25
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 Infniti® Vitrectomy Probes

The Inniti® system supports two different vitrectomy probes: the 20 gaugeInniti®
vitrectomy probe, and the 23 gaugeInniti® UltraVit® probe. Each probe is a sterile,
single-use, vitreous cutter which provides for aspiration and cutting. An irrigating
cannula is provided in each pak to allow for bimanual irrigation. The 20 gauge
Inniti® vitrectomy probe can be used with, as a separate accessory, an irrigation
sleeve to allow for simultaneous coaxial irrigation. This sleeve is not for use with the
23 gauge Inniti® UltraVit® probe.

The 23 gauge Inniti® UltraVit® probe supports higher cut rates by utilizing an

additional pneumatic actuation line.

Each probe is completely preassembled and requires no lubrication or cleaning prior
to surgery. These guillotine vitreous cutters are intended for single use only.

20 Gauge Infiniti® Vitrectomy Probe

Irrigating Cannula

Optional
Irrigation ®

Sleeve

23 Gauge Infiniti® UltraVit® Probe

Irrigating Cannula

Figure 2-23 VITRECTOMY PROBES - The 20 gauge Infniti® vitrectomy probe operates at up to 800 cpm
and can be used with an optional irrigation sleeve. The 23 gauge Infniti® UltraVit® probe operates at up to
2500 cpm and utilizes two pneumatic lines. Both handpieces are packaged with an irrigating cannula.

2.26 8065751606
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 WARNINGS!
Do not test or operate vitrectomy probes unless tip of probe is immersed in
BSS ® sterile irrigating solution or distilled water or is in surgical use. Irreparable
damage to the handpiece and tip can result if run dry.

After lling and testing, and before surgical use, verify that the probe i s prop -
erly actuating and aspirating. This may require lowering cut rate to achieve
good visualization. The port should always remain in open position in footpedal
position 1. If cutting port is partially closed while in position 1, replace the probe.
Prior to entry into the eye, and with tip of probe in sterile irrigating solution,
the surgeon should step on the footpedal for visual verication that the probe
is cutting; alternatively, press the Test button on the Vitrectomy Setup Screen: if
the cutter is observed to not fully close, or does not move when the probe is
actuated, replace the probe.
• If cutting port is parti ally closed while idle, replace the probe.
• If air bubbles are observed in the aspiration line or exiting the probe tip during
priming, replace the probe.
• If a reduction of cutting capability or vacuum is observed during the surgical
procedure, stop immediately and replace the probe.

8065751606 2.27
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 Bipolar Coagulation Handpieces
• Bipolar Coagulation Forceps are lightweight and ergonomically designed to
reduce hand fatigue as well as to provide precise control and safety. The forceps
are available with a wide variety of tip styles.

• Bipolar Coagulation Brushesare available in a wide variety of congurations:

straight, curved, tapered, and widestroke. All disposable bipolar accessories are
available both with and without cords.

Coagulation Cords are available in disposable and reusable congurations.

See your Alcon representative for a complete listing of products and accessories.

Figure 2-24 Single use bipolar brush

2.28 8065751606
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FLUIDIC MANAGEMENT SYSTEM

The Fluidic Management System (FMS) is an interface between the Inniti®

console and the surgical handpiece. It is used to regulateBSS® irrigating uid to
the handpiece, aspirate debris from the handpiece, monitor irrigation and aspiration
pressure, and deposit the debris in a sealed drainage bag for disposal. This single
assembly contains a rigid plastic uidic chamber, non-invasive pressure/vacuum
sensor, drain bag, irrigation (clear) and aspiration (blue stripe) tubing, and a clear
tubing with spike for connection to the bottle ofBSS® irrigating solution. The type
of FMS inserted is automatically identied by the system when it is inserted into
the uidics module. Inserting the FMS into the console uidics module establishes

uidics system connections, contributing to quick and easy surgical setup.

Inniti® FMS
This is the srcinal FMS. The aspiration line has a blue stripe.

Intrepid® FMS
The Intrepid® FMS is designed to enhance microcoaxial techniques. The aspiration
line is tinted blue.

AquaLase® FMS
The AquaLase® FMS offers an additional tubing (black stripe) for connection to
the bottle of AquaLase® Solution CE. The user can also utilize either theInniti® or
Intrepid® FMS used in conjunction with standaloneAquaLase® kits with Injection
Line.

Figure 2-25 The Infniti® Ultrasound Fluidic Management System (FMS)

8065751606 2.29
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INFINITI® AQUALASE® BALANCED SALT SOLUTION BOTTLE

When performing an AquaLase® liquefaction device procedure, theInniti® Vision

System must be equipped with anAquaLase® bottle containing BSS® sterile irrigating
solution. This solution is emitted in warm high energy pulses from the tip of the
handpiece.

During the setup procedure the bottle is inserted into its receptacle on the front of the
console, with its alignment arrow at the 12 o'clock position, and turned clockwise 1/4
turn to secure it in position

CAUTION
To avoid damaging the bottle, take care not to overtighten.

To remove the bottle, press it in and turn counterclockwise before pulling it out from
AquaLase®
its receptacle. The spike on the black-striped tubing is inserted into the
®
bottle and then connected to theAquaLase handpiece.

Figure 2-26 The AquaLase® Balanced Salt Solution Bottle

2.30 8065751606
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CONSUMABLE PAK CONFIGURATIONS

The family of Inniti® paks consist of various combinations of uidic management

systems (FMS), handpiece tips, infusion sleeves, and other components.AquaLase®
complete paks include a bottle ofAquaLase®/Balanced Salt Solution. Consumable
items used with the Inniti® Vision System during surgery are designed to be used
once and then discarded, unless labeled otherwise.

Please contact your Alcon Sales representative for complete up-to-date listings, and
Inniti® paks contain
for in-service information prior to initial use of Alcon paks. All
Directions for Use (DFU). It is important to read and understand the DFU's prior to

use.
NOTE: If an inconsistency exists between the instructions in the operator's
manual and the Directions For Use (DFU) supplied with a consumable pak o r
accessory, follow the DFU.

Custom Pak® Surgical Procedure Pack Congurations

To better serve our customers we offer the opportunity for surgeons to specify a
Custom Pak® surgical procedure pack for their own individual needs. Please contact your
Custom Pak®
Alcon Sales representative for more information on how to design your own
surgical procedure pack.

WARNINGS!

Mismatch of consumable components and use of settings not specially adjusted for a
particular combination of consumable components may create a patient hazard.
Do not use paks that have exceeded the expiration date.

Sterile disposable medical devices should not be reused! These components have
been designed for one time use only; do not reuse.

The equipment used in conjunction with the Alcon disposables constitutes a

complete surgical system. Use of disposables other than Alcon disposables may
affect system performance and create potential hazards, and if it is determined to
have contributed to the malfunction of the equipment under contract, could result
in the voidance of the contract and/or invoicing at prevailing hourly rates.

In all cases, the instrument setup instructions contained in the manual should be
thoroughly understood prior to using any of the pak congurations.

Read all package label material printed on the consumable paks prior to their
use.

8065751606 2.31
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 Infniti® U/S Fluidic Management System Paks
When performing a phacoemulsication procedure, one of the Inniti® U/S family of
paks with handpiece tip is used. The pak can contain all the items listed below:

• Fluidic Management System (FMS) - This single assembly consists of

irrigation (clear) and aspiration (striped) tubing, a plastic reservoir/pump
device, and a drainage bag (maximum capacity of 500 cc). Inserting the
FMS into its console receptacle establishes theInniti® uidic system,
allowing quick and easy surgical setup.

• U/S Tip with Tip Holder/Wrench - The tip attaches to the ultrasonic

handpiece. Securely
assembly, then removetighten the tipfrom
the wrench with the
thetall-in-one tip wrench/
ip. Several tip designs
are available.

• Infusion Sleeve with BSI - This single-piece silicone sleeve ts over
the handpiece tip to provide irrigation into the eye, protection to the
surrounding tissues, and uidic balance. One infusion sleeve contains a
bubble suppression insert (BSI); a second infusion sleeve is included to
be used with the I/A handpiece/tip.

• Test Chamber - The test chamber is a small elastomeric cap that ts over
the handpiece tip to facilitate a functional irrigation and aspiration check
of the handpiece and instrument prior to surgery.

• I/A Tip Wrench - A separate wrench is required to securely fasten the

I/A tip to its handpiece, and also to remove the tip when the surgery is
completed.

• Tray Support Cover - The tray support cover is a sterile plastic bag that is
placed around the instrument tray and support arm. The cover is used to
form a pouch in the tray to provide storage for the handpiece and tubing
during surgery.

• Directions for Use (DFU) - Instructions for setup and removal of pak
contents (not shown).

2.32 8065751606
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 Infniti® AquaLase® Fluidic Management System Paks
When performing a lens extraction procedure with the AquaLase® handpiece, a
single-use Inniti® AquaLase® pak is used. This pak can contain all the items listed
below:

• Fluidic Management System (FMS) - This single assembly consists of

irrigation (clear), aspiration (blue striped), andAquaLase® (black striped)
tubing; a plastic reservoir/pump device, and a drainage bag (maximum
capacity of 500 cc). Inserting the FMS into its console receptacle establishes
the Inniti® uidic system, allowing quick and easy surgical setup.

®
• AquaLase Liquefaction®Tip
attaches to the with integral Tip Holder/Wrench - The tip
AquaLase handpiece. Securely tighten the tip with the
all-in-one tip wrench/assembly, then remove the wrench from the tip.

• Infusion Sleeve - This single-piece silicone sleeve ts over the handpiece
tip to provide irrigation into the eye, and uidic balance. A second infusion
sleeve is included to be used with the I/A handpiece/tip.

• Test Chamber - The test chamber is a small elastomeric cap that ts over
the handpiece tip to facilitate a functional irrigation and aspiration check
of the handpiece and instrument prior to surgery.

• I/A Tip Wrench - A separate wrench is required to securely fasten the

I/A tip to its handpiece, and also to remove the tip when the surgery is
completed.

• Tray Support Cover - The tray support cover is a sterile plastic bag that is
placed around the instrument tray and support arm. The cover is used to
form a pouch in the tray to provide storage for the handpiece and tubing
during surgery.

!
• AquaLase® Balanced Salt Solution Bottle - Liquefaction solution.

• Directions for Use (DFU) - Instructions for setup and removal of pak
contents (not shown).

8065751606 2.33
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 ®
INFINITI VIDEOVERLAY SYSTEM (optional item)

Overview

The Inniti® VideOverlay (IVO) system accepts operating parameters from theInniti®
Vision System and overlays that information onto video accepted from the microscope
camera. The IVO system then outputs a video signal to a monitor and/or VCR for
retrospective viewing.

There are two models of IVO available: Standard and High Denition. The text below describes
the Standard IVO. For a complete description of the High Denition IVO, please refer to Figure

2-31 and the operator's manual addendum which accompanied the High Denition IVO.
The Standard IVO will accept either Composite or S-Video inputs in either NTSC or PAL
format (auto detecting). The IVO is powered by an external power supply. The external
power supply can operate from a 100 VAC to 240 VAC source, and provides an output of 12
VDC at 1.25 amps to power the IVO.

WARNINGS!
• Do not remove VideOverlay cover; there are no user-serviceable parts inside. Refer
servicing to qualied service personnel.
• Do not simultaneously touch the VideOver lay enclosure and the patient.

CAUTIONS
• Do not use multiple portable socket outlets with this system.
• Use only Alcon-supplied serial cable to connect Infniti® Vision System to IVO.

NOTES:
• This unit is not a medical device and should be located/stored with other video
equipment (i.e., VCR, monitor, etc.).
• When connected to the Infniti® Vision System, the IVO system does not increase the
leakage current of the Infniti® Vision System.
• The Infniti® VideOverlay system is for information purposes only, and is not intended to
substitute for the Infniti® Vision System display.

POWER MMC COMM PAL NTSC

MMC Sensor
On = MMC Card Detected NTSC Video Source
Off = MMC Card Not Detected

Send & Receive

PAL Video Source
On = Active

Figure 2-27 VideOverlay Front Panel

2.34 8065751606
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 COMPOSITE S-VIDEO
VIDEO
INFINITI™
POWER

ON
12VDC
IN OUT IN OUT 1.25A
OFF

Figure 2-28 VideOverlay Rear Panel

Setup For Standard IVO

(for HD IVO refer to Figure 2-31 and documentation that came with HD kit)
1. Ensure electric power to all systems is turned OFF. Attach the 12 V end of the external
power supply to the IVO system.

2. Attach the appropriate wall outlet adapter (USA, United Kingdom, Australia, or Europe)
to the AC end of the external power supply, and plug it into an appropriate wall outlet
(see Figure 2-29).

3. The IVO can operate using either Composite Video inputs/outputs or S-Video inputs/
outputs. Appropriate cables should be used to congure the IVO. Connect the microscope
camera output to the Composite or S-Video input of the IVO (see Figure 2-30).

NOTE: If the microscope camera output has an RCA or BNC connector, connect the
camera output to the VideOverlay Composite input. Do not use an adapter cable to
connect the camera output to the VideOverlay S-Video input or loss of color will occur.

4. Connect the Composite or S-Video output of the IVO to a monitor or a VCR. The
video output selected must be the same conguration as that used for the video input
(Composite or S-Video).

5. With the video output connected to a monitor, turn the monitor and microscope camera
power ON, and leave the IVO power OFF. If the video input and output cables are
connected properly, the microscope camera image will appear on the monitor.

6. Connect the serial cable between the IVO and Infniti® Vision System (see Figure 2-30).

7. Turn Inniti® Vision System power ON. Turn IVO power ON with its rear panel switch.
The MMC light and either the PAL or NTSC Video source light should be illuminated (if
not illuminated, check power supply connections).

®
8. With the Inniti system touchscreen interface running, make sure the Send & Receive
light blinks (if not blinking, check serial cable).

9. Observe the monitor video display. The Inniti® Vision System logo should appear (see
Figure 2-30) (if the Inniti® Vision System logo does not appear, check serial cable
connections). If the system does not operate correctly, contact an Alcon Technical Service
representative.
8065751606 2.35
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 USA, Japan, China United Kingdom Australia Europe

External Power Supply

Figure 2-29 Wall Outlet Adapters

Camera Infiniti® Vision System Rear Panel

Eye

Camera output to IVO input

(S-Video or Composite Video)

Serial cable from

NOTE: On the IVO you must use either Infiniti® Vision System
Composite in/out or S-Video in/out. to IVO
Do not use use C-in/S-out, or S-in/C-out.
To Wall Outlet
COMPOSITE S-VIDEO
VIDEO
INFINITI™
POWER

ON
12VDC
1.25A
IN OUT IN OUT OFF External
Power Supply
IVO Rear Panel

IVO output (Composite Video or S-Video)

to VCR or Monitor input

VCR output
VCR to Monitor input Infiniti® Logo

Monitor

Figure 2-30 Standard VideOverlay Connection Diagram

2.36 8065751606
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 HD Camera Infiniti® Vision System Rear Panel
with Component Video

Eye

Serial cable from

®
Infiniti Vision System
to HD VideOverlay To Wall Outlet

Monitor

External
Power Supply
Sony PDW-70MD

HD & SD COMPONENT S-VIDEO CVBS

ANTENNA
HD-SDI OUT
SD-SDI
6.0VDC
2.1A ON
IN

PWR OFF
Y Cb CR USB RS232 CONFIG
IN OUT

HD VideOverlay

Figure 2-31 High Denition VideOverlay Connection Diagram

8065751606 2.37
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 INFINITI® VISION SYSTEM OPERATOR INTERFACE

FRONT DISPLAY PANEL AND TOUCH SCREEN

The Inniti® Vision System front display panel andtouch screen has a at, non-glare
surface, and is mounted above the console. For ease of viewing the display panel
swivels and rotates, and it folds down into a protected position for storage.

Control buttons are located within the active touch

screen area. There are two basic types of pushbuttons
on the display screen: up/down arrow buttons and
momentary buttons. The user can press and hold the
up/down arrow buttons until the desired adjustment is
complete, and he can press the momentary buttons with
a single push-and-release to activate a function.

The Inniti® Vision System emits an audible tone

to indicate button activation. Activation of a valid
touchscreen button or remote control button results in
a valid key tone; an invalid button results in an invalid
Figure 2-32 TheInfniti ® Vision
key tone, and sometimes its icon symbol is ghosted to System Front Display Panel and
indicate an invalid function. Touch Screen

There are three types of display screens: the Setup screen, Surgery screens, and Dialogs.
• The Setup screen is used to prepare for surgery; i.e., priming the uidic
management system and testing the handpiece.
• Surgery screens contain special surgical settings for each of the current surgical
procedures. Pressing the touch screen buttons (or footswitch or remote control)
allows the user to adjust the settings for his current step.
• Dialogs are displayed as a result of selecting an option from the Custom drop list
(i.e., System, About, Doctor, etc.) or pressing the Metrics or Footswitch button.
Dialogs enable the user to view and modify system settings, doctor settings, and
some surgical settings. There is another class of dialogs that are displayed when
the user needs to be advised or warned of a situation, or to indicate progress on a
function in the Setup screen.

Initialization Screen

Setup Screen Custom

Surgery Screens

OZil® NeoSoniX® U/S AquaLase® Irrigation/Aspiration Capsule Wash** Coagulation Vitrectomy

• Continuous •Continuous • Continuous • I/ACut
• Pulse •Pulse • Pulse • Cut I/A
• Burst •Burst • Burst
• Custom Pulse* •Custom Pulse* • Custom Pulse*

* Custom Pulse is enabled/disabled through the Advanced tab in the Custom/Doctor dialog.
** Capsule Wash is enabled/disabled through the Steps tab in the Custom/Doctor dialog.

Figure 2-33 Navigating the Infniti® Vision System User Screens

2.38 8065751606
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SETUP SCREEN AND ITS FUNCTIONS

The Setup screen is displayed when one of the following occurs:

• The system is powered up and initialization is successful.
• The screen is explicitly invoked by pressing the Setup button from a Surgery screen.
• The FMS is removed while in a surgery screen other than Coagulation.
• The handpiece tip is changed in a surgery screen and the user indicates on the
resulting popup message that he selects the Setup screen.
• A handpiece is selected in a surgery screen and the handpiece is not tuned.
• A valid FMS is inserted while the user is in a surgery screen.

The Setup screen is divided into three sections. At the top is the Main Window, below
that is the Setup Status Window, and below that are the Setup Steps.
1. Main Window
The Main Window consists of buttons and readouts that are used to set up the system
and then perform surgery (see Figure 2-34). The Setup Main Window is the same in
most areas as the Surgery Main Window discussed later.

1.1 Doctor Name 1.4 Procedure Type

1.2 Handpiece Type 1.5 Cataract Grade
1.3 Tip Type

1. Main Window

1.9 Custom Button

1.8 Footswitch Button

1.7 Metrics Display

or I/A Tip Type

2. Setup Status Window 1.6 Irrigation Controls

3. Setup Steps

Figure 2-34 Functional Areas of the Setup Screen

8065751606 2.39
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1.1 Doctor Name
The Doctor Name button displays the currently-selected doctor. When pressed, and
also when system is rst turned on, this button displays a drop list of all the doctors
entered in the system. The rst doctor at the top of the list is the Alcon Settings
doctor, which contains all the Alcon defaults. Listed in the second position from
the top is the Add Doctor selection which allows the user to add a new doctor to the
list. The remaining doctors will be listed with the most-recently-selected doctor in
the third position from the top, or if enabled in theCustom/System drop list menu,
alphabetically.

When a doctor is selected (other than Add Doctor), the following occurs:
• The drop list collapses and the selected doctor name is displayed.
• The surgical handpiece, phaco tip, procedure, and I/A tip are selected in
accordance with the following:
- The I/A tip is changed to that last used by the doctor.
- If no handpiece is connected, the surgical handpiece, tip, and procedure are
changed to those last used by the doctor, or the defaults selected in Doctor
Settings.
- If the currently-selected handpiece is connected but not tuned, the selected
handpiece does not change. The tip and procedure change to those last used by
the doctor for the selected handpiece. If the tip or procedure do change, a dialog
is displayed notifying the doctor that the tip and/or procedure have changed.
- If the currently-selected handpiece is tuned, the selected handpiece and tip
do not change. The procedure changes to that last used by the doctor for the
selected surgical handpiece and tip.
• The Cataract Grade is set to the doctor’s default.

Add Doctor

When Add appears.

keyboard Doctor isThe
selected fromenter
user can the doctor dropname
a doctor’s list, aindialog window with
the designated box using the
alphanumeric keypad. When a doctor’s name is typed and the OK button is pressed,
the dialog window disappears and the doctor name is saved with Alcon’s default
parameters (names are not case-sensitive). When a new doctor is successfully saved,
he becomes the current doctor and is entered in the third position from the top, or if
enabled in the Custom/System drop list menu, alphabetically.

1.2 Handpiece Type

The Handpiece Type button displays the currently-selected surgical handpiece: Ozil®
torsional (OZil), NeoSoniX® (Neo), Ultrasound (U/S), orAquaLase® (AqL). Pressing
this button displays a drop list of available surgical handpieces. When a handpiece is
selected, the following occurs:
• The drop list collapses and the selected handpiece is displayed.
• The surgical tip and procedure are changed to those last used by the doctor for the
selected handpiece. The current surgical steps in the Surgery Menu are replaced
with the steps associated with the newly selected procedure, and the rst step is
entered.

During setup, the handpiece selection will automatically correspond to the installed
handpiece. Automatic selection of the handpiece is disabled when the case is started.

2.40 8065751606
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 The system has two surgical connectors for Ozil® torsional, NeoSoniX®, and U/S
handpieces; however, only one connector can be used at one time. There is a third
connector for an AquaLase® handpiece, and it can be connected at the same time as an
Ozil® torsional, NeoSoniX®, or U/S handpiece.

If handpieces are plugged into both of the Ozil® / NeoSoniX® / U/S connectors, the
message “Two handpieces detected. Remove a handpiece.” will appear. The message
can be dismissed by pressing the OK button; however, U/S power will not be available
until one of the handpieces is removed.

1.3 Tip Type

The Tip Type button displays the currently-selected surgical tip. When pressed,
this button displays a drop list of available tips for the selected handpiece. The tips
displayed in the drop-down menu have been color-coded to assist in differentiating
between 0.9 mm and 1.1 mm tips. The 0.9 mm tips are listed in purple, and the 1.1
mm tips are listed blue. When a tip is selected, the following occurs:
• The drop list collapses and the selected tip is displayed.
• The Procedure Type is changed to that last used by the doctor for the selected
handpiece and tip.
• If there are unsaved changes to surgical parameters, a dialog will be displayed
giving the user the option either to save or discard the changes, or just cancel the
dialog. If the dialog is canceled, the surgical tip is not changed.

Each doctor selects the available tips offered at the top of the surgery screen for the
selected handpiece. The tips offered for each doctor are enabled or disabled from the
Custom Copy/Delete feature.

1.4 Procedure Type

The Procedure
When pressed,Type
thisbutton
buttondisplays
displaysthe currently-selected
a drop surgical
list of the available procedurefor
procedures name.
the
selected handpiece tip. When a procedure is selected, the following happens:
• The drop list collapses and the procedure is selected.
• If there are unsaved changes to surgical parameters, a dialog will be displayed
giving the user the option to save or discard these changes, or just cancel the
dialog. If the dialog is canceled, the procedure is not changed.

Procedures can be customized by using the Custom Copy/Delete feature.

1.5 Cataract Grade

The Cataract Grade button displays the currently selected cataract grade: 1, 2, 3, or
4. When selected, this button displays a drop list of the four cataract grades. When a
new cataract grade is selected, the following occurs:
• The drop list collapses and the selected cataract grade is displayed.
• The cataract grade is enunciated.
• Surgical step parameters that are dependent upon the cataract grade are updated
with the parameter values specied for the new cataract grade.

8065751606 2.41
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1.6 Irrigation Controls
• Irrigation/Continuous Irrigation and PEL Indicators - Pressing the bottle height
readout will toggle the readout from "Irrigation" to "Continuous Irrigation" and
back to "Irrigation" again. Continuous irrigation can also be activated several
other ways as described on the next page.

The Patient Eye Level (PEL) readout indicates the number of centimeters
below the FMS that the patient’s eye is located. The PEL is programmed in the
Custom/Doctor menu. When the PEL is set to a value other than 0, “PEL= xx” is
displayed in the lower-right corner of the box.

WARNING!
Avoid setting the patient above the FMS. Operating with the patient above the
FMS will result in a lower irrigation pressure than indicated on the display, and
possible underventing.

• Irrigation Pressure Bar Display - This bar display is a visual indication of the
irrigation pressure as measured by the uidics mechanism, irrespective of the IV
pole position.

