Ivent201 - Manual de Usuario (001-099)

GE Healthcare
iVentTM201
User’s Reference Manual
Revision: 13
VersaMed, a General Electric Company, doing business as GE Healthcare.
Calling for Help
Owner’s Record
The model number and serial number of your iVentTM201 are located on the rear panel of
your ventilator. Record the serial number in the space below in case service or support is
necessary.
Model Number:
Serial Number:
Customer Service
If you have a ventilator problem you cannot solve and you purchased your ventilator directly from GE,
call:
US number 800-345-2700 - Customer Service
If you have a ventilator problem that you cannot solve and you purchased your ventilator from an
authorized GE distributor, please contact your distributor directly to report the problem.
TABLE OF CONTENTS
1 INTRODUCTION .................................................................................................................................................. 1
Introduction .......................................................................................................................................................................................... 3
How to Use This Manual ................................................................................................................................................................. 4
Looking at the iVent™201 .............................................................................................................................................................. 5
Cautions and Warnings .................................................................................................................................................................. 7
Symbols and Labels .......................................................................................................................................................................... 8
Performance Parameters ........................................................................................................................................................... 12
Specifications.................................................................................................................................................................................... 13
Monitored Data Range, Resolution and Accuracy .......................................................................................................... 13
Size and Weight ............................................................................................................................................................................... 15
Ventilation Modes ........................................................................................................................................................................... 15
Environmental Specifications.................................................................................................................................................... 16
Power Supply .................................................................................................................................................................................... 16
O2 Supply Specifications ............................................................................................................................................................. 17
Ventilation Performance and Controlled Parameters ................................................................................................... 17
Pulse Oximetry Specifications................................................................................................................................................... 18
Standards and Safety Requirements .................................................................................................................................... 19
User Adjustable Alarms ................................................................................................................................................................ 22
Additional Alarms and Indicators ............................................................................................................................................ 23
Waveforms and Diagnostics Packages ............................................................................................................................... 23
Intended Use ..................................................................................................................................................................................... 25
Use of the iVentTM201 With MRI ............................................................................................................................................. 25
MRI Conditional Tests Specifications ..................................................................................................................................... 29
2 SETTING UP ....................................................................................................................................................... 31
Introduction ....................................................................................................................................................................................... 32
Power Connection .......................................................................................................................................................................... 32
External Power ................................................................................................................................................................................. 32
Internal Battery ................................................................................................................................................................................ 35
Oxygen Supply ................................................................................................................................................................................. 38
High Pressure Oxygen supply ................................................................................................................................................... 38
Low Pressure Oxygen Supply .................................................................................................................................................... 39
Patient Circuit ................................................................................................................................................................................... 40
Disposable Patient Circuit ........................................................................................................................................................... 41
Reusable Patient Circuit ............................................................................................................................................................... 41
Dual Limb Patient Circuit ............................................................................................................................................................. 42
Circuit Resistance ........................................................................................................................................................................... 44
I
Other Connections ......................................................................................................................................................................... 44
HME ....................................................................................................................................................................................................... 44
MDI ......................................................................................................................................................................................................... 44
Using the iventTM201 with heated humidification (1.4 Stepper Based models only) ....................................... 44
PneUmaTIC Nebulizer ................................................................................................................................................................... 46
Pulse Oximeter ................................................................................................................................................................................. 46
Remote Alarm ................................................................................................................................................................................... 49
Sensor Line Maintenance............................................................................................................................................................ 49
Patient Connection......................................................................................................................................................................... 49
Filters .................................................................................................................................................................................................... 49
Air Inlet Filter ..................................................................................................................................................................................... 50
Bacterial Filter................................................................................................................................................................................... 50
Chemical, Biological, Radiological and Nuclear Filter.................................................................................................... 50
Operational Case ............................................................................................................................................................................ 51
The iVentTM201 User Interface .................................................................................................................................................. 51
Controls and Power Up ................................................................................................................................................................ 52
The Front Panel ................................................................................................................................................................................ 52
Silence.................................................................................................................................................................................................................. 52
Manual Breath ................................................................................................................................................................................................. 53
Hold ....................................................................................................................................................................................................................... 53
Clear...................................................................................................................................................................................................................... 53
LED Indicators .................................................................................................................................................................................................. 53
The Screen ......................................................................................................................................................................................................... 54
3 OPERATING THE IVENTTM201 – SETTING MODES AND PARAMETERS...................................................... 57
Introduction ....................................................................................................................................................................................... 59
Operation of the iVentTM201 ...................................................................................................................................................... 59
Power Up and Weight Selection .............................................................................................................................................. 59
O.V.T ...................................................................................................................................................................................................... 60
Standby and Patient Ventilation .............................................................................................................................................. 61
Changing Ventilation Mode........................................................................................................................................................ 62
Common Parameters.................................................................................................................................................................... 64
Changing Ventilation Paramters – Overview ..................................................................................................................... 65
The Selection Interface................................................................................................................................................................. 66
Adjusting the Breath Rate ........................................................................................................................................................... 67
Adjusting the Tidal Volume ......................................................................................................................................................... 69
Breath Types ..................................................................................................................................................................................................... 70
Adjusting Pressure.......................................................................................................................................................................... 71
Adjusting FiO2 .................................................................................................................................................................................. 73
Adjusting Peak Flow....................................................................................................................................................................... 74
Adjusting Pressure Support Ventelation .............................................................................................................................. 76
II
Adjusting PEEP.................................................................................................................................................................................. 78
Adjusting Trigger Sensitivity....................................................................................................................................................... 79
Adjusting Inspiratory Time .......................................................................................................................................................... 80
Adjusting Rise Time ........................................................................................................................................................................ 82
Adjusting Flow Termination (Esens) ........................................................................................................................................ 84
4 THE MAIN MENU............................................................................................................................................... 87
Introduction ....................................................................................................................................................................................... 89
Navigating the Main Menu ......................................................................................................................................................... 89
Alarm Settings .................................................................................................................................................................................. 90
Advanced Settings ......................................................................................................................................................................... 91
Sigh Breath ........................................................................................................................................................................................ 91
Easy Exhale™ .................................................................................................................................................................................... 93
Oxygen Supply ................................................................................................................................................................................. 94
High Option ....................................................................................................................................................................................................... 95
Alarm Messages .............................................................................................................................................................................................. 96
Low + Monitoring Option ............................................................................................................................................................................. 97
Low Option......................................................................................................................................................................................................... 97
None Option ...................................................................................................................................................................................................... 98
Adaptive Peak Flow........................................................................................................................................................................ 98
Humidifier Setting ........................................................................................................................................................................... 99
Pulse Oximetry ...............................................................................................................................................................................100
Pneumatic Nebulizer ...................................................................................................................................................................102
Set Time and Date ........................................................................................................................................................................103
Restore Default Settings ............................................................................................................................................................105
Default parameters Settings ...................................................................................................................................................106
Show Graphs ...................................................................................................................................................................................108
Browse Waveforms......................................................................................................................................................................108
Select Range ...................................................................................................................................................................................110
Show Trends ....................................................................................................................................................................................112
Selecting Trends To Display .....................................................................................................................................................114
Browsing Trends ............................................................................................................................................................................115
Show Loops .....................................................................................................................................................................................117
Show Mechanics ...........................................................................................................................................................................119
Pulse Oximetry Screen................................................................................................................................................................120
Pulse Oximetery Alarms .............................................................................................................................................................122
Show Log Book ..............................................................................................................................................................................123
Display................................................................................................................................................................................................124
O.V.T. ...................................................................................................................................................................................................127
Maintenance ...................................................................................................................................................................................127
III
5 ADAPTIVE BI-LEVEL ........................................................................................................................................ 129
Introduction .....................................................................................................................................................................................131
About Adaptive Bi-Level.............................................................................................................................................................131
Guide to Adaptive Bi-Level .......................................................................................................................................................131
Indications and Warnings .........................................................................................................................................................132
Indications ........................................................................................................................................................................................132
Warnings...........................................................................................................................................................................................132
Setup ...................................................................................................................................................................................................132
Adaptive Bi-Level Alarm Settings ..........................................................................................................................................134
Other Alarm Options....................................................................................................................................................................134
Adjusting Adaptive Bi-Level Parameters ...........................................................................................................................134
Adaptive Bi-Level Window ........................................................................................................................................................135
Easy Exhale ......................................................................................................................................................................................137
Optimizing the Patient Ventilator Interface ......................................................................................................................137
Resolving Patient Ventilator Dysynchrony ........................................................................................................................137
Excessive Ventilation ...................................................................................................................................................................137
Excessive Leak ...............................................................................................................................................................................137
Non-Triggered Breaths (Inspiratory Trigger Failure).....................................................................................................138
Excessive Triggering (auto cycling): ......................................................................................................................................138
I:E Cycling Dysynchrony .............................................................................................................................................................138
Premature I:E Cycling ..................................................................................................................................................................138
6 ALARMS............................................................................................................................................................ 141
Introduction .....................................................................................................................................................................................143
How Alarms Work .........................................................................................................................................................................143
Responding to an Alarm ............................................................................................................................................................143
Alarm settings ................................................................................................................................................................................144
Changing Individual Alarm Settings .....................................................................................................................................145
Setting the Respiratory Rate Alarm ......................................................................................................................................146
Setting the Minute Volume Alarm ........................................................................................................................................................ 147
Setting the Pressure Alarm...................................................................................................................................................................... 148
Setting the Apnea Time Alarm ............................................................................................................................................................... 149
Setting the FiO2 Alarm .............................................................................................................................................................................. 150
Setting the Leak Alarm .............................................................................................................................................................................. 151
Auto Settings ...................................................................................................................................................................................152
Alarm Options .................................................................................................................................................................................153
Setting the Alarm Volume ........................................................................................................................................................................ 154
Setting the Inverse I:E Ratio Alarm ....................................................................................................................................................... 154
Setting the Tidal Volume Not Delivered Alarm ............................................................................................................................... 155
Disabling or Enabling the Patient Circuit Disconnect Alarm .................................................................................................... 156
Guide to Alarm Definitions and Priorities ...........................................................................................................................158
IV
Alarms Test ......................................................................................................................................................................................167
The Sensor Failure Alarm ..........................................................................................................................................................169
Patient Disconnect Alarm .........................................................................................................................................................170
Patient Circuit Failed Alarm......................................................................................................................................................170
7 CARE, MAINTENANCE AND TESTS ............................................................................................................... 171
Introduction .....................................................................................................................................................................................173
Cleaning and Maintenance ......................................................................................................................................................173
Cleaning the Ventilator...............................................................................................................................................................174
Planned Maintenance .................................................................................................................................................................174
Storage Planned Maintenance ...............................................................................................................................................176
The O.V.T............................................................................................................................................................................................176
The Maintenance Screen...........................................................................................................................................................176
Calibration ........................................................................................................................................................................................176
O2 Calibration ............................................................................................................................................................................................... 177
Ventilator Verification tests ......................................................................................................................................................179
Required Equipment and Supplies: ...................................................................................................................................................... 180
Starting the VVT ............................................................................................................................................................................................ 181
The Alarm Sound Test ................................................................................................................................................................................ 181
Pressure Tests ............................................................................................................................................................................................... 182
Flow Tests........................................................................................................................................................................................................ 182
O2 Tests............................................................................................................................................................................................................ 182
Battery Test .................................................................................................................................................................................................... 183
Watchdog Timer Tests .............................................................................................................................................................................. 183
VVT Completion ............................................................................................................................................................................................ 183
Configuration Screen ..................................................................................................................................................................184
Choosing a Different Startup Screen ...................................................................................................................................184
Setting the Startup Weight .......................................................................................................................................................185
Default FiO2 Setting .....................................................................................................................................................................185
VersaMed Service Functions ...................................................................................................................................................186
Communication Port ...................................................................................................................................................................186
Communication Rate ..................................................................................................................................................................186
Localization......................................................................................................................................................................................186
Total Operating Hours ................................................................................................................................................................188
APPENDIX A: GLOSSARY .......................................................................................................................................... 191
APPENDIX B: WARRANTY ........................................................................................................................................ 199
Warranty ...........................................................................................................................................................................................201
APPENDIX C: OPERATING THEORY ........................................................................................................................ 203
Operating Theory ..........................................................................................................................................................................205
V
Theory ................................................................................................................................................................................................205
Ambient Air Filter...........................................................................................................................................................................205
CBRN Filter (optional) ...................................................................................................................................................................205
Low Pressure O2 Adapter and Filter (optional) ...............................................................................................................205
Air/Oxygen Blending System ...................................................................................................................................................205
Inlet Manifold ..................................................................................................................................................................................205
Turbine Unit .....................................................................................................................................................................................206
Turbine Pressure Sensor ............................................................................................................................................................206
Turbine Valves ................................................................................................................................................................................206
Over Pressure Relief Valve ........................................................................................................................................................206
Airway Flow and Pressure Sensors ......................................................................................................................................206
Pressure Switch .............................................................................................................................................................................206
Inlet and Outlet Mufflers ............................................................................................................................................................206
APPENDIX D: THEORY OF BREATH DELIVERY ...................................................................................................... 211
Breath Delivery...............................................................................................................................................................................213
Patient Triggering .........................................................................................................................................................................213
Breath Types ...................................................................................................................................................................................214
Adaptive Flow and Adaptive I-Time .....................................................................................................................................215
Mandatory Volume Control Breath ......................................................................................................................................216
Pressure Control Breath.............................................................................................................................................................217
Manual Mandatory Breath .......................................................................................................................................................218
Patient Pressure Support Breath ...........................................................................................................................................218
Patient Spontaneous Breath ...................................................................................................................................................219
Summary ..........................................................................................................................................................................................220
APPENDIX E: VENTILATION MODES....................................................................................................................... 223
Assist/Control Mode.....................................................................................................................................................................225
Definition ...........................................................................................................................................................................................225
Available Breath Types ...............................................................................................................................................................225
Description .......................................................................................................................................................................................225
Parameters Setting ......................................................................................................................................................................226
Synchronized Intermittent Mandatory Ventilation Mode...........................................................................................226
Definition ...........................................................................................................................................................................................226
Available Breath Types ...............................................................................................................................................................226
Description .......................................................................................................................................................................................226
Continuous Positive Airway Pressure Mode .....................................................................................................................228
Definition ......................................................................................................................................................................................................... 228
Available Breath Types .............................................................................................................................................................................. 228
Description...................................................................................................................................................................................................... 228
VI
Apnea Back-Up Ventilation ......................................................................................................................................................229
Open Loop Mode ...........................................................................................................................................................................229
Adaptive Bi-Level Mode .............................................................................................................................................................230
APPENDIX F: HOLD FUNCTION AND STATIC MECHANICS MEASUREMENTS .................................................. 233
Front Panel Controls ....................................................................................................................................................................235

