Knightstar 330 Bi-Level Ventilator: Service Manual
Knightstar 330 Bi-Level Ventilator: Service Manual
Knightstar 330 Bi-Level Ventilator: Service Manual
Bi-Level® Ventilator
2
Table of Contents
Chapter 1: General Information .......................................................................................1
Warnings, Cautions, and Notes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -3
Service Manual Illustrations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -3
Symbols and their Definitions - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -4
System Setup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -5
Performance Specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -6
Displayed Patient Parameters - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -6
Circuit Resistance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -6
Noise- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -6
Electrical Characteristics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -6
External Battery Time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -6
Environmental Requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -7
Physical Characteristics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -7
Chapter 2: Theory of Operation .......................................................................................8
Safety Features - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -8
KnightStar 330 Operating Modes - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11
Modes/Settings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12
System Description - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 14
Control Panel Display - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 14
Control Panel Buttons- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 14
Control Panel Indicators- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 16
Chapter 3: Modes of Operation ......................................................................................17
Stand-by Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 17
Power On - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 17
Delay/Ramp - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 18
Power Off - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 18
Therapy Modes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 18
Breath Detection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 19
User Interface Display- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 20
Alarm Control - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 20
Breath Detection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 21
Sensitivity Adjustments - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 22
Inspiratory Sensitivity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 22
Expiratory Sensitivity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 22
Rise Time- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 24
Chapter 4: Service and Repair ........................................................................................25
i
KnightStar 330 Connectors and Setup - - - - - - - - - - - - - - - - - - - - - - - - - - 25
Cleaning the KnightStar 330 - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 26
Connecting Device Components - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 27
Performance Verification - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 28
Unit Disassembly - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 28
Re-assembly - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 40
Overlay Replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 46
Chapter 5: Final Test ....................................................................................................... 49
Serial Number Transfer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 53
Chapter 6: Troubleshooting ........................................................................................... 54
Chapter 7: KnightStar 330 Service Spare Parts ............................................................ 57
Appendix A: US Control Panel Configuration ............................................................... 59
Appendix B: Alarm Types and Conditions ..................................................................... 61
Appendix C: Working with the RS-232 Sub-D Connector ............................................ 66
Appendix D: Symbols Seen on the KnightStar 330 Display ........................................ 67
Appendix E: KnightStar 330 Setup Checklist ................................................................ 69
Appendix F: KnightStar 330 Settings ............................................................................ 72
Appendix G: Service Information .................................................................................. 74
Appendix H: Limited Warranty ...................................................................................... 75
Index ................................................................................................................................. 77
ii
Chapter 1: The Puritan Bennett KnightStar 330 is a continuous bi-level ventilator that
General provides noninvasive ventilation for the treatment of respiratory
insufficiency and obstructive sleep apnea that may occur in the home. It is
Information also indicated for the treatment of respiratory failure in institutional
environments. It is intended to assist the ventilation of spontaneously
breathing patients who are over 30 kg (66 pounds) in weight . Read this
manual and the KnightStar 330 Clinician’s Manual thoroughly before
operating the device. They provide service, repair, and technical information
concerning the operation and performance of the Puritan Bennett KnightStar
330 bi-level ventilator.
• Monitors pressure, tidal volume, respiratory rate, air leaks, peak flow,
and the I:E ratio.
• Audible and visual indicators alert users to power failure, system leaks,
device performance.
1
KnightStar 330 bi-level Tubing and proximal
ventilator pressure line
Puritan
Bennett
KnightStar 330
Bi-level Ventilator
It is recommended to use the KnightStar 330 with 6-ft (1.8 m) or 8-ft (2.4 m)
tubing and Puritan Bennett Breeze™, or ADAM™interfaces.
2
In the I/E PAP mode the system tracks patient breathing effort and provides
two levels of pressure—a higher level of pressure for inspiration (normal
operating range of 3 to 30 cmH2O) and a lower pressure for expiration
(normal operating range of 3 to 20 cmH2O).
In the A/C mode, the system delivers the same two levels of pressure as
described for the I/E PAP mode with the addition of a backup breath rate
(normal operating range of 3 to 30 breaths per minute) and an I:E ratio
(normal operatnig range of 1:1.0 to 1:4.0).
When the Lockout mode is active, these settings are available to the patient:
the Delay Time, Ramp Time, and Ramp Starting Pressure.
Warnings, The following words found in this document have special significance.
Cautions, and Warning
Notes Means that there is a possibility of injury or death.
Caution
Means that there is the possibility of damage to the device
or other property.
NOTE:
Indicates information of particular interest for more efficient
and convenient operation.
Service Manual Throughout the manual, illustrations and photographs show the International
Illustrations configuration of the KnightStar 330 (control panel with International
symbols). Refer to Appendix A: US Control Panel Configuration for an
illustration of the control panel found on United States models, and a
description of each of the controls.
3
Symbols and their
Definitions
Alarm condition
CE Mark: This device complies with the requirements of Medical Device Directive
93/42/EEC concerning medical devices
Max
4
System Setup This section describes how to prepare the KnightStar 330 system for use.
Warning
Be careful when handling the KnightStar 330 during or
immediately after use. Under specified conditions, some
surfaces of the unit may become hot to the touch. This is a
normal occurrence and is typical of this type of device.
In the sleep lab, the optional remote control enables control and monitoring
away from the device. Connection between the remote control and the
KnightStar 330 unit is made using a cable that attaches to the rear of the
device.
5
Performance Working Pressure: 3 to 30 cmH2O (1 cmH2O = 0.98 hPa)
Specifications Pressure Limit:40 cmH2O
Static Pressure Regulation: 4 to 30 cmH2O
CPAP ±0.5 cmH2O
Bi-Level ±1.0 cmH2O
External Battery Direct current power from a 12-volt external battery pack can operate the
Time KnightStar 330. The 32 ampere-hour external battery provides power for at
least 8 hours. The 7 ampere-hour external battery provides power for 3
hours. If needed, cables are available for connecting the KnightStar 330 to a
car or truck cigarette lighter outlet.