• Bottle Height and Adjustment Arrows- The bottle height readout is representative of
the actual bottle height, respective to the PEL. The adjustment arrows are pressed to
adjust the IV pole height, and thus change the irrigation pressure value and readout.

t
H eigh
Bottle

L)
(PE
evel
ye L
nt E
Patie

Figur e 2- 35 BOTTLE HEIGHT MEASUREMENT - Bottle height for gravity-fed irrigation is

measured from the center of the drip chamber to the patient's eye. Default
bottle height is 95 cm above the center of the round aspiration pressure
sensor in the FMS. PEL is measured from the aspiration pressure sensor
to the patient's eye.

2.42 8065751606
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 Irrigation Control
Irrigation operates on a gravity-feed principle from the IV bottle to the FMS to the
handpiece. The console's irrigation valve is normally closed when the uidic interface
device is inserted. In most modes of operation irrigation begins owing when the
footpedal transitions from position 0 to position 1.

Irrigation pressure is increased or decreased by raising or lowering the IV pole that

holds the irrigation bottle. Default height for Ultrasound is 95 cm , and for I/A modes
is 78 cm, measured from the center of the drip chamber to the center of the FMS
aspiration pressure sensor; for Anterior Vitrectomy mode it is 55 cm. Patient Eye
Level (PEL) is measured from the FMS aspiration pressure sensor to the patient’s
eye. Maximum bottle height of 110 cm results in maximum irrigation pressure. In the
event of power loss, bottle position is maintained; however, if the unit is turned off
using the Standby switch, the IV pole automatically retracts to its storage position.

Continuous Irrigation
Continuous irrigation is available in all applicable surgical steps and allows for
continuous irrigation of the eye during surgery by opening the irrigation valve.
Changing a doctor or handpiece shuts off continuous irrigation, allowing exchange
of irrigation and aspiration tubing between handpieces without loss of irrigation
solution. Continuous irrigation is not available in Setup or Coagulation modes.

The continuous irrigation feature is normally turned off. Continuous irrigation can be
toggled from "Irrigation" to "Continuous Irrigation" and back to "Irrigation" again by
using the four methods described below:
- Press the bottle height readout on the display.
- Use the remote control's Parameter Selection button to select the Irrigation

- windowaon
Program the display,
footswitch thenfor
button press the Enter key
the Continuous on the remote
Irrigation control.
function, then press
down on the designated footswitch button.
- Custom/Doctor/General tab/Continuous Irrigation can be turned On to activate
continuous irrigation when the footpedal is depressed. It can be turned off using
one of the other three methods.

When continuous irrigation is on, footswitch treadle range 1 is eliminated, and ranges
2 & 3 are expanded.

NOTE: Before switching handpieces it is advised to turn continuous irrigation

off, after exiting the eye, to close the irrigation valve and prevent excess BSS®
sterile irrigating solution from owing out of the han dpiece.

1.7 Metrics Display

The Metrics display is available in the surgery screen during lens removal steps.
®
During surgical
gures shown in procedures utilizing
this box display U/S Ultrasound andNeoSonix
Time and Average Power. modes
Duringthe
an metrics
AquaLase® procedure the metrics gures shown are AquaLase® Time, Pulses, and
Average Magnitude. For theOzil® mode it shows Cumulative Dissipated Energy.
When the Metrics box is pressed, the Metrics dialog is displayed, and the metrics
readouts can be reset to 0. The display will close when Reset is pressed.

8065751606 2.43
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Fi gu re 2-36 METRICS DIALOG SCREEN - Metric denitions are listed below.
U/S
U/S Total Time: Sum of Phaco Time and Torsional Time.
U/S Total Equivalent Power in Position 3:
CDE
U/S Total Time
Total U/S energy in footpedal position 3 (both phaco and torsional) calculated as:
Cumulative Dissipated Energy:
(Phaco Time x Average Phaco Power) + (Torsional Time x 0.4 x Average Torsional Amplitude)
The factor 0.4 represents approximate reduction of heat dissipated at the incision as compared to conventional phaco.
Phaco
Phaco Time: Total time phaco power was active. This records the phaco On-time, displayed in minutes and seconds.
Average Phaco Power: Average phaco power over the time when phaco power was applied. For example, if Ultrasound
Burst mode was selected and 100 mS burst pulses at 70% stroke were generated once a second, the Average Power
would record 70%.
Average Phaco Power in Position 3: Average phaco power over the time when phaco power was applied in footpedal
position 3. This takes into account the U/S modulation aspects, resulting in a signicantly lower reading than Average
phaco Power. For example, if Ultrasound Burst mode was selected and 100 mS burst pulses at 70% stroke were
generated once a second, the Average Power in Position 3 would record 7%.
Torsional
Torsional Time: Total time torsional power was active. This records the torsional On-time in minutes and seconds.
Average Torsional Amplitude:Average torsional amplitude over the time when torsional power was applied. For
example, if OZil Burst mode was selected and 100 mS burst pulses at 70% amplitude were generated once a second,
®

the Average torsional amplitude would record 70%.

Average Torsional Amplitude in Position 3: Average torsional amplitude over the time when torsional power was
applied in footpedal position 3. This takes into account the U/S modulation aspects, resulting in a signicantly lower
reading than Average Torsional Amplitude. For example, if Ultrasound Burst mode was selected and 100 mS burst pulses
at 70% amplitude were generated once a second, the Average Torsional Amplitude in Position 3 would record 7%.
Eqv. Avg. Torsional Amplitude in Position 3: Average U/S energy in footpedal position 3 calculated as:
0.4 x Average Torsional Amplitude in Position 3.
NeoSoniX
NeoSoniX Time: Total time NeoSoniX® mode was active, On-time recording in minutes and seconds.
Average NeoSoniX Power: Average amplitude only when NeoSoniX mode was active.
®

Fluidics
Aspiration Time: Total time the system was aspirating.
Estimated Fluid Used:An estimation of the volume of uid aspirated based on system settings and time.
AquaLase
AquaLase Time: Total time when AquaLase® mode was active, displayed in minutes and seconds. This is a s ummation
of all pulse On-times while in AquaLase® mode.
AquaLase Number of Pulses: Total number of AquaLase® mode pulses used in the case.
Avg. AquaLase Magnitude: Average magnitude only when AquaLase® mode was active.
Avg. AquaLase Magnitude in Position 3: Average magnitude over the time in footpedal position 3 when AquaLase ®

mode was active. This takes into account the burst control which sets the duty cycle. For example, if an 80% amplitude
was used and a 60% burst (duty cycle) was set, Average Magnitude in Position 3 would record 48%.
Case Time:The timer starts (Case Begin) when rst step is chosen and footpedal is depressed. The timer stops (Case
Ended) when the FMS and all active handpieces are removed (U/S,NeoSoniX®, AquaLase®, and OZil® handpieces).
The timer pauses when system is placed in Set-up mode (Case is Inactive).

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1.8 Footswitch Button
The Footswitch button is a graphical representation of the currently-installed
footswitch (either Inniti® or Accurus®/Legacy® footswitch). The current footpedal
position (0, 1, 2, or 3) is displayed in the center of the footswitch. Right/left and up/
down arrows appear in the box whenever a momentary switch is activated.

When the Footswitch Button is pressed, the Footswitch Buttons dialog (see Figure
2-37) or Footswitch Treadle dialog (see Figure 2-38) appear. These dialogs allow the
user to view and modify the current settings of the footswitch. Switching between the
Buttons and Treadle dialogs is performed by pressing the corresponding tab on the
viewing screen.

Figure 2-37 FOOTSWITCH BUTTONS DIALOGS - Pressing the Footswitch Button pulls up a dialog
that corresponds to the footswitch connected to the Infniti® Vision System. Pressing the
Buttons tab activates one of these dialogs; on the left is the Infniti® footswitch, and on
the right is the Accurus®/Legacy® footswitch. Pressing a button next to a switch activates
a drop-down list, as shown in these images, with functions that can be selected for that
footswitch button.

Figu re 2-38 FOOTSWITCH TREADLE DIALOGS - Pressing the Footswitch Button pulls up a dialog
that corresponds to the footswitch connected to the Infniti® Vision System. Pressing the
Treadle tab activates one of these dialogs; on the left is the Infniti® footswitch, and on the
right is the Accurus®/Legacy® footswitch. The buttons on the screen allow you to adjust
the treadle settings to your own personal preferences.

8065751606 2.45
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 Treadle
Function Adjustment Method Type of Adjustment Description of Function

Vibration Horizontal Bar with Minimum to Maximum Treadle vibration level applied at
Up/Down Arrow Keys Vibration both upward and downward treadle
movement.

Button Selection On Vibration active during upward and

downward treadle movement.
Vibration not active during upward
Off and downward treadle movement.
Detent Firmness Horizontal Bar with Minimum to Maximum Firmness (0 Detent rmness for all detents of the
Up/Down Arrow Keys to 100% of maximum rmness) footswitch.
Span 1 Value Adjust with Percentage value (0 to 26) such The span of footpedal position 1.
Up/Down Arrow Keys that the total of Span 1, Span 2, When the rst set of arrow keys
and Span 3 equal 95% (the rst is used to increase or decrease
5% is always reserved for the 0
position) the span 2or
increased start position,by
decreased span
the 1same
is
amount.
Span 2 Value Adjust with Percentage value (19 to 95), such The span of footpedal position 2.
Up/Down Arrow Keys that the total of Span 1, Span 2, When the rst set of arrow keys
and Span 3 equal 95% is used to increase or decrease
the span 2 start position, span 2 is
decreased or increased by the same
amount. When the second set of
arrow keys is used to increase or
decrease the span 3 start position,
span 2 is increased or decreased by
the same amount.
The span of footpedal position 3.
Percentage value (0 to 50), such When the second set of arrow keys
Span 3 Value Adjust with that the total of Span 1, Span 2, is used to increase or decrease
Up/Down Arrow Keys and Span 3 equal 95% the span 3 start position, span 3 is
decreased or increased by the same
amount.

Table 2-2 PROGRAMMING THE FOOTSWITCH TREADLE - This table describes all the objects in
the Footswitch Treadle tab, accessed by pressing the Footswitch Button in the display
screen’s Main Window.

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1.9 Custom Button
The Custom button enables the user to view and modify system settings, doctor
settings, and some surgical settings. When theCustom button is pressed, a drop list
menu appears with the following options (see Figure 2-39). When one of the options
is selected from the menu, the respective dialog for that option is displayed and the
drop list menu disappears. If no selection is made, the drop list menu disappears after
about ve seconds.

The following describes the purpose of each drop list menu item, the function of
the controls in its dialog, and how the selections are invoked. The selections may be
invoked whether the footswitch treadle and/or a footswitch button is depressed or not

depressed, and the

list menu items footswitch
provide is functional
the user when
with options the dialog
relating is displayed.
to viewing, The
copying, drop
deleting,
modifying, backing up, and restoring doctor/system settings.

• Doctor
• Save
• Copy/Delete
• System
• Sound
• AqL Occlusion
• About
• Shutdown

1.9 Custom Button

1.9.1 through 1.9.8

Custom Drop List Menu

Figure 2-39 Setup Screen with Custom Drop List Menu

8065751606 2.47
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1.9.1 Doctor
The Doctor Settings dialog is invoked when the user presses Doctor on the Custom
drop list menu (see Figure 2-40). The Doctor Settings dialog enables the user to view
and modify surgeon preferences for the currently-selected doctor.

The dialog has Save and Cancel buttons. When Save is selected, all settings changed
since the dialog was invoked are saved to persistent storage, the doctor dialog closes,
and the settings take immediate effect. If the current doctor is the Alcon Settings
default, the changes take immediate effect, but they are not saved to persistent
storage; the changes are temporary. If Cancel is selected, the whole doctor dialog
closes and the system returns to its prior settings.

Figure 2-40 Doctor Settings Dialog Screen - General Tab

General Tab

• Continuous Irrigation
Continuous irrigation is applicable for lens removal, I/A, and vitrectomy
surgical steps. When Continuous Irrigation is set to On (enabled), continuous
irrigation will be active following the rst footpedal depression. When activated
“Continuous Irrigation” is displayed in the irrigation section of the Main Window,
and the continuous irrigation On tone is generated. When transitioning to another
step of the same surgical type, continuous irrigation remains activated. When
transitioning to a step that is a different surgical type, continuous irrigation is
inactivated but then re-activated when the footpedal is depressed (except for
Coagulation).

• Footswitch Position One Tone

When enabled, irrigation On tone will sound when transitioning from footpedal
position 0 to 1 in any phaco, I/A, or vitrectomy step. Irrigation Off tone will
sound when transitioning from footpedal position 1 to 0. This feature is mutually
exclusive with Continuous Irrigation, as both cannot be enabled at the same time.

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 • Vitrectomy Bottle Height Maintenance
If the Vitrectomy Bottle Height Maintenance feature is enabled, and during
vitrectomy surgery the footpedal is depressed, upon a transition to a non-
vitrectomy step a conrmation dialog will appear. If the user conrms the
desire to begin irrigation pressure maintenance, the irrigation pressure level
used in the vitrectomy step will be maintained, and the following rules will be
in effect until 1) a Vitrectomy step is reentered and then the desire to continue
irrigation pressure maintenance is denied, or until 2) the Vitrectomy Bottle
Height Maintenance feature is disabled in the Doctor Settings Dialog, or until 3)
a new doctor is selected with the Vitrectomy Bottle Height Maintenance feature
disabled, or until 4) the surgery ends:

- Iftothe PEL is changed,

maintain the IV
the irrigation pole height will be adjusted up/down as needed
pressure.
- The user can manually change the irrigation pressure using the remote,
footswitch buttons, or touchscreen buttons. If the user manually changes the
irrigation pressure while in the Surgery mode, the new irrigation pressure
value will be maintained until the surgery ends.
- Manual changes to irrigation pressure will not be saved to the doctor database.
- The IV pole height will be automatically moved when the Setup mode is
entered, and to accommodate prime/tune/test while in Setup mode. When
Surgery mode is re-entered, the irrigation pressure will revert back to the
value being maintained for Vitrectomy Irrigation Pressure Maintenance.
- The IV pole height will be automatically moved when a Fill step is activated.

• Vitrectomy Setup
When the Anterior Vitrectomy step is entered, an automated Vitrectomy Setup
screen appears. This automated screen assists the user through the proper set up
and test of the selected vitrectomy probe. If the doctor does not want the screen to
guide him through the vitrectomy handpiece setup procedure when the Anterior
Vitrectomy step is entered, press the Off button.

• Ozil® Torsional Before Phaco

The Inniti® system has an ON/OFF setting called “OZil Torsional Before Phaco”
in the General tab of the Doctor Settings dialog that affectsOzil® Pulse and

Torsional Phaco Pause Torsional Phaco

Time
Repeat
Torsional Before Phaco Turned ON

Phaco Torsional Pause Phaco Torsional

Time
Repeat
Torsional Before Phaco Turned OFF

Figure 2-41 OZil® Torsional Function Before Phaco

8065751606 2.49
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 Burst modes. When the “OZil Torsional Before Phaco” feature is turned ON, the
torsional pulse of U/S energy leads the phaco (longitudinal) pulse, then there is
a pause before repeating. When turned OFF, the progression is phaco/torsional/
pause/repeat (as in prior software releases).

This feature is illustrated in the Figure 2-41. The top portion depicts the pulse
sequence in which torsional comes before phaco; the bottom portion depicts the
sequence in which phaco comes before torsional.

• PEL
The Patient Eye Level (PEL) indicates the number of centimeters below the FMS

that the patient’s

compensate eyePEL.
for the is located. The IV pole height is automatically adjusted to

• Default Grade
Indicates the initial cataract grade that will be selected when a doctor is selected.

• Infusion Pressure Drop

When the acquired value of the irrigation pressure sensor is below the value
specied for the Infusion Pressure Drop, the system will display an advisory
dialog. When this setting is 100%, this feature is disabled.

• Reux Offset
The software limits reux pressure to a level equal to the current infusion pressure
plus the value specied for the Reux Offset, or the maximum infusion pressure
the system is capable of, whichever is less.

• Vent Time Adjustment

A vent time adjustment feature is used to tailor the degree of venting pressure at
the tip that is adjusted in response to a vent (transition from footswitch position
2 to position 1). There are three settings: 0, 1, and 2. Zero is the default which
provides unmodied venting performance. Settings 1 and 2 increase the net
pressure experienced at the handpiece tip after a vent.

2.50 8065751606
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 Steps Tab

According to doctor's preferences the Irrigation Footswitch, Coag, Vit, and Fill steps
can be placed at different locations in the surgery step sequence by enabling these
buttons.

• Irrigation Footswitch Before Phaco Steps

The Irrigation Footswitch step can be placed before phaco steps in the surgery
step sequence by pressing the Enable button.

• Capsule Wash
®
TheWhen
Capsule Wash the
enabled, stepCap
usesWash
the step
AquaLase mode to clean the posterior capsule.
is placed before the last I/A step for all
®
procedures. The AquaLase handpiece must be primed and tuned prior to use.
Unlike the regular AquaLase® step, there is no burst control, and PPS maximum
and Magnitude Limit are different.

• Coag Before Phaco Steps - Coag After I/A Steps

The Coag step can be placed before the phaco steps and/or after the I/A steps in
the surgery step sequence by enabling these buttons. The Power and Fixed/Linear
settings in the Coag Before Phaco Steps are unique, and are not shared with other
coagulation steps.

• Vit Before I/A Steps - Vit After I/A Steps

The Vit step can be placed before and/or after the I/A steps in the surgery step
sequence by enabling these buttons.

• Fill Before I/A Steps - Fill After I/A Steps

The Fill step can be placed before and/or after the I/A steps in the surgery step
sequence by enabling these buttons. If Irrigation Fill is enabled in System
Settings, this step will be Irrigation Fill.

Figure 2-42 Doctor Settings Dialog Screen - Steps Tab

8065751606 2.51
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 Defaults Tab

Selecting this tab allows the user to select default settings for the active surgeon,
shown in the upper right corner of the screen (in this case the active surgeon is Alcon
Settings). Enabling the options in this screen will activate the selected Handpiece,
Tip, and Procedure each time the associated doctor name is activated. If Defaults are
not enabled, the doctor's settings will return to those "last used."

Figure 2-43 Doctor Settings Dialog Screen - Defaults Tab

Advanced Tab

Selecting this tab from within the Doctor Settings screen allows the user to enable or
disable the Custom Pulse feature, and to change the settings for theOZil® IP feature.

• Custom Pulse
Use this button to enable or disable the Custom Pulse feature in phaco steps.
(Refer to the Ultrasound (U/S) mode of operation section of this manual for
details on the Custom Pulse feature.)

Figure 2-44 Doctor Settings Dialog Screen - Advanced Tab

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 OZil® IP
Use these controls to adjust settings for the OZil® IP (Intelligent Phaco) feature (see
Figure 2-44). The settings allow the user to specify theOZil® IP control parameters
used in the enabled steps.

This OZil® IP feature can be enabled or disabled for individual phaco steps. In
addition, the OZil® IP settings can be tailored for each cataract grade. (Refer to the
OZil® Mode of Operation in this manual for instructions on enabling and disabling
this feature.) The settings specied in this screen are applied to the phaco steps for
which the OZil® IP feature is enabled.

Cataract
• of
Each the Grade ® IP settings can be established as a function of cataract grade.
OZil

• Vacuum Threshold (% of Vacuum Limit)

The Vacuum Threshold setting determines the percentage of the vacuum limit
set value at which the OZil® IP feature is activated and its specied phaco power
is applied. When vacuum reaches and/or exceeds the vacuum threshold, then
the OZil® IP feature, if enabled, is activated. When the vacuum drops below the
vacuum threshold value, then theOZil® IP feature is deactivated.

• Phaco Pulse On Time

The Phaco Pulse On Time species the on-time of an applied phaco pulse during
activation. These phaco pulses are applied at 10 pulses per second until either
the vacuum level falls below the threshold or the total accumulated pulse time
exceeds 200 mS. OZil® IP functionality can be turned off for a particular cataract
grade if the Phaco Pulse On Time is set to Off.

• Longitudinal / Torsional Ratio

The Longitudinal / Torsional Ratio establishes the applied phaco power level
relative to the applied torsional amplitude. This ratio is expressed as a decimal
fraction and ranges from 0.7 to 1.0.

8065751606 2.53
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1.9.2 Save
The Save dialog can be invoked when a change has been made to the current surgical
parameters and the user selects the Save option from theCustom drop list menu. If
there are no unsaved changes, the Save button is disabled.

The Save dialog provides the user with three buttons: Save, Discard Changes, and
Cancel. If the Save button is pressed, the changes are saved to the current doctor. If
Discard Changes is selected, the unsaved changes to the surgical parameters for the
current doctor will be discarded and the dialog will be closed. If Cancel is selected,
surgical parameters will not be saved to the current doctor and the dialog will close.

The
When Alcon
AlconSettings doctor
Settings is theiscurrent
the factory default
doctor, and cannot
the Save be permanently
dialog provides the userchanged.
with three
buttons: Save As, Discard Changes, and Cancel. If the Save As button is pressed, a
keyboard appears allowing the user to add a new doctor. Once the new doctor is added,
the changes are saved to the new doctor. Settings can be saved for up to 100 doctors. If
Discard Changes is selected, the unsaved changes will be discarded and the dialog will
be closed. If Cancel is selected, changes will not be saved and the dialog will close.

1.9.3 Copy/Delete
The Copy/Delete dialog is opened when the user selects Copy/Delete from the
Custom drop list menu (see Figure 2-45). The Copy/Delete dialog allows the users to
perform these actions:
• Copy data from the Inniti® Vision System to a data card (backup).
• Copy data from a data card to the Inniti® Vision System (restore).
• Save changes previously made to surgical parameters.
• Copy, delete, and rename groups of doctor settings on the Inniti® Vision System.
These settings include 1) surgical parameters for handpieces, tips, procedures, and
steps; and 2) doctor preferences.
• Add, Remove, Rename, and change the order of steps.
• Select available tips to be offered at top of surgery screen for current doctor/handpiece.

Source Pane Destination Pane

Hierarchy Levels

Info Window (2)

Source Level Buttons

Figure 2-45 Copy/Delete Dialog

2.54 8065751606
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 In the Copy/Delete dialog two hierarchies are shown: the left hierarchy is the source
pane invoked with the Copy button, and the right hierarchy is thedestination pane.
The source pane can be manipulated using the source level buttons below it (Save,
Save As, Edit, Reset, Delete, Rename). The destination pane cannot be similarly
manipulated. The Info Window, immediately below each hierarchy, provides
additional information about the selected hierarchy level.

Upon entry to the Copy/Delete dialog, the hierarchy of the source pane (on the left
side) reects the current surgical procedure. The destination hierarchy (on the right
side) is not expanded and the destination pane is INFINITI.

Data Hierarchy
The rst level of the hierarchy is either INFINITI or DATA CARD.

The second level under DATA CARD is either Full Backup or Doctors. The level
under Full Backup is the doctor backup name, and all doctors included in that full

BACKUP / DELETE / RESTORE EXERCISE

3.
Data card must be blank before beginning this procedure. Restore TEST DOC data from data card to Infniti ®
console.
1. Backup data from Infniti ® console to data card. 3.1 Press the Custombutton, then Copy/Delete.
1.1 Press Doctor Name (Alcon Settings ) button in upper- 3.2 Press top-left source pane button to select DATA CARD .
left corner of screen. 3.3 Press Doctorsand select TEST DOC.
1.2 Select Add Doctorfrom drop down list, type TEST DOC 3.4 Press top-right destination pane button to select INFINITI.
on keyboard, then press OK. 3.5 Press the Restorearrow button in the top-center of the
1.3 Select U/S handpiece, Cataract Grade 1, and press screen. The system restores the TEST DOC data from
Surgery button to enter surgery screen. Select the data card to the Infniti® console.
Ultrasound Continuous , and set Power Limit to 50. 3.6 Press Exit to leave Copy/Delete screen and return to
1.4 Press the Custombutton, then Save. The dialog "Save surgery screen.
changes to the surgical step parameters of the current 3.7 To verify transfer of TEST DOC cataract grade 1 settings
doctor?" appears. Press the Save button to save new to Infniti® console, press Alcon Settings , select TEST
doctor settings. DOC, select U/S handpiece, press Cataract Grade 1
1.5 Insert data card into its slot on the right side of the button, Ultrasound Continuous , and verify Power Limit
Infniti® console below the speaker. is 50.
1.6 Press the Custombutton, then Copy/Delete.
1.7 Press the top-left source pane button to select INFINITI. 4. Delete TEST DOC data from data card and Infniti ®
Select TEST DOC. console.
1.8 Press the top-right destination pane button to select 4.1 Press the Custombutton, then Copy/Delete.
DATA CARD . 4.2 Press top-left source pane button to select DATA CARD .
1.9 Press the Backup arrow button in the top-center of the 4.3 Press Doctorsand select TEST DOC.
screen. The system archives the TEST DOC data from 4.4 Press Deletein the lower-left corner of the screen. The
the Infniti® console to the data card. dialog "Delete doctor backup on Data Card" appears.
Press the OK button.
2. Delete TEST DOC data from Infniti ® console. 4.5 Press the top-left source pane button to select INFINITI.
2.1 Press Deletein the lower-left corner of the screen. The Select TEST DOC.
dialog "Delete selected doctor setting? It is currently in 4.6 Press Deletein the lower-left corner of the screen. The
use" appears. Press the OK button. dialog "Delete selected doctor setting? It is currently in
2.2 Press Exit to leave Copy/Delete screen and return to use" appears. Press the OK button.
surgery screen. 4.7 Press top-left source pane button to select INFINITI.
2.3 Press Alcon Settingsand verify TEST DOC has been Press its "+" button to ensure TEST DOC is no longer
deleted from Infniti® console drop down list. on Infniti® console.
4.8 Remove data card from its slot.