Static Compliance Measurements ........................................................................................................................................235
Static Compliance.........................................................................................................................................................................235
Respiratory Time Constant .......................................................................................................................................................236
Performing a Static Respiratory Mechanics Measurement ......................................................................................236
Clinical Considerations ...............................................................................................................................................................237
End Expiratory Hold .....................................................................................................................................................................237
Performing and End Expiratory Hold Maneuver ............................................................................................................238
Reviewing Static Mechanics and Intrinsic PEEP Measurements ............................................................................238
RR/Vt Ratio .......................................................................................................................................................................................239
APPENDIX G: ACCESSORIES .................................................................................................................................... 241
Disposable Breathing Circuit ...................................................................................................................................................243

Instructions for Use..................................................................................................................................................................................... 244
Instructions for Use With a Pneumatic Nebulizer ......................................................................................................................... 245
Reuseable Patient Breathing Circuit ....................................................................................................................................245
Contents........................................................................................................................................................................................................... 245
Warnings and Cautions ............................................................................................................................................................................ 245
Sterilization and Duration of Use .......................................................................................................................................................... 246
Phthalates ....................................................................................................................................................................................................... 246
Instructions for use ..................................................................................................................................................................................... 247
Instructions for use with the humidifier............................................................................................................................................. 247
Cleaning and Sterilization ........................................................................................................................................................................ 248
Reassembly .................................................................................................................................................................................................... 249
Dual Limb Patient Circuit Adapter.........................................................................................................................................250
Kit Contents .....................................................................................................................................................................................250
Phthalates ........................................................................................................................................................................................251
Installation........................................................................................................................................................................................251
Installing the Exhalation Valve............................................................................................................................................................... 252
Installing the Patient Circuit .................................................................................................................................................................... 252
Extended Battery ..........................................................................................................................................................................254
To replace the battery: ...............................................................................................................................................................254
Specifications..................................................................................................................................................................................256
MRI Extension Tubing Set for Patient Breathing Circuit ..............................................................................................256
Warnings...........................................................................................................................................................................................256
VII
Instructions for Use ......................................................................................................................................................................258
Instructions for Use With the Humidifier ...........................................................................................................................258
Transport Mounting Panel ........................................................................................................................................................259
Kit Contents .....................................................................................................................................................................................259
Installation........................................................................................................................................................................................259
Support Arm for Breathing Circuit ........................................................................................................................................261
connecting the Patient circuit to the Support Arm .......................................................................................................261
Roll Stand ..........................................................................................................................................................................................262
Mounting the iVentTM201 On The Roll Stand ....................................................................................................................262
Dismounting the iVentTM201 From The Roll Stand ........................................................................................................262
Connecting the optional Battery Holder Accessory P/N: M1162050....................................................................263
APPENDIX H: REMOTE ALARM PINOUT ................................................................................................................. 265
APPENDIX I: PART NUMBERS AND ACCESSORIES ............................................................................................... 269
INDEX ......................................................................................................................................................................... 275
VIII
1 INTRODUCTION
This chapter contains the following sections:
Introduction Page 3
Specifications Page 13
Intended Use Page 25
Use of the iVentTM201 With MRI Page 25
1
1 Introduction
INTRODUCTION
The iVentTM201 is a compact, portable, multi-featured, microprocessor-controlled

ventilator, which has the versatility and capability of larger and more costly
ventilators.
A turbine-powered air source and a rechargeable internal battery provide
freedom from wall air and power outlets. An intuitive turn-and-click Control
Knob, quick-choice pushbuttons, and a bright, well-organized easy-to-read
screen, allow for rapid control and continuous real-time monitoring of patient
ventilation.
Alarm settings are fully adjustable. Optional Waveform and Diagnostic Software
package displays pressure and flow waveform data, loops, trends, and logged
totals in a variety of graphical and numerical modes.
The iVentTM201 supports the following modes:
 Assist/Control (A/C)
o Volume Controlled A/C
o Pressure Controlled A/C
 Synchronized Intermittent Mandatory Ventilation (SIMV)
o Volume Controlled SIMV (Vctrl SIMV)
o Pressure Controlled SIMV (Pctrl SIMV)
 Continuous Positive Airway Pressure (CPAP)
 Pressure Support Ventilation (PSV)
NOTE Certain modes are optional features and may not be operational in some
iVentTM201 models
In addition, the iVent™201 has the following advanced features:

 Quick setup enabled by Preset Parameters according to Patient Weight
 Adaptive Peak Flow™ and Adaptive I-Time to adapt to patient flow demand
during volume control breath delivery or to maintain a 1:2 I:E ratio in the
event of no patient flow demand.
 Rise time is adjustable
 The iVent™201 s Adaptive Bi-Level feature enables leak-tolerance for
facemask ventilation or other specialized high-leak tube ventilation
 Easy Exhale™ is an advanced feature when PEEP>0 is selected, designed to
shorten expiratory time and reduce risk of auto-PEEP.
 Firmware is upgradeable via a PC connection
 The iVent™201 is designed to operate according to specifications in any
physical orientation, such as during transport use
3
HOW TO USE THIS MANUAL
The iVent™201 must only be operated by authorized medical personnel certified

trained in the use of this product. It must be operated according to the
instructions provided in the Operator’s Manual.
The manual is primarily organized according to available screens, menus, options
and settings and begins with a look at the hardware, including power
considerations and patient circuit setup.
Study the manual with the iVent™201 in close proximity, along with a patient
circuit (preferably with a test lung and Rp20 resistor). Become comfortable with
the Control Knob and the front panel buttons.
The user interface consists of three primary screens/menus:
 The Main Screen
 The Main Menu
 The Mode Menu
Almost every function or operation of the iVent™201 is accessible through one of
the Main screen menus. Be aware of the notes, warnings, and cautions marked in
bold print.
Refer to the index and the Table of Contents to assist you in finding information.
For more information about the Adaptive Bi-Level feature see About Adaptive Bi-
Level, page 131.
4
1 Introduction
LOOKING AT THE IVENT™201
5
3
4
Figure 1: Front View of the iVent™201
Item Number Description
1 Display
2 Keypad
3 Control Knob
4 Exhalation valve luer inlet
5 Ventilator outlet
6 Sensor line luer inlets
7 Nebulizer outlet
5
1
2 3
17
16
4
15 5
6
14
7
8
13
9
12
10
11
Figure 2: Back View of the iVent™201

Item Number Description
1 Carrying handle
2 Keyboard connector
3 Remote alarm connector
4 External screen connector
5 LAN connector*
Do not remove connector cap. This connection
port is not in use
6 AC cable clip
7 RS 232 connectors (COM1 and COM2)
8 On/off switch (with cover)
9 High pressure oxygen inlet connector
6
1 Introduction
10 4 x Battery pack screws

11 Internal battery handle
12 DC fuse
13 AC fuses
14 DC cord connector
15 Grounding pin
16 AC cord connector
17 Cooling fan
CAUTIONS AND WARNINGS
CAUTION The iVentTM201 is a restricted medical device to be operated by

qualified medical personnel under the direction of a qualified medical
practitioner
Always perform a complete Operation Verification Test (O.V.T.) when

connecting a new patient circuit to the ventilator, and before using it
on a patient. Standard facility policy should be followed.
Using the iVentTM201 in combination with devices such as humidifiers

or filters can increase the pressure gradient across the breathing
system. Make sure that such devices do not produce excessive
resistance to the airflow provided by the iVentTM201.
The iVentTM201 must not be operated immediately following storage

or transport outside the recommended operation condition
The iVentTM201 internal battery contains lead and must be disposed of

in accordance with local ordinances and environmental regulations.
Do not connect the O2 supply when equipment is not in use.
The remote alarm should be considered secondary to the ventilator’s

primary alarm system.
Verify the remote alarm device functionality before use
The remote alarm connector should be connected to a nurse station

device on a low voltage less than 24Vdc and compliant with IEC
60601-1.
The factory default setting for Leak Alarm is set to Off. Users must
manually set the leak alarm to enable it.
WARNING The iVentTM201 is a life-sustaining device. Do not rely solely on the

ventilator performance: always make sure an alternative source of
ventilation is available. Clinical supervision of the patient is
7
mandatory.
Qualified medical personnel should visually monitor patients on
life-support ventilation. Life-threatening conditions may arise that
might not activate alarms,
To prevent explosion hazard, do not use the ventilator in the
presence of flammable anesthetics.
Do not cover the iVentTM201 while it is in use. Make sure that the
iVentTM201 is positioned so that its inlet ports and cooling vents
are open to freely circulating air.
SYMBOLS AND LABELS
Symbol Meaning
Indicates that you should “Refer to documentation for

further information.” Refer to manual per IEC 601-1
Potential equalization (Ground) point
Direct Current ( DC) and Alternating Current (AC)
Type BF equipment, per IEC 601-1
MR conditional per ASTM 2503-05
Nebulizer
Sensor line luer inlets
Ventilator outlet
Exhalation valve luer inlet
8
1 Introduction
Location Label
AC Connector AC IN 100-240V
50-60Hz 1.6A
AC Fuses 2xT3.15AL (250V)
Air Inlet INLET AIR

FILTER
DO NOT
OBSTRUCT
COOLING
Cooling Fan
FAN
DO NOT
OBSTRUCT
Connector DC IN
12-15V
8.5A
T15A (250V)
DC Fuse
Device ID
Device Product
Ethernet
Connector (not
on all units)
External Display
Connector
9
High Pressure
Oxygen Inlet
Keyboard
Connector
Power Pack
Fuse T15A (250V)
Power Switch
ON
OFF
Remote Alarm REMOTE

Connector
ALARM
Serial RS-232
Communication
Connector
10
1 Introduction
Power Pack
(inside) POWER PACK
P/N : 503A0012
Caution: This Power Pack contains a sealed Lead -
Acid Battery. Disposal of this unit should be
according to Environmental Safety Requirements for
Lead-Acid batteries.
VersaMed
11
PERFORMANCE PARAMETERS
Ventilation Component Parameters/ Unit of Accuracy