Rated Input Voltage: 12 V
Rated Input Current: 6.0 A
Rated Input Power: 140 W
6
Environmental Operating Temperature: +41° F to +104° F (+5° C to +40° C)
Requirements Humidity:15 to 95% noncondensing
Altitude: 0 to 8,000 ft (0 to 2,438 m)
Storage Temperature: -40° F to +158° F (-40° C to +70° C)
Humidity: 10 to 100% condensing
Physical Device Size: 3.75 in x 8.25 in x 5.62 in (9.52 cm x 20.95 cm x 14.27 cm)
Characteristics Device Weight: 2.7 lbs (1.21 kg)
Device Airway Volume: 65 mL
Tube Airway Volume: 695 mL (6 ft/1.8 m) or 927 mL (8 ft/2.4 m)
7
Chapter 2: The device is a micro-controller-based design employing a 2-pole/3-phase,
Theory of high frequency blower powered by a universal switching power supply. The
device controls can be set via the top panel keyboard and LCD or via the RS-
Operation 232 interface. Internal memory stores waveform, compliance log, and error
log information that can be downloaded to a computer.
A gross particulate filter provided at the air inlet filters the incoming air. Use
of a high efficiency bacterial filter at the air outlet is recommended for
optimal device performance. A patient circuit of 6 or 8 feet with proximal
pressure tube provides delivery of air to the patient and pressure feedback to
the device.
The device operates in three distinct modes; CPAP, I/E, and A/C. CPAP
provides continuous positive airway pressure up to 20 cmH2O. I/E PAP and
A/C modes provide two pressure levels; an exhale pressure level of up to 20
cmH2O and an inhale pressure level of up to 30 cmH2O. The A/C mode also
provides a backup breath rate if the patient stops breathing or the patient’s
breath rate drops below the set value. When in I/E PAP and A/C modes, the
device monitors the flow to determine if the patient is inhaling or exhaling.
The detection is performed using a mass flow sensor connected to a pitot
tube at the blower outlet. The sensor output is then connected to an analog
hardware circuit that sends inhale and exhale triggers to the micro-
controller. The sensitivity of the breath detection set by the user is adjusted
by the micro-controller. Five settings each for inspiratory and expiratory
sensitivity are provided for clinician selection. The micro-controller also
monitors the analog flow signal to determine tidal volume and leak. Altitude
compensation of the flow is accomplished by using an internal barometer
that adjusts the flow value in software.
Safety Features Several features have been designed into the device to protect the patient and
user from injury following a single fault condition.
8
Controls protection - A lockout mode allows the clinician to limit patient
access to settings except for comfort features (ramp, delay). There is no
auto-scrolling of setting selections; the selection advances one step with
each button press.
Power off protection - The on/off button must be depressed for three seconds
to power off the device.
See Figure 3 for flow chart of the micro-controller for this bi-level
ventilator.
9
Bi-Level Device Air Inlet/
Filter
AC Power Patient
Power Outlet Patient
Main 85 to Supply
Blower Driver Blower Outlet/
Filter Circuit
Patient
264VAC Flowmeter
Pressure
Current Input
Measurement Tube
DC Power Flow Sensor
External
Battery
12 VDC
Micro-Controller Trigger
Circuit
Blower Control
Currrent Analysis
Cooling
Fan
Flow and Volume
LCD Analysis/Triggering/ Control
Module Patient Compliance/
Altitude Flow Data
Keyboard Compensation Atmospheric
Module Pressure
Switches Pressure Analysis / Sensor
& LEDs Leak Compensation/
Proximal
RS 232, IE Altitude Pressure
Pressure
trig, prog Limitation
Sensor
enable
Program Audible
Data
Memory Alarm
Storage
Real Time
Alarm
Clock &
Battery
Battery
10
KnightStar 330 The KnightStar 330 operates in one of three modes as shown in Table 1.
Operating Modes
Mode Description
A/C I/E PAP with an adjustable respiratory rate and I:E ratio. If the device is unable to track breathing efforts, or the
patient’s spontaneous respiratory rate falls to or below the prescribed backup rate, the device will cycle at the
prescribed levels of pressure and I:E ratio. If the backup rate cycles for five continuous breaths, the f symbol
will appear on the lower left corner of the display, and the yellow LED will illuminate. The symbol f will be
displayed and the yellow LED will remain lit until the patient breathes on his or her own. When the backup rate
is cycling, the patient data for the “f” and “I:E” will be the prescription parameter values.
I/E PAP Inspiratory/Expiratory Positive Airway Pressure with default to EPAP. This occurs when no inspiration is
detected for the average inspiration period plus five seconds. Upon reaching this condition the device will
default to the selected EPAP setting (setting range is 3 -20 cm H2O). When the device is at EPAP pressure for
the average exhalation time plus 5 seconds, the patient data will also default to the given values. When an
inspiration event is detected, the device will resume normal operation. During the default condition the patient
data will be as follows:
f = 0 bpm
P = EPAP setting
Vt = 0 liters
Leak = 0 L/min
V = 0 L/min
I:E = 1:0.0 ratio
CPAP Continuous Positive Airway Pressure: Pressure is continuously delivered at the set level.
11
Modes/Settings Each mode enables a different set of system settings. Table 2 lists the modes
and their respective settings. Table 3 shows the KnightStar 330 Initial
Factory Settings.
Table 2: Modes/Settings
Start pressure
Leak setting
12
Table 3: KnightStar 330 Initial Factory Settings
FUNCTION SETTING
MODE A/C
EPAP 3
Resp rate 10
I Sensitivity 3
E Sensitivity 3
Rise time 3
Volume 3 (maximum)
Delay time 0
Ramp time 0
NOTE:
Refer to Table 4: Top Panel Buttons and Appendix F:
KnightStar 330 Settings for information on changing device
settings.
13
System The following section describes control features of the KnightStar 330.
Description
Control Panel The Liquid Crystal Display (LCD, shown in Figure 4) provides an easy-to-
Display read format for mode, settings, and patient parameters. A backlight
illuminates the display when the Mode or Settings button is pressed. The
display will remain illuminated for approximately 60 seconds after the last
button push.
Control Panel The top panel controls are shown in Figure 4 and their features are listed in
Buttons Table 4.
PURITAN BENNETT
TM
1
2
3
Yellow
Green Red
14
Table 4: Top Panel Buttons
Mode Scroll through various modes: CPAP, I/E PAP, A/C (if the Lockout mode is inactive).
1
2
3
Leave Settings Leave Settings mode if adjusting settings.