8065751606 2.55
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 backup are displayed. The level under Doctors is the doctor backup name, and all
doctors that have been individually backed up are displayed.

The second level under INFINITI is the doctor name. When the doctor name is
selected, there is a third level which may be a handpiece, step, or preference. When a
handpiece is selected, the fourth level is either an I/A tip or a phaco tip. When an I/A
tip is selected, the fth level is an I/A step. When phaco tip is selected, the fth level
is a phaco procedure, and the sixth level is a phaco step.

Collapse/Expand Buttons
The Collapse button (–) is displayed to the left of each non-selected level in the

hierarchy.
the selectedTouching this
label. The buttonbutton
Expand hides all lower
( ) is
+
levels,tomaking
displayed the leftthe
of label at thatfor
each level level
which a lower level exists. Touching this button opens the node selection drop-down
menu for the next lower level.

Label Selection Button

Each hierarchy level is a button which displays a drop-down menu of possible labels
for that level when touched. Selecting an item from this list collapses all lower levels,
changes to the selected label, and opens the drop-down menu for the next lower level.
The system provides a visual indication in all levels to indicate there are unsaved
parameters.

Copy/Delete - Handpiece Tip Selections

To ease setup, the system supports the ability to show only doctor-selected tips in the
Tip Selection Dropdown display, at the top of the surgery screen, for the selected doctor
and handpiece. Enabling /disabling occurs within this copy/delete screen where an
enabled tip is highlighted while a disabled tip is grayed out. Disabled tips do not appear
in the Tip Selection Dropdown display, nor do they appear in the Tip Selection Menu in
the Defaults tab of the Doctor Settings Dialog.

Figure 2-46 Copy/Delete Dialog with Enabled and Disabled Tips - For the selected
doctor and handpiece, tips colored white are enabled and will be shown in surgery
screen's Tip Selection Dropdown list, while grayed out tips w ill not be shown.

2.56 8065751606
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 Copy Button
The Copy button, located above and between the left and right hierarchies, is used to
copy data from the source (left) node to the destination (right) node. When the Copy
button is touched the action taken is determined by the source and destination.

The button is labeled Copy when the source node is a surgeon, and the destination
node is a surgeon. The button is labeled Back Up when the source node is INFINITI,
and the destination node is DATA CARD. The button is labeled Restore when the
source node is the DATA CARD, and the destination node is INFINITI.

Info Window
The Info Window, immediately below each hierarchy, provides additional informa-
tion about the selected node. If a Backup doctor node or doctor node is selected, the
Info Pane displays the date and time at which the parameters were archived and the
software release. If the selected node has lower level nodes, the Info Pane provides a
preview of the lower level nodes.

Source Node Manipulation Buttons

The Save, Save As, Edit, Reset, Delete, and Rename buttons are used to manipulate
the source node. The destination node cannot be similarly manipulated.

• Save - When parameters have been changed during surgery, this button can be
pressed to update the procedure type with the new settings.
• Save As - This button is pressed to save current settings under a new procedure
type name using the on-screen keyboard.
• Edit - To edit the steps of a procedure type, press this button to open an editing
dialog. The sequence, names, icons, and number of steps can be manipulated in

• this dialog
Reset using
- Reset dataitstoDelete,
systemRename, Add As, and Edit buttons.
default settings.
• Delete - When enabled this button can be pressed to delete the highlighted label.
• Rename - When this button is enabled it can be pressed to activate an on-screen
keyboard. Typing in a new name will replace the old name.

8065751606 2.57
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1.9.4 System
The System Settings dialog is invoked when the user selects System from the Custom
drop list menu. This dialog enables the user to view and modify the current system
settings such as Language, Remote Channel, IV Pole Extender, Alphabetize Doctor
Menu, Irrigation Fill, Date, and Time. System settings apply to all doctors, and
remain in effect until modied; the settings are not lost when the system is powered
down. The System Settings dialog has a Save button and a Cancel button. If Save is
selected, the current settings are saved to persistent storage, the dialog closes, and
the settings take immediate effect. If Cancel is selected, the dialog closes and any
changes made to the system settings are neglected.

Setting Remote Channel

The remote channel displayed in the System Settings dialog is for display only. To
change the remote channel, press the Remote Channel button to bring up the remote
control graphic with instructions to change the remote channel; this screen must be
displayed while changing the remote channel. The newly-selected remote channel
takes effect immediately. Pressing Cancel on the System Settings dialog returns the
system to its previously-saved remote channel.

Figure 2-47 System Settings Dialog

IV Pole Extender
The Inniti® system supports the use of theAlcon® IV pole extender. This extender
has two hooks. Use of the upper hook extends the upper and lower limits of the
IV pole by 32 cm (increased from 110 cm to 142 cm, and 13 cm to 45 cm). The
maximum PEL is -39 cm.

Use of the IV pole extender applies to all users. Once the extender is physically
attached to the system it must be enabled through the System Settings dialog, and the
upper hook must be used by all users.

Enabling the use of the extender is done by depressing the IV Pole Extender button in
the System Settings dialog. This brings up the IV Pole Extender Settings dialog where
the extender can be “Installed” or “Not Installed.” When Installed is selected, the

2.58 8065751606
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 Figure 2-48 IV Pole Extender Settings

system automatically compensates for the additional height and the upper hook must
be used. There is no need to adjust the PEL setting to account for the extender. When
Installed is selected, the Maximum Pole Height setting feature is enabled, allowing
the user to adjust the IV pole maximum height. This feature is used to protect against
inadvertent damage to overhead structures. When the "Move IV Pole when adjusting
height" is set to “Move,” then the IV pole tracks to the maximum pole height setting
while the adjustment is made.

WARNINGS!
Once the IV pole extender is installed, the upper hook is to be used. Do not change

bottle
IV height
bottle to thebylower
manually
hook hanging the bottle
will introduce on the
an error lower
in the hook. Manually
displayed loweringand
height indication the
negatively impact the performance of the Infusion Pressure Drop detection feature,
causing false indications at low bottle levels.

Empirical numbers for bottle heights are not a replacement for competent surgical
technique. The surgeon should visually and physically monitor intraocular pressure.

Alphabetize Doctor Menu

When enabled, the doctor names presented in a drop list at the top of the Setup and
Surgery screens are alphabetized, starting after Alcon Settings and Add Doctor. If not
enabled, the doctor last-used is presented after Alcon Settings and Add Doctor.

Irrigation Fill
When enabled, irrigation is activated without reux to ll handpiece. The result is that
the Irrigation Fill step replaces the Fill step, in all instances, for all users of the console.

8065751606 2.59
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1.9.5 Sound
The Sound dialog is invoked when the user selects Sound from the Custom drop list
menu. The Sound dialog enables the surgeon to set a volume level for all tones and
voice conrmations.

The volume levels are set individually. When an individual button is selected, the
volume level adjustment will pertain only to the selected tone. Each selection; except
for Vacuum Level, Phaco Occlusion, and Coagulation Power; may be turned Off
so that no tone will be heard. Pressing the Play Sound button emits a sample of the
volume level selected.

Figure 2-49 Sound Settings Dialog

1.9.6 AqL Occlusion

The AquaLase ®
Occlusion feature is invoked when the user selectsAql Occlusion
from the Custom drop list menu. The AquaLase® Occlusion feature enables the
surgeon to specify parameters (Magnitude and Burst) for reduction ofAquaLase®
power at the onset and full occlusion duringAquaLase® surgery steps. The Total
Power Reduction readout is the product of the Magnitude and Burst settings.

Figure 2-50 AquaLase® Occlusion Settings Dialog

2.60 8065751606
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 The AquaLase® Occlusion feature can be enabled and disabled by pressing the
appropriate button in this menu. When enabled, a button in the surgery screen's
horizontal Adjust bar indicates whether occlusion watch is off or on, and user is able
to press this button to turn it on or off.

1.9.7 About
The About dialog is invoked when the user selects About from the Custom drop list
menu. The About dialog displays the software and hardware revisions for system
mechanisms, is for display only, and may not be modied by the user. Pressing OK
closes the About dialog and returns the system to its prior state.

Figure 2-51 About Dialog

1.9.8 Shutdown
Pressing the Shutdown button invokes a message asking if the user wants to
Shutdown system? Pressing the Cancel button in the dialog returns the system to its
prior state; pressing OK turns standby power off. To turn system power off the user
must then press the power switch at the bottom of theInniti® Vision System rear
panel.

8065751606 2.61
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2. Setup Status Window
This area of the Setup Screen is used to display current system status during the
setup phase of operation, and is for display only (see Figure 2-52). The user is alerted
to situations like handpiece status (“Tuned,” “Not Tuned,” etc.), prime status, and
type of FMS. The user can also be alerted when a remote control battery is low,
or the AquaLase®/Balanced Salt Solution bottle is inserted. This area is also used
for pictures to help the user perform a procedure (i.e., luers being connected to a
handpiece).

If a valid FMS is not inserted, “No FMS” is displayed in the Setup Status area,
and the Prime FMS, Fill, and Test Handpiece Setup Steps are unavailable. Text is

displayed in the Setup Status area indicating “Insert FMS. . .”

When a valid FMS is inserted, “Calibrating FMS” is displayed while the uidics
mechanism performs a test of the aspiration pressure sensor. If the test fails, a dialog
is displayed and the FMS is rejected. If the test succeeds, the FMS type and “Not
Primed” is displayed, and the Prime FMS and Fill Setup Steps are available. The Test
Handpiece button is not available until the system is primed and a valid handpiece is
connected to the system.

2. Setup Status Window

Figure 2-52 Functional Area of the Setup Status Window

2.62 8065751606
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3. Setup Steps
This area of the Setup Window is used for initiating setup functions as well as
activating the surgery screen (see Figure 2-53). At power-up the system enters the
grayed-out Setup Screen with the Doctor Name dropdown list displayed. One of the
doctor names must be selected to continue with the system setup. After a doctor is
selected the complete Setup Screen appears, and the Prime FMS button is highlighted.
NOTE: It is important to follow the setup sequence as indicated on the Infniti®
Vision System display screen and/or as written in section three of this operator's
manual. Not following the directions could lead to priming failures.

3.1 Prime FMS Button

The Prime FMS button may be selected as long as a valid FMS is installed,
regardless of current prime and tune status. With the irrigation and aspiration
luer ttings connected together, the priming sequence is 1) raise the IV pole, 2)
draw uid, and 3) vacuum/vent check. When selected, the Prime FMS button is
highlighted, metrics are reset to 0, and a priming dialog box is invoked which
contains the following:
• Progress bar to show the progress of the draw uid priming sequence.
• Vacuum bar as well as the actual vacuum value to show the vacuum check
progress and actual vacuum value.
• Text message indicating “Drawing Fluid…”, “Checking Vacuum…”
• Two buttons; one for Advance to Vacuum Check, and another for Cancel.

Once the prime sequence is initiated and the system is raising the IV pole or drawing
uid, then pressing Advance to Vacuum Check on the dialog will immediately skip
to the vacuum/vent check. Once the prime sequence is initiated it can be aborted by
pressing Cancel or by removing the FMS.

When the priming and vacuum checks are completed successfully, the prime status
becomes “Primed” and the Fill Button is highlighted.

3. Setup Steps

3.3 Test Handpiece Button

3.2 Fill Button
3.1 Prime FMS Button 3.4 Surgery Button

Figure 2-53 Functional Areas of the Setup Steps Window

8065751606 2.63
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3.2 Fill or Irrigation Fill Button
The Fill button is automatically highlighted when the priming sequence has
completed successfully (if Irrigation Fill is enabled in System Settings, this button
will be Irrigation Fill). Pressing the Fill Button activates the uidics system
to ll the handpiece. During the ll process a text message indicating “Filling
Handpiece….” appears on the screen. Also displayed is a dialog with a Cancel
button and an Advance To Test button. (Note that the Advance to Test button is
ghosted if the conditions for testing are not met.)

Once the ll sequence is initiated it can be aborted by pressing Cancel or by removing
the FMS, whereby the Fill dialog closes and the Fill Button remains highlighted. If

Advance To Test
dialog closes and is
thepressed, or if the system
Test Handpiece is is
function left to proceed to completion, the Fill
selected.

The Fill step activates both irrigation and reux to clear air bubbles from the uidics
system. If Irrigation Fill is enabled, irrigation is activated without reux.

3.3 Test Handpiece Button

The Test Handpiece button may be selected only when the FMS is primed and the
selected handpiece is inserted. In addition, if anAquaLase® handpiece is selected,
the AquaLase® bottle must be inserted.

The Inniti® Vision System allows anAquaLase® and a U/S, NeoSoniX®, or Ozil®
torsional handpiece to be connected at the same time, but the user must perform
the Test Handpiece sequence for each handpiece; once when the U/S orNeoSoniX®
handpiece is selected, and once when theAquaLase® handpiece is selected.

When the Test Handpiece button is selected the test handpiece dialog will display
progress of the ow check with a vacuum bar as well as the actual vacuum value.
A Cancel button also appears. Once the test sequence is initiated, it can be aborted
by the user by pressing Cancel or removing the FMS, or it can be left to proceed to
completion. For the AquaLase® handpiece only, a momentary collapse of the test
chamber is normal.

Upon successful completion of the handpiece test sequence, the system exits the
Setup Screen and enters the appropriate Surgery Screen.

3.4 Surgery Button

If the Surgery button is pressed the system goes to the appropriate Surgery Screen as
determined by the procedure selected. The rst surgery step for the doctor’s procedure
is entered.

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SURGERY SCREEN AND ITS FUNCTIONS

The Surgery Screens contain the buttons, readouts, and controls that allow the user to
perform surgical functions. This screen is displayed when one of the following occurs:
• The Surgery button is pressed from the Setup Screen.
• The Test Handpiece function is completed in the Setup Screen and no other
connected handpieces are “Not Tuned.”

The Surgery Screen is divided into three sections (see Figure 2-54). At the top is
the Main Window, below that is the Surgery Control Window, and below that is
the Surgery Menu. Depending on the handpiece, procedure type, and surgery step

selected, the Surgery

corresponding Screen is updated
to the selections. with
Although the buttons
several and surgical
representative parameters
surgery screens are
shown in this section of the manual, screens showing all handpiece/procedure/steps
are not shown.

1. Main Window
The buttons in the Surgery Main Window for U/S are nearly the same as the buttons
in the Setup Main Window (see Setup Screen earlier in this section of the manual for
descriptions). The Main Window for I/A, Coagulation, and Vitrectomy are discussed
later in this section.

Depending on the active surgery step, the buttons available in the Main Window vary;
however, the behavior of a button is consistent, regardless of the surgery step from
which it is pressed. All buttons are available regardless of whether the footpedal and/or

Doctor Name Procedure Type

Handpiece Type Cataract Grade
Tip Type

1. Main Window

Custom Button

Footswitch Button

Metrics Display

2. Surgery Control Window Irrigation Controls

3. Surgery Menu

Figure 2-54 Functional Areas of the Infniti® Vision System Surgery Screen - This screen
is for the Ultrasound Continuous mode of operation. Other modes of operation look similar
to this, but may have more or fewer buttons and surgical parameters corresponding to
the surgery step.

8065751606 2.65
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 a footswitch button is depressed or not depressed, and the functionality provided by
the footswitch will continue.
• Doctor Name
When a new doctor is selected, the system setup is changed to the settings
associated with the newly-selected doctor.
• Handpiece Type, Tip Type, Procedure Type, and Cataract Grade
These selections along the top row of the Main Window are displayed during
U/S, NeoSoniX®, Ozil®, and AquaLase® steps. The selections change during I/A,
Vitrectomy, and Coagulation steps.
• Irrigation Controls, Metrics Display, Footswitch Button, and Custom Button
These selections along the second row of the Main Window are displayed in all step

types. Their descriptions, except for Metrics, are the same as in the Setup Screen.
2. Surgery Control Window
This window contains an Information Bar. Surgical parameters are situated above and
below the bar. Parameters related to the uidics, vacuum, and aspiration ow rate are
located below the bar. Parameters related to the chosen mode, for example ultrasound
power, are located above the bar. Parameters above the bar are independent of the
uidics parameters. The content of these areas is determined by the active surgical step.

The actual values for certain parameters are shown using Display Bars. With the
exception of the Vacuum parameter, the upper limits of the Display Bars are equal
to their maximum settings. For the Vacuum parameter, if the vacuum limit is set to
650+, then the upper limit does not exist; otherwise, the upper limit is equal to the
vacuum limit setting.

Display Bar Limit Box with Adjustment Arrows

Mode Button

2.2 Surgery Controls

2. Surgery Control Window
2.3 Adjust Button and
Information Bar
2.1 Fluidics Controls

Figure 2-55 Surgery Control Window - Above the Adjust bar is the area reserved for
Surgery Controls, and below the bar is the area reserved for Fluidics Controls. This
Surgery Control Window is used to adjust system settings with the up/down arrows, and
to observe current performance levels on the Display Bars. Depending on the mode of
operation, the Adjust Button is used to adjust other settings.

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 Saving Modications to Surgical Parameters
Each surgery step has surgical parameter values that are established by default.
During surgery the user may change surgical parameters in any of the steps. Any
parameter changes made may be explicitly saved by the user using the Save option
in the Custom drop list. Also, if there are unsaved changes to the surgery steps and
the user changes the doctor, phaco handpiece, phaco tip, I/A tip, or lens removal
procedure, a dialog box appears asking the user to save or discard any unsaved
changes. Powering down the system automatically dismisses any unsaved changes.

2.1 Fluidics Controls

Below the Information Bar in the Surgery Control Window are the Fluidics Controls.

These parameters
Surgery Controls. are always
Fluidics vacuumare
Controls and aspiration
available andsteps
in all are independent of the
but Coagulation.

2.2 Surgery Controls

For Phaco steps, the area above the Information Bar contains the Surgery Controls
for U/S functions. The surgery controls available are dependent on the type of lens
removal step and mode selected. The possible parameters are a power bar to display
a real-time representation of the actual power level, a linear/xed button to toggle
between linear (/) or xed (-) footswitch-controlled power, and limit boxes with
adjustment arrows to display and set maximum or minimum settings (see Table 2-3).

The Mode button in the top-center of this area displays the current mode (continuous,
pulse, custom pulse, burst) for the step. The mode can be changed by pressing
the Mode Button and selecting another from a drop list. Depending on the current
handpiece the mode selections are:
• Ozil®Continuous • NeoSoniX®Continuous • Ultrasound Continuous • Vit Cut I/A
• Ozil®
Pulse • NeoSoniXPulse
®
• Ultrasound Pulse • Vit I/A Cut
® ®
• Ozil
Burst • NeoSoniXBurst • Ultrasound Burst
®
• Ozil Custom Pulse • NeoSoniX® Custom Pulse • Ultrasound Custom Pulse

For AquaLase®, Irrigation/Aspiration, Coagulation, and Capsule Wash, the top-center

of this area displays the current mode, but is not a button.

8065751606 2.67
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 Ultrasound, NeoSoniX®, AquaLase®, Coagulation, Vitrectomy
Power % Power Limit Burst % Burst % Time pps % Time On On ms On ms Off ms Amplitude Threshold Cut Rate Cut Rate
Bar Linear/Fixed Time On On Limit Box Box Box Limit Limit Box Box cpm Bar Limit Box
Button Bar Linear/Fixed
MODE Button

Ultrasound
Continuous X X

Ultrasound
Pulse X X X X

Ultrasound
Burst X X X X

U/S
Custom Pulse X X X X

NeoSoniX®
Continuous X X X X

NeoSoniX®
Pulse X X X X X X

NeoSoniX®
Burst X X X X X X

NeoSoniX®
Custom Pulse X X X X X X

®
AquaLaseX* X* X X X

Coagulation X X

Vitrectomy X X

* For AquaLase® these labels are Magnitude instead of Power.

OZil®
Mode Phaco Power/ Torsional Amplitude

% Limit On ms Limit Off ms Limit On % Off PPS

Bar Linear/Fixed Linear/Fixed Linear/Fixed ms Time On ms
Button Button Button Limit

OZil®
Continuous X X

OZil®
Pulse X X X X

OZil®
Burst X X X X

®
OZil
Custom Pulse X X X X

Table 2-3 PARAMETERS IN SURGERY CONTROLS AREA - The top half of the Surgery Control Win -
dow contains surgery con trols; uidics controls are in the lower half. Listed here are the
operating parameters in the surgery controls section for identied surgical modes.

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 Lower and Upper Limits
The system now allows for lower limits to be established for any parameter setting in
which linear mode is supported. This lower limit can be set between 0 and the upper
limit. Once a linear footpedal position is entered, the parameter starts at the lower
limit and increases to the upper limit at the end of that footpedal position.

To adjust the lower limit, touch the active bar graph; an adjustment window appears
on top of the value being adjusted (see Figure 2-56). Press the up and down arrows
to select the desired lower limit setting, then press OK. (Lower and upper limits can
both be adjusted in this window. The upper limit can also be adjusted in the surgery
screen without entering this adjustment window.)

The lower limit setting is shown in the surgery screen below the lower-left corner of
the bar graph.

Figure 2-56 Lower and Upper Limits - This is an example of an adjustment window with
upper and lower linear control limits that is displayed by pressing an active bar graph;
in this case the Torsional Amplitude bar graph was pressed.

2.3 Adjust Button and Information Bar

When the Adjust button is pressed, the Display Bar is depicted with buttons
representing the current settings of each of the Adjust parameters. The Adjust
parameters may be changed at this time. If the parameter is a drop down type, when
the parameter button is pressed, a drop down list appears and the user can select the
option desired. If the parameter is a toggle type, when the parameter button is pressed,
the value will be toggled. The Display Bar can be removed manually by pressing the
Adjust Button again, or by waiting ve seconds and it will be disappear automatically.

The Display Bar is available in all surgery steps except Coagulation.

Dynamic Rise - The value in the display bar indicates the current rise time for the
aspiration pump rate adjustment at occlusion onset. The Dynamic Rise setting can
vary from –2 to 4, in increments of 1. When Dynamic Rise -2 is displayed in the
Adjust Bar, it indicates that the rise time in aspiration pump rate adjustment is

8065751606 2.69
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 slowest. When Dynamic Rise 4 is displayed in the Adjust Bar, it indicates that the rise
time in aspiration pump rate adjustment is fastest. The Alcon default setting is 0.

WARNING!
The use of Dynamic Rise setting 1, 2, 3, or 4 may result in aspiration levels (volumes)
exceeding irrigation ow. This may cause chamber shallowing or collapse which may
result in patient injury.

Occlusion Watch Off/On - Occlusion Watch is enabled in the Custom/AqL Occlusion

menu. When enabled it can be turned on and off in this information bar. When
Occlusion Watch On is displayed in the Adjust Bar, it indicates that auto-attenuation
of occlusion-based power is active. When Occlusion Watch Off is displayed in the
Adjust Bar, it indicates that auto-attenuation of occlusion-based power is inactive.

Status Icons - These icons indicate the presence and status of the active handpiece,
FMS, and bottle of AquaLase® BSS® sterile irrigating solution.

OZil® IP Icon - When the OZil® IP feature is enabled for a particular surgical step,
this icon is colored and animated; when disabled, this icon is greyed out. Pressing
this icon button displays theOZil® IP dialog which allows the feature to be enabled/
disabled for the currently-active surgical step. Refer to theOZil® IP Feature later in
this section of the manual.

2.4 Surgery Controls Window with I/A Steps

All I/A steps contain the same Fluidics Controls for vacuum and aspiration. The
Surgery Controls area above the Display bar does not contain any surgical parameters,
but does display a mode indicator showing Irrigation/Aspiration.

2.5 Surgery Controls Window with Vitrectomy Steps

All Vitrectomy steps contain Surgery Controls for cut rate parameters, and Fluidics
Controls for vacuum and aspiration parameters. The Surgery Controls area also
contains a Mode Button indicating the current Vitrectomy step type (Vitrectomy I/A
Cut or Vitrectomy Cut I/A).