Range Measure
Displayed
Page
Set
Respiratory rate 1-12 bpm 1 Y Y 67
12-80 2
Inspired Tidal Volume 50-2000 mL 10% Y N 69
Measurement
Exhaled Tidal Volume 50-300 mL 10 mL or N Y NA

Measurement +15%
300-2000 whichever is
greater
+10%
Inspiratory Pressure Limit 5 to 80 cmH2O 5 Y Y 71
Inspiratory Time 0.2 to 3 or sec. 10% Y Y 80
Adaptive I-
Time
Peak Flow up to 120 or L/min 10% Y Y 74
Adaptive
Flow
Peak Flow (Spontaneous) up to 180 L/min 10% Y Y 74
Oxygen Mix (FiO2) 21 to 100% 10% of the Y Y 73
set value or
3% absolute
whichever is
greater
PEEP 0 to 40 cmH2O 1 or 10%, Y Y 78

whichever is
greater
Trigger sensitivity 1 to 20, off L/min Y Y 79
-0.5 to –20, cmH2O
off
PSV 0 to 60 cmH2O 10% Y Y 76
Positive Pressure relief 80 cmH2O N N NA
valve
Controlled Pressure 5 to 80 cmH2O 5 Y Y NA
Flow Termination 10-90 % +10% Y Y 84
Rise Time Mid, High, NA Y Y 82
Max, Auto
FiO2 at power up 21%, 40%, Y Y 185
60%, 100%
(selectable)
12
1 Introduction
SPECIFICATIONS
MONITORED DATA RANGE, RESOLUTION AND

ACCURACY
The following section describes the various specifications and parameters of the
iVentTM201.
Parameter Range, resolution, accuracy
Breath type Range: Type: - Control, assist, patient, sigh

Resolution: N/A
Accuracy: N/A
Respiratory Rate Range: 0 to 150/min
Resolution: 1/min
Accuracy: 1 for 1 to 12/min
2 for 12 to 150/min
Exhale tidal volume Range: 0 to 5000 mL
Resolution: 1 mL
Accuracy: 10 mL or 15% (whichever is
greater)
for 0 to 300 mL
10% for 300 to 5000 mL
Exhaled Minute Volume Range: 0 to 99.9L
Resolution: 0.1 L
Accuracy: 10%
Peak flow Range: 0 to 140 L/min
Resolution: 1 L/min
Accuracy: 10%
PIP (Peak Inspiratory Range: 0 to 99 cmH2O
Pressure) Resolution: 1 cmH2O
Accuracy:  2 (+ 5 % of reading) cm H2O
Inspiratory time Range: 0 to 3.0 sec
Resolution: 0.1 sec
Accuracy: 10%
I:E ratio Range: 1:11 to 3:1
Resolution: 0.1 for 1:1 to 1:5
1 for 1:5 to 1:11 and 3:1 to 1:1
Accuracy: 0.1
Delivered O2% Range: 21 to 100%
13
Resolution: 1%
Accuracy: 5%
Flow Leak Range: 0 to 100%
Resolution: 1%
Accuracy: 15%
Mean Airway Pressure Range: 0 to 99 cmH2O
Resolution: 1 cmH2O
Accuracy:  2 (+ 5 % of reading) cmH2O
Resistance (dynamic) Range: 0 to 99.9 cmH2O/L/s
Resolution: 0.1 cmH2O/L/s
Accuracy:  (2 + 20% of actual value)
cmH2O/L/s
Compliance (dynamic) Range: 0 to 99.9 ml/cmH2O
Resolution: 0.1 ml/cmH2O
Accuracy:  (2 +20% of actual value)
ml/cmH2O
RR/Vt-Rapid Shallow Range: 0 –200 /min*L
Breathing Index (RSBI) Resolution: 1 /min*L
Accuracy:  (5 + 20% of actual value). /min*L
Static compliance Range: 0 to 99 ml/cmH2O
Resolution: 1 ml/cmH2O
Accuracy:  (2 + 20 % of actual value).
ml/cmH2O
Auto PEEP Range: 0 to 99 cmH2O
Resolution: 1 cmH2O
Accuracy:  2 (+ 5 % of reading) cmH2O
Plateau Pressure Range: 0 to 99 cmH20
Resolution: 1 cmH20
Accuracy: +2(+5% of reading) cmH20
Time Constant Range: 0.0 to 9.9 sec
Resolution: 0.1 sec
Accuracy: 20%
14
1 Introduction
SIZE AND WEIGHT
Parameter
Height: 13” / 33 cm
Width: 9.5” / 24 cm
Depth: 10.3” / 26 cm
Screen: 8.4” / 21.3 cm
diagonal
Weight 18.3 lb/8.3 kg
(without battery)
Battery Weight 6.2lb/2.8kg
Extended Battery 10.1 lb / 4.6 kg
Weight
Overall Weight 24.5 lb/11.1 kg
Overall Weight (with 27.8 lb/12.6 kg
extended Battery)
VENTILATION MODES
 Assist/Control (A/C)
o Volume Controlled (A/C)
o Pressure Controlled (A/C)
 Synchronized Intermittent Mandatory Ventilation (SIMV)
o Volume Controlled SIMV (Vctrl)
o Pressure Controlled SIMV (Pctrl)
 Continuous Positive Airway Pressure (CPAP) with Pressure Support Ventilation
(PSV)
NOTE Certain modes are optional and might not be operational in all
iVentTM201 models
15
ENVIRONMENTAL SPECIFICATIONS
Parameter
Operating Temperature 0 to +50 °C / +32 to +122 °F

Storage Temperature Without battery: -15 to +70 °C / +5 to +158
°F
With battery: -15 to +30 °C / +5 to +86 °F
Relative Humidity 15 to 95% @ 30 °C / 86 °F
Water and Dust IP-54 (Splash proof)
Resistance
Atmospheric Pressure 430 - 825 mmHg (up to 15,000 feet)
Vibration IEC 68-2-6, IEC 68-2-34
MIL-STD-810E
Shock IEC 68-2-27 (100 g)
MIL-STD-810E
Total External Sound 40 – 45 dBa at one meter
Level
POWER SUPPLY
Parameter
External AC 100 to 240 V, 50-60 Hz, max 1.6 A.

External DC Battery 12 to 15 V max 8.5 A.
Internal Battery Sealed Lead-Acid, 12 V 8 Ah (rechargeable)
Recharge Time Over 8 hours, <1 Ampere
Operating Time (internal Up to 2 hours (varies with ventilation
battery) parameters)
Extended Battery Sealed Lead-Acid, 12 V, 12 Ah (rechargeable)
Extended Battery Over 24 hours, <1 Ampere
recharge time:
Operating Time (extended Up to 4 hours (varies with ventilation
Operating Time (external Up to 8 hours (varies with ventilation
16
1 Introduction
O2 SUPPLY SPECIFICATIONS
Parameter
High Pressure Pressure Range 40 –75psi (2.8-5.1 bar).

Warning: The exact oxygen pressure which the
iVentTM201 uses depends on the version you
have. Check the back label (shown in Figure 11)
for the pressure levels of your unit.
Low Pressure Maximum flow 15L/min or 0.5 psi
VENTILATION PERFORMANCE AND CONTROLLED

PARAMETERS
Parameter
Respiratory Rate 1 – 12 ±1, 12 – 80 ± 2 bpm

Tidal Volume 50-2000 mL
Accuracy of Tidal Volume ±10% or ±10 mL whichever is greater
Delivery
Accuracy of Exhale Tidal ±15% above 100 mL from actual reading
volume Measurement or ±10 cc below 100 mL
Inspiratory Pressure Limit 5 to 80 ±5 cmH2O
Inspiratory Time Adaptive TimeTM or 0.2 to 3 ±10% sec
Peak Flow (PIF) Adaptive FlowTM or to 120 ±10% L/min
Spontaneous to 180 ±10% L/min
Oxygen Mix (FiO2 ) 21% to 100% ±10% of the set value or ±3%
absolute, whichever is greater
PEEP 0 to 40 ±1 cmH2O or ±10%, whichever is
greater
Trigger Sensitivity 1 to 20 L/min Flow, Off
- 0.5 to – 20 cmH2O Pressure, Off
PSV 0 to 60 ±10% cmH2O
Positive Pressure Relief 80 cmH2O
Valve
Pneumatic Nebulizer 5 to 240 minutes
Controlled Pressure 5 to 80 cmH2O ±5 cmH2O
FiO2 at Power up 21%, 40%, 60%, 100% (configurable)
Configurable Humidifier HME (10 minute), Heated (1 minutes), Off
Setting (Purging Cycle)
17
PULSE OXIMETRY SPECIFICATIONS
Oxygen Saturation Range: 0 to 100%

Pulse Rate Range: 18-300 pulse par a minute
Measurement Wavelengths: Red- 660 nanometers at 3m W nominal
Infrared – 910 nanometers at 3m W nominal
SpO2 Accuracy: No motion (adult, pediatrics) + 2 digits
(70-100%)(+1SD) Motion (adult, pediatrics) + 2 digits
Low Perfusion (adult, pediatrics) + 2 digits
Heart Rate Accuracy: No motion (18-300 BPM): + 3 digits
- adult, pediatrics
Motion (40-240 BPM): + 3 digit
- adult, pediatrics:
Low Perfusion (40-240 BPM)
+ 3 digits
- adult, pediatrics:
Operating Temperature: 0°C to 50°C (32°F to 122°F)
Storage Temperature: -20°C to +50°C (-4°F to 122°F)
Power Consumption 60mW – typical operation
Dimensions: 2.1’’ x 0.8’’ x 0.6’’ (53 x 201 x 15mm)
Weight: 75g (including 6’ and connector)
Shock Ruggedness Immersion: Per IEC 86-2-27
Vibration Ruggedness Mil-STD-810C, method 514-2
Immersion:
Sensors: Disposable and reusable sensors (8000 series)
manufactured by Nonin and labels for Patients
ranging from pediatrics to adults.
18
1 Introduction
STANDARDS AND SAFETY REQUIREMENTS
The iVentTM201 meets or exceeds the following international standards:
EN/IEC 60601-1 Medical Electrical Equipment – General requirements

for safety
EN/IEC 60601-1-2 Medical Electrical Equipment - Part 1: General
requirements for safety 2. collateral standard:
Electromagnetic Compatibility - requirements and tests
EN/ IEC 60601-1-6 General requirements for basic safety and essential
performance - Collateral standard: Usability
EN/IEC 60601-2-12 Medical Electrical Equipment – Particular Requirements
for the Safety of Lung Ventilators - Critical Care
Ventilators
UL 60601-1 Medical Electrical Equipment, part1: General
Requirements for Safety
ASTM F1246 Standard Specification for Electrically Powered Home
Care Ventilation.
ISO 10651-2 Lung Ventilators for medical use – Particular
requirements for Home Care Ventilators
19
DISPLAYED PARAMETERS
The following table presents the displayed parameters and indicates whether the
displayed values are set, measured or both.
Unit of
Displayed
Parameter Measure
Set
Rate bpm + +
Ventilation Mode + +
Oxygen Concentration FiO2 + +
Inspiration to Expiration +
time ratio I:E ratio
Inspiratory Time (Itime) sec + +
Sensitivity Values cmH2O/LPM + +
(Triggers): Pressure and
Flow
Pressure Support cmH2O +
Ventilation (PSV)
Flow termination (Esens) % +
Rise time (drive) + +
Alarm Pressure / Limit cmH2O + +
Pressure
Positive End Expiratory cmH2O + +
Pressure (PEEP)
Exhaled Minute Volume L +
Peak Inspiratory Pressure cmH2O +
Pressure/Flow Wave +
Forms
Electrical Power Source +
(Ext./Int.)
SpO2 % +
Heart rate Bmp +
In Adaptive Bi-Level
Mode:
IPAP (Ins Pressure) cmH2O + +
EPAP (Exp. Pressure) cmH2O + +
Tidal Volume (estimated) mL +
Leak (estimated)* LPM +
Rise Time Setting sec +
Non-Displayed Additional
Parameters
20
1 Introduction
Unit of
Displayed
Parameter Measure
Set
Sigh Breath Setting +
Humidifier Setting (purge +
cycle)
Nebulizer Settings (time) Hr: min + +
* In SW version 19.18.01 estimated leak in adaptive Bi-Level mode is presented in %
21
USER ADJUSTABLE ALARMS
Value Range
Respiratory rate High: 4-80 bpm