Mode
On + Autoclear When the KnightStar 330 is in the Stand-by mode (plugged in to AC power but not
button operating), you can press the “On,” “Mode,” and Up arrow buttons and
Mode + combination hold for approximately 20 seconds to clear the updatable “flash” memory, and
restore the default values. Within approximately 20 seconds after simultaneously
releasing the buttons, the user will recognize that this process is occurring by the
“Xs” that appear on the display (in place of the patient ID) during Power On Self
Test (POST).
Mode + Lockout mode If the Lockout mode is active, the patient may only change the delay, start pressure,
and Toggle and ramp duration functions.
To change the Lock or Unlock position, hold the Mode button and the up arrow
together for approximately 2 seconds.
Settings If the Lockout mode is inactive, you may scroll through all of the available
parameters. If the Lockout mode is active, you may only scroll through the patient-
settable parameters (delay, start pressure, ramp duration).
Display In AC or I/E mode, when the main display screen is shown, pressing this button
Secondary displays V and I:E ratio if there are no active alarms.
Screen
15
Control Panel The KnightStar 330 control panel has visual indicators (shown in Figure 5)
Indicators that illuminate in response to specific device or tubing circuit problems.
1
2
3
Red
Yellow
Green
Control Indicators
(LEDs)
16
Chapter 3: Device Operation consists of the following modes: Stand-by, Power On,
Modes of Power Off, Delay/Ramp, and Therapy.
Operation
Stand-by Mode Once the AC power cord is connected, the device enters Stand-by Mode.
The device performs a self-test to verify the integrity of the firmware,
hardware, and stored data. Defined in Appendix B: Alarm Types and
Conditions, these tests include the following:
Power On The device powers on by pressing the On/Stand-by Switch, then displays
copyright notice, company name, and firmware version. Each time the
device is turned on, the device performs the following tests:
3. LED test
17
Delay/Ramp Upon completion of the power on sequence, the device begins the delay/
ramp function (if a delay and/or ramp are set), and then commences delivery
of the set therapy mode.
Power Off The device powers off (returns to Stand-by Mode) when the On/Stand-by
Switch is pressed for three seconds. The device retains all settings in
memory during periods when the unit is powered off.
Therapy Modes CPAP Mode: The device will implement CPAP by producing a
continuous pressure at the CPAP level. Pressure will be continuous in the
range of 3 to 20 cm H2O. In this mode, the device will continue to track
respiration rate, tidal volume, leak rate and I/E ratio of the patient.
Bi-level (I/E) Mode : While tracking patient breathing efforts in I/E PAP
mode, the device provides two levels of pressure: a higher level of pressure
for each inhale event (3 to 30 cm H2O) and a lower level of pressure for each
exhale event (3 to 20 cm H2O).
If the device is unable to track patient breathing effort in bilevel mode, the
KS 330 defaults to the modes shown in Table 5 in response to the stated
conditions.
The time of the average inhalation period Device cycles to the EPAP level and
plus five seconds is exceeded while at the remains at this level until it detects an
IPAP level inhalation trigger.
Upon detecting an inhale trigger the device resumes normal I/E PAP mode
operation supporting all detectable spontaneous breathing at the prescribed
pressure levels.
18
Assist with Control (A/C) Mode : A/C Mode provides the same
ventilatory characteristics as I/E mode as long as the patient’s respiratory
rate (RR) is higher than the set frequency. If the patient’s spontaneous RR
drops below the prescribed RR, the device will cycle at the prescribed IPAP
and EPAP levels, respiratory rate, and I:E ratio (the A/C default condition).
When the patient’s spontaneous RR returns to a rate higher than the
prescribed RR, the device will resume tracking of the patient’s spontaneous
respiratory rate and will continue to provide pressure at the IPAP and EPAP
levels.
Breath Detection When in I/E PAP and A/C modes, the device responds to detected breathing
by adjusting pressure levels. The device detects flow with a pitot tube, mass
flow sensor, and analog trigger circuit to detect inhalation and exhalation.
An inhalation trigger occurs when the flow exceeds a fixed threshold set by
the inhale sensitivity. An exhalation trigger occurs when the difference
between the instantaneous flow and the flow from an earlier time is less than
the threshold set by the exhalation sensitivity. When the device shifts from
inhalation to exhalation or exhalation to inhalation, the device incorporates a
refractory period to prevent auto-cycling due to additional flow triggers.
NOTE:
Autocycling refers to a delivered breath that was not
initiated by the patient.
The inhalation detection is determined by comparing the high pass and low
pass filtered flow signal to the delayed signal and to a fixed inhalation
threshold. If the delayed signal (from the 0.93Hz filter) is greater than the
fixed threshold, the inhalation detection works as just the reverse of the
exhalation threshold, triggering an inhalation when the filtered flow signal
goes more positive than the delayed signal. If the delayed signal is less than
the fixed threshold, the flow signal is compared to the fixed threshold.
19
Exhalation sensitivity: The device provides 5 exhalation sensitivity
settings across a range. The setting of 1 is the most sensitive exhalation
trigger, 5 is the least sensitive.
The exhalation detection is determined by comparing the high pass and low
pass filtered flow signal with a delayed copy of itself. The signal is more
positive than the delayed signal during the inhalation, but when it crosses to
less than the delayed signal the exhalation is triggered. The 0.93Hz low pass
filter determines the delay. The amplitude of the delayed signal, which is
determined by the gain setting in series with the 0.93Hz filter sets the
threshold.
User Interface Displayed Parameters: The device displays four measured parameters
Display continuously and simultaneously during operation in I/E PAP and A/C
modes:
• The respiration rate (f) in breaths per minute (BPM)
Pressing the Up Arrow/Alarm Mute switch when the unit is operating in I/E
PAP or A/C modes, and no alarm condition is present, the device displays
the following parameters for 5 seconds:
• Peak flow (V ) in liters per minute (LPM)
Alarm Control The device includes an audible alarm capable of an adjustable sound level
and can produce 85 dB(A) sound pressure level at a distance of one meter.
20
The audible alarm function is provided on a separate alarm PCBA, which
connects to the main PCBA via a 10-pin double row header.
Pin # Function
1 Ground
6 Ground
10 Ground
The alarm processor takes commands from the main PCBA processor via the
I2C interface for the alarm controls (including sound level). The PIC
processor can control its onboard audible alarm and the red and yellow
LED's on the membrane keypad. It is powered at maximum volume on the
alarm PCBA with +13.5V nominal with a 5mA current limit. The alarm is
equipped with a lithium power source. This allows the alarm to function
during power outages or failure of the main PCBA.