2.6 Surgery Controls Window with Coagulation Steps

All Coagulation steps contain just one surgical parameter: Power. This parameter
is displayed in the upper portion of the Surgery Control Window. This window also
contains a mode indicator showing Coagulation.

The Power and Fixed/Linear settings in Pre-Phaco Coagulation (enabled in Steps tab
of Custom/Doctor dialog) are unique and are not shared with other coagulation steps.

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3. Surgery Menu
The Surgery Menu consists of the buttons at the very bottom of the surgery display
(see Figure 2-57). These buttons represent all the surgery steps for the currently
selected surgery mode, plus a Setup button to quickly return to the Setup screen.

The Surgery Menu allows up to 10 visible buttons across the bottom of the surgery
display screen. The Setup button is always on the far left, followed by up to 7 buttons
corresponding to the lens removal and I/A steps. The last two buttons are for the
coagulation and anterior vitrectomy steps. The Setup, coagulation, and anterior
vitrectomy buttons are xed, however the 7 buttons corresponding to lens removal
and I/A steps are scrollable to the left and right. This scrolling is necessary since more

than 7 lens removal and I/A steps may be specied.

The lens removal steps correspond to the selected tip, procedure, and handpiece. The
I/A steps correspond to the selected I/A tip and procedure. When selecting the step
that is furthest left (e.g. next to the Setup button) or furthest right (e.g. next to the
stationary coagulation button), the lens removal and I/A steps will scroll so that all
steps before or after the selected step, respectively, can be seen.

3. Surgery Menu

Lens Removal Steps I/A Steps

3.1 Setup Button Coag Step Vit Step

3.2 Procedural Step Buttons 3.3 Stationary Step Buttons

Figure 2-57 Surgery Menu - At the bottom of the display screen is the Surgery Menu.
The buttons in this area allow the surgeon to control the surgical step progression.

8065751606 2.71
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3.1 Setup Button
When the Setup button is pressed, the user will be taken to the Setup screen. To enter
the Setup screen the footpedal must be released, and the footswitch buttons must not
be activated.

3.2 Procedural Step Buttons

When a surgery step is selected, its button is highlighted with a frame, and the

surgical parameters
In addition, for the
the Surgery surgery
Main step isare
Window displayed
updated withinthe
thebuttons
Surgerythat
Control Window.
are applicable
for the selected step.

Step changes in lens removal and I/A modes are allowed regardless of footpedal
position. A step change into Coag or Vit is allowed with the footpedal depressed, but
the footpedal must be released to exit.

Procedural Steps
The Inniti® Vision System provides operational surgical steps to support efcient
lens removal. Each step allows for the adjustment of surgical parameters such as
power, aspiration, and vacuum settings according to doctor preferences. These steps
are arranged in sequential order from left to right across the bottom of the screen to
provide a complete surgical procedure of different settings associated with different
aspects of the procedure. Complete procedures can be saved for future use without
having to re-program the instrument. Coag and Ant Vit steps can be added to the
procedural sequence by enabling them from the Doctor Settings dialog (see 1.9.1). U/S ,
Aql, and I/A steps can be added or deleted from the Copy/Delete dialog (see 1.9.3).

The procedural steps are selectable from the unit’s front display screen, from the remote
control unit, or from the footswitch. Step changes will result in voice conrmation.
(The user has the ability to turn this feature off via theCustom/Sound menus.)

Preset operating parameters for each step are programmed into the system as "Alcon
Settings." These default operating parameters can be temporarily modied by using
the front panel or remote. These parameters can then be permanently saved by using
the Custom/Save/Save As option.

3.3 Stationary Step Buttons

Steps are always present to support Coag and Ant Vit. These two steps are selectable
from the display screen and remote control, but can be exited using either the display
screen, remote control, or footswitch (if footswitch button programmed for Step+,
Step-, or Step±) when pedal is in position 0 or 1.

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SURGERY MODES

Ultrasound (U/S) Mode of Operation

When the U/S handpiece is selected, irrigation, aspiration, and phaco power are provided
to the handpiece tip. Phaco power is dened as being proportional to ultrasound
displacement of the phaco tip. Amplitude of the ultrasound displacement of the phaco tip
is proportional to the ultrasound power displayed on the console front panel. The user
has the ability to adjust the aspiration rate, vacuum levels, and phaco power at any time
during the surgical procedure via their respective adjustment arrows or remote control.

Power
The phaco Power Limit is increased or decreased via the front panel in increments
of 5% from a minimum of 0% to a maximum of 100%. The amount of phaco power
delivered to the handpiece is controlled by one of two methods: linear or xed
footpedal control.

• If linear footpedal control is selected (diagonal button graphic), the power readout
button indicates the maximum power available in footpedal position 3. In footpedal
position 3, power starts at the lower limit and increases linearly until power reaches
the upper limit at full footpedal depression. To change the lower and upper limits,
press the active power bar to bring up the adjustment window, then press the up or
down arrows which will increase or decrease the lower and upper limits.

• If xed footpedal control is selected (horizontal button graphic), the Power Limit
button indicates the power applied in footpedal position 3. To increase or decrease
power, the arrow buttons must be pressed. The selected power is fully activated
on transition of the footpedal into and throughout position 3.

OFF (position 0)

IRRIGATION (position 1)

DAL
TPE IRR + ASPIRATION (position 2)
FOO
IRR + ASP + PHACO POWER (position 3)

FOOTSWITCH ASSEMBLY

Power
• Linear or Fixed Power

Timing
• Continuous: Continuous Power with No Rest Period
• Pulse: Adjustable Pulse Rate Setting
Adjustable Duty Cycle
• Burst: Decreasing
Fixed On-Time
Off-Time
• Custom Pulse: Fixed, Increasing, or Decreasing On-Time
Fixed or Decreasing Off-Time

Figure 2-58 U/S Footpedal Control - Phaco power is delivered with the power and
timing methods listed above when the footpedal enters, and then travels through,
footpedal position 3.

8065751606 2.73
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 Timing
Phaco power is delivered to the phaco tip through a variety of timing congurations
when in footpedal position 3. Depending on the mode selected the timing can be
continuous, or can include moments of rest between power pulses.

Figure 2-59 The Ultrasound Continuous Surgery Screen

• Ultrasound Continuous - This mode of operation provides continuous phaco

power to the handpiece.

Figure 2-60 The Ultrasound Pulse Surgery Screen

• Ultrasound Pulse - When operating in this mode of operation, phaco power is

turned On and Off at a frequency determined by the pulse rate setting in pulses
per second (pps), and on a duty cycle adjustable by the operator (% Time On).

2.74 8065751606
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 Figure 2-61 The Ultrasound Burst Surgery Screen - This is an example of the screen
when the footpedal is depressed into footpedal position 3 and is delivering power for less
than 20 ms. The Smart Pulse text ickers under the Power bar when power is delivered
for less than 20 ms.

• Ultrasound Burst - Ultrasound Burst control allows xed or linear controlled

phaco power in footpedal position 3. The power is delivered in bursts, separated by
off-times. The timing of the burst and off-times occur for an operator-set duration.

- The duration of each burst (On ms) can be increased or decreased by pressing
the up or down arrows.

- The off-time between each burst (Off ms), during which no phaco power is
applied, is 2.5 seconds (2500 ms) at the beginning of footpedal position 3. The
user can adjust the minimum off-time (Off ms) at the bottom of footpedal position
3 from between 500 to 0 ms (0 ms results in continuous phaco power). When in
footpedal position 3 the readout displays the actual off-time.

Smart Pulse
When in footpedal position 3, and the duration of ultrasound pulse becomes less than
20 ms, a proprietary algorithm becomes active. This is indicated by the Smart Pulse
message appearing on the screen below the Power bar (see Figure 2-61).

When the algorithm is active, ultrasound power will be generated at 10% or half
of the commanded power, whichever is lower, prior to the application of the main
power pulse. This low-powered pulse contributes a negligible amount of energy
to the procedure, but it allows the electronic equipment to determine the optimum
operating parameters for the main power pulse, thus making it more efcient, even
for the shortest duration of ultrasound. The Smart Pulse algorithm can be active in
Pulse, Burst, or Custom Pulse modes when used with the U/S,NeoSoniX®, or OZil®
torsional handpieces. The minimum duration of the main pulse in ultrasound is 5 ms;
the minimum duration of torsional pulse is 20 ms.

8065751606 2.75
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 Figure 2-62 The U/S Custom Pulse Surgery Screen

• Ultrasound Custom Pulse - When operating in this mode of operation, phaco

power is turned On and Off for a period of time determined by the milliseconds
(ms) selected by the user (On ms - Limit / Off ms - Limit) and the position of the
footswitch in position 3. This screen can only be accessed if it is enabled in the
doctor's preferences (Custom/Doctor/Advanced/Custom Pulse Enable).

- The on-time can be xed at the selected setting throughout position 3, set to
increase from one-fth the set limit (ms) at the beginning of position 3 to the set
limit at the end of position 3, or set to decrease from ve times (ms) the set limit
at the beginning of position 3 down to the set limit at the end of position 3.

- The off-time can be xed at the selected setting throughout position 3, or set to
decrease from 2500 ms at the beginning of position 3 down to the set limit at the
end of position 3. When not in footpedal position 3 the user setting is displayed;
when in position 3 the actual value reported by the subsystem is displayed.

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 NeoSoniX® Mode of Operation

When the NeoSoniX® handpiece is selected, irrigation, aspiration, phaco power and sonic
oscillations are provided by the handpiece. In this mode of operation phaco power and
sonic oscillations alternately turn On and Off. The
user has the ability to adjust the aspiration rate, nic
o
S cillations
vacuum levels, phaco power, and sonic oscillations s
O
(via Amplitude/Threshold settings) at any time o
Phac
during the surgical procedure via their respective
adjustment arrows or remote control.

Power
The phaco Power Limit is increased or decreased via the front panel in increments
of 5% from a minimum of 0% to a maximum of 100%. Power to the handpiece is
controlled by one of two methods: linear or xed footpedal control.

• If linear footpedal control is selected (diagonal button graphic), the power readout
button indicates the maximum phaco power delivered with the footpedal fully
depressed. In footpedal position 3, power starts at the lower limit and increases

OFF (position 0)

IRRIGATION (position 1)

DAL
TPE IRR + ASPIRATION (position 2)
FOO
IRR + ASP + PHACO POWER (position 3)
+ SONIC OSCILLATIONS

FOOTSWITCH ASSEMBLY

Power and Sonic Oscillations

• Linear or Fixed Phaco Power
• Fixed Sonic Oscillations when U/S Power Threshold Reached

Timing
• Continuous: Continuous Power with No Rest Period
• Pulse: Adjustable Pulse Rate Setting
Adjustable Duty Cycle
• Burst: Fixed On-Time
Decreasing Off-Time
• Custom Pulse: Fixed, Increasing, or Decreasing On-Time
Fixed or Decreasing Off-Time

Figure 2-63 NeoSoniX® Footpedal Control - Phaco power and sonic oscillations are
delivered with the power and timing methods listed above when the
footpedal enters, and then travels through, footpedal position 3.

8065751606 2.77
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 linearly until power reaches the upper limit at full footpedal depression. To change
the lower and upper limits, press the active power bar to bring up the adjustment
window, then press the up or down arrows which will increase or decrease the
lower and upper limits.

• If xed footpedal control is selected (horizontal button graphic), phaco power is

fully activated on transition of the footpedal into and throughout position 3. To
increase or decrease power, the arrow buttons must be pressed.

• Sonic oscillations are activated when phaco power reaches or exceeds the (phaco
power) Threshold set on the screen. At that point sonic oscillations are activated at

the
the Amplitude set on the
Threshold setting, screen.
sonic If phaco will
oscillations powernotcontrol is xed,
turn On; and is lower
alternatively, than
if phaco
power control is xed, and is higher than the Threshold setting, oscillations turn
On when the footpedal enters position 3.

Timing
Phaco power and sonic oscillations are delivered to the phaco tip through a
variety of timing congurations when in footpedal position 3. Depending on the mode
selected the timing can be continuous, or can include off-times between power/sonic
pulses.

• NeoSoniX® Continuous - This mode of operation provides continuous phaco

power and sonic oscillations (if Threshold reached) to the handpiece.

Figure 2-64 The NeoSoniX® Continuous Surgery Screen

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 Figure 2-65 The NeoSoniX® Pulse Surgery Screen

• NeoSoniX® Pulse - When operating in this mode of operation, phaco power and
sonic oscillations are turned On and Off with a frequency determined by the pulse
rate setting in pulses per second (pps), and on a duty cycle adjustable by the
operator (% Time On). Sonic oscillations are applied at the limit value specied in
the Amplitude box when phaco power meets or exceeds the power value specied
in the Threshold box.

Figure 2-66 The NeoSoniX® Burst Surgery Screen

• NeoSoniX® Burst - NeoSoniX® Burst control allows xed or linear controlled

phaco power and sonic oscillationsin footpedal position 3. The power is delivered
in bursts, separated by off-times. The timing of the burst and off-times occur for an

operator-set duration.
- The duration of each burst (On ms) can be increased or decreased by pressing
the up or down arrows.

- The off-time between each burst (Off ms), during which no phaco power or
sonic oscillations are applied, is 2.5 seconds (2500 ms) at the beginning of
8065751606 2.79
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 footpedal position 3. The user can adjust the minimum off-time (Off ms) at
the bottom of footpedal position 3 from between 500 to 0 ms (0 ms results in
continuous power). When in footpedal position 3 the readout displays the actual
off-time reported by the subsystem.

Figure 2-67 The NeoSoniX® Custom Pulse Surgery Screen

• NeoSoniX® Custom Pulse - When operating in this mode of operation, phaco

power and sonic oscillations are turned On and Off for a period of time
determined by the time (ms) selected by the user (On ms - Limit / Off ms - Limit)
and the position of the footswitch in position 3. This screen can only be accessed
if it is enabled in the doctor's preferences (Custom/Doctor/Advanced/Custom

Pulse Enable).
- The on-time can be xed at the selected setting throughout position 3, set to
increase from one-fth the set limit (ms) at the beginning of position 3 to the set
limit at the end of position 3, or set to decrease from ve times (ms) the set limit
at the beginning of position 3 down to the set limit at the end of position 3.

- The off-time can be xed at the selected setting throughout position 3, or set to
decrease from 2500 ms at the beginning of position 3 down to the set limit at the
end of position 3. When not in footpedal position 3 the user setting is displayed;
when in position 3 the actual value reported by the subsystem is displayed.

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 OZil® Mode of Operation

When the OZil® torsional handpiece is selected, irrigation, aspiration, phaco power and
ultrasonic oscillations are provided by the handpiece. In this mode of operation phaco
power and ultrasonic oscillations alternately turn On
onic
and Off. Amplitude of the ultrasound and torsional as
lt r cillations
displacement of the phaco tip is proportional to the U s
O
ultrasound power and torsional amplitude displayed
ha co
on the console front panel. The user has the ability P
to adjust the aspiration rate, vacuum levels, phaco
power, and torsional amplitude (ultrasonic oscillations) at any time during the surgical

procedure
of the OZilvia
® their respective adjustment arrows or remote control. For best perfor
mance
torsional handpiece, use tips recommended by your Alcon representative.

Power/Amplitude
The Phaco Power Limit and Torsional Amplitude Limit are increased or decreased via
the front panel in increments of 5% from a minimum of 0% to a maximum of 100%.
Power/Amplitude to the handpiece is controlled by one of two methods: linear or
xed footpedal control.

• If linear (increasing) footpedal control is selected (rising diagonal button graphic),

the Limit buttons indicate the maximum phaco power and ultrasonic oscillations
(Torsional Amplitude) delivered with the footpedal fully depressed.In footpedal
position 3, power and oscillations start at the lower limit and increases linearly until

OFF (position 0)

IRRIGATION (position 1)

DAL
TPE IRR + ASPIRATION (position 2)
FOO
IRR + ASP + PHACO POWER (position 3)
+ ULTRASONIC OSCILLATIONS

FOOTSWITCH ASSEMBLY

Power
• Linear or Fixed Phaco Power
• Increasing or Fixed Torsional Amplitude

Timing
• Continuous: Continuous Power with No Rest Period
• Pulse: Adjustable Pulse Rate Setting
Adjustable Duty Cycle
• Burst: Fixed On-Time
Decreasing Off-Time
• Custom Pulse: Fixed, Increasing, or Decreasing On-Time
Fixed or Decreasing Off-Time

Figure 2-68 OZil® Footpedal Control - Phaco power and ultrasonic oscillations are
delivered with the power and timing methods listed above when the footpedal enters,
and then travels through, footpedal position 3.

8065751606 2.81
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 power reaches the upper limit at full footpedal depression. To change the lower and
upper limits, press the active power bar to bring up the adjustment window, then
press the up or down arrows which will increase or decrease the lower and upper
limits.

• If xed footpedal control is selected (horizontal button graphic), the Limit

buttons indicate the phaco power and ultrasonic oscillations delivered throughout
footpedal position 3. To increase or decrease power, the arrow buttons must be
pressed.

Timing

Phaco power
variety and ultrasonic
of timing oscillations are delivered to the phaco tip through a
congurations when in footpedal position 3. Depending on the
mode selected the timing can be continuous, or can include off-times between phaco/
torsional pulses.

Figure 2-69 The OZil® Continuous Surgery Screen

• OZil® Continuous - When the Phaco Power default setting is set to 0 (no phaco
power), then only torsional ultrasonic oscillations at the preset Torsional
Amplitude are delivered, for 100% of the time, to the handpiece tip. This allows
the user to have continuous torsional ultrasonic oscillations if so desired. If U/S
power is added, then this mode of operation provides 20% of its duty cycle for
phaco power, then torsional ultrasonic oscillations for the remaining 80% when
in footpedal position 3, and repeats this cycle over and over again as long as the
footpedal is in position 3. This produces continuous U/S alternations between
phaco power and torsional amplitude.

The user can select between xed (horizontal button display) or linear (diagonal
button display) Phaco Power, and xed or increasing Torsional Amplitude when
in footpedal position 3 by pressing their associated buttons.

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 Figure 2-70 The OZil® Pulse Surgery Screen

• OZil® Pulse - When operating in this mode of operation, phaco power and
ultrasonic oscillations turn On and Off at a frequency determined by the pulse rate
(pps) setting, and on a duty cycle adjustable by the operator (% Time On). The
remaining pulse time, or percent time Off, is an off-time. The sum of phaco duty
cycle and torsional duty cycle cannot exceed 100%.

For example, in the gure above the entire cycle of phaco, torsional, and off-
time is 100 ms duration because of the selected pulse rate of 10 pps. Duration
of the phaco, therefore, is 100 ms X 10% = 10 ms, and duration of the torsional
is 100 ms X 50% = 50 ms. The remaining 40 ms is an Off period. Note that the
Off period follows application of torsional ultrasound, while torsional ultrasound
follows application of phaco immediately with no pause.

If Phaco Power Limit (see gure below) and/or Torsional Amplitude Limit are set
to zero, then there are no phaco nor torsional contributions to the pulse, and the
duty cycles (% Time On) are not adjustable.

Figure 2-71 Phaco Duty Cycle (% Time On) Not Adjustable

8065751606 2.83
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 Figure 2-72 The OZil® Burst Surgery Screen

• OZil® Burst - When operating in this mode, phaco burst is followed immediately
by torsional burst, followed by an off-time. Duration of the phaco burst is
determined by the setting on the panel, for example 30 ms in the gure above;
duration of the torsional burst is 70 ms. Duration of the off-time is determined by
the footpedal in position 3. At the beginning it is equal to 2500 ms, and gradually
reduced as the footpedal is depressed. When the footpedal is depressed all the
way, the off-time will be equal to that set on the panel – 30 ms in the given
example.

If Phaco Power Limit and/or Torsional Amplitude Limit are set to zero, then there
are no phaco or torsional contributions to the burst, and the duty cycles (On ms)
are not adjustable.

• OZil® Torsional Before Phaco

The Inniti® system has an ON/OFF setting called “OZil Torsional Before Phaco”
which affects the order of the phaco and torsional pulses/bursts in theOZil® Pulse
and Burst modes. This feature has been previously described in the "General Tab"
section of the manual.

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 • OZil® Custom Pulse - When operating in this mode of operation, phaco power
and ultrasonic oscillations are turned On and Off for a period of time determined
by the time (ms) selected by the user (On ms - Limit / Off ms - Limit) and the
position of the footswitch in position 3. The system repeats this sequence of
events: phaco power on then off-time, ultrasonic oscillations on then off-time.
This screen can only be accessed if it is enabled in the doctor's preferences
(Custom/Doctor/Advanced/Custom Pulse Enable).

Figure 2-73 The OZil® Custom Pulse Surgery Screen - In this mode of operation there
is a repeating sequence of events as follows: phaco power, then an off-time, ultrasonic
oscillations, then an off-time. The Phaco Power Limit and Torsional Amplitude Limit set
the strength of each. The duration of each is set with the On ms - Limit and O ff ms - Limit
settings.

- The on-time can be xed at the selected setting throughout position 3, set to
increase from one-fth the set limit (ms) at the beginning of position 3 to the
set limit at the end of position 3 (rising diagonal button graphic), or set to
decrease from ve times (ms) the set limit at the beginning of position 3 down
to the set limit at the end of position 3 (falling diagonal button graphic).

- The off-time can be xed at the selected setting throughout position 3, or

set to decrease from 2500 ms at the beginning of position 3 down to the set
limit at the end of position 3 (falling diagonal button graphic). When not in
footpedal position 3 the user setting is displayed; when in position 3 the actual
value is displayed.

8065751606 2.85
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 OZil® IP Feature
This feature can be enabled when performing surgery in the OZil® phaco mode. It is
used to intelligently deliver energy combinations of phaco (longitudinal) power of
equal or less magnitude when a programmable vacuum threshold is exceeded. These
additional longitudinal pulses are applied only as necessary to enhance the delivery
of energy, and continue until the vacuum drops below the Trigger or the maximum
number of pulses has been reached.

While in the OZil® mode of operation, theOZil® IP feature can be enabled or disabled
for each individual phaco step by pressing theOZil® IP button icon located in the
Information Bar (see Figure 2-74). When pressed, theOZil® IP dialog appears (see
® ®
Figure
disabled2-75). OZil IP for the current OZil step is enabled by pressing the
by pressing Ondialog
the Off button. Press the OK button to close theOZil® IP button;
or it will be automatically dismissed after about three seconds of inactivity.

OZil® IP Button Icon

Figure 2-74 Surgery Screen with OZil® IP Enabled - When enabled for the current step,
the OZil® IP button icon is colored and animated (when not enabled it is dull and gray).
The user can press the button icon to pull up the OZil® IP dialog, shown below.

Figure 2-75 OZil® IP Dialog - This dialog is used to turn the OZil® IP feature On (enabled)
and Off (disabled).

2.86 8065751606
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 When the OZil® IP feature is enabled, theOZil® IP button icon is colored and
animated for the current step. WhenOZil® IP is disabled for the selectedOZil® phaco
step, the OZil® IP button icon is grayed out.

The OZil® IP settings are specied, and can be changed, in the Advanced tab of the
Custom/Doctor dialog (see the description of the Advanced tab earlier in this section
of the manual). These settings are user-adjustable so the user can specify the vacuum
limit at which the OZil® IP feature is activated, and the amount of pulsed phaco power
that is delivered when activated. In addition, theOZil® IP settings can be tailored for
each cataract grade.

®
Even though
be turned Offthe
forOZil IP feature
a particular may grade.
cataract be enabled forturned
If it is a particular
Off forsurgical step,cataract
a particular it can
grade (turned Off by adjusting the Phaco Pulse On Time to Off) and the user presses
the OZil® IP button icon, then the user is notied that the OZil® IP feature has been
turned Off for that cataract grade (see Figure 2-76). The advisory instructs the user
how to turn it On if desired.

Figure 2-76 OZil® IP Dialog - This dialog shows that OZil® IP feature is turned Off for this
cataract grade. To turn it On for this cataract grade, it must rst be enabled in the Custom
/ Doctor / Advanced window.

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 AquaLase® Liquefaction Mode of Operation

When the AquaLase® handpiece is selected, irrigation, aspiration, and liquefaction

energy are provided by the handpiece.

The Magnitude Limit, Pulse Rate, and Burst % are increased or decreased via the
front panel adjust arrows in increments of 5% from a minimum of 0% to a maximum
of 100%. Power to the AquaLase® handpiece is controlled by one of two methods:
linear or xed footpedal control of magnitude.
• If Fixed is selected, the output setting is displayed in the Magnitude Limit box. To
increase or decrease magnitude, press the arrow buttons. The selected magnitude

•
is fully activated on transition of the footpedal into position 3.
If Linear control is selected, the Magnitude Limit box indicates the maximum
output available. In footpedal position 3, magnitude starts at the lower limit and
increases linearly until power reaches the upper limit at full footpedal depression.
To change the lower and upper limits, press the active control bar to bring up
the adjustment window, then press the up or down arrows which will increase or
decrease the lower and upper limits.