Low: 1-77 bpm
Minute volume High: 1-99 L/min; off
Low: 0-60 L/min
Inspiratory pressure High: 4-80 cmH2O
Low: 1-77 cmH2O
Apnea 5-120 seconds
FiO2 High: 22-100%
Low: 21-99%
Leak 0-100%
Low Tidal Volume Off or 15%-85%
Delivered
Volume Limit Reached 100-2000 mL
Inverse I:E Ratio ON/OFF
Patient Circuit Disconnect ON/OFF
(AB-Level mode, for other
modes – optional)
Alarm Volume 1-10
SpO2 High: 60-100
Low: 59-99
Heart Rate High: 50-175
Low: 40-150
22
1 Introduction
ADDITIONAL ALARMS AND INDICATORS
The following table shows Additional Alarms.
Alarms
Low O2 Pressure
AC Power Disconnect
Low Battery
Empty Battery
Battery Disconnect or
Damaged
Over Temperature
Check Sensor
Tube Disconnect
Sensor Disconnect
Patient Disconnect
Service Notice
High PEEP
Need Cal (Calibration)
Patient Circuit Failed
SpO2 Patient
Disconnect
SpO2 Sensor
Disconnect
SpO2 Reading Failed
The following table shows additional Indicators and Icons.
Indicators
Battery Charge
Alarm Silence Icon & Timer
Work Hour Counter
Date and Time
LEDs: ON, Charge, Alarm
Power Source Icon
Breath Type: Mandatory, Spontaneous,
Assist, Hold, or Sigh
Zeroing
Purging
100% O2 suction mode
External DC
23
WAVEFORMS AND DIAGNOSTICS PACKAGES
Pressure, Flow, and Volume Waveforms Software Package includes the following:
 Real Time Pressure and, Flow Waveforms
 Waveform History Browsing
 Trending of Monitored Data
 Respiratory Diagnostics Software Package
 Pressure, Flow and Volume Loops
 Lung Mechanics (Compliance-static and dynamic, Resistance, Mean Airway
and Plateau Pressure)
24
1 Introduction
INTENDED USE
The iVent™201 MR Conditional is a portable, computer controlled, electrically

powered intensive care ventilator intended to provide continuous or intermittent
ventilatory support for the care of individuals who require mechanical ventilation.
Specifically, the ventilator is applicable for use with adult through pediatric
patients, who require invasive or non-invasive assistance via the following
general modes of ventilatory support, as prescribed by an attending physician:
 Assist/Control (Pressure Controlled or Volume Controlled)
 SIMV (Pressure Controlled or Volume Controlled)
 CPAP/PSV
The iVent™201 MR Conditional ventilator is suitable for use in the ICU and all
other hospital areas, including Magnetic Resonance (MR) environment, not to
exceed a 3.0 Tesla static magnetic field, in all hospital-type facilities, alternate
care sites, transport, emergency and in the home environment. The iVent™201
MR Conditional ventilator is MR conditional.
The optional non-invasive Pulse Oximeter is intended for non-invasive monitoring
of oxygen saturation and pulse rate and is suitable for use in all above mentioned
areas, excluding MR environments.
The iVent™201 MR Conditional ventilator is a restricted medical device intended
for use by qualified, trained personnel under the direct supervision of a physician.
USE OF THE IVENTTM201 WITH MRI
The iVent™201 ventilator (serial number 15 000 and higher) is classified as MR

conditional for 1.5T and 3T MR scanners. This means that the iVentTM201 is safe to
use in the MR environment if the operation conditions specified in this section are
met.
For the MRI conditional specifications refer to MRI Conditional Tests
Specifications, on page 29 of this document.
CAUTION The iVentTM201 ventilator should not be subjected to field strength

greater than 100 Gauss and must be kept outside of 100 Gauss
perimeter.
NOTE The iVentTM201 MR Conditional has been demonstrated to pose no known

hazards in MR Environment under specified conditions of use. However, MR
image quality may degrade when working with the ventilator in a specific MR
suite. It is recommended to perform a pre-qualification image quality test to
ensure an acceptable level of image quality. For more details contact your
local sales representative
25
The facility must map and permanently mark the 100 Gauss strength line on the
floor with a durable tape. VersaMed Gauss line warning floor label (Versamed P/N
350C0323-01, GE P/N M1218236), shown in Figure 3 below can be used to
emphasize the location of the 100 Gauss line.
Figure 3: 100 Gauss Line Warning Floor Label
Figure 4: MRI Warning Card
26
1 Introduction
MR Class
MR conditional per ASTM 2503-05
WARNING Use of the ventilator other than as instructed may result in injury to
the patient or personnel.
Connect the potential equalization pin on the back of the ventilator to the
CAUTION
ground during battery (DC power) operation
Before using the MR suite, remove the green cover and the attached metal
chain from the high-pressure oxygen fitting.
To avoid degrading image quality, do not use the static mechanics

function during MRI scanning.
Use of the ventilator other than as instructed may cause damage to the
MR scanner
If the ventilator is placed on a roll-stand or a moving cart lock the

ventilator cart's wheel to prevent inadvertent movement.
The ventilator is attracted to the magnet if it is brought within 100 Gauss

field line of the MR magnet. If there is a risk of personnel moving the
ventilator, it should be tethered to the wall, or placed within a retaining
box affixed to the floor.
The SpO2 option is not intended for use in the MR environment.
Use of the ventilator other than as instructed may cause the ventilator to
malfunction, and may cause permanent damage to the ventilator.
NOTE To avoid degrading image quality, do not use the static mechanics function
during MRI scanning and Connect the potential equalization pin on the back
of the ventilator to the ground during battery (DC power) operation
If the standard patient circuit is not long enough when the ventilator is
placed outside the 100 Gauss boundary we offer the following options:
P/N M1173406 3.8m/ 12.5 Ft PATIENT CIRCUIT.
P/N M1173617 MRI PATIENT CIRCUIT
The only metal GEHC accessories that are acceptable for use within the MRI
Suite are the following:
P/N M1206572 GCX OXYGEN CYLINDER HOLDER, MRI CONDITIONAL
27
P/N M1162046 OXYGEN CYLINDER HOLDER, MRI CONDITIONAL
P/N M1206571 GCX iVENTTM201 ROLL STAND MRI CONDITIONAL
P/N M1162044 ROLL STAND AND MOUNTING BRACKET, MRI-CONDITIONAL
P/N M1162051 BEDRAIL MOUNTING MECHANISM
The iVentTM201 was tested with the Magnetom Trio, a Siemens Medical Solution
scanner under 3 Tesla, horizontal static magnetic field. For the test specifications
refer to MRI Conditional Tests Specifications below.
The outcomes of the test results were:
 There was no detectable magnetic attraction of the ventilator when placing
the iVentTM201 close to the 100 Gauss line.
 The operation of the ventilator was not affected when adhering to the
instructions as described above.
 The ventilator demonstrated minor visible RF interference (zipper
interference) which is detectable in some MR images. This effect varies from
site to site due to variation in MR shielding and should be evaluated by the
site radiologist.
28
1 Introduction
MRI CONDITIONAL TESTS SPECIFICATIONS
The iVent™201 MR conditional has been performed to demonstrate that there are
no known hazards in a specified MR environment with specified conditions.
The specified MR environment was:
Model: Magnetom Trio, Siemens Medical Solutions, Erlangen, Germany, 3

Tesla, horizontal static magnetic field, active shielded
Image frequency: 123.192952 MHz
Gradient System: max. 40 mT/m, Slew rate: 200 mT/m/ms
Software: Numaris/4, syngo MR 2004A 4VA25A
Coil: Body coil for transmitting & receiving signals
Field Strength: 3 Tesla
Spatial gradient: 0.12 mT/m
dB/dt 200mT/m/ms
RF: 13-231 Watts
SAR: 0.2 – 92.2
Spin echo: SE 2D
Time of echo (TE): 20 ms
Time of repetition 1000 ms
(TR):
Field of view (FoV): 400 x 400mm
Matrix 256 x 256 pixel
FoV phase: 100%
Flip angle 90°
Bandwidth/ Pixel: 100 Hz
Slice thickness: 5 mm
No. of slices: 1
Slice orientation: Coronal
No. of averages: 1
Phase encoding: Right –left (RL)
iVent™ 201 configuration during the test:

Ventilation Type: SIMV Volume Control
Tidal Volume: 500mL
PEEP: 5 cmH20
FiO2: 50
Power source: AC and battery
Distance from 100 Gauss (approximately 3 meters from the isocenter, this field
isocenter: strength must be measured with a gauss meter)
29
2 Setting up
2 SETTING UP
Introduction Page 32
Power Connection Page 32
Oxygen Supply Page 38
Patient Circuit Page 40
Other Connections Page 44
Patient Connection Page 49
Filters Page 49
Operational Case Page 51
The iVentTM201 User Interface Page 51
Controls and Power Up Page 52
31
INTRODUCTION
This section shows you how to set up the iVentTM201, and includes the following:
 Connecting to external AC or DC power
 Using the internal battery
 Verifying power condition
 Charging the battery, and proper recharging procedure
 Connecting to cylinder, central supply-system, or low-pressure oxygen
 Connecting the breathing circuit
 Installing heated humidification
 Connecting a pneumatic nebulizer
 Connecting a pulse oximeter
 Installing filters at the ventilator’s inlet and outlet
 Packing the unit in its optional transportation case
POWER CONNECTION
EXTERNAL POWER
The iVentTM201 can use either external alternating current (AC) or direct current
(DC) power. Both AC and DC inputs are located on the back panel of the
ventilator (see Figure 5). A hospital grade AC power cord is supplied
CAUTION Before connecting the ventilator to an AC or DC outlet, verify that the

external power supply is the correct voltage and frequency.
NOTE When connecting to an external battery use P/N M1162000
Connect one end of the AC or DC cord to the ventilator and the other to the
power outlet
WARNING To prevent electrical shock hazards, connect the power cord to a

properly grounded power outlet.
32
2 Setting up
Figure 5: External AC and DC power supply sockets. The AC power cord is connected to
the power inlet and fastened with the clip.
NOTE To prevent accidental disconnection of the AC power cord, secure it

with the cable clip
WARNING If the power cord is damaged, worn, or frayed, replace it

immediately
NOTE Before you turn off the iVentTM201 change the mode to Standby
mode (Page 61)
When the ventilator is in operation, icons at the bottom section of the screen
indicate the power state (Figure 6).
33
Figure 6: On-Screen Power Status Indicator
Icon Icon Name Power State
Power
When the iVentTM201 is connected to an AC
power supply, the screen shows a 3-pronged
power outlet icon.
Power
When disconnected from the AC power supply,
disconnect
the 3-pronged outlet icon is displayed with a red
“X” throughout.
DC power
When connected to an external DC power supply
connected
such as a battery, the screen shows “EXT” in blue
and AC
power
connected.
No External
When disconnected from the DC power supply,
battery
the screen shows “No EXT” in black
connected
CAUTION If the screen flashes “EXT” in red, the external battery voltage is low.
Replace the battery at once. Ensure adequate power is immediately
available
If the external battery connector is removed from the iVentTM201 IT MUST REMAIN
DISCONNECTED FOR 40 SECONDS before plugging it back in.
NOTE The iVentTM201 is designed to switch off the external DC battery if the
external battery voltage drops below 10 volts, in order to prevent
damage to the external battery. Some batteries may pose a fire hazard if
discharged below specified minimum charge levels. Because the
ventilator draws variable current while it is operational, the voltages
34
2 Setting up
provided by external batteries may change. To prevent switch-offs from

the external battery due to normal fluctuations in DC voltages, the
iVentTM201 is programmed to average the external DC voltage reading
over time. Therefore, if the user disconnects the external battery, the
ventilator interprets this as a dying battery and switches off the external
DC source for power. To re-enable input from the external battery
source, the user must leave the external battery disconnected for 40
seconds before reconnecting the external battery
INTERNAL BATTERY
The ventilator switches to an internal battery when it detects a loss of external

power. When fully charged, the internal battery can supply approximately 1 to 2
hours of power, under typical conditions and settings.
NOTE The extended internal battery can supply approximately 3 to 4 hours of

power under typical conditions and settings
CAUTION The iVentTM201 should only be used with a properly functioning battery.
The battery is automatically charged when attached to an external power source,

whether the ventilator is operating, in Standby mode, or switched off.
Batteries should undergo a full recharge procedure:
 Prior to initial use
 After prolonged storage
 Every 3 months during normal use
 If after 8 hours charging, the battery indicator fails to indicate a full charge
Indicator Colors Description Remarks
Green
Battery is fully charged
Gray/Green Indicator moves