Breath Detection When in I/E PAP and A/C modes, the device monitors the breath detection
triggers to determine if the patient is inhaling or exhaling. The actual
detection is done with analog hardware. The sensitivity of the breath
detection is adjusted by the micro-controller. The micro-controller monitors
the analog flow signal and breath trigger signals to determine tidal volume
and leak. An analog signal from the flow sensor is connected to the micro-
controller analog input 0 (Pin 5).
21
Sensitivity An important part of the KnightStar 330 is its adjustable triggering
Adjustments sensitivity for both inspiration and expiration.
Inspiratory A setting of 1 is the most sensitive setting on the KnightStar 330 and a
Sensitivity setting of 5 is the least sensitive setting.
NOTE:
Autocycling refers to an automatically delivered breath that
was not initiated by the patient.
Expiratory The chart shown in Figure 6 illustrates the effects of changing the expiratory
Sensitivity sensitivity on the KnightStar 330.
A setting of 1 is the most sensitive setting, and it causes the KnightStar 330
to cycle into the expiratory phase quickly. A setting of 5 is the least
sensitive, and inspiratory flow needs to diminish significantly before the
KnightStar 330 cycles into the expiratory phase. The longer it takes for the
device to cycle into the expiratory phase, the greater the potential tidal
volume delivered to the patient.
22
Figure 6: Effects of changing the expiratory sensitivity on
the KnightStar 330.
23
Rise Time The following graph depicts the “Rise-time” for settings 1, 3, and 5.
24
Chapter 4:
Service and
Repair
KnightStar 330 The following table identifies materials and tools needed for service and
Connectors and repair.
Setup
25
Cleaning the Thoroughly clean the exterior of the KnightStar 330 before servicing or
KnightStar 330 repairing the unit with a 10% bleach and water solution or equivalent.
NOTE:
The outlet air filter, L-6108 on the KnightStar 330 test
equipment must be replaced at least once every 2 months.
The connectors on the back of the KnightStar 330 are shown in Figure 8.
RS-232 Battery
Mains/AC power connector
power connector
NOTE:
Personal computers (PCs) used with the KnightStar 330
must be approved according to the requirements of UL
1950 or EN 60950.
26
External Battery Connector: Used for connecting an optional external
12V battery, or for use with a 12 V cigarette lighter adapter when
Mains/AC power is not available.
Connecting Device Upon connecting the KnightStar 330 for the first time, review the device
Components components. (See Figure 9.)
Air outlet
Test Setup:
1. Ensure that the KnightStar 330 is placed in such a manner that there is
at least 1 inch of clearance at the back of the unit.
2. Connect one end of the Mains/AC power cord into the rear panel of the
KnightStar 330, and the other end into an Mains/AC wall outlet.
27
3. Attach patient circuit, P/N Y-261000-27, and optional air filter, P/N L-
6108, to air outlet.
NOTE:
To perform a functional test prior to disassembling the unit,
refer to Chapter 5: Final Test.
28
2. Assure work station is clean.
Caution
Before handling circuit boards with ICs inserted, the
operator must be grounded preventing static discharge to
sensitive components. Place the ground strap from the
static control station around the operator’s wrist before
handling static sensitive components/assemblies.
NOTE:
The following assembly drawings refer to Y-KS330-XX.
29
Figure 11: KnightStar 330 assembly drawing (page 1).
30
Figure 12: KnightStar 330 assembly drawing (page 2).
Disassembly Steps.
31
Figure 13: Removing the housing screws from KnightStar 330.
3. While holding both housing halves together, turn the unit over and
place the unit onto its bottom.
32
5. Lay the top housing to the back side of the unit and carefully remove
the LCD overlay ribbon cable from the PCBA.
Ribbon cable
PCBA Replacement.
1. Remove the LCD display, ITEM 16, from the Main PCBA. Using
needle nose pliers, for each of the four plastic snap fit connectors,
pinch the ends together and gently pull the corner of the display over
the connectors.
J4 pins
Snap-fit connectors
Figure 16: Removal of the LCD display.
Caution
Take care not to damage the J4 connector pins.
33
2. Remove the mylar LCD insulator, ITEM 17, and keep for the re-
assembly of the unit.
Mylar LCD
insulator
3. Disconnect the 10" silicone tube, ITEM 12, from the “P2” flow sensor
tap on the Main PCBA.
4. Disconnect the 4-1/4" silicone tube, ITEM 13 from the “P1” flow
sensor tap on the Main PCBA.
34
NOTE:
Verify that all three silicone tubes remain attached to the
outlet connection.
6. Remove the Main PCBA, ITEM 30, from the chassis by removing the
two PCBA screws, ITEM 8.
35
7. Disconnect the blower wire from the J3 connector on the Main board.
8. Disconnect the fan wire from the J8 connector on the Main board.
36
9. Remove and keep the Lexan shield, ITEM 47, for re-installation.
10. Gently pull up on the Alarm PCBA, ITEM 31, to remove it from the
main PCBA.
NOTE:
If the battery or either of the two PCBAs is being replaced,
dispose of the used items in accordance with local
regulations.
37
11. To reinstall the board, go to Board re-installation section on page 42.
Blower Replacement.
1. Remove the pitot tube, ITEM 19, blower housing bellows, ITEM 15,
and screen, ITEM 20, from the blower. These items will be needed
later for re-assembly.
2. Remove the bottom housing, ITEM 1, from the unit by grasping two
chassis stand-offs, and gently pulling the chassis, ITEM 5, from the
bottom housing.
5. Remove ferrite snap, ITEM 40, from blower wire. Keep ferrite snap for
re-assembly.
38
6. Guide blower wire through chassis hole.
39
Fan Replacement.
1. Separate the cooling fan assembly, ITEM 22, and the fan adhesive
foam, ITEM 23 from the chassis.
NOTE:
Ensure that all of the old foam has been removed from the
square recess corner of the chassis before attempting to
install the new fan and adhesive.
2. Apply new fan adhesive foam, ITEM 23, onto the bottom side of the
new cooling fan assembly, ITEM 22, opposite the fan label.
3. Attach cooling fan assembly into the square recess in the corner of the
chassis, with the label side of the fan facing up and wires to the upper
left corner.
4. Attach the fan ferrite, ITEM 40, at the mid-point of the fan wires.
1. Place the suspension muffler, ITEM 21, into the case foam with open
slots in the foam and bottom portion of the muffler lined up.