Liquefaction energy is delivered to the AquaLase® handpiece tip through a variety of

timing congurations when in footpedal position 3. Depending on the mode selected
the timing can be in pulses, or can be in bursts of pulses which include off-times
between sets of pulses.

PPS - The pulse frequency, or pulses per second (PPS) may be set using the up/down
keys. PPS can be adjusted in increments of 5 from 10 to 50, and then jumps to 75.

• Fixed control - When Fixed is selected liquefaction energy is supplied at the

selected pulse rate upon transition of the footpedal into position 3.

Burst - Burst percentage indicates the percentage of a xed time period that is spent
applying pulses of liquefaction energy, and may be adjusted in 5% increments using
the control labeled "Burst." The remainder of the time period is spent off. When the
limit is set to 100% the pulses are uninterrupted.
NOTE: Burst is limited to a maximum of 67 % when PPS is set to 75.

• Fixed control - When Fixed is selected liquefaction energy is supplied at the

selected burst upon transition of the footpedal into position 3.

• Linear control - If Linear is selected, the Burst Limit box indicates the maximum
output available. Upon transition to footpedal position 3, burst starts at the lower
limit and increases linearly until power reaches the upper limit at full footpedal
depression. To change the lower and upper limits, press the active control bar to
bring up the adjustment window, then press the up or down arrows which will
increase or decrease the lower and upper limits.

2.88 8065751606
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 Figure 2-77 The AquaLase® Surgery Screen

OFF (position 0)

IRRIGATION (position 1)

L
EDA
OTP
IRR + ASPIRATION (position 2)
FO
IRR + ASP + AQUALASE® (position 3)

FOOTSWITCH ASSEMBLY

Figure 2-78 AquaLase® Footpedal Control - Liquefaction energy is delivered with the mag-
nitude and timing methods listed above when the footpedal enters footpedal position 3.

WARNINGS!
Use of the OZil® torsional, Infniti® NeoSoniX ®, U/S, or AquaLase® handpiece in the absence
of irrigation ow and/or in the presence of reduced or lost aspiration ow can cause
excessive heating and potential thermal injury to adjacent eye tissues.

Appropriate use of Infniti® Vision System parameters and accessories is important for
successful procedures. Use of low vacuum limits, low ow rates, low bottle heights, high power
settings, extended power usage, power usage during occlusion conditions (beeping tones),
failure to sufciently aspirate viscoelastic prior to using power, excessively tight incisions,
and combinations of the above actions may result in signicant temperature increases at
incision site and inside the eye, and lead to severe thermal eye tissue damage.

Use of an ultrasonic handpiece other than the OZil® torsional, Infniti® NeoSoniX ®, or U/S
handpiece, or use of a handpiece repaired without Alcon authorization, is not permitted, and
may result in patient injury, including potential shock hazard to patient and /or operator.

The U/S tips supplied in the Infniti® Vision System pak are only to be used on the OZil®
torsional, Infniti® NeoSoniX ®, or U/S handpieces. Each U/S tip is intended to be used only
once per case, and then disposed of according to local governing ordinances.
Use 0.9 mm U/S tips e xclusively with 0.9 mm infusion sleeves. U se 1.1 mm U/S and 1.1
mm liquefaction tips exclusively with 1.1 mm infusion sleeves. Mismatching U/S tips and
infusion sleeves may create potentially hazardous uidic imbalances.

Directing energy toward non-lens material may cause tissue damage.

8065751606 2.89
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 Irrigation/Aspiration Mode of Operation

I/A provides gravity-fed irrigation and simultaneous peristaltic aspiration for use with
I/A handpieces and tips. I/A control supports all surgical steps except coagulation.

In Irrigation/Aspiration mode there are only two footpedal positions. Irrigation is

provided in footpedal positions 1 and 2; Aspiration is provided in footpedal position
2. To change the lower and upper linear limits in footpedal positon 2, press the active
power bar to bring up the adjustment window, then press the up or down arrows which
will increase or decrease the lower and upper limits.

All I/A steps contain vacuum and aspiration Fluidics Control Parameters. These
parameters are displayed in the portion of the Surgery Control Window below the
Adjust bar. The Surgery Control Window above the Adjust bar does not contain any
surgical parameters, but does contain an indication of the step type (i.e. Irrigation/
Aspiration).

The following is an example of an I/A step surgery screen with the Adjust bar
displayed.

Figure 2-79 The Irrigation/Aspiration Surgery Screen

OFF (position 0)

IRRIGATION (position 1)

DAL
TPE
FOO IRR + ASPIRATION (position 2)

FOOTSWITCH ASSEMBLY

Figure 2-80 Irrigation/Aspiration Footpedal Control

2.90 8065751606
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 Vacuum Control
The operator can adjust the vacuum limit using the front display panel or the remote.
The adjustable vacuum limit range is 0 to 650+ mmHg, where 650+ is limited by
atmospheric pressure.

• Fixed Vacuum Control - Fixed vacuum control provides a xed vacuum limit
when aspirating in footpedal position 2.

• Linear Vacuum Control - Linear vacuum control provides linear control of

vacuum in footpedal position 2 where the actual vacuum limit is proportional to
the footpedal position. The upper vacuum limit is the set vacuum limit displayed.

Aspiration Control
The operator can adjust the aspiration limit using the front display panel or the
remote. The adjustable aspiration limit range is 5 to 60 cc/min.

• Fixed Aspiration Control- Fixed aspiration control provides a xed aspiration

ow rate when in footpedal position 2.

• Linear Aspiration Control - Linear aspiration control provides linear control of

aspiration ow rate in footpedal position 2 where the ow rate is proportional to
the footpedal position.

Fill Mode of Operation for Irrigation/Aspiration

The Fill step can be added before and/or after the I/A steps. When transitioned into
the Fill step, irrigation and reux will be enabled simultaneously for up to 10 seconds
(if Irrigation Fill is enabled in System Settings, this step will be Irrigation Fill, and
irrigation will be enabled without reux). It is recommended to add the Fill step
before the rst I/A step to facilitate removal of air from the I/A handpiece. Adding
the Fill step after the last I/A step will simplify cleaning of the I/A tip and handpiece.
Refer to Custom/Doctor in section 1.9 for details of how to add/remove the Fill step.

8065751606 2.91
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Coagulation (Coag) Mode of Operation

The Coagulation mode provides approximately 1 MHz frequency bipolar coagulation

to drive Alcon brush and forceps up to the preset limit upon travel through footpedal
position 2. The preset lower and upper limits are the available percentage of maximum
available coagulation power from 0% to 100%. To change the lower and upper linear limits
in footpedal positon 2, press the active power bar to bring up the adjustment window, then
press the up or down arrows which will increase or decrease the lower and upper limits.

The Power and Fixed/Linear settings in Pre-Phaco Coagulation (enabled in Steps tab
of Custom/Doctor dialog) are unique and are not shared with other coagulation steps.

In Coagulation mode there are only two footpedal positions. In footpedal position
2 coagulation is displayed and an audible tone is initialized. As in all other steps,
settings in Coag are retained in memory so that when re-entering the Coagulation
step, the previous settings are displayed.

• Fixed Coag Control - provides bipolar coagulation at the preset limit when the
footpedal enters position 2.

• Linear Coag Control - The control power is varied linearly from the lower limit to
the upper limit. Power begins when entering footpedal position 2 and ends when
the footpedal is fully depressed.

Figure 2-81 The Coagulation Screen

OFF (position 0)

OFF (position 1)

TPEDAL
FOO COAGULATION (position 2)

FOOTSWITCH ASSEMBLY

Figure 2-82 Coagulation Footpedal Control

2.92 8065751606
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 WARNINGS!
• Do not use the coagulation function on patients wit h pacemakers or implanted
debrillatory devices. If electrosurgery is used on patients with implanted
cardiac pacemakers or debrillatory devices or pacemaker electrodes, be
aware that irreparable damage to the pacemaker or debrillatory device
and its function may occur and lead to ventricular brillation. Please
check with the pacemaker or debrillatory device manufacturers for their
recommendations.

• Failure of the HF surgical equipment (coagulation circuitry) could result in

an unintended increase of output power.

CAUTION
The Infniti® Vision System is not protected against the effects of debrillator
discharge.

8065751606 2.93
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 Anterior Vitrectomy Mode of Operation

The Anterior Vitrectomy (Ant Vit) mode is used to drive a pneumatically operated
vitrectomy cutter. The Cut Rate is adjustable from 10 to 800 cuts per minute for the
20 gauge Infniti® vitrectomy probe, and from 10 to 2500 cuts per minute for the 23 gauge
Infniti® UltraVit® probe. Fixed and linear control of aspiration and vacuum is provided
in both Vitrectomy Cut I/A and Vitrectomy I/A Cut control modes. The currently-selected
vitrectomy probe is displayed in a button at the top of the vitrectomy surgery screen.
When pressed, a drop down list of available vitrectomy probes appears. When a probe
is selected the drop down list collapses and the selected probe is displayed.

Aleft
switch on the footswitch may be assigned to enable and disable the Vit Cutter (the
horizontal switch is an exception). When the Vit Cutter is disabled, I/A functionality
in footpedal positions 2 and 3 is unchanged, but the Vit Cutter does not cut, and the
message “Vit Cutter Disabled” is displayed. The assigned Vit Cutter switch may be
pressed in footpedal positions 1, 2, or 3, and the function takes effect immediately.

• Vitrectomy Cut I/A - Irrigation is provided in footpedal position 1; irrigation and

guillotine-motion cutting in position 2; and irrigation, cutting, and aspiration in
position 3.

• Vitrectomy I/A Cut - Irrigation is provided in footpedal position 1; irrigation and

aspiration in position 2; and irrigation, aspiration, and cutting in position 3. The
operator can adjust the preset aspiration and vacuum limits using the adjustment
control buttons on the control panel or on the remote control.

OFF (position 0) OFF (position 0)

TPEDAL
IRRIGATION (position 1) IRRIGATION (position 1)
FOO IRR + CUTTING (position 2) IRR + VACUUM / ASPIRATION (position 2)
IRR + CUT + VACUUM / ASPIRATION (position 3) IRR + VAC / ASP + CUTTING (position 3)

FOOTSWITCH ASSEMBLY Vitrectomy Cut I/A Vitrectomy I/A Cut

Figure 2-83 Anterior Vitrectomy Footpedal Control

Figure 2-84 Anterior Vitrectomy Screen With Vit Probes In Drop Down List

2.94 8065751606
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 Figure 2-85 Anterior Vitrectomy Surgery Screen Using 20 Gauge Infniti® Vitrectomy Probe

Figure 2-86 Anterior Vitrectomy Surgery Screen Using 23 Gauge Infniti® UltraVit® Probe

8065751606 2.95
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 Anterior Vitrectomy Setup Screen
When the Anterior Vitrectomy step is entered, the Vitrectomy Setup screen
appears (see Figure below) unless turned Off in the Doctor Settings screen. This
setup screen assists the user through the proper set up and test of the selected probe.

The Switch Probe button allows the user to change selected probes if the desired
probe is not displayed (this button appears only if hardware forUltraVit® probe
upgrade is installed). After performing a procedural step, pressing the Next Step
button brings up the screen for the next step. TheFill button allows the user to
prime the irrigation and aspiration tubings and ll a test vessel for proper testing
of the probe. Pressing theTest button initiates an automated test sequence which

veries
reduced secure
cut ratepneumatic
for visualconnections, then
verication of applies
probe pneumatic activation at a
cutting.

Figure 2-87 Vitrectomy Setup Screen

2.96 LAST PAGE OF THIS SECTION 8065751606

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 SECTION THREE
OPERATING INSTRUCTIONS

INTRODUCTION

This section details a recommended setup and check-out procedure for the Inniti®
Vision System. The steps on the following pages cover preparation for cataract lens
removal surgery including irrigation and aspiration, coagulation, and vitrectomy using
Alcon-supplied paks.

The Inniti® Vision System, including Alcon-approved consumables and accessories,

constitutes a complete surgical system and is intended exclusively for use by licensed
ophthalmic surgeons and their surgical teams. These surgical teams are experienced
at conducting phacoemulsication procedures in a properly maintained surgical
environment (qualied personnel, availability of backup equipment) and are familiar
with the operation of the equipment used as outlined in operator’s manuals and
directions for use (setup/checkout procedures to be completed before the surgical
procedure; processing of reusable devices; maintenance; etc.).

The procedures are divided into two columns and presume a surgical team of three
people: Surgeon and ScrubNurse in the sterile eld, and a Circulating Nurse in
the non-sterile eld. In the left column a directive is given; in the right column the
responsible team member is identied.

Any problems pertaining to setup and check-out procedures should rst be directed to
the Troubleshooting section of this manual. If questions still exist, contact the Alcon
Technical Services Department or your local Alcon representative.

POWER UP SEQUENCE

When the Power switch is turned on, and the Standby switch is pressed, the Inniti®
Inniti®
logo screen appears while the system performs its self-test diagnostics. The
Vision System is capable of detecting and reporting a wide range of fault and error
conditions. Many of these are checked during the power up procedure. If a fault is
detected during power up, the instrument becomes non-operational until the failure/
problem is corrected. Upon successful completion of the self-tests, the system enters
the Setup screen.

8065751606 3.1
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INITIAL SYSTEM SETUP

1. Matching the red dot on the footswitch cable connector to the red dot on Circulating Nurse
the footswitch, plug cable into footswitch. Place footswitch on the oor.
Ensure treadle and switches are not depressed/activated.

2. Plug main power cord into a suitable wall outlet or receptacle. Turn Circulating Nurse
Power switch ON located at the bottom of the rear panel next to the
power cord (this switch remains ON in the I position). Turn system
power ON using the Standby switch located at the top of the rear panel.

CAUTION
Do not use multiple portable socket outlets with this system.

WARNING!
Keep clear of the IV pole w hen it is in motion to prevent skin, hair, and/or
clothing from becoming trapped in the IV pole mechanism. The IV pole
moves during power on/off, priming, and bottle height adjustments.

3. Extend the IV pole hook. Do not extend while IV pole is in motion. Circulating Nurse

4. The grayed-out Setup screen appears with the Doctor Name dropdown Circulating Nurse
list displayed. Press a Doctor Name button (Alcon Settings) to select an
available doctor, or add a doctor by following the steps presented on the
display. If desired, select a Handpiece, Tip, and Procedure Type.

5. Inspect the O-rings on the Ultraow™* I/A handpiece tip. If damaged, Circulating Nurse
the O-rings must be replaced using theUltraow™* O-ring tool prior to
sterilization.

6. Sterilize the instruments according to hospital procedure. Circulating Nurse

CAUTION
The U/S, OZil® torsional, NeoSoniX®, and AquaLase® handpieces
must be at room temperature before use. Allow handpiece to air cool
after steam autoclave (at least 15 minutes). Never immerse in liquid
to cool.

3.2 8065751606
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STANDARD PHACOEMULSIFICATION SETUP

Prepare Contents of U/S Surgical Pak

1. Extend instrument tray out from the right or left side of console. Pull to Circulating Nurse
extend wire loop on tray.

2. If remote control is to be used during surgery, place it in the instrument Circulating Nurse
tray well. Verify remote control is functional by slightly raising or
lowering the IV pole.

3. Peel lid from U/S surgical pak and aseptically transfer contents to sterile Circulating Nurse
eld.

4. Drape the tray support cover over the tray, remote control, and support Scrub Nurse
arm. Push tray support cover downward through open wire loop to form
pouch.

5. Grasp Fluidic Management System (FMS), remove paper band from Scrub Nurse
irrigation/aspiration (I/A) tubing, uncoil tubing and place in pouch.

6. Hold FMS by handle, angle it toward the lip on bottom of uidic module, Scrub Nurse
and press top forward to insert into housing, all in one motion. Ensure
that the drain bag hangs freely, and that tubing does not fall out of pouch.

7. Remove band from irrigation drip chamber tubing and aseptically Scrub Nurse
present drip chamber to Circulator.

8. Accept the drip chamber. Spike the irrigation bottle and hang it from the Circulating Nurse
irrigation pole. Squeeze drip chamber until it lls approximately 2/3 to
3/4 full.

CAUTION
IV pole rises automatically. To avoid stretching d rip chamber
tubing, and possibly pulling drip chamber out of bottle, tubing must
hang freely with no interference on left side of console.

WARNING!
Do not exceed maximum capacity of drain bag (500 ml). Excessive
pressure can result from exceeding drain bag maximum capacity and
potentially result in a hazardous condition for the patient.

8065751606 3.3
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Prime, Vacuum, and Vent Test

9. Connect the blue aspiration tubing luer to the white irrigation tubing luer. Scrub Nurse

10. The setup screen is automatically entered at startup or upon removal of Scrub Nurse or
the FMS after completion of a procedure. If not in setup screen, press the Circulating Nurse
Setup button, or access the setup screen via the remote control.

11. Press Prime FMS on the setup screen or Enter on the remote control. Scrub Nurse or
The IV pole automatically goes to the priming position and the system Circulating Nurse
performs three functions: prime, vacuum test, and vent test.

NOTE: After completion of priming, the vacuum test is performed. This

is immediately followed by a vent test. After successful completion of
vacuum and vent tests the prime status indicator will change from U/S
FMS Not Primed (red) to U/S FMS Primed (blue).

If the vacuum or vent test is not successful the system will display an
advisory.

3.4 8065751606
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U/S, OZil® Torsional, or NeoSoniX® Handpiece Setup and Test

12. Thread U/S tip onto U/S, OZil® torsional, or NeoSoniX® handpiece. Scrub Nurse
Tighten rmly using the tip wrench. Remove tip wrench and retain
for future tip removal. If tip is not securely attached, an error may be
generated and/or inadequate tuning will occur.

US TIP/WRENCH ASSEMBLY

U/STIP WRENCH

Figure 3-1 U/S Tip/Wrench Assembly

Mackool** series ultrasonic tips contain a polymer tubing. This necessary

part of the Mackool** tip provides additional thermal and uidic advantages.

polymer tubing

Mackool** Round Tip Mackool** Kelman® Tip

Figure 3-2 Mackool** Tips

WARNING!
Check for the presence and correct position of the polymer tubing on the
Mackool** tips. Never attempt to remove the tubing. Use of the Mackool**
tips without polymer tubing may result in a hazardous condition for the
patient.

CAUTION
Do not use the disposable tip wrench for subsequent cases; stripping
of the tip wrench may occur.

13. Thread infusion sleeve containing the BSI onto handpiece over the U/S Scrub Nurse
tip. Match the proper color coding between the tip and sleeve. Adjust
sleeve so it clears bevel on tip by approximately 1-2 mm, and orient port
holes correctly.

14. Connect irrigation and aspiration tubing to U/S, OZil® torsional, or Scrub Nurse
NeoSoniX® handpiece.

8065751606 3.5
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15. Remove protective cap from connector by retracting the sheath of Scrub Nurse
the connector and releasing cap. Line up red dot on handpiece cable
connector with red dot onInniti® Vision System front panel and plug
cable into console connector.

Figure 3-3 Protective Cap Removal

16. Hold handpiece with tip pointed down into test chamber. Press Enter Scrub Nurse
on the remote control (or Circulator press Fill on the setup screen). Fill
test chamber completely and slide it over end of handpiece. Ensure no
air bubbles are present in test chamber. Press handpiece into tray pouch
with tip pointed up. Ensure tubing is not kinked.

Place handpiece
vertically in pouch
formed with drape

Slide test chamber

over handpiece tip

BSS® irrigating fluid

in test chamber

Figure 3-4 Preparing Test Chamber and Placing Handpiece in Pouch.

3.6 8065751606
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 WARNINGS!
If stream of uid is weak or absent w hile lling test chamber, good uidics
response will be jeopardized. Good clinical practice dictates the testing
for adequate irrigation and aspiration ow prior to entering the eye.

Ensure that the tubings are not occluded during any phase of operation.

When using a bimanual procedure, ensure the irrigation handpiece and

settings have sufcient ow characteristics. Use of irrigation handpieces
or settings with insufcient ow characteristics may result in a uidic
imbalance and may cause a shallowing or collapsing of the anterior
chamber.

17. Press Enter on the remote control (or Circulator press Test Handpiece Scrub Nurse or
on the setup screen). After a very brief and successful tuning of the Circulating Nurse
handpiece, ow check will follow automatically. After a successful ow
check, the tune status indicator will change from Not Tuned (red) to
Tuned (green). The system will then advance to the surgery screen.

The IV pole returns to its last selected height, but if no memory has been
selected it returns to its default position.

WARNINGS!
If the handpiece test chamber is collapsed after tuning, there is
a potential of low irrigation ow through the handpiece and may
result in a uidic imbalance. This, in turn, may cause a shallowing or
collapsing of the anterior chamber.

Good clinical practice dictates testing for adequate irrigation, aspiration

ow, reux, and operation as applicable for each handpiece prior to
entering eye.

8065751606 3.7
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STANDARD AQUALASE® SYSTEM SETUP

Prepare Contents of AquaLase® Surgical Pak

1. Extend instrument tray out from the right or left side of console. Pull to Circulating Nurse
extend wire loop on tray.

2. If remote control is to be used during surgery, place it in the surgical tray Circulating Nurse
well. Verify remote control is functional by slightly raising or lowering
the IV pole.

3. Peel lid from AquaLase® surgical pak and aseptically transfer contents to Circulating Nurse
sterile eld.

4. Drape the tray support cover over the tray, remote control, and support Scrub Nurse
arm. Pull to extend wire loop on tray. Push drape downward through
open wire loop to form pouch.

5. Grasp Fluidic Management System (FMS), remove paper band from all Scrub Nurse
tubing, uncoil tubing and place in pouch.

6. Hold FMS by handle, angle it toward the lip on bottom of uidic Scrub Nurse
interface module, and top press forward to insert into housing, all in one
motion. Ensure that the drain bag hangs freely, and that tubing does not
fall out of pouch.

7. Insert AquaLase®/Balanced Salt Solution bottle into bottle receptacle Circulating Nurse

on front panel,
inserting bottle,then push
etched and rotate
arrow 1/8must
on bottle turn clockwise to secure.
be in alignment withWhen
top of
receptacle.

8. Aseptically present drip chamber/irrigation tubing to Circulator. Scrub Nurse

9. Accept the drip chamber. Spike the irrigation bottle and hang it from the Circulating Nurse
irrigation pole. Squeeze drip chamber until it lls approximately 2/3 to
3/4 full.

CAUTION
IV pole rises automatically. To avoid s tretching drip chamber
tubing, and possibly pulling drip chamber out of bottle, tubing must
hang freely with no interference on left side of console.

Do not exceed maximum capacityWARNING!

of drain bag (500 ml). Excessive
pressure can result from exceeding drain bag maximum capacity and
potentially result in a hazardous condition for the patient.

3.8 8065751606
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Prime, Vacuum, and Vent Test

10. Connect the blue aspiration line luer to the white irrigation line luer. Scrub Nurse

11. The setup screen is automatically entered at startup or upon removal of Circulating Nurse
the FMS after completion of a procedure. If not in setup screen, press the
Setup button.

12. Press Enter on the remote control (or Circulator press Prime FMS on the Scrub Nurse
setup screen). The IV pole automatically goes to the priming position
and the system performs three functions: prime, vacuum test, and vent
test.

After completion of priming, the vacuum test is performed. This is

immediately followed by a vent test. After successful completion of
vacuum and vent tests the prime status indicator will change from
AquaLase® FMS Not Primed (red) toAquaLase® FMS Primed (green).

If the vacuum or vent test is not successful the system will display an
advisory.

8065751606 3.9
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AquaLase® Handpiece Setup and Test

13. Prepare AquaLase® handpiece for use as described in theAquaLase® Staff

handpiece DFU.

14. Install AquaLase® tip onto AquaLase® handpiece. Tighten rmly using Scrub Nurse
the tip wrench. Remove tip wrench and retain for future tip removal.

15. Install infusion sleeve over tip and onto end of AquaLase® handpiece. Scrub Nurse
Adjust sleeve so it clears bevel on tip by approximately 1 mm, and orient
port holes correctly.

16. Connect irrigation, aspiration, and black-striped AquaLase® tubing to the Scrub Nurse
AquaLase® handpiece.

17. Grasp black-striped AquaLase® tubing spike from the pouch and spike Scrub Nurse
the AquaLase®/Balanced Salt Solution bottle.

18. Remove protective cap from connector by retracting the sheath of Scrub Nurse
the connector and releasing cap. Line up red dot on handpiece cable
connector with red dot onInniti® Vision System front panel connector
and plug cable into console connector.