Battery partly discharged
downward in 10%
increments
Gray / Red At 10%, the indicator
Low battery
changes to red
Gray Below 7%, the indicator
Empty battery
changes to gray
CAUTION The battery for the iVentTM201 is a critical component. It should be

replaced only with batteries supplied by VersaMed. If the user has
been qualified by VersaMed to service the iVentTM201, the battery may
35
be substituted and programmed according to the VersaMed Service
Manual and only with the battery specified in those notes
Full Recharge Procedure
CAUTION “Low Battery” or “Empty Battery” alarm appears, the internal battery must
y recharged, as described below
Continued usage of the battery after the “Empty Battery” alarm appears may
disable the battery’s charging capability and/or lead to battery failure. Ventilation
parameters may not be met in this condition.
NOTE The full recharge procedure first empties the battery of all its charge.
Charging it to capacity then allows for proper calibration of the battery
gauge.
To perform a full recharge procedure:

1. Plug the AC power cord into the ventilator. Verify that the amber Charge LED
is lit.
2. Allow the unit to charge for at least 10 hours.
NOTE If the Extended battery is in use, charge the unit for at least 24 hours
3. Switch on the ventilator. When the Weight Selection window appears, select
the 70kg patient weight setting.
4. Set the pressure alarm to 60 (cmH20).
5. Connect the ventilator with a patient circuit to the Rp20 resistor and test
lung.
6. Press Start on the ventilator (See page 59) for directions on starting the
iVentTM201.)
7. Adjust the tidal volume (Vt) so that a PIP (peak inspiratory pressure) of 40 is
attained on each breath – for example, a value of 850.
8. Disconnect the power cord. The AC Disconnect alarm sounds and a pop-up
window appears. Press the red Silence button on the keypad to
remove the pop-up window and silence the alarm.
9. Allow the ventilator to run off the battery continuously. When the Empty
Battery alarm sounds, clear it by pressing the red Silence button on the
keypad.
10. Place the unit in Standby mode (Page 61), then switch it off. Connect the AC
power cord.
11. Let the unit charge for at least 10 hours.
36
2 Setting up
NOTE If Extended battery is in use, charge the unit for at least 24 hours.
If after a full recharge, the battery indicator fails to reach Full, or a Low or Empty
Battery alarm displays, then the battery pack must be replaced.
Battery Pack Replacement
The following procedures explain how to replace the battery pack.

1. Disconnect the unit from the external power.
2. With a #1 Phillips-head screwdriver, remove all four screws from the battery
pack plate (Figure 7, Figure 8).
Figure 7: Unscrewing the Battery Pack Figure 8: Unscrewing the Extended Battery Pack
3. Using the handle, pull the Battery Pack out
Figure 9: Removing the Battery Pack Figure 10: Removing the Extended Battery Pack
4. Carefully slide the new battery pack into the chassis. Be sure it is
properly aligned.
5. Firmly and carefully push the battery back into place, making certain
the female connector at the front end of the pack plugs into the
ventilator.
6. Reattach the four screws.
37
7. Charge the battery by following the instructions in Full Recharge Procedure,
page 36.
OXYGEN SUPPLY
The iVentTM201 can use medical-grade oxygen from either

 A high-pressure source such as a central supply system or cylinder at 40-75
psi (2.8-5.1 bar).
WARNING The exact oxygen pressure which the iVentTM201 requires when
connected to medical grade oxygen depends on the version you have.
Check the back label (Shown in Figure 11) for the pressure levels of your
unit.
 A low-pressure oxygen source -- oxygen concentrator or flow meter device -

using the optional Low Pressure Oxygen Enrichment System (M1161007,
M1162020, M1162022)
When connecting the iVentTM201 to an oxygen supply, ensure that the correct
type of oxygen source is selected in Advanced Settings. [Main
Screen/Menu/Advanced Settings/Oxygen Supply (Pressure)] (See page 94). The
factory default is High pressure.
WARNING The O2 system must be calibrated every 6 months
We recommend calibration every 3 months to ensure the O2 system integrity. For

instructions for performing the O2 calibration see O2 Calibration Page 177.
HIGH PRESSURE OXYGEN SUPPLY
If using pressurized oxygen, connect the oxygen supply to the oxygen O2 inlet
connector at the back of the ventilator (Figure 11).
WARNING To prevent explosion hazard always ensure the oxygen connector is free
from oil.
CAUTION Verify that the oxygen supply is at the correct pressure before connecting to
the O2inlet.
When the unit is ventilating the measured concentration of delivered oxygen can
be viewed on the Alarm Settings screen (See page 145).
38
2 Setting up
Figure 11: The Oxygen Inlet Connector
CAUTION When using the iVentTM201 with a pressurized oxygen supply, the accuracy of
the oxygen concentration should be verified periodically with an external
calibrated oxygen analyzer
LOW PRESSURE OXYGEN SUPPLY
Connecting a low pressure O2 supply Adapter requires a low pressure O2

filter/adapter, fitted with a 22mm female port.
To connect the low pressure oxygen supply:
1. Remove the air inlet filter by turning it counterclockwise. Then install the Low
Pressure O2 filter/adapter with a clockwise turn.
2. You are now ready to connect the Low Pressure O2 Supply Adapter to the air
inlet port of the ventilator (Figure 12).
39
Figure 12: Low Pressure O2 Supply Adapter and Filter Installed
3. Be sure that the Low +M or Low option is selected under Oxygen Supply
(Pressure) in the Advanced Settings menu (See page 91).
CAUTION Do not attempt to use the FiO2 option above 60% when using a low pressure
oxygen supply
When not using a low pressure O2 supply, the Low Pressure O2 Filter must
NOT be used, as the 22mm port is easily blocked.
When the Low + M option is the selected in the Advanced Settings window, the
measured FiO2 level is displayed in the Main window of the screen.
PATIENT CIRCUIT
There are three ways to connect a patient circuit to the iVentTM201: using a
disposable patient circuit, a reusable patient circuit, or a dual limb patient circuit.
Consult a physician and an authorized VersaMed dealer for the appropriate
patient circuit that suits the patient’s needs.
Warning Only patient circuit accessories approved by VersaMed or authorized

by VersaMed dealers should be used with the iVentTM201.
40
2 Setting up
DISPOSABLE PATIENT CIRCUIT
The disposable patient circuit consists of an inspiratory limb with a connector at

one end of corrugated tubing, and a one-way valve connected to the Patient Wye
at the other end (Figure 13).
Figure 13: Patient Circuit Connections (Breathing Circuit)
The Patient Wye contains a flow sensor which is connected by two sensor tubes
to the luer connectors on front of the ventilator.
The Expiratory Limb fastens to the Patient Wye and leads to the Exhalation Valve,
which connects to a blue tube, the Control Line, and leads back to the ventilator
front panel. (See Figure 1)
To connect a disposable patient circuit:
1. Twist the knurled connector of the inspiratory limb onto the ventilator outlet.
The connector should fit snugly.
2. Connect the Flow Sensor tubing (the clear tubes) to their connectors. Ensure
correct connection of the Male and Female luer connectors on the flow
sensor tubing.
3. Connect the external Exhalation Valve control tube (the blue tube) to its
connector (marked with a blue dot).
4. Ensure that all connections are secure and airtight. Perform an Operation
Verification Test (O.V.T.), as described on page 60.
REUSABLE PATIENT CIRCUIT
The reusable patient circuit contains the same components as the disposable
circuit. It should be sterilized by a stem autoclave. The Versamed reusable Patient
Circuit can be sterilized up to 40 cycles.
CAUTION Prior to use, examine the patient circuit carefully. Should any damage,
discoloration or other abnormality appear on any part of the patient circuit, do
not use it. Replace the patient circuit.
41
To connect a reusable patient circuit:
1. Twist the knurled connector of the Inspiratory limb onto the Ventilator outlet.
The connector should fit snugly.
2. Connect the Flow Sensor tubing (the clear tubes) to their connectors. Ensure
correct connection of the Male and Female luer connectors on the flow
sensor tubing.
3. Connect the Exhalation Valve control tube (the blue tube) to its connector
(marked with a blue dot).
4. Ensure that all connections are secure and airtight. Perform an Operation
Verification Test (O.V.T.), as described in on page 60.
DUAL LIMB PATIENT CIRCUIT
The dual limb patient circuit contains two corrugated tubes, which can be used
as either inspiratory or expiratory limbs. The expiratory limb is connected to
external Exhalation valve, which is then connected to the iVentTM201.
To connect a dual limb patient circuit:
1. Connect the Exhalation valve and its accessories to the ventilator
2. Connect the Tubing.
NOTE The instructions provided below only refer to devices in which the
Transport Mounting plate (P.N.M1169908) is installed. For additional
information regarding Transport Mounting plate refer to your local
customer support.
To install the exhalation valve

1. Facing the device insert the Exhalation valve adapter into the handle on the
right side of the Transport Mounting plate, and guide the adapter into its
place.
2. Insert the Captive screw into the screw-hole on the adapter side, and screw it
in with a flat screwdriver.
3. Connect the Exhalation valve holder to the Exhalation Valve adapter. Verify
that the Exhalation Valve holder is firmly connected.
There are three ways to connect the adapter:
42
2 Setting up
Figure 14: Exhalation Valve Positions
The Exhalation valve is now connected and ready to use. The next step involves
installing the tubing to the ventilator.
To install the patient circuit:
1. Assemble the PEEP control tube by connecting one end to the barb fitting of
the exhalation valve and the other end to the barb fitting of the reusable Luer
fitting.
2. Connect the assembled PEEP control tube by securing the luer lock fitting to
the Exhalation valve luer inlet, which is marked with a blue dot on the front
panel of the ventilator (see figure 1, item number 4).
3. Secure the multi-use one way valve to the ventilator patient outlet (see figure
1, item number 5)
4. Connect the patient circuit inspiratory limb to the one way valve sitting on
the ventilator patient outlet and the expiratory limb to the exhalation valve.
5. If appropriate, fit the patient wye to the inspiratory and expiratory patient
circuit tubes.
6. Secure the flow sensor to the patient wye and connect the 2 sensor lines to
the ventilator sensor line luer inlets (see figure 1, item number 6).
Note: even though the luer lock fittings at the end of the flow sensor
sampling lines are non-interchangeable, it is good practice to verify that the
left (while facing the ventilator) male luer connector connects to the fitting on
the flow sensor which is closest to the patient
WARNING Before connecting a patient to the ventilator with a new circuit, you
must perform a complete Operational Verification Test (O.V.T.) as
described on page 60
43
CIRCUIT RESISTANCE
It is important to check the inspiratory and expiratory resistance specification of

the patient circuits used with the iVentTM201 ventilator to ensure they do not
exceed the following limits when adding attachments or other components or
subassemblies to the breathing circuit:
 O.6 KPA (6cmH2O) at 60 L/min for adult patients.
 O.5 KPA (5cmH2O) at 30 L/min for pediatric patients.
OTHER CONNECTIONS
HME
If required, a Heat and Moisture Exchanger may be placed between the flow
sensor and the patient connection.
CAUTION A contaminated HME filter can impede the ventilator’s Patient Disconnect
alarm detection. Do not use any filter that appears to be discolored or filled
with water.
NOTE Adding attachments, components or sub-assemblies to the iVentTM201

breathing circuit may increase the pressure gradient.
MDI
To administer medication, install an adapter for MDI treatment between the flow
sensor and the patient connection.
USING THE IVENTTM201 WITH HEATED

HUMIDIFICATION (1.4 STEPPER BASED MODELS
ONLY)
The following procedures explain how to connect the iVentTM201 to a heated

humidifier.
To use the iVentTM201 with a heated humidifier:
1. Disconnect the Inspiratory Limb from the ventilator outlet of the iVent201
and reconnect it to the humidifier outlet.
2. Remove the one-way valve from the Patient Wye and reconnect the tube.
44
2 Setting up
3. Connect the one-way valve to one end of a 1-2’ length of 22mm corrugated
tubing.
4. Connect the other end of the tubing to the ventilator outlet. Fasten the one-
way valve to the humidifier inlet. Be sure the directional arrow on the valve is
pointing towards the patient end of the circuit.
5. Connect the Male and Female clear sensor tubing connectors to the Male
and Female luer inlets on the front of the iVent201 as described above in
Patient Circuit, page 40.
6. Connect the blue Expiratory Sensor tube to the luer connector marked with a
blue dot on the front of the ventilator.
Figure 15: The iVentTM201 shown connected to a Fisher and Paykel Heated Humidifier Model MR850
Figure 16: Heated Humidifier Connections
NOTE If not using a heated wire circuit, placement of a water trap at the
45
lowest point of the Inspiratory Limb is highly recommended.
Follow the humidifier manufacturer’s instructions for the operation of

the humidifier.
If a heated wire circuit is required, use the VersaMed inlet equipment