40
NOTE:
If the blower is being replaced, order P/N
Y-103017-00. Record blower lot code number onto the
Product Experience Report, or equivalent.
3. Put screen, ITEM 20, into the ribbed end of blower housing bellows,
ITEM 15. Install the ribbed end of the blower housing bellows with
screen over air outlet of blower assembly.
41
Figure 24: Screen and ribbed end of the blower housing bellows.
4. Install Chassis, ITEM 5, over case foam and blower assembly, and into
base, routing blower assembly wires through hole in chassis dome.
5. Pull the blower housing bellows through the chassis hole. The long end
of the bellows should be completely visible through blower outlet
opening in chassis.
Chassis hole
7. Re-install the ferrite snap, ITEM 40, onto the blower wires at
approximately the midpoint of the wire.
Board re-installation.
NOTES:
If the Alarm PCBA has failed, replace it with P/N Y-101931-
00C. Record the new serial number on the Product
Experience Report, or equivalent.
42
1. Install the internal battery, ITEM 32, if needed, onto the Main PCBA.
Record the Main board serial number onto the Product Experience
Report, or equivalent.
NOTE:
The battery is designed to last the life of the product.
Caution
Ensure Alarm PCBA connector pins are aligned properly
with connector on Main PCBA. Misalignment during
assembly could result in severe damage.
3. Place the Lexan shield, ITEM 47, on the backside of the Alarm PCBA,
ITEM 31, taking care to ensure that it is placed squarely between the
Alarm and Main PCBAs.
43
6. Slide pitot tube, ITEM 19, into blower housing bellows, ITEM 15, and
drop into its notch on the side of the base. Double check that all
silicone tube connections have been maintained.
7. Re-attach 10" silicone tube, ITEM 12, to the flow sensor nozzle “P2”
facing towards the back of the main PCBA. Attach 4-1/4" silicone
tube, ITEM 13, to the flow sensor nozzle “P1” facing towards the
curved front of the main PCBA. Ensure tubing is fully seated on taps.
44
8. Tuck the blower ferrite to the lower left of the pressure
sensor.
Blower ferrite
Figure 27: Fitting the blower ferrite near the lower left of the
pressure sensor.
9. Attach 1-1/4" silicone tube, ITEM 14, to the pressure transducer on the
main PCBA.
10. Place main PCBA, ITEM 30, onto chassis while carefully routing the
long silicone tubing through tubing guides on chassis dome to front of
unit. Allow a generous loop of tubing towards back of unit. Avoid any
kinks in the tubing. Align main PCBA with the chassis support posts.
Make sure the alarm PCBA drops into notches on the chassis. Align the
blower wire and ferrite to ensure main PCBA seats onto the chassis.
45
NOTE:
For board replacements, the S/N will need to be written to
the main board using the service communications kit. See
section on "Serial Number Transfer."
Overlay 1. Remove old overlay (membrane switch), ITEM 3, from the top
Replacement housing, ITEM 2.
2. Wipe down top housing around overlay slot with isopropyl alcohol.
Remove paper backing from new overlay. Insert the ribbon cable from
the overlay through the cover slot from the front.
3. Carefully apply the overlay into the cover recessed area. Make sure the
overlay completely adheres to the cover.
Final Assembly.
NOTE:
During final assembly steps, take extra care not to kink the
silicone tubing or the overlay ribbon cable. Ensure that the
fan wiring and ferrite do not interfere with the seating of the
board.
1. Mount main PCBA to chassis with two (2) screws, ITEM 8. Torque to
5 in. lbs. Make sure all three silicone tubes are not kinked and are
firmly connected.
2. Re-apply the mylar LCD insulator, ITEM 17, onto top of main PCBA
over LCD stand-offs. Mount LCD Assembly, ITEM 16, onto Main
PCBA by lining up with header connector J4 and stand-offs. Snap into
46
place. DO NOT PRESS ON LCD SCREEN WHEN INSTALLING
THE LCD ASSEMBLY.
NOTE:
If the LCD assembly is being replaced with a new LCD
assembly, remove the protective plastic liner from the LCD
screen.
3. Mount the top housing over the main assembly. Tuck overlay ribbon
cable under PCBA. Carefully line up the tongue and groove of the
base, housing, and pitot tube as well as the three (3) connectors on the
backside of the unit coming through the housing. Make sure LCD is
lined up with display window properly.
Figure 28: Back to front view of mounting the housing over the
main assembly.
47
Figure 29: Installing the top housing.
4. Hold unit together and flip upside down. Using screws, ITEM 18, and
Phillips screwdriver, screw the top and bottom of the unit together.
Torque to 15 in. lbs.
5. Remove inlet baffle, ITEM 6, and replace old inlet filter, ITEM 10,
into back of base as shown on print. Re-install inlet baffle over the
filter in the base by snapping it into place.
6. Plug in unit and turn on. Listen for alarm and look for startup display to
verify operation. Turn unit off and unplug.
48
Chapter 5: Final Test: Setup.
Final Test
1. Ensure that the KnightStar 330 is placed in such a manner that there is
at least 1 inch of clearance at the back of the unit.
2. Connect one end of the Mains/AC power cord into the rear panel of the
KnightStar 330, and the other end into an Mains/AC wall outlet.
3. Attach patient circuit, P/N Y-261000-27 and air filter P/N L-6108 to air
outlet.
Figure 30: Attaching the outlet air filter and tubing to the
KnightStar 330 air outlet.
NOTE:
For each of the following tests, fill out the KnightStar 330
setup checklist found in Appendix E: KnightStar 330 Setup
Checklist.
49
Functional Test.
Warning
Be careful when handling the KnightStar 330 during or
immediately after use. Under specified conditions, some
surfaces of the unit may become hot to the touch. This is a
normal occurrence and is typical of this type of device.
NOTE:
If locked, unlock KnightStar 330, by pressing the Mode
button and the Up arrow at the same time. Hold for
approximately 2 seconds. Verify that the LCD arrow has
moved from the Locked position to the Unlocked position.
1. With the unit turned on, use the Mode button to select the CPAP
mode.
3. In the CPAP mode, use the Settings button to scroll to the prescription
pressure. Use the up or down arrow and set the pressure to 3 cmH2O.
Verify that the blower motor speed has decreased.