19. Hold handpiece with tip pointed down into test chamber. Press Enter Scrub Nurse
on the remote control (or Circulator press Fill on the setup screen). Fill
test chamber completely and slide it over end of handpiece. Ensure no
air bubbles are present in test chamber. Press handpiece into tray pouch

with tip pointed up. Ensure that tubing is not kinked.

WARNING!
If stream of uid is weak or absent while lling test chamber, good uidics
response will be jeopardized. Good clinical practice dictates the testing
for adequate irrigation and aspiration ow prior to entering the eye.

3.10 8065751606
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20. Press Enter on the remote control (or Circulator press Test Handpiece on Scrub Nurse
the setup screen). After a very brief and successful tuning of the handpiece,
ow check will follow automatically. For the AquaLase® handpiece, a
momentary collapse of the test chamber is normal. After a successful
ow check, the tune status indicator will change from Not Tuned (red) to
Tuned (green). The system will advance to the surgery screen.

The IV pole returns to its last selected height, but if no memory has been
selected it returns to its default position.

WARNING!
Use of the U/S, OZil® torsional, NeoSoniX®, or AquaLase® handpiece in
the absence of irrigation ow and/or in the presence of reduced or lost
aspiration ow can cause excessive heating and potential thermal injury
to adjacent eye tissues.

If the handpiece test chamber is collapsed after tuning, there is

a potential of low irrigation ow through the handpiece and may
result in a uidic imbalance. This, in turn, may cause a shallowing or
collapsing of the anterior chamber.

Good clinical practice dictates testing for adequate irrigation, aspiration

ow, reux, and operation as applicable for each handpiece prior to
entering eye.

8065751606 3.11
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IRRIGATION/ASPIRATION HANDPIECE SETUP

1. Remove the blue luer aspiration line and white luer irrigation line from Scrub Nurse
the U/S, OZil® torsional, NeoSoniX®, or AquaLase® handpiece and
connect to the I/A handpiece.

2. This step is required when using Ultraow™* I/A handpiece with

threaded tip adapter.

Attach sterile I/A tip to I/A handpiece using tip wrench supplied in the Scrub Nurse
phaco pak.

CAUTION
Use of a tool other than Alcon tip wrench may cause damage to the
I/A tip and handpiece.

Thread infusion sleeve, without bubble suppression insert (BSI), over Scrub Nurse
the I/A tip until sleeve clears the tip’s aspiration opening. Orient the
irrigation port holes on the sleeve.

3. Press Fill until uid streams from both irrigation and aspiration ports (if Circulating Nurse
Irrigation Fill is enabled in System Settings, uid will only stream from
irrigation port). Ensure no air bubbles remain in irrigation or aspiration
pathways before continuing procedure.

WARNING!
If stream of uid is weak or absent while lling test chamber, good uidics
response will be jeopardized. Good clinical practice dictates the testing
for adequate irrigation and aspiration ow prior to entering the eye.

3.12 8065751606
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ANTERIOR VITRECTOMY PROBE SETUP
(using Vitrectomy Setup screen)

When the Anterior Vitrectomy step is entered, the Vitrectomy Setup screen
appears (see Figure below) unless turned Off in the Doctor Settings screen. This
setup screen assists the user through the proper set up and test of the selected probe.

If the Vitrectomy Setup screen is turned Off, you can eitherturn the Vitrectomy
Setup screen On (Custom/Doctor/General), or proceed to ANTERIOR
VITRECTOMY PROBE SETUP (without using Vitrectomy Setup screen).

Figure 3-5 Vitrectomy Setup Screen - The Switch Probebutton allows the
user to change selected probes if the desired probe is not displayed; this
button appears only if hardware forUltraVit® probe upgrade is installed.
After performing a set up step, pressing the Next Step button brings up

the screen for the next step. The Fill button allows the user to prime the
probe and to ll a test vessel for proper testing of the probe. Pressing the
Test button initiates an automated test sequence which veries secure
pneumatic connections, then applies pneumatic activation at a reduced
cut rate for visual verication of probe actuation.

1. Peel lid and aseptically transfer contents of pak to sterile eld. Circulating Nurse

2. Press the Ant Vit step button; the Vitrectomy Setup screen appears. Circulating Nurse/
Scrub Nurse
NOTE: In the next few steps the user will be instructed to press buttons
on the display screen. These buttons can be pressed on the display screen,
or they can be activated u sing the Forward/Back Arrow keys and Enter
key on the remote control.

3. Verify probe type - If desired probe is not displayed, press theSwitch Circulating Nurse/
Probe button to select probe being used. PressNext Step button. Scrub Nurse

4. Connect to console Vit ports - For 20 gauge Inniti® vitrectomy probe, Scrub Nurse
connect clear tubing connector to left Vit port. For 23 gaugeInniti®
UltraVit® probe, connect black and purple tubing connectors to left and
right Vit ports, respectively. PressNext Step button.

8065751606 3.13
For Reference Only
5. Connect aspiration tubing - Disconnect FMS irrigation and aspiration Scrub Nurse
tubing connectors from lens removal handpiece. Connect FMS blue
aspiration tubing connector to probe's blue aspiration tubing connector.
Press Next Step button.

6. Connect irrigating cannula - Connect FMS white irrigation tubing connector Scrub Nurse
to irrigating cannula, or optionally for a 20 gaugeInniti® vitrectomy
probe, to an irrigation sleeve added to probe's tip. PressNext Step button.

7. Press Fill then press Test - Priming of the vitrectomy probe is required Scrub Nurse
prior to use. With tip of probe and irrigating cannula in a cup of sterile
uid, press the Fill button. Ensure all air bubbles have been removed
from all tubing connected to the probe prior to use.

Verify probe actuation - While observing cutting port of probe, held Scrub Nurse
under surface of sterile uid, press the Test button. The system intitiates
an automated test sequence conrming secure connections and facilitates
visualization of probe cutter by applying a brief period of reduced cut rate.
The cutter should fully open and close when actuated. Press the Exit button.

8. The Vitrectomy Cut I/A or I/A Cut surgery screen appears on the front Circulating Nurse
display panel. Switching between Cut I/A and I/A Cut is done with the
Mode button at top center of surgery screen.

9. Press Irrigation Control up/down keys on the remote control (or Scrub Nurse/
Circulator press Bottle Height Adjustment Arrows on the setup screen) Circulating Nurse
to adjust bottle height. Vitrectomy probe is ready.

WARNINGS!
Do not test or operate vitrectomy probes unless tip of probe is
immersed in BSS ® sterile irrigating solution or distilled water or is
in surgical use. Irreparable damage to the handpiece and tip can
result if run dry.

After lling and testing, and before surgical use, verify that the probe
is properly actuating and aspirating. This may require lowering cut
rate to achieve good visualization. The port should always remain in
open position in footpedal position 1. If cutting portsi partially closed
while in position 1, replace the probe. Prio r to entry into the eye, a nd
with tip of probe in sterile irrigating solution, the surgeon should
step on the footpedal for visual verication that the p robe is cutting;
alternatively, press the Test button on the Vitrectomy Setup Screen:if
the cutter is observed to not fully close, or does not move when

the probe is actuated, replace the probe.

• If cutting port is parti ally closed while idle, replace the probe.
• If air bubbles are observed in the aspiration line or exiting the
probe tip during priming, replace the probe.
• If a reduction of cutting capability or vacuum is observed during
the surgical procedure, stop immediately and replace the probe.

3.14 8065751606
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ANTERIOR VITRECTOMY PROBE SETUP
(without using Vitrectomy Setup screen)

To set up the vitrectomy probe without using the Vitrectomy Setup screen,
follow the instructions below.

1. Peel lid and aseptically transfer contents to sterile eld. Circulating Nurse

2. Press the Ant Vit step button; the vitrectomy surgery screen appears. Circulating Nurse/
Scrub Nurse
3. If desired probe is not displayedin the button at the top of the vitrectomy Circulating Nurse/
surgery screen, press the button to select probe being used. Scrub Nurse

4. For 20 gauge Inniti® vitrectomy probe, connect clear tubing connector Scrub Nurse
to left Vit port. For 23 gaugeInniti® UltraVit® probe, connect black and
purple tubing connectors to left and right Vit ports, respectively.

5. Disconnect FMS irrigation and aspiration tubing connectors from lens Scrub Nurse
removal handpiece. Connect FMS blue aspiration tubing connector to
blue connector of vitrectomy probe.

6. Connect FMS white irrigation tubing connector to irrigating cannula, Scrub Nurse
or optionally for a 20 gaugeInniti® vitrectomy probe, to an irrigation
sleeve added to probe's tip.

7. Priming of the vitrectomy probe is required prior to use, and can be Scrub Nurse
performed using one of two methods.With tip of probe and irrigating
cannula in a cup of sterile uid:

• Independently use
1 to remove air irrigation
bubbles bythe
from depressing
probe’s the footpedal
irrigation line,toand
position
then use
reux to remove air bubbles from the probe’s aspiration tubing.
• Use the Fill command, if enabled in Doctor Settings, to simultaneously
remove air bubbles from the irrigation and aspiration lines, then return
to Ant Vit mode.
Ensure all air bubbles have been removed from all tubing connected to
the probe prior to use.

8. Testing of the vitrectomy probe should be performed prior to use. With Scrub Nurse
tip of probe and irrigating cannula in a cup of sterile uid, depress
footpedal to the cut position and observe probe's cutting port (to facilitate
visualization, reduce cut rate). The cutter should fully open and close
when actuated, and remain open when footpedal is released to position 0.

9. Switching between Cut I/A and I/A Cut is done with the Mode button at Circulating Nurse
top center of surgery screen.

10. Press Irrigation Control up/down keys on the remote control (or Scrub Nurse/
Circulator press Bottle Height Adjustment Arrows on the setup screen) Circulating Nurse
to adjust bottle height. Vitrectomy probe is ready.

– Always observe Warnings on previous page –

8065751606 3.15
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COAGULATION HANDPIECE SETUP

1. Using aseptic techniques, plug new or sterilized handpiece cable Scrub Nurse
connectors into Inniti® Vision System front connector panel.

2. Plug connector into new or sterilized coagulation handpiece. Scrub Nurse

3. Coagulation handpiece is ready.

3.16 LAST PAGE OF THIS SECTION 8065751606

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 SECTION FOUR
CARE AND MAINTENANCE

INTRODUCTION

This section of the manual is designed to inform the operator of basic care and
maintenance of the instrument. If a problem occurs on the instrument, contact
Alcon Technical Support or your local Alcon representative and give details of the
breakdown circumstances and effects. If there is an error message, write down the
number and message exactly as it appears on the screen. From these elements, a
specialized technician will evaluate the problem and determine the maintenance

requirements.
For optimum performance, it is the user’s responsibility to schedule preventive
maintenance service on the system and its accessories at least one time each year.
Alcon’s Field Service Engineers are trained and equipped to provide the highest
quality of workmanship.
CAUTION
There are no operator replaceable parts other than the fuse. Contact Alcon
Technical Services for all servicing issues .

WARNING!
The Infniti® Vision System battery can only be serviced by a factory-trained Alcon
service engineer. Access by untrained personnel can lead to injury.

8065751606 4.1
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UPON COMPLETION OF THE DAY'S SURGERY SCHEDULE

STEP ONE: Clean handpieces, cables, forceps, etc., as instructed in DFU's supplied
with each accessory.

WARNING!
If in the medical opinion of the physician a patient with a prion related disease
undergoes a high risk procedure, the instrument should be destroyed or be
processed according to local requirements.

STEP TWO: Remove irrigation bottle from hanger and set aside. Remove spike from
irrigation bottle and discard tubing.

STEP THREE: Eject FMS and discard.

STEP FOUR: Flip the irrigation bottle holder to its storage position.

STEP FIVE: Select Custom/Shutdown from the Surgery Screen. Select OK. IV pole
will go down to storage position before unit shuts off.

or

Press Standby power switch located at top of rear panel to remove operating power
from the system. IV pole will go down to storage position before unit shuts off.

WARNING!
Keep clear of the IV pole when it is in motion to prevent skin, hair, and/or clothing
from being trapped in the IV pole mechanism.

STEP SIX: Turn the Main power switch OFF. It is located at the bottom of the rear
panel above the power cord.

STEP SEVEN: Disconnect the power cable from the wall receptacle and wind the
cable around the cord wrap.

4.2 8065751606
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 STEP EIGHT: Inspect, and if required, clean footswitch bottom cover and under rear
section of treadle with water, alcohol, or mild soap and water. Remove any debris (see
Figure 4-1).
CAUTION
Debris, including uid residue, stuck on footswitch bottom or under rear section
of treadle may cause temporary malfunction of the footswitch.

Clean and remove debris from

this
fromarea under
bottom the treadle, and
of footswitch.

Figure 4-1 Footswitch Cleaning -Clean under rearsection of footswitch treadle toremove
debris that can interfere with its operation.

STEP NINE: If required, the console panels, the footswitch, and the remote control
may be wiped with alcohol, mild soap and water, or any germicidal solution that is
compatible with the plastic parts.

CAUTIONS
• Do not clean console or accessories using solvents, abrasives, or any cleaner
that is not compatible with plastic parts made of GE Cycoloy CU 6800 and
LEXAN 920A. Damage may result.
• Avoid spilling BSS® solution, or moisture of any kind, around the electrical
handpiece connectors.

STEP TEN: Place the footswitch and cable in its drawer at the bottom of the front
panel.

8065751606 4.3
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CARE AND CLEANING

The following tips are recommended for proper care of the Inniti® Vision System:
• The console panels, the footswitch, and the remote control may be wiped with
alcohol, mild soap and water, or any germicidal solution that is compatible with
the plastic parts; instructions begin on the prior page.
• The touch screen may be cleaned with a soft, non-abrasive cloth towel and a mild
commercially-available window cleaner. Apply the cleaner to the towel rather
than the touch screen.
• Follow cleaning and maintenance schedules outlined in this section of the manual.
• Periodically check chassis appearance.
• Pay attention to correct operation of controls, connectors, and indicators.
• Damaged hardware must be replaced to ensure safe operation. Call Alcon
Technical Services for assistance.

WARNING!
A qualied technician must perform a visual inspection of the following components
every twelve months:
• Warning Labels (see section one of this manual)
• Power Cord
• Fuses
In case of a deciency, do not use the system; call Alcon Technical Services.

A qualied technician must check ground continuity for leakage current every
twelve months to ensure they are within the applicable standards (for example:
EN60601-1/IEC601-1). Values must be recorded, and if they are above the applicable
standards, do not use the system; call Alcon Technical Services.

4.4 8065751606
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STERILIZATION INSTRUCTIONS

Please consult the accompanying Directions For Use (DFU) for cleaning, reprocessing, and
sterilization instructions for Alcon approved reusable accessories. The DFU will provide the
recommended time and temperature guidelines for steam autoclave cycles performed by Alcon, Inc.
The sterility assurance level achieved with these parameters must be validated by each surgical
facility. Please refer to Association for the Advancement of Medical Instrumentation (AAMI)
Standards or your facility’s standard procedures for the most current specications.

Additionally, per the Sterilizer Equipment Manual, the sterilizer reservoir is to be lled with distilled
or deionized water.

NOTE: The reusable items will withstand steam autoclave cycles at 134° C (273°F). Due to
the variations found in steam autoclaves and the variable bioburden on devices
in clinical use, it is not po ssible for Alcon to provide specic parameters to ensure
an adequate sterility assurance level. Validation of the individual autoclave, and
verication of the sterility assurance level achieved with a given steam sterilization
cycle, must be performed by each surgical facility. Please refer to below AAMI
Standards or your facility’s standard procedures for the most current specications.

8065751606 4.5
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FUSE REPLACEMENT

1. Turn the Main power switch OFF. It is located at the bottom of the rear panel
above the power cord. Unplug power cord from power source.

2. Insert a at surfaced instrument into opening located just below the fuse drawer.

3. Gently push tab up until it releases fuse drawer.

CAUTION

The tab must be pressed gently to ensure it does not break.

4. Remove the fuse drawer from the fuse module.

5. Gently remove and replace fuses. Contact Alcon Technical Services for the correct
rating and size.

6. Reinsert fuse drawer. A snap is heard when it is secured inside module.

7. Plug power cord into power source.

4.6 LAST PAGE OF THIS SECTION 8065751606

For Reference Only
 SECTION FIVE
TROUBLESHOOTING

INTRODUCTION

Table 5-1 is a general troubleshooting guide that addresses symptoms/observations

and what the operator can do to try and solve the observed problem. Figure 5-4 and
Table 5-2 are presented as aids to rapid location of failed or malfunctioning parts or
components in the Inniti® Vision System; they are not meant to replace standard
troubleshooting methods. In all cases, should the corrective actions not provide the
desired result, call your Alcon Technical Services Department.

Equipment Malfunction
The system communicates equipment malfunctions through the display of Advisories,
Warnings, and Faults based on the level of severity. Listed below is a general
sequence of events for each.

Advisories
An advisory is a message to the user (see Figure 5-1). The advisory may require user
intervention, or it may be for information purposes only. When an advisory condition
is detected, the following occurs:
• A tone is generated.
• A dialog is displayed indicating the advisory.

Figure 5-1 ADVISORIES SCREEN - This is a typical example of an Advisories dialog.

8065751606 5.1
For Reference Only
 Warnings
Warnings are generated to indicate a non-system fault (see Figure 5-2). When a
warning is detected, the following occurs:
• A tone is generated.
• Affected mechanisms are placed in a safe state.
• A dialog is displayed indicating the warning.

Figure 5-2 WARNINGS SCREEN - This is a typical example of a Warnings dialog.

Faults
System faults are the result of an exceptional condition resulting from an error or a
hardware failure that renders the software unable to carry out a requested service, or
one that results in unacceptable risk (see Figure 5-3). When a system fault is detected,
the following occurs:
• A tone is generated.
• All mechanisms are disabled.
• A dialog is displayed indicating the fault. If the fault occurs during system
initialization, shutdown, or when the touchscreen graphics software is unavailable,
the fault dialog will be displayed in English.
• All requests for functions are ignored, including key activations.

Figure 5-3 FAULTS SCREEN - This is a typical example of a Faults dialog.

5.2 8065751606
For Reference Only
 No message is displayed, but Follow the Problem Conditions table
unable to setup and operate as in this section of the operator’s man-
described in this operator's manual ual. If unable to fix the problem, or
Problem
and other applicable labeling. if the problem is not described in
Encountered
the troubleshooting table, contact
Alcon Technical Support or your
local Alcon representative.

Unit displays an Advisory number Follow the Advisories troubleshoot-

and message. These messages ing table in this section of the oper-
are displayed within a dialog box ator’s manual. If unable to fix the
and have a green border. problem, write down the Advisory
number and message exactly as it
appears on the screen, then con-
tact Alcon Technical Support or
your local Alcon representative.

Unit displays a Warning number Write down the Warning number and
and message. These messages message exactly as it appears on the
are displayed within a dialog box screen, then contact Alcon Technical
and have a yellow border. Support or your local Alcon repre-
sentative. Some or all of the functions
could be disabled . Do not use unit
unless the case is already started
and no back-up is available.

Unit displays a System Fault Write down the Fault number and
number and message. These message exactly as it appears on the
messages are displayed within a screen, then contact Alcon Technical
dialog box and have a red border. Support or your local Alcon repre-
sentative. Discontinue use of unit
until the problem is resolved.

Figure 5-4 TROUBLESHOOTING GUIDE - When a problem is encountered, refer to this chart rst.

8065751606 5.3
For Reference Only
 PROBLEM CONDITIONS

SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

Test chamber does not ll— 1. Restriction to irrigation inow. 1. Check for kinks in irrigation line or
insufcient irrigation. twisted infusion sleeve.
2. Bottle too low or handpiece too 2. Put bottle at 78 cm and put handpiece
high. at patient eye level.
3. Drip chamber not adequately lled 3. Squeeze drip chamber until 2/3 to
with uid. 3/4 full.
4. Clogged handpiece or tips. 4. Check handpiece and tips.

5. Drip chamber valve stuck. 5. Tap drip chamber with nger to free
ball valve.
6. Faulty Fluidic Management System 6. Replace FMS.
(FMS).

Vacuum check failure. 1. Improper FMS insertion. 1. Reinsert FMS.

Advisory 162
2. IRR and ASP fittings are not 2. Ensure both fittings are tightly
connected together securely. connected together.
3. Drip chamber not 2/3 to 3/4 full. 3. Flush irrigation line a nd fill drip
chamber halfway using Fill button
in Setup mode. Reprime.
4. Test chamber not on handpiece, or 4. Secure test chamber tightly onto
not secured tightly onto handpiece. handpiece.
5. Priming with HP attached. 5. Remove HP, then connect blue and
white luer ttings together.
6. Cracked blue luer tting. 6. Check tting and replace FMS as
necessary.
7. Faulty FMS. 7. Replace FMS.

Vent test failure or vacuum and vent 1. Restriction in irrigation or aspiration 1. Check kinked irrigation or aspiration
check failure. lines. lines or twisted tip cap sleeve.
Advisory 161, 164
2. Machine insufciently primed. 2. Press Test to reprime.
3. Drip chamber vent valve stuck. 3. Tap drip chamber with nger to free
ball valve.
4. Faulty FMS. 4. Reinsert FMS. Replace FMS if
problem persists.

Ultraow™* I/A handpiece leaking at 1. Loose tip. 1. Retighten tip.

tip and handpiece connection.
2. Damaged O-ring. 2. Retest. Inspect O-rings and replace,
as necessary. To replace:
• Using the specia l O-ring tool,
remove damaged O-ring.
•into
Rollplace
new on
O-ring
tip. off tool and roll it
3. Leak in tubing. 3. Replace tubing.

Table 5-1 PROBLEM CONDITIONS - Listed in this table are problem conditions that may be observed. The
observedSymptom is followed by the Probable Cause and its Corrective Action.

5.4 8065751606
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 SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

System does not power-up. 1. Main power switch in OFF position. 1. Turn main power switch near power
cord to ON position.
2. Blown power fuse. 2. Replace power fuse near power cord.

Test chamber collapses after tuning 1. Clogged handpiece or tips. 1. Check handpiece and tips irrigation
completed—does not rell. ow.
2. Drip chamber valve stuck. 2. Tap drip chamber with nger to free
ball valve.
3. Restriction to irrigation ow. 3. Check for kinks in irrigation line or
twisted infusion sleeve.
4. Wrong sleeve on tip. 4. Check for proper sleeve and tip size.

Backow regurgitation. Machine insufciently primed. Reprime.

Insufcient aspiration. 1. Loose blue luer ttings. 1. Reconnect securely.

2. Damaged O-ring (Ultrafow ™* I/A 2. Inspect O-ring and replace, as
handpiece only). necessary.

3. Clogged tip. 3. • Flush tip with sterile water or BSS®

sterile irrigating solution. Retest.
• Replace tip. Retest.
4. Kinked or damaged tubing. 4. Check tubing and/or replace FMS.
5. Cracked blue luer tting. 5. Check tting and/or replace FMS.

Test Handpiece Failed: Loose Tip. Loose tip. Retighten and retune.

Test Hand piece Failed: Tuning in Air. Attempted to tune tips in presence Fill test chamber completely. Retune.
of air.

Prime Complete / Test Handpiece 1. Faulty Handpiece. 1. Replace handpiece. Retest.

Failed.
2. Faulty Connector. 2. Unplug, reinsert into socket, retest.
3. Faulty tip. 3. Remove tip and replace if faulty.
Retighten. Retest.

4. Other. 4. Record the failed code number and

contact Alcon Technical Services
Department.
5. Aqu aLas e handpiece injection
®
5. Flush path with syringe and s terile
path clogged. uid.

No tune or loss of U/S power. 1. Handpiece tuned while hot. 1. Retune.

2. Loose tip. 2. Retighten and retune.

3. HP connector not seated correctly. 3. Disconnect and reinsertHP connector.

4. Faulty handpiece. 4. Try alternate handpiece.

8065751606 5.5
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 SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

Irrigation does not stop. System in Continuous Irrigation mode. Turn Continuous Irrigation off.

Air in irrigation line causing bubbles. 1. Drip chamber not sufciently full. 1. Fill drip chamber 2/3 to 3/4 full.
Flush irrigation line in Free Flow or
footpedal position 1.
2. Air in line or handpiece. 2. Tap handpiece 2-3X during ow test.

3. Loose irrigation luer tting. 3. Check irrigation line and reseat.

4. Improper priming. 4. Reprime per setup procedure.

Ant Vit probe does not work at all (no 1. Faulty probe. 1. Replace probe.
movement).
2. An actuation line lling with BSS® 2. Check for correct tubing connections,
uid due to improper setup. then replace probe.

Ineffective or poor Vit cutting. 1. Port not closing fully as the inner 1. Reduce cutting speed until port
cutter moves. closes completely.
2. Kinked, damaged or loose actuation 2. Check for damaged or kinked tubing;
tubing. straighten if necessary. Tighten any
loose luer ttings. Replace probe
if visual inspection shows any
damaged components.
3. Faulty probe (activated in air instead 3. Replace probe.
of uid).