(Patient Wye with one-way valve and exhalation valve. Replace the
VersaMed inspiratory tubing with the heated wire tubing.
WARNING To prevent water and/or secretions from entering the sensor

tubing, always keep the patient sensor tilted upward.
PNEUMATIC NEBULIZER
If required, a pneumatic nebulizer may be connected to the machine.
NOTE 100% oxygen is used as a driver gas for the nebulizer. Thus an external
high-pressure oxygen supply must be connected to the machine to
enable the nebulizer operation.
To activate the nebulizer you need to select the High option under
Oxygen Supply in the advance menu (See page 95)
To connect a nebulizer device:

1. Connect the Nebulizer tube to the Nebulizer outlet on the front panel. The
Nebulizer icon is still displayed in gray at the lower bar of the display,
showing that the nebulizer is connected but not activated (Figure 17).
Figure 17: nebulizer Icon
2. Install the Nebulizer with the required medication to the patient circuit after
the Patient Wye and the Flow Sensor.
3. Connect the other side of the Nebulizer tube to the nebulizer.
4. To activate the Nebulizer see page 102.
PULSE OXIMETER
The pulse oximeter and accessories are indicated for continuous non-invasive
monitoring of oxygen saturation (SpO2) and pulse rate (measured by the SpO2
sensor). The pulse oximeter and accessories are intended for use with adult and
46
2 Setting up
pediatric patients in hospital, hospital types facilities, mobile/ transport functions,

and home environments.
A pulse oximeter can be connected to the iVentTM201 ventilator allowing the

operator to continuously monitor patient’s oxygenation saturation on the
iVentTM201 screen.
WARNING Use only Nonin manufactured pulse oximeter sensors. Using other
manufacturer’s sensors can result in improper oximeter performance.
Explosion Hazard: Do not use the pulse oximeter in an explosive atmosphere

or in the presence of flammable anesthetics or gasses.
Carefully route cables and connections to reduce the possibility of

entanglement and strangulation.
The SpO2 device do not meet defibrillation-proof requirement per IEC 60601-
1.
Do not sterilize the SpO2 device. Refer to the cleaning instructions included in
the sensor instruction.
Do not use the pulse oximeter in the MRI environment.
To connect the pulse oximeter to the iVentTM201 ventilator:

1. Remove the Pulse Oximeter sensor and the unit connector cable from the kit.
One end of the unit connector is gray and connects to the sensor. The other
end of the unit connector cable has two connectors, a Keyboard connector
and an RS-232 connector (Figure 18).
Figure 18: The Pulse Oximeter Connectors
2. Connect the Pulse Oximeter sensor to the gray end of the Unit Connector
cable (Figure 19).
47
Figure 19: Pulse Oximeter Sensor
3. At the rear panel of the iVentTM201 device, connect the following:

 The Keyboard connector to the Keyboard port.
 The RS-232 connector to the RS-232 port (COM1 or COM2), located on the
right side of the device. (Figure 20).
Keyboard
Connector
LAN Remote Alarm

Connector
RS-232
Connectors:
COM1
COM2
Figure 20: iVentTM201 Rear Panel
You can connect the RS-232 to any communication port. The iVentTM201 sets the
communication automatically. To configure the communication port see page
186.
48
2 Setting up
REMOTE ALARM
The iVentTM201 can be connected to a remote alarm system via the Remote
Alarm Connection port on the back panel shown in Figure 20.
Using Normally Opened (NO) or Normally Closed (NC) signals, this connection port
allows alarm signal activation in locations remote from the ventilator triggered by
ventilator alarm conditions. For connector details see Appendix H: Remote Alarm
Connector.
WARNING Connect the Remote Alarm Cable only to its designated port marked
accordingly.
NOTE The iVentTM201 is supplied with the Remote Alarm port covered (See Figure 20).
Unscrew the cover to connect the Remote Alarm cable.
The LAN port is not in use and should be covered with the plastic cap at all
times
SENSOR LINE MAINTENANCE
The iVentTM201 monitors the sensor lines and periodically sends pressurized air
through the lines to clear them of any accumulated material. It is possible for
secretions and/or condensation to accumulate. Should this occur:
1. Do not attempt to clean sensor lines while a patient is connected to the
iVentTM201.
2. Disconnect the sensor lines from the connectors on the iVentTM201.
3. Insert the end of a syringe into one end of the sensor line and discharge air
through it until the line is clear of condensation or secretions.
4. Re-attach the sensor lines.
PATIENT CONNECTION
When connecting the patient, make sure the Patient Wye is positioned so that the
flow sensor tube connections are on top.
Angle the Patient Wye downward to help prevent fluid accumulation.
FILTERS
WARNING Do not use the iVentTM201 without the air-inlet filter and a bacterial filter
before the patient circuit.
49
AIR INLET FILTER
The air inlet filter (part no. M1161007 )screens out particulate matter from
ambient air (Figure 21).
Figure 21: Air Inlet Filter
WARNING Failure to use an air inlet filter may result in severe damage to the
internal components of the iVentTM201.
The air inlet filter must be replaced every 500 hours or every thirty days of
operation. See page 173 for air filter maintenance procedures.
BACTERIAL FILTER
A user-supplied bacterial filter prevents contamination of the patient circuit

components, and prevents bacteria, excessive humidity and liquids from entering
the iVentTM201.
WARNING Failure to use an adequate bacterial filter may cause severe damage
to internal pressure and flow sensors, which may result in ventilator
failure.
CHEMICAL, BIOLOGICAL, RADIOLOGICAL AND

NUCLEAR FILTER
In the event of environmental contamination by hazardous or toxic substances,

the air-inlet filter should be replaced with an optional CBRN canister. CBRN
canisters are designed for first-response protection against nuclear, toxic, or
biological particulate material and chemical vapors, gases, and mists/aerosols
and tear gas.
50
2 Setting up
The CBRN filter fits into the iVentTM201 via an optional air inlet adapter (item
M1161967). Remove the air inlet filter from the iVentTM201 by turning it
counterclockwise. Then fasten the air inlet adapter to the CBRN filter by twisting
it on clockwise. Finally, screw the CBRN canister with the adapter into the air inlet
adapter.
Figure 22: CBRN Filter
OPERATIONAL CASE
With an optional soft case (item M1161883 )(Figure 23) the iVentTM201 can be
operated in bad weather conditions, such as rain or snow. Padding and
protected ventilation ports enable full function in a variety of situations.
Figure 23: Soft Case
THE IVENTTM201 USER INTERFACE
It is important to invest time to acquaint yourself with the iVentTM201 and how the
Control Knob is integrated with the screen and the operation of the iVentTM201.
Connect a test lung with an Rp20 resistor and patient circuit. Switch on the unit,
and navigate through the features discussed in this section. Rotating the Control
Knob at the menu level allows for easy, automatic selection of ventilation modes.
Choosing the best parameter for a patient is as easy as switching on the
iVentTM201 and selecting the patient’s ideal body weight.
51
CONTROLS AND POWER UP
THE FRONT PANEL
Located above and to the right of the ventilator outlet, is the rotational Control
Knob, which allows control of and access to all the ventilator functions via the
LCD screen. Turn the knob to change a value, or navigate through a menu screen
or through a list of choices. Press the knob and the iVentTM201 responds with a
tactile click and with audible feedback – to select or confirm a choice, or to
access another menu.
Where a numeric value is required, selection is done by rotating the dial to move
a virtual slider bar, spin button, or counter, in increments calibrated precisely
along the full range of values. In some settings menus, one press of the knob is
enough to instantly select or confirm a value, which thereafter immediately
returns you to the previous screen.
Five dedicated keys are positioned below the LCD (Figure 24):
Figure 24: the iVentTM201 Front Panel
Silence
Silence is used to immediately mute the audible alarm and minimize the
corresponding red message pop-up window. A two-minute timer is activated and
displayed in the lower right corner of the display instead of the time-date field,
alongside the silenced alarm icon (Figure 25).
One short press on the Silence key resets the time to 2 minutes. Press the Silence
key for one second and it re-activates pending alarms.
52
2 Setting up
Figure 25: Status Window After Alarm Has Been Silenced
Manual Breath
Manual Breath delivers a single breath at the set tidal volume or pressure. In
CPAP/PSV ventilation mode, where there is no definition for machine breath, the
Manual Breath is set according to the default volume control for the specified
patient weight chosen at startup.
Hold
Hold activates and/or cancels the hold maneuver. Press the button once to
initiate an inspiratory hold maneuver, which allows the calculation of static
compliance. Press it twice to initiate an end to the expiratory hold maneuver,
which allows the calculation of intrinsic PEEP. For more details see page 235.
Clear
Clear has several functions. Press it to perform the following:

 Clear the screen of its current selection and return the operator to the
previous screen or menu selection – just like the Escape key on a computer
keyboard.
 Minimize any red alarm-warning pop-up window and mute the alarm sound
for 30 seconds. If clear is pressed again within 30 seconds, an alarm warning
pop-up window appears.
 When Clear is pressed and held, all corrected alarm messages (displayed in
green) are cleared.
LED Indicators
Three LED (light emitting diode) indicators provide a quick indication of power and
alarm status:
 The red alarm LED blinks rapidly when the iVentTM201 detects an alarm
condition.
53
 The amber charge LED lights to indicate that the iVentTM201 is connected to
external power.
 The green on LED indicates that the power is switched on.
The Screen
The LCD screen is organized to allow rapid access to the ventilator’s functions.
The monitoring or control of any critical parameter is performed with ease.
 Baseline indicators and alarms – emergency alerts and alert status
indicators, power and battery states, date and time, and the Menu access
button -- are all displayed along the bottom of the screen indicators.
 Set values are displayed in black
 Measured and calculated values are displayed in blue -- flashing values
indicate that a set value was not obtained.
Here is a quick overview of the most important screens:
The Main Screen (Figure 26) is the first screen displayed when the iVentTM201 is
placed in Standby or Start Mode.
The slider gauge along the left side of the screen displays the real-time measured
Peak Inspiratory Pressure below a digital readout of the last peak inspiratory
pressure value.
On the top left of the screen, a large shows the total measured respiratory rate in
breaths per minute in large blue numbers. The selected/default respiratory rate
is shown in smaller black numbers below. Proceed to the Respiratory Rate
option to enable and change the number of breaths per minute.
Beside the Respiratory Rate option, there is also the Tidal Volume option. This
displays the exhaled Tidal Volume and allows adjustment to the set Tidal Volume.
(See page 69 for more details about the Tidal Volume display.)
On the top right of the screen is the Mode Selection option, which shows the
current ventilation mode. This option allows you to change modes (See page 62).
Selecting and clicking on a mode brings up the appropriate Mode screen for the
selected ventilation mode. Use this screen to view or adjust ventilation
parameters.
When the ventilator is operating, the middle section of the Main screen displays
pressure/flow waveforms. The optional waveforms package permits a host of
possible display characteristics. (See page 108 for a guide to the waveform
package.)
54
2 Setting up
Figure 26: The Main Screen
If a pulse oximeter is connected to the iVentTM201 the SpO2 levels and Heart rate
are displayed on the lower right side of the screen (Figure 27).
Figure 27: The Main Screen With the Pulse Oximetry Monitoring Window
55
Notes:
56
3 Operating the iVentTM201 – Setting Modes and Parameters
3 OPERATING THE IVENTTM201 –