5. Use the Settings button to scroll to the alarm volume, and set it to 1.
6. Turn the KnightStar 330 off by pressing the ON/OFF button for 3
seconds. Wait for the motor to stop rotating.
50
8. Turn on the KnightStar 330 and let it run for approximately 3
minutes. Verify that the LEAK alarm indicator L is illuminated,
and that the audible alarm activates. See the lower left corner of the
display.
3. After a short time, the KnightStar 330 should begin to cycle between
IPAP (20 cmH2O) and EPAP (10 cmH2O).
5. Record the IPAP and EPAP pressures listed in Table 8. Decrease IPAP
and EPAP pressure settings in 3 cmH2O intervals until IPAP set
pressure is 14 cmH2O, and EPAP set pressure is at 4 cmH2O. Record
both the IPAP, and EPAP output pressure at each interval.
IPAP 20 17 14
EPAP 10 7 4
51
NOTE:
The output pressure should be within 1 cmH2O in any of the
pressure settings. For accurate readings, ensure that the
manometer has recently been calibrated in accordance with
the manufacturer’s recommendation.
Delay Test.
1. Use the Mode button and scroll to the I/E PAP mode. Use the Settings
button and scroll to the delay functions. Set delay time for 5 minutes.
2. Use the Settings button to scroll to the START Pressure settings. Set
the START pressure to 4, and press the Mode button.
3. Scroll to the I/E PAP screen, and press the Delay/Ramp button. Use the
manometer to verify that the pressure has dropped to 4 cmH2O.
4. Verify that the delay symbol appears on the KnightStar 330 display.
1. In the I/E PAP mode, set the low pressure alarm to 1 cmH2O above the
EPAP pressure. Remove the tubing from the patient pressure port. The
low pressure alarm should sound.
52
Power Failure Indicator Verification.
2. Verify that the audible alarm and red LCD activate. To mute the alarm,
press the alarm mute button.
Serial Number 1. For all unit repairs which includes a new KnightStar 330 main board,
Transfer the unit serial number must be downloaded onto the main board. To
accomplish this task, order the KnightStar 330 Service Software, P/
N Y-103012-00 and the KnightStar 330 Service Communication
Cable, P/N Y-103086-00A.
53
Chapter 6: Any unusual system event results in any or all of the following:
Troubleshooting • Displayed error code
• Audible alarm
• Logged error code (contents of error log may be downloaded using ser-
vice software)
To mute an alarm for one minute, press the Alarm Silence button.
• A high priority alarm is indicated by a flashing red LED, along with an
audible alarm that beeps 5 times at intervals of ten seconds.
No airflow out of Display turns on? Motor turns on? Motor runs on
device another board?
54
Table 9: Troubleshooting Checklist
Low airflow out of Air leaking around Pressure port/line Device deplays high
device pitot and motor? obstructed? pressure
55
Table 9: Troubleshooting Checklist
10, 11 (SPI failure) Alarm test failure Flash failure Replace main board
47 Frequency error Does it reset if Can’t reset? Pressure Replace main board
mask is on? sensor failure
56
Chapter 7: The KnightStar 330 Service repair kits and order numbers are identified in
KnightStar 330 the following table. Where applicable, item numbers from the assembly
drawings in Chapter 4: Service and Repair are provided for reference.
Service Spare
Parts
5 Chassis Y-101616-00A
20 Screen Y-102272-00A
57
Table 10: List of Spare Parts (continued)
40 Ferrite Y-102951-000
58
Appendix A:
US Control
Panel
Configuration PURITAN BENNETT
TM
Mode Set
Delay Alarm
Ramp Silence
59
Table 11: KnightStar 330 US Model Top Panel Buttons
Mode Scroll through various modes: CPAP, I/E PAP, A/C (if the Lockout mode is inactive).
Mode
Leave Settings Leave Settings mode if adjusting settings.
Mode
On + Autoclear When the KnightStar 330 is in the Stand-by mode (plugged in to AC power but not
button operating), you can press the “On,” “Mode,” and Up arrow buttons and
Mode + combination hold for approximately 20 seconds to clear the updatable “flash” memory, and
restore the default values. Within approximately 20 seconds after simultaneously
releasing the buttons, the user will recognize that this process is occurring by the
“Xs” that appear on the display (in place of the patient ID) during Power On Self
Test (POST).
Mode + Lockout mode If the Lockout mode is active, the patient may only change the delay, start pressure,
and Toggle and ramp duration functions.
To change the Lock or Unlock position, hold the Mode button and the up arrow
together for approximately 2 seconds.
Settings If the Lockout mode is inactive, you may scroll through all of the available
parameters. If the Lockout mode is active, you may only scroll through the patient-
Set settable parameters (delay, start pressure, ramp duration).
Delay
Ramp
60
Appendix B:
Alarm Types
and Conditions
Table 12: Event Conditions
Type Condition Produces Logging Actions
occurs when: Alarm code
ROM checksum ROM checksum Always 1 Activate internal malfunction alarm. Turn off
does not match all device activity.
internal checksum
during POST.
RAM error Device writes Always 4 Activate internal malfunction alarm. Turn off
pattern to RAM all device activity.
during POST and
read pattern does
not match.
Stack overflow Stack is Always 5 Activate internal malfunction alarm. Turn off
overwritten. all device activity.
Spurious More than 2 Always 7 Activate internal malfunction alarm. Turn off
interrupt interrupts detected, all device activity.
which are not
defined.
Key stuck Keypad checked at Always 8 Activate internal malfunction alarm. Turn off
power on. If any all device activity.
key is pressed,
alarm sounds and
unit shuts down.
Alarm test PIC read during Always 9 Activate internal malfunction alarm. Turn off
failure post, and alarm all device activity.
test failure bit is
set.
SPI read failure SPI read returned As defined 10 Condition is logged. If failure occurred during
non-ready status POST at start-up, the internal malfunction
following a flash alarm is activated and all device activity
read operation. ceases.
SPI write failure SPI write returned As defined 11 Condition is logged. If failure occurred during
non-ready status POST at startup, the internal malfunction
following a flash alarm is activated and all device activity
write operation. ceases.
61
Table 12: Event Conditions (continued)
Type Condition Produces Logging Actions
occurs when: Alarm code
Invalid date/ Invalid date or time As defined 31 On reset, the device will read the RTC and
time detected during check for a valid date/time. If the device
POST. detects an invalid date/time, it will use the
last date/time associated with the last log
entry or the default date. If no other date is
available, set a flag and do a reset. This will
disable "turnon" if date/time is still invalid
after reset.