“Calibration failed. Vitrectomy cut rate Internal pneumatics valve calibration Continue vitrectomy procedure with
will be limited to 800 cpm” Advisory has failed. limited cut rate and contact Alcon
is displayed at power up. Error code Technical Services Department.
752 or 753.

Remote control does not work. 1. Remote and system set on different 1. Verify system channel selection and
channels. remote channel select are set to same
channel (A, B, C, or D).
2. Batteries discharged. 2. Replace batteries in remote control.

IV pole does not retract completely System error. Turn system on, wait until system
upon shutdown. powers up, then turn system off using
Standby power switch located on upper
rear panel.

Footpedal not responding properly. 1. Footpedal was pressed when system 1. Release footpedal and power off
was powered up, or footpedal system. Make sure footswitch is
was pressed when footswitch was properly connected to system, and
plugged in. turn power back on, with footpedal
in full up position.
2. Footswitch connector not seated 2. Disconnect and reconnect footswitch
properly. cable connector.
3. Debris or BSS® uid residue under 3. Clean and remove debris.
rear section of treadle.
4. Console malfunction. 4. Disconnect and reconnect footswitch
cable connector.
5. Faulty footswitch. 5. Replace footswitch.

5.6 8065751606
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 SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

“Please Install Footswitch” Advisory 1. Improperly connected or discon- 1. Verify proper insertion of footswitch
is displayed. Error code 460. nected footswitch. connector (while footpedal/treadle is
in full up position).
2. Footswitch connector not seated 2. Disconnect and reconnect footswitch
properly. cable connector.
3. Faulty footswitch. 3. Replace footswitch.

System Fault occurs; entire system System Fault has several possible Carefully record all text appearing in
inoperative, red screen with stop sign causes. Fault screen, on display. Press and
is displayed. hold Standby switch for a few seconds

to turnthen
dark, system
turnoff, wait until
system back screen
on togoes
see
whether fault clears. Contact Technical
Services.

AquaLase® handpiece test failed. 1. Short circuit error. 1. Replace handpiece.

2. Open circuit error. 2. Ensure AquaLase® uid is owing
to handpiece.
Replace handpiece.
3. Flow obstruction. 3. Ensure AquaLase® uid is owing
to handpiece.
Flush injection ow path per hand-
piece DFU and verify uid exits tip.

Aqua Lase ® handpiece leak at tip 1. Loose tip. 1. Reapply wrench and tighten tip.
interface.
2. Missing or damaged gasket. 2. Replace tip.

Diminished pulsing performance. AquaLase® uid container near empty. Replace AquaLase® uid container.

Low irrigation ow. Irrigation sleeve too distal. Move sleeve so holes are proximal to
tip are.

“Doctor data invalid, U/S Occlusion, Dr. User restores, or selects Doctor Name Save data. U/S Occlusion settings will
XXXX” Advisory is displayed. that contains U/S Occlusion settings be removed.
Error code 471. which are no longer available.

8065751606 5.7
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 ADVISORIES

ERROR ERROR
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED

160 Advisory xxx: Reinsert FMS. Replace FMS if 278 Advisory xxx: Replace handpiece. If problem
problem persists. persists after restarting system, contact Alcon
Technical Services.
161-164 Advisory xxx: Please check ttings and reprime.
Replace FMS if problem persists. 279 Advisory xxx: Unknown handpiece detected.
165-167 Advisory xxx: Flow obstruction. Please check 280 Advisory xxx: Unsupported handpiece detected.
handpiece free ow.
281 Advisory xxx: Cautery comp lian ce error. If
169 Advisory xxx: Irrigation pressure is low. Please problem persists after restarting system, contact
check bottle and ttings. Alcon Technical Services.

170 Advisory xxx: Reux terminated. Reux uid 282 Advisory xxx : Coagulator error. If problem
volume depleted. persists after restarting system, contact Alcon
Technical Services.
171 Advisory xxx: Excessive pressure in drain bag.
Replace FMS. 350 Advisory xxx: Footswitch failure detected. Check
footswitch, clean under rear section of treadle and
175-176 Advisory xxx: Infusion pressure sensor calibra- remove debris if present. (Reference maintenance
tion error. Remove FMS. If problem persists section of Operator’s Manual.) Ensure treadle is
contact Alcon Technical Services. not depressed then reset footswitch. If condition
persists, contact Alcon Technical Services.
180 Advisory xxx: Invalid FMS ID. Replace FMS.
351 Advisory xxx: Footswitch failure detected. Check
181 Advisory xxx: Excessive Ambient Light. Unable and reset footswitch. If condition persists, con-
to calibrate FMS ID sensors. tact Alcon Technical Services.

182 Advisory xxx: Excessive Ambient Light. Unable 352 Advisory xxx: Footswitch failure, replace foot -
to read FMS ID. switch.
183 Advisory xxx: Remove MultiPak FMS? See 353 Advisory xxx: Footswitch failure detected. Check
MultiPak Directions-For-Use. and reset footswitch. If condition persists, con-
tact Alcon Technical Services.
250 Advisory xxx: Tuning in air. 450 Advisory xxx: Footswitch is depressed. Release
251 Advisory xxx: Insert handpiece. footswitch before pressing Prime FMS, Fill, or
Test Handpiece.
252 Advisory xxx: Multiple handpieces detected.
Remove a handpiece. 451 Advisory xxx: Can not recognize footswitch.
Please check footswitch connection and reset
254 Advisory xxx: Loose tip. footswitch. If condition persists, contact Alcon
Technical Services.
256-270 Advisory xxx: Replace handpiece. If problem
persists after restarting system, contact Alcon 460 Advisory xxx: Please install footswitch.
Technical Services.
461 Advisory xxx: Infniti ® backup power service
271 Advisory xxx: Two handpieces detected. Re- needed, contact Alcon Technical Services.
move a handpiece.
463 Advisory xxx: Invalid language(s) found during
272-274 Advisory xxx: Replace handpiece. If problem initialization. One or more installed languages
persists after restarting system, contact Alcon may not be available.
Technical Services.
464 Advisory xxx: The language specied by system
276 Advisory xxx: Ultrasound error. Release treadle settings is invalid.
and retry. If problem persists after restarting
system, contact Alcon Technical Services. 465 Advisory xxx: The tune sequence was inter -
277 Advisory xxx: Handpiece disconnected while rupted by removal of the handpiece.
applying U/S power. Release treadle then insert 466 Advisory xxx: AquaLase® handpiece test failed.
and tune handpiece. Handpiece tune failed. CheckAquaLase® hand-
piece connection.

Table 5-2 ERROR CODES - Listed in this table are error codes shown on the Infniti® Vision System
display panel when the system detects a problem. The error codes are separated between
Advisories, Warnings, and Faults.
5.8 8065751606
For Reference Only
 ADVISORIES

ERROR ERROR
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED

467 Advisory xxx: Replace FMS with an AquaLase® 570 Advisory xxx: AquaLase® handpiece failed.
FMS to allow tuning of the AquaLase® hand- Replace AquaLase® handpiece.
piece.
571 Advisory xxx: AquaLase® Error. Release trea-
468 Advisory xxx: The AquaLase® tune sequence dle, check uid container and retry. If problem
was interrupted by removal of the AquaLase® persists replace AquaLase® handpiece.
container.
572 Advisory xxx: AquaLase® handpiece disabled.
469 Advisory xxx: Doctor data corrupted. Retest handpiece.
471 Advisory xxx: Doctor data invalid, U/S Occlusion, 573 Advisory xxx: Aqua Las e® Error. Release
Dr. XXXX. treadle and retry. If problem persists contact
Alcon Technical Services.
473 Advisory xxx: Inserted handpiece does not
match selected handpiece. Change selected 574 Advisory xxx: AquaLase® handpiece disabled.
handpiece before proceeding. Check AquaLase® handpiece connection and
retest the handpiece.
474 Advisory xxx: AquaLase® handpiece test failed.
Retry test. If problem persists contact Alcon 575 Advisory xxx: Unknown AquaLase handpiece
Technical Services. detected.
475 Advisory xxx: CPU Battery should be replaced. 580 Advisory xxx: Replace AquaLase® container.
Contact Alcon Technical Services. Meanwhile,
you may proceed with surgical cases. 582 Advisory xxx: Aqua Las e® Error. Release
treadle and retry. If problem persists contact
476 Advisory xxx: Invalid console serial number. Alcon Technical Services.
Contact Alcon Technical Services.
583 Advisory xxx: AquaLase ® pressure failure.
478 Advisory xxx: Inserted handpiece does not Check uid container and retry. If problem
match selected handpiece. Change selected persists contact Alcon Technical Services.
handpiece before proceeding.
650 Advisory xxx: IV Pole jammed. Check for ex-
550-551 Advisory xxx: AquaLase® handpiece test failed. ternal obstacles. Pole may not have achieved
Retry test.Services.
Technical If problem persists contact Alcon desired height.
651 Advisory xxx: The IV pole cannot attain the
552 Advisory xxx: AquaLase® handpiece test failed. requested height due to the PEL setting.
Replace AquaLase® Fluid Container. If problem
persists contact Alcon Technical Services. 750 Advisory xxx: Pneumatic pump leakage. If
problem persists, contact Alcon Technical
553 Advisory xxx: AquaLase® handpiece test failed. Services.
Check uid container and retry test. If problem
persists contact Alcon Technical Services. 751 Advi sory xx x: Lo w pre ss ure. System is
charging…
554 Advisory xxx: AquaLase® handpiece test failed.
Tighten tip and check all uid connections. If 752,753 Advisory xxx: Calibration fai led. Vitrectomy
problem persists, replace tip. cut rate will be limited to 800 cpm.

555 Advisory xxx: AquaLase® handpiece test failed.

Flush handpiece injection pathway using ush
adaptor. If problem persists, replaceAquaLase®
handpiece and/or uid container.
556,558 Advisory xxx: AquaLase® handpiece test failed.
Check uid container and retry test. If problem
persists contact Alcon Technical Services.
559 Advisory xxx: AquaLase® handpiece test failed.
Check uid container and retry test. If problem
persists replace AquaLase® handpiece.
560 Adv isory xxx: AquaLase® handpiece test
failed. Check AquaLase® handpiece and retry
test. If problem persists replace AquaLase ®
handpiece.

8065751606 5.9
For Reference Only
 WARNINGS FAULTS

ERROR ERROR
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED

100-152 Warning xxx: Fluidics not available. Restart 400 System Fault xxx: Please restart system.
system. If problem persists after restarting
system, contact Alcon Technical Services. 401 System Fault xxx: Bus failure.
200-233 Warning xxx: Ultrasound and Coagulation not 402 System Fault xxx: 24 V Out of Tolerance.
available. Contact Alcon Technical Service.
403 System Fault xxx: Software error.
300-331 Warning xxx: Footswitch OK, but not avail -
able. Restart system. If problem persists after 404 System Fault xxx: Corrupt/Missing File.
restarting system, contact Alcon Technical
Services. 405 System
Version.Fault xxx: Incompatible Software
441 Warning xxx: AC power lost. System is shut -
ting down. 406 System Fault xxx: Failed software installation.
500-544 Warning xxx: AquaLase® not available. If this
function is required, restart system. If problem
persists after restarting system, contact Alcon
Technical Services.

600-635 Warning xxx: IV Pole not available. Restart

system. If problem persists after restarting
system, contact Alcon Technical Services.
Use external IV Pole.
700-740 Warning xxx: Vitrectomy and AquaLase® not
available. If these functions are required, re-
start system. If problem persists after restart-
ing system, contact Alcon Technical Services.

5.10 LAST PAGE OF THIS SECTION 8065751606

For Reference Only
 SECTION SIX
ACCESSORIES AND PARTS

In this section of the Inniti® Operator's Manual is a list of Alcon-approved accessories and
replacement items. Use of non-approved accessories cannot be permitted.

Please contact the Alcon Sales Department for in-service information prior to initial use of
handpieces, accessories, or paks.

For additional information, please contact the Alcon Sales Department.

Phone: Write:
(800) 862-5266 or Alcon, Inc.
(817) 293-0450 6201 South Freeway
Ask for Customer Service Fort Worth, TX. 76134-2099

INTERNATIONAL: Please contact your local Alcon Sales Ofce.

8065751606 6.1
For Reference Only
CATALOG NUMBER DESCRIPTION

8065741085. . . . . Ultrasound FMS, 30° Round, 0.9 mmABS® Tip

8065741086. . . . . Ultrasound FMS, 45° Round, 0.9 mmABS® Tip
8065741087. . . . . Ultrasound FMS, 30°Kelman®, 0.9 mm ABS® Tip
8065741088. . . . . Ultrasound FMS, 45°Kelman®, 0.9 mm ABS® Tip
8065741089. . . . . Ultrasound FMS, 30° Round, 1.1 mmABS® Tip
8065741090. . . . . Ultrasound FMS, 45° Round, 1.1 mmABS® Tip
8065741091. . . . . Ultrasound FMS, 30°Kelman®, 1.1 mm ABS® Tip
8065741092. . . . . Ultrasound FMS, 45°Kelman®, 1.1 mm ABS® Tip
8065741093. . . . . Ultrasound FMS, 30° Round, 0.9 mm FlaredABS® Tip
8065741094. . . . . Ultrasound FMS, 45° Round, 0.9 mm FlaredABS® Tip
8065741095. . . . . Ultrasound FMS, 30°Kelman®, 0.9 mm Flared ABS® Tip
8065741096. . . . . Ultrasound FMS, 45°Kelman®, 0.9 mm Flared ABS® Tip
8065741097. . . . . Ultrasound FMS, 30° Round, 1.1 mm FlaredABS® Tip
8065741098. . . . . Ultrasound FMS, 45° Round, 1.1 mm FlaredABS® Tip
8065741099. . . . . Ultrasound FMS, 30°Kelman®, 1.1 mm Flared ABS® Tip
8065741100. . . . . Ultrasound FMS, 45° Kelman®, 1.1 mm Flared ABS® Tip
8065750266. . . . . Ultrasound FMS, 30˚ Round, 0.9 mm Mackool** Tip
8065750267. . . . . Ultrasound FMS, 45˚ Round, 0.9 mm Mackool** Tip
8065750268. . . . . Ultrasound FMS, 30˚ Kelman®, 0.9 mm Mackool** Tip
8065750269. . . . . Ultrasound FMS, 45˚ Kelman®, 0.9 mm Mackool** Tip
8065750274. . . . . Ultrasound FMS, 30˚ Round, 1.1 mm Flared Mackool** ABS® Tip
8065750275. . . . . Ultrasound FMS, 45˚ Round, 1.1 mm Flared Mackool** ABS® Tip
8065750276. . . . . Ultrasound FMS, 30˚ Kelman®, 1.1 mm Flared Mackool** ABS® Tip
8065750277. . . . . Ultrasound FMS, 45˚ Kelman®, 1.1 mm Flared Mackool** ABS® Tip
®
8065750278. . . . . Ultrasound FMS, 30˚ Round, 0.9 mm Tapered ABS® Tip
8065750279. . . . . Ultrasound FMS, 45˚ Round, 0.9 mm Tapered ABS Tip
8065750280. . . . . Ultrasound FMS, 30˚ Kelman®, 0.9 mm Tapered ABS® Tip
8065750281. . . . . Ultrasound FMS, 45˚ Kelman®, 0.9 mm Tapered ABS® Tip
8065750282. . . . . Ultrasound FMS, 30˚ Round, 0.9 mm Tip
8065750283. . . . . Ultrasound FMS, 45˚ Round, 0.9 mm Tip
8065750284. . . . . Ultrasound FMS, 30˚ Kelman®, 0.9 mm Tip
8065750285. . . . . Ultrasound FMS, 45˚ Kelman®, 0.9 mm Tip
8065750286. . . . . Ultrasound FMS, 30˚ Round, 1.1 mm Tip
8065750287. . . . . Ultrasound FMS, 45˚ Round, 1.1 mm Tip
8065750288. . . . . Ultrasound FMS, 30˚ Kelman®, 1.1 mm Tip
8065750289. . . . . Ultrasound FMS, 45˚ Kelman®, 1.1 mm Tip
8065751035. . . . . Intrepid® Ultrasound FMS, 0.9 mm Ultra Tip
8065751036. . . . . Intrepid® Ultrasound FMS, 1.1 mm Ultra Tip
8065751039. . . . . Intrepid® Ultrasound FMS, 30° Kelman®, 0.9 mm Mini-Flared Tip, 0.9 mm Ultra
8065751040. . . . . Intrepid® Ultrasound FMS, 45° Kelman®, 0.9 mm Mini-Flared Tip, 0.9 mm Ultra

8065750157. . . . . 20 gaugeInniti® Vitrectomy Pak with Infusion Cannula

8065801351. . . . . Coaxial Anterior Vitrectomy Irrigation Sleeve - Reusable
8065750352. . . . . Coaxial Anterior Vitrectomy Irrigation Sleeve - Single Use
8065751196. . . . . 23 gauge Inniti® UltraVit® Vitrectomy Pak with Infusion Cannula

6.2 8065751606
For Reference Only
CATALOG NUMBER DESCRIPTION

0065-0796-40 . . . . . . . . AquaLase® Complete Pak CE

0065-0796-14 . . . . . . . . AquaLase® Complete Pak US
8065750846. . . . . . . . . . AquaLase® Kit with Injection Line, 1.1mm Tip
8065750893. . . . . . . . . . AquaLase® Kit with Injection Line, 1.1mm MI Tip
8065750904. . . . . . . . . . AquaLase® Kit with Injection Line, 1.1mm MI Tip,Kelman®
0065-0795-81 . . . . . . . . AquaLase® Solution CE (90 ml)

8065740842. . . . ... . . .Small Parts Kit, 0.9 mm MicroSmooth® High Infusion Sleeve
8065740872. . . . ... . . .Small Parts Kit, 1.1 mm MicroSmooth® High Infusion Sleeve
8065750159. . . . ... . . .Small Parts Kit, 0.9 mm MicroSmooth®
8065750160. . . . ... . . .Small Parts Kit, 1.1 mm MicroSmooth®
8065750517. . . . ... . . .Small Parts Kit, 0.9 mm MicroSmooth® Ultra Infusion Sleeve
8065750518. . . . ... . . .Small Parts Kit, 1.1 mm MicroSmooth® Ultra Infusion Sleeve
8065750519. . . . ... . . .Small Parts Kit, 1.1 mm MicroSmooth® Micro Infusion Sleeve

8065814301. . . . . . . . . . Ultraow™* IA Tip STR

8065814401. . . . . . . . . . Ultraow™* IA Tip CRVD
8065814501. . . . . . . . . . Ultraow™* IA 45°
8065814601. . . . . . . . . . Ultraow™* IA 90°
8065814701. . . . . . . . . . Ultraow™* IA 1200
8065814801. . . . . . . . . . Ultraow™* CNL STTL
8065814901. . . . . . . . . . Ultraow™* Luer
8065-A001-01. . . . . . . . Ultraow™* I/A Box
405-184. . . . . . . . . . . . . Ultraow™* Tool/0-rings
ULTRA O-RNG RPL . .Replacement O-ring
8065817002. . . . . . . . . . Ultraow™* Tip Protector, Standalone

355-1009 . . . . . . . . . . . .I/A Tip 0.5 mm

356-1007 . . . . . . . . . . . .I/A Tip 0.3 mm Small Bore
356-1009 . . . . . . . . . . . .I/A Tip 0.3 mm Small Bore Mod
356-1010 . . . . . . . . . . . .I/A Tip 0.3 mm Bent
356-1020 . . . . . . . . . . . .I/A Tip 0.3 mm Bent & Sand Blast
8065740970. . . . . . . . . .Silicone I/A Tip, Straight
8065740969. . . . . . . . . .Silicone I/A Tip, Bent
8065751012. . . . . . . . . . Intrepid® I/A Tip 0.3 mm
8065751013. . . . . . . . . . Intrepid® I/A Tip 0.3 mm Bent

8065817001. . . . . . . . . .Straight Tip, .3 mm

8065817201. . . . . . . . . .45° Bent Tip, .3 mm
8065817301. . . . . . . . . .90° Bent Tip, .3 mm
8065817501. . . . . . . . . .Irrigation Only Luer
8065817601. . . . . . . . . .Curved Tip, .3 mm
8065817801. . . . . . . . . .Threaded Tip - STTL
8065814101. . . . . . . . . . Ultraow™* IA Handpiece Comp
8065814201. . . . . . . . . . Ultraow™* IA Handpiece Only

8065751606 6.3
For Reference Only
CATALOG NUMBER DESCRIPTION

0065-0795-90 . . . . . . . .Balanced Salt Solution US (90 ml)

8065740749. . . . . . . . . .TurboHex Wrench
8065803602. . . . . . . . . .Instrument Sterilization Tray

8065750121. . . . ... . . .Handpiece, Inniti® Ultrasound

8065750120. . . . ... . . .Handpiece, Inniti® NeoSoniX®
8065750193. . . . ... . . .Handpiece, AquaLase®
8065750469. . . . ... . . .Handpiece, OZil® Torsional

8065750184. . . . . . . . . .Footswitch, Inniti®

8065740240. . . . . . . . . .Footswitch, Accurus®/Legacy®
8065750403. . . . . . . . . .Footswitch, Enhanced Inniti®

8065750468. . . . . . . . . .Remote Control, Inniti®

20000TP . . . . . . . . . . . .Transfer Pouch, Remote Control
8065740759. . . . . . . . . .IV Pole Extender

8065128402. . . . . . . . . .Bipolar Cable, 12 ft. Silicone, IEC-601

8065129002. . . . . . . . . .Bipolar Cable, 12 ft. Disp. Ster IEC-601
8065129101. . . . . . . . . .Forceps, Curved Jewelers/Iris
8065129301. . . . . . . . . .Forceps, Coaptation
8065129501. . . . . . . . . .Forceps, Straight Jewelers/Iris
8065804001. . . . . . . . . .Brush, 18 Gage, Straight
8065804201. . . . . . . . . .Brush, 20 Gage, Straight
8065804601. . . . . . . . . .Brush, 18 Gage, Curved
8065806701. . . . . . . . . .Brush, 18 Gage, Widestroke
8065807901. . . . . . . . . .Brush, 23 Gage, Tapered

8065751606. . . . . . . . . .Manual, Operator’sInniti®

8065750238. . . . . . . . . .Manual, Service Inniti®
8065750254. . . . . . . . . . Inniti® Data Card (MMC)
8065750232. . . . . . . . . .VideOverlay,Inniti®
8065751495. . . . . . . . . . VideOverlay, High Denition, Inniti®
8065751181. . . . . . . . . .Upgrade Ki t, Inniti® Wireless VideOverlay
8065751182. . . . . . . . . .Upgrade Ki t, Inniti® Wireless Network
8065751482. . . . . . . . . .Upgrade Kit, Inniti® UltraVit®
8065750243. . . . . . . . . .Cover, Dust,Inniti®

6.4 LAST PAGE OF THIS SECTION 8065751606

For Reference Only
 SECTION SEVEN
INDEX

Symbols Bubble suppression insert . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.22