SETTING MODES AND
PARAMETERS
Operation of the iVentTM201 Page 59
Common Parameters Page 64
57
INTRODUCTION
The iVentTM201 offers advanced capabilities for adjusting ventilation parameters

for each mode. In this section you learn how to:
 Start the ventilator
 Choosing a patient weight
 Test the patient circuit
 Choose a mode of ventilation
 Use the Mode screen and the Menu screen to change parameters
 Understand breath data returned by the iVentTM201
 Reset parameters to default values
OPERATION OF THE IVENTTM201
The following section describes the various functions and capabilities for
operating the iVentTM201.
POWER UP AND WEIGHT SELECTION
If you have installed a patient circuit then you are ready to begin operating the
iVentTM201. To turn on the power, press the green ON/OFF switch on the rear
panel.
When power is turned on, the software performs a self-test. Once the boot up
process completes (after approximately thirty seconds) you hear a beep and the
screen (Figure 28) asks you to select the patient’s body weight, which sets the
default ventilation parameters.
Figure 28: The Patient Weight Selection Pop-Up Window
59
NOTE Parameters for all the iVentTM201’s possible ventilation modes are set when
you choose a patient weight upon startup. For a view of the default
parameters according to weight, refer to Table 1: Default Start Parameters for
Volume Ventilation for 10 kg to 70 kg through Table 4, page 107.
The default selection for patient weight range for the iVentTM201 is 70+kg. This
may be changed using the Configuration utility described on page 185.
As a safety measure, within a few seconds after the patient weight selection pop-
up window appears, the iVentTM201 generates airflow to see if resistance is
encountered in the patient circuit, which means that the patient is connected.
NOTE This is an optional feature, not available in all iVentTM201 units.
 If the iVentTM201 detects resistance, it sounds an alarm and begins

ventilating in SIMV pressure control mode at a rate of 15 breaths per minute,
P(INSP) 20 and a PEEP of 5.
 If the iVentTM201 detects no airway resistance, it enters Standby mode.
During this state, if flow is detected in the patient circuit the iVentTM201
performs an auto-start.
O.V.T
The patient circuit must be tested each time it is connected, so if you are
reconnecting a patient circuit or using a new one, you must perform the
Operational Verification Test (O.V.T.). This test, which takes less than one minute,
checks the integrity of the breathing circuit and audible alarm functionality.
Two plastic caps for covering the ends of the patient circuit are required for the
O.V.T. They are included with all patient circuits offered by Versamed.
To perform an O.V.T.:
1. Rotate the Control Knob until the O.V.T. option is selected in bright blue.
2. Press the Control Knob until you hear a click. The O.V.T. Instructions pop up
window appears (Figure 29).
60
Figure 29: The Initial O.V.T Pop-Up Window
3. Follow the instructions on the screen. Use the plastic caps to seal off the
following:
 The patient Wye sensor, and
 The exhalation valve
4. Press the knob to begin the test. A pop-up window appears which indicates
the test has begun.
5. After several seconds, another pop-up window appears and instructs you to
remove the cap on the exhalation valve leaving the cap on the Wye
outlet.
6. After the ventilator performs further testing, it sounds an alarm. If you can
hear the alarm, press the Control Knob to complete the O.V.T. If remote
alarm is connected verify the alarm is activated in remote station.
Once the iVentTM201 has successfully completed the O.V.T., the patient circuit and
ventilator are ready for use.
If the O.V.T. fails:
1. Verify that both Flow Sensor tubes are properly and snugly connected to the
correct luer ports on the front of the iVentTM201. (Note: Remember that two
lines go to the patient Wye connectors, and the blue line goes to the
Expiratory Valve Control connector.) Repeat the test.
2. If the O.V.T. fails once again, then replace the patient circuit.
3. If after replacing the patient circuit, the O.V.T. still fails, try re-calibrating the
ventilator. If calibration fails to correct the O.V.T. failure, immediately remove
the ventilator from service and contact a Versamed approved technician.
STANDBY AND PATIENT VENTILATION
When you have selected the weight, the iVentTM201 enters Standby, ready to
ventilate the patient with a press of the Control Knob. By default iVentTM201
starts up in SIMV Volume control.
To start ventilation from Standby mode:
61
Return to the Main screen, rotate the Control Knob until the Start option is
selected, then press the Control Knob.
To return the ventilator to Standby mode:
1. Return to the Main screen, turn the Control Knob to select the Mode
Selection option on the top right of the LCD display, and press the Control
Knob.
2. At the bottom of the drop-down menu is Standby. Dial the knob until
Standby is selected and press. Then select the Yes option in the
Confirmation window and press the knob. The ventilator suspends
operation.
NOTE Always return the iVentTM201 to Standby mode before powering down
CHANGING VENTILATION MODE
The Mode Selection option is on the top right side of the LCD display (Figure 30):
Figure 30: The Mode Selection Menu Selected
To change the mode, turn the Control Knob to select the Mode Selection option,
then press. The Ventilation Modes menu pop-up window appears (Figure 31)
which offers six options including Standby:
62
Figure 31: The Ventilation Modes Selection Pop-Up Menu Window
NOTE Depending on which iVentTM201 model you have

purchased, not every mode may be available.
Turning the Control Knob moves the selected bar through the choices. When the
required mode is selected, press the knob to accept it. A parameter screen is
displayed where you can either accept the default ventilation parameters or
change any of them.
For example, to change to SIMV pressure control mode from SIMV volume
control mode:
1. Make sure that you start from the Main screen
NOTE To return to the Main screen, press the clear key on the keypad below the display.
This returns you to all previous screens until you return to the Main screen.
2. From the Main screen, turn the Control Knob to select the Mode Selection
option, as shown in Figure 30. By default, the iVentTM201 starts in SIMV
Volume Control, abbreviated “SIMV Vctrl.”
3. Press the Control Knob and the Parameters screen appears. Turn the knob
clockwise one click to select Pressure Control (Figure 32):
63
Figure 32: Pressure Control Option Selected
4. Press the knob to accept the selection. The SIMV Pressure Control
Parameters screen appears (Figure 33).
Figure 33: The SIMV Pressure Control Parameters Screen
5. Note that Accept is automatically selected, which makes it possible to accept

the default parameters immediately and go directly into patient ventilation.
This is after you have verified that the patient settings are correct.
NOTE The user must press Accept to change both the mode and the parameters.
COMMON PARAMETERS
This section details how to change:

 Breath rate
64
 Tidal volume
 Pressure limit
 Oxygen level
 Peak flow
 Pressure support
 PEEP
 Triggers
 Inspiratory time
 Rise Time
 Flow Termination – Exhale sensitivity (Essens)
CHANGING VENTILATION PARAMTERS – OVERVIEW
CAUTION Only a fully qualified professional should change these settings
The iVentTM201 provides two different ways to change ventilation parameters:

through the Main screen and through the Mode Parameters screen.
NOTE To quickly change an individual parameter setting, the fastest way is

through the Main screen. If you need to adjust several settings at once,
navigate to the Mode Parameters screen and make each required
adjustment. When you have set each parameter, you can accept all of
them at once.
To change ventilation parameters through the Main Screen:

1. Return to the Main screen -- if you are not already there, press the Clear
button until you return to it.
2. Turn the Control Knob to select the parameter you want to adjust.
3. Press the Control Knob.
4. Adjust the setting to the required value.
5. Press the Control Knob again to confirm your changes and return to the Main
screen.
To change ventilation parameters through the Mode Parameter Screen:
1. From the Main window, choose the Mode Selection option and select the
required ventilation mode. The Parameters screen appears.
2. Dial the Control Knob to select the particular setting you wish to change.
3. Press the knob to display the setting’s control window.
4. Turn the knob until the parameter has been changed to the required level or
value.
65
5. Press the knob again to save the setting. You are returned to the Parameters
screen.
6. Continue through the other parameter options, and choose and change until
you have set all the values you want. Once you have finished, select
Accept at the bottom of the screen. Press the knob and your new
selections are saved.
NOTE To abort the selection process and return the parameter to the previously
chosen value, press the Clear button
To change ventilation parameters through the Default Setting Option:

See page 105 Restore Default Settings, for instructions
CAUTION Selecting Restore Defaults resets ALL values to their default state, including
the Ventilation mode (SIMV Volume Control). For more information about
restoring defaults. See page 105 Restore Default Settings
THE SELECTION INTERFACE
Most of the quantitative parameters are presented in the form of an oval dial with
black numerals – in the iVentTM201 black numbers represent Set values – on solid
teal. Turning the Control Knob increases or decreases the selected value as
indicated by the black numerals inside the oval. A dark blue ribbon indicator
moves around the periphery of the oval to show the scale of the selected value.
Recommended ranges are outlined in green, while values outside the
recommended ranges are outlined in red. As a precaution, if a setting you are
inserting exceeds or fails to meet recommended settings for the patient weight, a
bright yellow Caution flag appears, as shown in Figure 34 below.
Figure 34: Example of Respiratory Rate exceeding the Recommended Value
Other parameter settings are adjusted on a slider gauge.
66
The chosen values are not operational until you confirm your selection by
pressing the Control Knob, which takes you back to the Main screen. The new
value(s) you have selected are shown in black.
NOTE To abort the selection process and return the parameter to the previously
chosen value, press the Clear button.
To return the selection of ALL ventilation parameters to their default levels for
a given patient weight see page 105.
ADJUSTING THE BREATH RATE
The following procedures explain how to adjust the breath rate, which is
measured in breaths per minute.
To adjust the breath rate during the ventilation:
1. From the top most left side of the Main screen select the Respiratory Rate
option (Figure 35).
Figure 35: Respiratory Rate Selected
Or select the Rate setting option from the Mode Parameter screen (Figure 36).
67
Figure 36: Respiratory Rate Selected on the Mode Parameter Screen
2. Press the Control Knob to display the Set Rate pop-up window (Figure
37).
Figure 37: The Set Rate Pop-Up Window
3. Turn the Control Knob to change the rate, measured in breaths per
minute. Notice that the calculated values for Breath Period,
Inspiratory Time, and Mandatory Minute Volume change
automatically.
4. After setting a new value, press the Control Knob to confirm and accept
the settings.
NOTE Certain modes and values described in this section are not
operational in all iVentTM201 models.
When the setting for Inspiratory Time is Adaptive, the value to reach
I.E. ratio 1:2 is displayed. Once this value reaches 2 seconds, it does
not change since the Adaptive Respiratory algorithm does not allow
Tinsp above 2 seconds.
When the setting for Inspiratory Time is Manual, the value is

continuously displayed at all breath rate values.
68
ADJUSTING THE TIDAL VOLUME
The Tidal volume is the amount of air inhaled and exhaled in a breath and can be
adjusted during the ventilation.
To adjust the tidal volume:
1. Select the Tidal Volume (or in Pressure Control select Volume Limit) setting
from the top middle section of the Main screen (Figure 38):
Figure 38: Tidal Volume Selected on the Main Screen
Or select Tidal Volume in the Parameters screen (Figure 39):
Figure 39: Tidal Volume Selected on the Parameters Screen
2. Press the Control Knob to display the Tidal Volume pop-up window (Figure
40).
69
Figure 40: The Tidal Volume Pop Up Window
3. Turn the Control Knob to change the Tidal Volume settings.

4. After setting a new value press the Control Knob to confirm and accept
the settings.
Changing the Tidal Volume affects the Mandatory Minute Volume. If a Manual
Peak Flow is set and does not deliver the set volume in the allotted inspiratory
time, then the display flashes. During operation of Adaptive Flow, spontaneous
and mandatory peak flows are displayed and cannot be changed.
Breath Types
The following section describes the various breath types which are each
represented by their own specific icon.
The Tidal Volume portion of the Main screen indicates the Exhale Minute Volume
(MV) on the left side of the window.
Figure 41: The Tidal Volume Window With the Breath Type Icon Displayed
The upper left corner of the Tidal Volume screen (Figure 41) also indicates the
type of breath delivered, by displaying one of several icons beside the exhale
volume, which are explained below
Figure Icon Description
Double Bar No measurement
70
Pink Fan Mandatory Assist Breath (patient initiated) - the

iVentTM201 has responded to patient initiation by
delivering a breath.
Blue Fan Mandatory Ventilator Breath (ventilator initiated) -

the iVentTM201 has delivered a breath without
patient initiation.
Green Sigh Sigh Breath
Pink Man Pressure Support Breath: In SIMV and CPAP/PSV

modes, the ventilator has delivered a patient
breath that has elevated the inspiratory pressure
above PEEP.
Green Z: Automatic Zeroing of Sensors:
The iVentTM201 has calibrated itself to ensure that
the sensors are measuring accurately.
Blue P Purge sensor lines function activated

Periodically, the iVentTM201 sends a puff of high-
pressure air through the sensor lines to clean them.
You can set the purging interval through the
Advanced Menu – Humidifier Settings (See page
99). This icon indicates that the Purge System is
now activated.
ADJUSTING PRESSURE
The pressure setting depends on the ventilation mode:

 When in a Volume Control ventilation mode you can adjust the maximum
acceptable pressure - P(Limit)
 When in Pressure control mode you can adjust the target pressure of the
ventilation - P(insp).
 When in Adaptive Bi-Level you can adjust the High pressure alarm – P(Alarm)
To adjust the pressure:
1. Select the option in the top right corner of the Main screen, below the
Mode Selection (Figure 42).
71
Figure 42: Pressure Limit Selected on the Main Screen
Or select the Pressure option in the Mode Parameters screen (Figure 43):
Figure 43: Pressure Limit Selected on the Mode Parameters Screen
2. Press the Control-Knob to display the Set Pressure pop-up window (Figure
44).
Figure 44: The Set Pressure Pop Up Window
72
3. Turn the Control Knob to choose the required numeric pressure value. The
high pressure alarm is adjusted automatically to the value PLimit + 5
cmH2O. It can also be set to any required value using the Alarm menu. For
more information see page 148.)
4. Press the Control Knob to confirm and save the settings.
ADJUSTING FIO2
The O2 percentage delivered to the patient is adjustable.