Multiple Watchdog reset As defined 32 When a watchdog reset occurs more than 3
watchdog occurs more than 3 times in 10 hours, the error will be logged
times in 10 hours. and treated as an internal malfunction alarm.
In that event, the unit will not restart.
Log full Compliance log fills Never 33 Log and turn on the yellow LED. Turn off the
up yellow LED when log is cleared.
Incipient power Power falls below As defined 34 Stop motor. Condition is logged, and an
loss 24 volts (usually attempt is made to restart the blower.
due to Backlight also turns off.
desynchronization).
RS232 Device receives Never 35 Send appropriate "@E4" response and log
command undefined condition.
command through
its serial port.
I2C error (I2 C) The I2C error bit is As defined 37 Retry read or write an additional two times. If
set. (I2 C) therapy isn’t provided, attempt to activate
internal malfunction alarm and turn off all
device activity. If therapy is already provided,
continue to provide therapy, and log error.
The screen will display the base address of
the particular unit that is causing the error.
These are as follows (write and read
respectively):
A0, A1 – Settings portion of settings
EEPROM
A2, A3 – Error Log portion of settings
EEPROM
A4, A5 – MFG EEPROM
D0.. D1 – RTC
D2 .. D3 – PIC Alarm Board
D6 – Failure bit on PIC set
D7 – Settings bit on PIC set
62
Table 12: Event Conditions (continued)
Type Condition Produces Logging Actions
occurs when: Alarm code
PIC system error Hardware error bit As defined 38 Try rereading PIC status register two more
set when reading times. If status bit continues to be set, then
the PIC status activate internal malfunction alarm. Turn off
register. all device activity.
Overvoltage Motor voltage is Always 40 Motor shuts down and internal malfunction
over 31 volts. alarm sounds.
MAX_DESYNCS More than 3 Always 44 When condition is logged, you get a high
desyncs in 30 priority malfunction alarm at full volume.
seconds. Attempts are still made to restart blower.
When the alarm is muted, the alarm is
cleared and the 44 error message goes away.
Barometer bad Barometer rails Always 45 Everything shuts down, and an internal alarm
high or rails low sounds.
when it is read.
Flow sensor bad Flow sensor rails Always 46 Everything shuts down, and an internal alarm
high with minimum sounds.
pressure or low for
60 seconds.
Frequency rail Frequency rails to As defined 47 In CPAP mode error indication appears on
high or low limit, screen. In I/E or A/C mode, high priority
while detecting alarm sounds, which will be reset if the
breaths for one condition goes away.
minute.
Note: All conditions that induce injury or prevent detection of injury have nonadjustable alarms. All other alarms are
suppressible or adjustable.
High pressure Pressure at mask Display shows 50 Reset if the pressure decreases to less than
rises above setting; P the alarm level and frequency is less than the
(0 causes alarm to Alarm maximum frequency limit.
be disabled.) Alarm audible? Yes.
is activated when LED? Yes.
high pressure Volume
condition persists adjust? Yes.
for at least 10
seconds.
63
Table 12: Event Conditions (continued)
Type Condition Produces Logging Actions
occurs when: Alarm code
Low pressure Pressure at mask Display shows 51 Reset if the pressure rises above the alarm
falls below setting: P limit, and/or frequency is above the lower
(0 causes alarm to Alarm frequency limit.
be disabled.) Alarm audible? Yes.
is activated when LED? Yes.
low pressure Volume
condition persists adjust? Yes.
for at least 10
seconds.
Leak Estimated leak rate Display shows 52 Reset if flow decreases to less than the alarm
rises above setting L setting.
(50–100 lpm). Alarm
Condition must audible? Yes.
persist for 60 LED? Yes.
seconds. Volume
adjust? Yes.
Overpressure Pressure greater Display shows 55 Reset if device powered down and then
than 40 cmH2O for ## powered up, provided device then operates
1/2 sec., power Alarm normally. (Motor will be immediately turned
fails, and an audible? Yes. off.)
internal LED? Yes.
malfunction occurs Volume
as defined in the adjust? No.
event table. Highest
volume
setting.
64
Table 13: Alarm Conditions
Alarm Reset
Type Priority Description Display
Volume Conditions
High pressure Medium Pressure at interface rises above P Adjustable Pressure decreases to
setting for 10 seconds; flashing 0–3: less than the alarm
yellow LED. 0=Off; limit.
3=Loudest
Low pressure High Pressure at interface falls below P Adjustable Pressure rises above
setting for 10 seconds; flashing 0–3: the alarm limit.
red LED. 0=Off;
3=Loudest
Leak High Estimated leak rate rises above L Adjustable Leak flow rate
setting for 60 seconds; flashing 0–3: decreases to less than
red LED. 0=Off; alarm limit.
3=Loudest
Log full Low Compliance log fills up. Yellow No alarm; Not Clear compliance log
LED is on. only an LED. applicable using PC.
Power Loss High Loss of Mains and external Display is Always Restore Mains or
battery power. Flashing red LED. blank enabled; external battery
Loudness=3 power.
Overpressure High Pressure > 40 cmH2O. Flashing 55 Always Plug in and unplug.
red LED. enabled; Reset if device
Loudness=3 functions normally.
65
Appendix C: A 9-pin sub-D connector located on the rear panel provides for RS-232 serial
Working with communications, modem control, remote control, I/E PAP digital triggering,
and control for programming and calibration. The RS-232 function will
the RS-232 operate at signal levels of at least 3 volts into a standard load at a data rate of
Sub-D 9,600 and 19,200 Baud. Applying 24 volts ±1 volt to pin 9 will enable
calibration EEPROM programming. This pin is used during calibration to
Connector enable the write function of the calibration data EEPROM (U3). Any voltage
less than 15VDC will not enable the EEPROM write function. The
calibration EEPROM contains calibration constants for pressure sensor,
barometric pressure, motor speed, and motor drive voltage, and flow Display
Back Light. During normal Bi-Level operation, pin 9 supplies a 0 or 5-volt
signal indicating inhalation trigger. All pins of the RS-232 connector can be
shorted together indefinitely without damaging the unit.
1 NC
2 TXD
3 RXD
4 NC
5 Ground
6 NC
7 NC
8 NC
9 Dual use I/E PAP trigger-out and program- enable
input.