Burst. .. . .. .. .. .. .. .. .. .. .. .. .. .. . .. .. . 2.75,2.79,2.84
®
20 gauge Infniti vitrectomy probe . . . . . . 2.26, 2.94, 3.13, 3.15 Burst % .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.88
23 gauge Infniti® UltraVit® pr obe. . . . . . . .2.2 6, 2.94, 3.13, 3.15 Buttons .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.38
% Time On .. .. . .. .. .. . .. .. .. .. .. .. .. .. .. .. ..2 .79, 2.83
C
A
Capsule wash . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.51
Abbreviation descriptions. . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3 Carea ndm aintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.1
Abbreviations used with theInfniti® V ision System . . . . . . 1.18 Caster wheels .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.4
Aboutd ialog... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.61 Catalog number.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. i
ABS®
..... .....
Accessories .. .. ........
.. .. .......
.. .. .....
.. .. .......
.. .. .....
.. .. .......
.. .. .... .2.21
2.2 Cataract grade . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.13, 2.63, 2.66
Cataract grade button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.41
Accessories and replacement items . . . . . . . . . . . . . . . . . . . . 6.1 Cataract grade key. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.16
Accessory equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3 Cataractl ensr emovals urgery. . . . . . . . . . . . . . . . . . . . . . . . . 3.1
Accurus®/Legacy® f ootswitch.. .. .. .. .. .. .. .. .. .. .. .. . 2.7 Cautions and Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.7
AC power connector. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5 CD/DVD drive .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.5
Addd octor .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.40 Change surgical parameters . . . . . . . . . . . . . . . . . . . . . . . . . 2.67
Adjust button and information bar . . . . . . . . . . . . . . . . . . . . 2.69 Check-outp rocedure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.1
Advanced tab . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.52 CirculatingN urse. .. .. . .. .. .. .. .. .. . .. .. .. .. .. .. .. . 3.1
Advisories.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5.1 Cleaning and sterilization instructions . . . . . . . . . . . . . . .4.4 , 4.5
Advisories, Warnings, and Faults . . . . . . . . . . . . . . . . . . . . . . 5.8 Coag Before Phaco steps . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.51
Alcon Laboratories, Inc. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . i Coagulationb rushes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.28
Alcon Sales Department . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6.1 Coagulation (Coag) mode of operation... ... ... ... ... .. 2.92
Alcon Technical Services Department . . . . . . . . . . . . . . . . . 1.16 Coagulation cords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.28
Alphabetizedoctorm enu . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.59 Coagulation footpedal control..... ..... ...... ...... .. 2.92
Amplitude. .. .. . .. .. .. .. .. .. . .. .. .. .. .. .. .. ..2 .78,2 .79 Coagulationforceps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.28
Anterior vitrectomy footpedal control . . . . . . . . . . . . . . . . . 2.94 Coagulation function. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.14
Anterior vitrectomy mode of operation . . . . . . . . . . . . . . . . 2.94 Coagulation handpieces . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.28
Anteriorv itrectomyp robes etup. . . . . . . . . . . . . . . . . . . . . . 3.13 Coagulationh andpieces etup . . . . . . . . . . . . . . . . . . . . . . . . 3.16
Anterior vitrectomy setup screen . . . . . . . . . . . . . . . . . . . . . 2.96 Coagulation power outputs . . . . . . . . . . . . . . . . . . . . . . . . . . 1.21
AquaLase® balanced salt solution. . . . . . . . . . . . . . . . . . . . . 2.30
AquaLase® balanced salt solution bottle. . . . . . . . . . . . . . . . 2.33 Collapse/Expand
Connector panel .b..uttons
.. .. ... . ... . ... . ... . ... . ... . .. ... . ... . ... . ... . ... . ... . ... . . 2.56
2.3
AquaLase®/BSS® bottle.. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.30 Connectors and outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
AquaLase® F MS .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2 .29, 3.9 Console.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.2
AquaLase® f ootpedal control . . . . . . . . . . . . . . . . . . . . . . . . 2.89 Console and accessories ..... ..... ..... ..... ...... ... 2.2
AquaLase® handpiece... .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.22 Consumable items. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.15
AquaLase® ha ndpiece setup and test. . . . . . . . . . . . . . . . . . . 3.10 Continuous . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.74, 2.78, 2.82
AquaLase® li quefaction mode of operation . . . . . . . . . . . . . 2.88 Continuous irrigation . . . . . . . . . . . . . . . . . . . . . 2.12, 2.43, 2.48
AquaLase® liquefactiont ip.. . . . . . . . . . . . . . . . . . . . . . . . . 2.33 Control buttons .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. 2.38
AquaLase® o cclusion . .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.60 Copy button.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.57
AquaLase® surgicalp ak .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 3.8 Copy/Deletedialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.54
AquaLase® s ystem setup.. .. .. .. .. .. .. .. .. .. .. .. .. .. . 3.8 Copy/Delete - h andpiece tip selections. . . . . . . . . . . . . . . . . 2.56
Aspiration bypass system . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.21 Cord wrap .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.5
Aspiration control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.91 Corrective actions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 .1, 5.4
Aspiration/Vacuum adjustments . . . . . . . . . . . . . . . . . . . . . . 1.11 Custom button. . . . . . . . . . . . . . . . . . 2.47, 2.58, 2.60, 2.61, 2.66
Custom drop list menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.47
B Custom Pak® surgical procedure pack. . . . . . . . . . . . . . . . . 2.31
Backup / Delete / Restore . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.55 Custom pulse. . . . . . . . . . . . . . . . . . . . . . . .2 .52, 2.76, 2.80, 2.85
Back up or restore system settings .. . . . . . . . . . . . . . . . . . . . 2.6 Cut I/A.. . .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. ..2 .94, 3.14
batteries are installed..... ...... ...... ...... ...... .. 2.17 Cut rate .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.94

battery
bimanual.. irrigation
.. .. .. .. .... ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . ..
. . .2.26
1.7 D
Bottleh anger.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.4 Data card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.18, 2.54, 2.6
Bottleh eight. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.42 Default grade.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.50
Bottle Height Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . 2.49 Debrillatory devices... ...... ...... ..... ..... ..... 1.14
Brush... ... ... ... ... ... ... ... ... ... ... ... ... ... . 2.92 Delete ... ... ... ... ... ... ... ... ... ... ... ... ... ... 2.57
Brushes ..... ..... ..... ...... ...... ...... ...... .. 2.28 Description .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.1
BSI ..... ...... ...... ..... ..... ..... ..... ..... .. 2.22 Detents .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.10
®
BSS irrigating uid .... ..... ..... ..... ..... ..... .. 2.30 DFU. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . viii, 2.32, 2.33, 4.5

8065751606 7.1
For Reference Only
Diagnostics .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 3.1 G
Dialogs .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.38
Dimensions .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 1.18 General information .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.1
Directions For Use (DFU) . . . . . . . . . . . . . . . . . . 2.32, 2.33, 4.5 General tab .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.48
Disassemblya ndc leaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.1 Groundconnector.. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. . 2.5
Display bar .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.69
Display panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .3, 2.38
H
Display screens .. .. .. . .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.38 Handpiece care .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. . 1.8
Doctor name .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.66 Handpiecesetup and test. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.5
Doctor name button.. .. .. .. .. .. .. .. .. .. .. .. .. .. .2 .40,3 .2 Handpieces, tips, and infusion sleeves . . . . . . . . . . . . . . . . . 2.19
Doctor name dropdown list. . . . . . . . . . . . . . . . . . . . . . . . . . 2.63 Handpiece tips. .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. 1.10
Doctor settings dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.48 Handpiece tip selections ..... ...... ...... ...... ..... 2.56
Doctor/system settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.47 Handpiece type .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. 2.66
Drip chamber . .. .. .. .. .. .. . .. .. .. .. .. .. .. .. .. ..3 .3, 3.8 Handpiece type button .. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.40
Drop list menu..... ..... ..... ..... ...... ...... .... 2.47 Hazardouss ubstances.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3
Dynamicr ise.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.69 Heel switches .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.7
High denition IVO ... ..... ...... ...... ..... ..... . 2.34
E
Edit ... ... ... ... ... ... ... ... ... ... ... ... ... ... .. 2.57
I
Electrical interconnections . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5 I/ACut. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . .. .. ..2 .94, 3.14
Electricalr equirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.18 I/Ahandpiece . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .24, 3.12
Electromagnetic emissions . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.4 I/Atips. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . .. .. ..1 .10, 2.24
Electromagnetic immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.5 I/Atipwrench.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .32,2 .33
EMCs tatement... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 1.4 Icons used with the Infniti® V ision System . . . . . . . . . . . . . 1.19
Enhanced Infniti® f ootswitch .. .. .. .. .. .. .. .. .. .. .. .. . 2.4 IEC standard .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 1.3
Enterk ey.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.17 Infniti®F MS... ... ... ... ... ... ... ... ... ... ... ... . 2.29
Environmental considerations. . . . . . . . . . . . . . . . . . . . . . . . . 1.3 Infniti® f ootswitch ... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.4
Environmentall imitations. . . . . . . . . . . . . . . . . . . . . . . . . . . 1.18 Infniti® AquaLase® p ak.. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.33
Equipment malfunction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.1 Infniti®p aks..... ... ... ... ... ... ... ... ... ... ... .. 2.31
Errorc odes. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5.8 Infniti® U/Sf amilyo fp aks. . . . . . . . . . . . . . . . . . . . . . . . . . 2.32
Error conditions .. .. . .. .. .. . .. .. .. .. .. .. .. .. .. .. .. . 3.1 Infniti® V ideOverlay (IVO) system . . . . . . . . . . . . . . .1. 14, 2.34
Exit button.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 3.14 Infniti® Vision System . . . . . . . . . . . . 1.1, 1.2, 1.3, 2.1, 2.4, 2.5,
. . . . . . . . . . . . . . . . . . . . . . . . 2.6, 2.7, 2.8, 2.10, 2.14, 2.15, 2.18
F
Infniti® V ision System operator interface. . . . . . . . . . . . . . . 2.38
Infniti® UltraVit® p robe . . . . . . . . . . . . . . .2. 26, 2.94, 3.13, 3.15
Fault and error
Faults.... conditions
... ... ... ... ..... . ..... . ..... . ..... . ..... . ..... . ..... . ..... . ..... . .. 3.1
5.2 Infniti® vitrectomy probe . . . . . . . . . . . . . .2.2 6, 2.94, 3.13, 3.15
Features of the Infniti® V ision System . . . . . . . . . . . . . . . . . . 1.2 Info window .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.57
Fill before/after I/A steps . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.51 Infusion pressure drop..... ..... ..... ..... ...... .... 2.50
Fill button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.64, 2.96, 3.14 Infusion sleeve . . . . . . . . . . . . . . . . . . . . . . . . . . 2.19, 2.22, 2.33
Fill mode of op eration for irrigation/aspiration . . . . . . . . . . 2.91 Infusions leevewithB SI. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.32
Fill step .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.91 Instrument tray .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. . 2.4
Fixed footpedal control. . . . . . . . . . . . . . . . . . . . . . . . .2 .10, 2.73 Intelligent phaco . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.53
Flow check .. . .. .. .. .. .. .. . .. .. .. .. .. .. .. .. .. .3 .7, 3.11 Interference with other devices. . . . . . . . . . . . . . . . . . . . . . . . 1.4
Fluidic Management System (FMS) . . . 2.2, 2.29, 2.32, 2.33, 3.3 Intrepid®F MS... ... ... ... ... ... ... ... ... ... ... ... 2.29
Fluidics Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.67 Irrigating cannula . . . . . . . . . . . . . . . . . . . . . . . . 2.26, 3.14, 3.15
Fluidics module.. .. .. .. .. .. . .. .. .. .. .. .. .. .. .. .. .. . 2.2 Irrigation/Aspiration footpedal control. . . . . . . . . . . . . . . . . 2.90
FMS. . . . . . . . . . . . . . . . . . . . . . . . . 2.2, 2.32, 2.33, 2.63, 3.3, 3.8 Irrigation/Aspiration handpiece setup. . . . . . . . . . . . . . . . . . 3.12
Footpedal.................................... ..... 2.7 Irrigation/Aspiration mode of operation . . . . . . . . . . . . . . . . 2.90
Footpedal control . . . 2.9, 2.73, 2.77, 2.81, 2.89, 2.90, 2.92, 2.94 Irrigation Control . . . . . . . . . . . . . . . . . . . . . . . . 2.15, 2.42, 2.66
Footpedal detents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.10 Irrigation ll .. .. .. .. .. .. .. .. .. .. .. .. .. . . 2.51, 2.59, 2.64
Footpedal positions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.9 Irrigation fo otswitch be fore p haco st eps. . . . . . . . . . . . . . . . 2.51
Footpedal switches .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.10 Irrigation sleeve . . . . . . . . . . . . . . . . . . . . . . . . . 2.26, 3.14, 3.15
Footswitch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4, 2.7, 4.3 Irrigation up or irrigation down . . . . . . . . . . . . . . . . . . . . . . 2.12
Footswitch button . . . . . . . . . . . . . . . . . . . . . . . . 2.10, 2.45, 2.66 IVO... ... ... ... ... ... ... ... ... ... ... ... ... ... .. 2.34
Footswitch cable connector.. .. .. .. .. .. .. .. .. .. .. ..2 .4,3 .2 IV pole. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4, 2.43
Footswitchc abler outing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.8 IV pole extender .. .. . .. .. .. .. .. .. .. .. .. . .. .. .. .. .. 2.58
Footswitch drawer.. .. . .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.4 IV pole height . .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. 2.49
Footswitches used with theInfniti® V ision System . . . . . . . 2.11
K
Forceps .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. .. ..2 .28, 2.92
Frontc onnectorp anel.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.3 Key tone .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.38
Front display panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .3, 2.38
Fuse drawer.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.5
Fuse replacement . .. . .. .. .. . .. .. .. .. .. .. .. .. .. .. .. . 4.6

7.2 8065751606
For Reference Only
L P
Labeling on Infniti® V ision System .. . . . . . . . . . . . . . . . . . 1.20 Pacemakers or implanted debrillatory devices.. .. .. .. .. 1.14
Label selection button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.56 Paks.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. ..1 .15, 2.31
Lens removal surgery .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.1 Parameter selection button . . . . . . . . . . . . . . . . . . . . . . . . . . 2.16
Limited warranty....... ..... ..... ..... ..... ..... .. 1.17 Parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6.1
Linear footpedal control . . . . . . . . . . . . . . . . . . . . . . . . .2 .9, 2.73 Patient Eye Level (PEL) . . . . . . . . . . . . . . . . . . . . . . . .2 .42, 2.50
List of gures ............................ ........... v Performance specications ...... ...... ...... ...... .. 1.18
Listo ft ables... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. ..v ii Phacoemulsication setup ...... ..... ..... ..... ..... .. 3.3
Logo screen.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 3.1 Phacoh andpieces .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. 2.19
Longitudinal/Torsional ratio . . . . . . . . . . . . . . . . . . . . . . . . . 2.53 Phaco power Limit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.73
Lower and upper limits . . . . . . . . . . . . . . . . . . . . . . . . .2 .69, 2.73 Phaco pulse on time .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.53
Plug in the footswitch..... ..... ...... ...... ...... ... 2.8
M Pole extender.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.58
Mackool** tip . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.10, 2.21, 3.5 Polymer tubing .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. 1.10
Magnitudel imit.. . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.88 Power module.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.5
Main powerswitch.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.5 Powero ff.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.61
Main window .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .39, 2.65 Power switch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .6, 3.1,3.2
Malfunction.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 5.1 Power up sequence.. .. . .. .. .. .. .. .. . .. .. .. .. .. .. .. . 3.1
Manual revision record. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .ii PPS. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .2 .79,2 .83
Metrics display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .43, 2.66 Preface..... ..... ..... ...... ..... ..... ..... ..... .. viii
MicroSmooth® i nfusion sleeves . . . . . . . . . . . . . . . . . .2 .22, 2.23 Pre-phaco coagulation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.92
Mode button .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.67 Preventive maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.1
Movingt hei nstrument. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4 Prime... ... ... ... ... ... ... ... ... ... ... ... ... ... .. 3.9
Multi Media Card (MMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.6 Prime FMS .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 3.4
PrimeF MSb utton.. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. 2.63
N Prime sequence.. .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. 2.63
Probablec ause .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5.4
Navigating the Infniti® Vision System user screens . . . . . . . 2.38
Problem ................................. ......... 5.1
NeoSoniX® burst .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.79
Problem conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.4
NeoSoniX® continuous .. . .. .. .. .. .. .. .. .. .. .. .. .. .. 2.78
Procedurals tepb uttons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.72
NeoSoniX® customp ulse.. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.80
Procedural steps. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. 2.72
NeoSoniX® f ootpedal control . . . . . . . . . . . . . . . . . . . . . . . . 2.77
Procedure type .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. 2.66
NeoSoniX® handpiece... .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.19
Procedure type button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.41
NeoSoniX® m ode of operation . . . . . . . . . . . . . . . . . . . . . . . 2.77
Product service .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. 1.16
NeoSoniX® p ulse.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.79
Next step button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .96, 3.13 Programming th efo otswitch tr eadle. . . . . . . . . . . . . . . . . . . 2.46
Program the footswitch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.7
Nurse... ... ... ... ... ... ... ... ... ... ... ... ... ... .. 3.1 Progressb ar.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.63
O Pulse. .. . .. .. .. .. .. .. .. .. .. .. .. .. . .. .. . 2.74,2.79,2.83
Pulser ate.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.88
Occlusiont ones.. . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . . 1.12
Occlusion watch off/on. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.70 R
Off ms .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. ..2 .75, 2.79
Rearp anel.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.5
Off-time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.76,2 .78,2 .80
Recycle .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 1.3
On ms .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. ..2 .75, 2.79 Reux ..... ..... ..... ...... ...... ..... ..... ..... 2.12
On ms - Limit / Off ms - Limit . . . . . . . . . . . . . . . . . . .2. 80, 2.85 Reux offset .......... ...... ...... ..... ..... ..... 2.50
On-time.. .. .. .. . .. .. .. .. .. .. .. .. .. .. .. .. .. ..2 .76, 2.80
Remote battery low. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.17
Operating instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.1
Remote channel.. .. .. .. .. .. .. . .. .. .. .. .. .. .. .. .. .. 2.58
Operator interface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.38
Remote control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 .18, 2.14
O-ring tool.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.25
Remote control batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.17
Oscillations.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .77,2.81
Remote control channel . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.18
OZil® I P.. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. . 2.52, 2.53, 2.87
Remote control keys and buttons . . . . . . . . . . . . . . . . . . . . . 2.15
OZil® I P dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .70, 2.86
Remote control settings dialog .. . . . . . . . . . . . . . . . . . . . . . 2.18
OZil®I P feature.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.86
Rename.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.57
OZil®I Picon.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.70
®
Replacementi tems .. .. . .. .. .. .. .. .. . .. .. .. .. .. .. .. . 6.1
OZil
OZil®Ifootpedal
P settingsc... .. ... . ... . ... . ... . ... . ... . ... . ... . ... . ... . ... . ... . ... . ... . .. 2.53
ontrol 2.81 Reset... ... ... ... ... ... ... ... ... ... ... ... ... ... . 2.57
OZil®m ode of operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.81 S
®
OZil t orsional handpiece. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.19
OZil® t orsional before phaco. . . . . . . . . . . . . . . . . . . . . . . . . 2.84 Salesd epartment. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. . 6.1
Save... ... ... ... ... ... ... ... ... ... ... ... ... ... .. 2.57
Savea s ... ... ... ... ... ... ... ... ... ... ... ... ... .. 2.57
Save dialog .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.54
Scrub nurse .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 3.1

8065751606 7.3
For Reference Only
Self-test.. .. .. .. .. .. . .. .. .. .. .. .. .. .. .. .. .. .. ..2 .1, 3.1 Tips ... ... ... ... ... ... ... ... ... ... ... ... ... ... .. 2.21
Separationdistances.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.6 Tip selection dropdown display . . . . . . . . . . . . . . . . . . . . . . 2.56
Service..... ..... ..... ..... ...... ...... ...... .... 1.16 Tip type.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.66
Servicingi ssues.. .. .. . .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 4.1 Tip type button .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. 2.41
Setting remote channel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.58 Tip wrench . .. .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .2 .32, 3.5
Setup and check-out procedure. . . . . . . . . . . . . . . . . . . . . . . . 3.1 Toe switches . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .7, 2.10
Setup button .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.72 Tones. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 .12, 2.6, 2.38, 2.60
Setup screen .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .38, 2.39 Torsionalamplitude . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.81
Setupstatuswindow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.62 Torsional before phaco . . . . . . . . . . . . . . . . . . . . . . . . .2 .49, 2.84
Setup steps .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.63 Touch screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .3, 2.38
Shipping.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 1.16 Tray support cover . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .32, 2.33
Shutdown .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 4.2 Troubleshooting .. .. . .. .. .. .. .. .. .. .. .. . .. .. .. .. .. . 5.1
Shutdownb utton.. .. . .. .. .. . .. .. .. .. .. .. .. .. .. .. .. 2.61 Troubleshooting guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.3
Shut down system.. .. .. .. .. . .. .. .. .. .. .. .. .. .. .. .. . 2.6 Tuning of the handpiece . . . . . . . . . . . . . . . . . . . . . . . . .3. 7, 3.11
Side panel.... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.6 Turn system power ON. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.2
Sleeves .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.22
Smart pulse .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.75 U
Software a nd hardware r evisions . . . . . . . . . . . . . . . . . . . . . 2.61 Ultraow™* I/A handpiece .. . . . . . . . . . . . . . . . . . . .2 .24, 3.12
Sonic oscillations .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.77 Ultrasonic oscillations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.81
Soundd ialog.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.60 Ultrasoundb urst. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. 2.75
Source node manipulation buttons . . . . . . . . . . . . . . . . . . . . 2.57 Ultrasound continuous . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.74
Speakers .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.6 Ultrasoundc ustomp ulse. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.76
Specications ........ ...... ...... ...... ...... .... 1.18 Ultrasoundp ulse.. .. . .. .. .. .. .. .. . .. .. .. .. .. .. .. .. 2.74
Standard IVO. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.34 Ultrasound (U/S) mode of operation ... ... ... ... ... ... . 2.73
Standbyp owers witch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.6 UltraVit® p robe . . . . . . . . . . . . . . . . . . . . . .2 .26, 2.94, 3.13, 3.15
Standby switch .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 .1, 3.2 Universal precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.4
Stationary step buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.72 U/S footpedal control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.73
Step advance/back. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.12 U/S handpiece. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . .. .. 2.19
Stepb uttons.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.72 U/S mode of operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.73
Steps... ... ... ... ... ... ... ... ... ... ... ... ... ... . 2.71 U/S tips .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.21
Steps tab... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.51 U/S tip with tip holder/wrench .. . . . . . . . . . . . . . . . . . . . . . 2.32
Sterilization instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.5
Surgery button. .. .. .. .. .. .. . .. .. .. .. .. .. .. .. .. .. .. 2.64 V
Surgeryc ontrols. .. .. .. .. .. . .. .. .. .. .. .. .. .. .. .. .. 2.67
Vacuum bar.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.63
Surgery control window .. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.66
Surgery menu.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.71 Vacuum
Vacuum control
range for.. I/A
.. ..tips
.. .... .... .... .... .... .... .... .... .... .... .... .. .... .... 1.10
2.91
Surgery modes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.73
Vacuumt est.. . .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. ..3 .4,3 .9
Surgery screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .38, 2.65
Vacuum threshold (% of vacuum limit) . . . . . . . . . . . . . . . . 2.53
Surgerys teps... .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.71
Vacuum tone .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 1.12
Surgicalp arameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.66
Vent test.. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. .. ..3 .4, 3.9
Surgical team. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.1
Vent time adjustment..... ..... ..... ...... ...... .... 2.50
Switchf unctions. .. .. .. .. .. . .. .. .. .. .. .. .. .. .. .. .. 2.10
VideOverlay .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 .14, 2.34
Switch probe button . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .96, 3.13
VideOverlay connection diagram . . . . . . . . . . . . . . . . . . . . . 2.36
Symptom.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 5.4
VideOverlayf rontp anel. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.34
System power .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 3.2
VideOverlayon/off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.13
System power off . .. . .. .. .. . .. .. .. .. .. .. .. .. .. .. .. 2.61
System setup.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 3.2 VideOverlay rear panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.35
System specications.. ......
Vit before/after I/A steps. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.51
...... ...... ...... .... 1.18
Vit cutter .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.94
Systemss ettingsd ialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.58
Vitc uttero n/off.. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. 2.13
System status.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 2.62
Vitrectomy bottle height maintenance . . . . . . . . . . . . . . . . . 2.49
T Vitrectomy footpedal control . . . . . . . . . . . . . . . . . . . . . . . . 2.94
Vitrectomy mode of operation . . . . . . . . . . . . . . . . . . . . . . . 2.94
Tableo fc ontents.. .. . .. .. .. . .. .. .. .. .. .. .. .. .. .. .. .. iii Vitrectomy probe . . . . . . . . . . . . . . . 1.11, 2.26, 2.94, 3.13, 3.15
Take-backs ystems .. . .. .. .. . .. .. .. .. .. .. .. .. .. .. .. . 1.3 Vitrectomy setup screen . . . . . . . . . . . . . . . . . . . . . . . .2 .96, 3.13
TechnicalSe rvicesD epartment. . . . . . . . . . . . . . . . . . . . . . . 1.16 Voice conrmations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60
Telephone .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. i Volume levels . .. .. .. .. .. .. .. .. .. .. .. .. . .. .. .. .. .. 2.60
Test button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 .96, 3.14
Test chamber . . . . . . . . . . . . . . . . . . . . . . . . .2 .32, 2.33, 3.6, 3.10 W
Test handpiece button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.64
Warnings.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 5.2
Threadedt ipa dapter.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.24
Warnings, cautions, and notes. . . . . . . . . . . . . . . . . . . . . . . . . viii
Threshold .. .. .. .. .. .. .. .. . .. .. .. .. .. .. .. .. ..2 .78, 2.79
Warranty..... ...... ...... ...... ...... ..... ..... . 1.17
Timing congurations.. . . . . . . . . . . . . . . . . . . . 2.74, 2.78, 2.82
Weight.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 1.18
Tips ... ... ... ... ... ... ... ... ... ... ... ... ... ... .. 2.19

7.4 LAST PAGE OF THIS SECTION 8065751606

For Reference Only