NOTE Adjusting FiO2 can be performed only when the Oxygen Supply -
High option is selected in the Advanced Setting menu (For more
information see page 95)
To adjust the FiO2:

1. Select the FiO2 setting from the top left of the Main screen (Figure 45).
Figure 45: FiO2 Selected on the Main Screen
Or select the FiO2 on the Mode Parameter screen (Figure 46):
73
Figure 46: FiO2 Selected on the Mode Screen
2. Press the Control Knob to display the FiO2 pop-up window (Figure 47).
Figure 47: The FiO2 Pop Up Window
3. Turn the Control Knob to adjust the FiO2 level. The range is 21% to 100%.
4. Press the Control Knob to confirm and accept the settings.
Changing the FiO2 percentage automatically changes the O2 alarm based on a
default margin of +20%, - 10% O2. The O2 alarm parameters can also be
adjusted from the Alarm Settings (See page 150.)
ADJUSTING PEAK FLOW
In volume control ventilation modes you can adjust the peak flow. You can also
set the ventilation to adaptive peak flow which matches the flow to the patient
spontaneous flow.
To adjust the peak flow:
1. Select the Peak Flow setting from the second row of options on the Main
screen (Figure 48):
74
Figure 48: Peak Flow Selected on the Main Screen
Or select the Peak Flow on the Mode Parameters screen (Figure 49):
Figure 49: Peak Flow Selected on the Mode Parameters Screen
2. Press the Control Knob to display the Peak Flow pop-up window (Figure 50).
75
Figure 50: The Set Flow Pop-Up Window
3. Turn the Control Knob to change the peak flow value.

4. To set the flow to Adaptive Flow™, turn the Control Knob counterclockwise
until Adapt is displayed.
If Adaptive Flow™ is selected, a blue icon with a black circled A is displayed on the
Main screen (Figure 51):
Figure 51: Adaptive Flow Icon
If a Manual Peak Flow is set, a transparent icon with a black circled M is

displayed on the Main screen (Figure 52).
Figure 52: Manual Peak Flow Icon
ADJUSTING PRESSURE SUPPORT VENTELATION
The Pressure Support Ventilation (PSV) during the ventilation is adjustable.

To adjust the PSV:
1. Select PSV setting from the second row of windows on the Main screen
(Figure 53):
76
Figure 53: PSV Selected on the Main Screen
Or select the PSV option in the Mode Parameters screen (Figure 54):
Figure 54: PSV Selected on the Mode Screen
2. Press the Control Knob. The PSV pop-up window appears:
Figure 55: The PSV Pop-up Window
3. Turn the Control Knob to adjust the PSV level.
77
NOTE The PSV value cannot be set to a value greater than P(Limit) – PEEP
or a maximum value of 60 cmH2O.
4. Press the Control Knob to confirm and accept the settings
ADJUSTING PEEP
The PEEP level of the patient is adjusted to a set value during the ventilation.
To adjust the PEEP:
1. Select PEEP from the second row on the Main screen (Figure 56):
Figure 56: PEEP Selected on the Main Screen
Or select the PEEP option in the Mode Parameters screen (Figure 57)
Figure 57: PEEP Selected on the Mode Screen
2. Press the Control Knob. The set PEEP pop-up window appears:
78
Figure 58: PEEP Pop-Up Window
3. Turn the Control Knob to adjust the PEEP level. The Inspiratory Pressure
limit above PEEP is shown at the bottom of the Setting pop-up window as
adjustments are made.
NOTE The PEEP value cannot be set higher than P(limit) – PSV or a maximum
value of 40 cmH2O.
ADJUSTING TRIGGER SENSITIVITY
When the patient's breathing is measured, and above the adjustable value, then
it is identified as spontaneous breath.
To adjust the triggers sensitivity:
1. Select the Triggers option from the bottom left section of the Main screen
(Figure 59):
Figure 59: Triggers Selected on the Main Screen
Or select the Triggers option in the Mode Parameters screen (Figure 60):
79
Figure 60: Triggers Selected on the Mode Parameters Screen
2. Press the Control Knob. Two sliding numeric gauges appear (Figure 61)
Figure 61: The Triggers Slider Gauges
3. Dial the Control Knob to select the required pressure value.

4. Press the Control Knob to confirm the pressure settings and select the Flow
gauge.
5. Dial to select the required Flow settings.
6. Press the Knob to confirm and accept the settings.
ADJUSTING INSPIRATORY TIME
The inspiration time is the time between the start of the inspiration until the
exhalation is started.
To adjust the inspiratory time:
1. Select the Inspiratory Time setting from the middle of the lower portion of the
Main screen (Figure 62):
80
Figure 62: Inspiratory Time Selected on the Main Screen
Or select the Inspiratory Time option on the Mode Parameters screen (Figure
63):
Figure 63: Inspiratory Time Selected on the Mode Parameters Screen
2. Press the Control Knob. The I. Time pop-up window appears (Figure 64)
Figure 64: The I Time Pop-Up Window
81
3. Turn the Control Knob to change the Inspiratory Time. Notice that the I:E
ratio is calculated as you adjust the value.
4. To return to Adaptive I. Time™, turn the Control Knob counterclockwise until
Adapt appears.
If Adaptive Inspiratory Time is selected a blue icon with black circled A is
displayed on the Main screen (Figure 66). If Manual Inspiratory Time is selected,
a transparent icon with black circled M is displayed on the Main screen (Figure
65).
Figure 65: Manual I Time Figure 66: Adaptive I Time
If a manual I time is set that does not allow for a 1:1 I:E Ratio, or does not allow
the set volume to be delivered within the set I time, then the display flashes
during the ventilation.
ADJUSTING RISE TIME
The iVentTM201 provides four possible values for Rise Time (drive): Mid, High, Max
or Auto. These options refer to the speed of the engine acceleration during the
inspiratory phase.
In Adaptive Bi-level you can adjust the rise time between 0.1 to 1.5 seconds.
NOTE The factory default value for rise time is “Auto”. It is recommended that this
setting not be changed
To adjust time value:

1. Select the Rise Time settings from the lower portion of the Main screen
(Figure 67):
82
Figure 67: Rise Time Selected on the Main Screen
Or select the Rise Time option in the Mode Parameters screen (Figure 68):
Figure 68: Rise Time Selected on the Mode Parameters Screen
NOTE The Rise Time option is located in the top left of the Mode
Parameters screen for Adaptive Bi-Level mode.
2. Press the Control Knob. The Rise Time pop-up window appears (Figure 69):
83
Figure 69: The Rise Time Pop Up Window
In Adaptive Bi-Level ventilation mode the rise time can be adjusted between 0.1
and 1.5 seconds (Figure 70).
Figure 70: The Rise Time pop up window in Adaptive Bi-level ventilation mode
3. Turn the Control Knob to select the required value.

ADJUSTING FLOW TERMINATION (ESENS)
The iVentTM201 terminates the pressure support breath delivery after flow drop
detection to an adjustable percentage of the peak flow. The flow termination
(exhale sensitivity) can be set between 10 to 90 percentages of the peak flow.
To adjust the flow termination:
1. Select the Esens option in the lower portion of the Main screen (Figure
71):
84
Figure 71: Esens Selected on the Main Screen
Or select the Esens option in the Mode Parameters screen (Figure 72):
Figure 72: The Esens Option Selected on the Mode Parameters Screen
2. Press the Control Knob. The Set Flow Term pop up window appears
(Figure 73):
Figure 73: The Set Flow Term Pop Up Window
3. Turn the Control Knob to change Flow termination percentages.

85
Notes:
86
4 The Main Menu
4 THE MAIN MENU
Navigating the Main Menu Page 89
Alarm Settings Page 90
Advanced Settings Page 91
Restore Default Settings Page 105
Show Graphs Page 108
Show Trends Page 112
Show Loops Page 117
Show Mechanics Page 119
Pulse Oximetry Screen Page 120
Show Log Book Page 123
Display Page 124
O.V.T. Page 127
Maintenance Page 127
87

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3 OPERATING THE IVENTTM201 – SETTING MODES AND PARAMETERS...................................................... 57

4 THE MAIN MENU............................................................................................................................................... 87

7 CARE, MAINTENANCE AND TESTS ............................................................................................................... 171

APPENDIX A: GLOSSARY .......................................................................................................................................... 191

APPENDIX B: WARRANTY ........................................................................................................................................ 199

APPENDIX C: OPERATING THEORY ........................................................................................................................ 203

Operating Theory ..........................................................................................................................................................................205

APPENDIX D: THEORY OF BREATH DELIVERY ...................................................................................................... 211

APPENDIX E: VENTILATION MODES....................................................................................................................... 223

APPENDIX F: HOLD FUNCTION AND STATIC MECHANICS MEASUREMENTS .................................................. 233

Front Panel Controls ....................................................................................................................................................................235

APPENDIX G: ACCESSORIES .................................................................................................................................... 241

Disposable Breathing Circuit ...................................................................................................................................................243

APPENDIX H: REMOTE ALARM PINOUT ................................................................................................................. 265

APPENDIX I: PART NUMBERS AND ACCESSORIES ............................................................................................... 269

INDEX ......................................................................................................................................................................... 275

This chapter contains the following sections:

Intended Use Page 25

Use of the iVentTM201 With MRI Page 25

The iVentTM201 is a compact, portable, multi-featured, microprocessor-controlled

In addition, the iVent™201 has the following advanced features:

The iVent™201 must only be operated by authorized medical personnel certified

LOOKING AT THE IVENT™201

Item Number Description

Figure 2: Back View of the iVent™201

10 4 x Battery pack screws

CAUTIONS AND WARNINGS

CAUTION The iVentTM201 is a restricted medical device to be operated by

Always perform a complete Operation Verification Test (O.V.T.) when

Using the iVentTM201 in combination with devices such as humidifiers

The iVentTM201 must not be operated immediately following storage

The iVentTM201 internal battery contains lead and must be disposed of

Do not connect the O2 supply when equipment is not in use.

The remote alarm should be considered secondary to the ventilator’s

Verify the remote alarm device functionality before use

The remote alarm connector should be connected to a nurse station

WARNING The iVentTM201 is a life-sustaining device. Do not rely solely on the

SYMBOLS AND LABELS

Indicates that you should “Refer to documentation for

Direct Current ( DC) and Alternating Current (AC)

Type BF equipment, per IEC 601-1

MR conditional per ASTM 2503-05

Sensor line luer inlets

Exhalation valve luer inlet

AC Fuses 2xT3.15AL (250V)

Air Inlet INLET AIR

Remote Alarm REMOTE

Ventilation Component Parameters/ Unit of Accuracy

Exhaled Tidal Volume 50-300 mL 10 mL or N Y NA

PEEP 0 to 40 cmH2O 1 or 10%, Y Y 78

MONITORED DATA RANGE, RESOLUTION AND

Parameter Range, resolution, accuracy

Breath type Range: Type: - Control, assist, patient, sigh

SIZE AND WEIGHT

Operating Temperature 0 to +50 °C / +32 to +122 °F

External AC 100 to 240 V, 50-60 Hz, max 1.6 A.

High Pressure Pressure Range 40 –75psi (2.8-5.1 bar).

VENTILATION PERFORMANCE AND CONTROLLED