66
Appendix D: The symbols shown in Table 15 appear on the KnightStar 330 display during
Symbols Seen operation of the device.
on the
KnightStar 330
Table 15: Display Symbols
Display
Symbol Symbol
Description
(USA) (Int’l)
Start-up Display Symbols
SN Serial number SN
Modes
Measured Parameters
f Respiratory rate f
P Current Pressure P
Vt Tidal volume Vt
L Leak Rate L
67
Table 15: Display Symbols (continued)
Symbol Symbol
Description
(USA) (Int’l)
ISENS Inspiratory sensitivity ISENS
Alarms
Alarm is muted
68
Appendix E:
KnightStar 330
Setup
Checklist
Pass Fail
Procedure
✔ ✔
General Exterior Appearance
Any dents, scratches, or loose parts that may indicate dropping or other abuse? ❑ ❑
Check for fluid residue in and around KnightStar 330 openings and housing joints. ❑ ❑
Ensure that the KnightStar 330 is placed in such a manner that there is at least 1 inch of clearance
at the back.
Connect one end of the Mains/AC power cord into the rear panel of the KnightStar 330, and the
other end into an Mains/AC wall outlet.
Turn the power button on. Both yellow and red indicators should flash for approximately 1 second; ❑ ❑
green stays lit
CAUTION: If an error code appears on the display, or an alarm stays activated following
system power-up, turn the power button off. Then turn the power button on; if the sys-
tem fails again, refer to the Troubleshooting section of this manual.
Functional Test
With the unit turned on, select the CPAP mode and an alarm volume of 0.
Set the CPAP prescription pressure to 3 cmH2O, then increase the pressure to 20 cmH2O. As the ❑ ❑
pressure increases, you should be able to hear the motor blower speed increase.
Turn the KnightStar 330 off and wait for the motor to stop rotating.
69
Table 16: KnightStar 330 Setup Checklist (continued)
Pass Fail
Procedure
✔ ✔
Turn the KnightStar 330 on and let it run for approximately 3 minutes. Verify that the LEAK alarm ❑ ❑
indicator L is illuminated, and that the audible alarm activates. See the lower left corner of
the display.
3. Attach calibration shell to end of patient circuit, and connect circuit to manometer.
After a short time, the KnightStar 330 should begin to cycle between IPAP (20 cmH2O) and EPAP ❑ ❑
(10 cmH2O).
Increase ESENS to 5. The KnightStar 330 should begin to cycle at a slower rate. ❑ ❑
Decrease IPAP and EPAP pressure settings in 3 cmH2O intervals until IPAP set pressure is 14
cmH2O, and EPAP set pressure is at 4 cmH2O. Make a note of both IPAP and EPAP output pressure
at each interval.
NOTE: Accuracy of measured output pressure is dependent on the specified/actual accuracy of the manometer. For proper
readings, ensure that the manometer has recently been calibrated in accordance with the manufacturer’s recommendation.
Increase ISENS to 5. The KnightStar 330 should not cycle to IPAP and should remain at EPAP ❑ ❑
pressure (10 cmH2O).
Delay Test
Set delay time for 5 minutes. Set the START pressure to 4; and press the Mode button.
70
Table 16: KnightStar 330 Setup Checklist (continued)
Pass Fail
Procedure
✔ ✔
Press the Delay/Ramp button and, using the manometer, verify that the pressure has dropped to 4 ❑ ❑
cmH2O.
Verify that the delay symbol appears on the KnightStar 330 display. ❑ ❑
In the I/E PAP mode, set the low pressure alarm to 1 cmH2O above the EPAP pressure. Remove ❑ ❑
tubes from the patient pressure port. Verify the low pressure alarm sounds.
While the KnightStar 330 is turned on and running, disconnect the Mains/AC power cord.
Verify that the audible alarm activates. To mute the alarm, press the alarm mute button. ❑ ❑
71
Appendix F:
KnightStar 330
Settings
IPAP Pressure during inspiration 3–30 cmH2O (increments of 1 Top panel, remote Only I/E
cmH2O) control, PC, modem or
A/C
EPAP Pressure during expiration 3–20 cmH2O (increments of 1 Top panel, remote Only I/E
cmH2O) control, PC, modem or A/C
Backup respiratory Rate of machine-initiated 3–30 bpm (increments of 1 Top panel, remote Only A/C
rate breaths bpm) control, PC, modem
I:E ratio Ratio of inhalation time to 1:1.0 to 1:4.0 (increments Top panel, remote Only A/C
exhalation times for backup 0.5) control, PC, modem
breath rate
Inspiration sensitivity Sensitivity at which devices 1–5 (1 most sensitive; 5 least Top panel, remote Only I/E
switches from EPAP to IPAP sensitive) control, PC, modem or A/C
Expiration sensitivity Sensitivity at which devices 1–5 (1 most sensitive; 5 least Top panel, remote Only I/E
switches from IPAP to EPAP sensitive) control, PC, modem or A/C
Rise-time Rate of pressure increase 1–5 (1 is the fastest setting; 5 Top panel, remote Only I/E
is the slowest) control, PC, modem or A/C
Alarm volume Loudness 0–3 (0=Off, 3=loudest) Top panel, remote All
control, PC, modem
Leak alarm Rate of air leaking before 50–100 liters per minute Top panel, remote All
alarm sounds (increments of 1 L/min); 0=Off control, PC, modem
Low pressure alarm Pressure below the prescribed 1 cmH2O below the IPAP Top panel, remote Only I/E
IPAP setting at which an setting to 1 cmH2O above control, PC, modem or A/C
alarm will sound EPAP (in increments of 1
cmH2O); 0 = Off.
High pressure alarm Pressure above the prescribed 1 cmH2O above the IPAP Top panel, remote Only I/E
IPAP setting at which an setting to 35 (in increments of control, PC, modem or A/C
alarm will sound 1 cmH2O); 0 = Off.
Delay time Time delay before automatic 0–30 minutes (in increments Top panel, remote All
device start of 5 minutes) control, PC, modem
Ramp duration Time from device start to 0–30 minutes (increments of Top panel, remote All
prescribed operating pressure 5 minutes) control, PC, modem
72
Setting Description Value Accessibility Mode
Start Pressure Pressure at which the unit 3–20 cmH2O (increments of 1 Top panel, remote All
starts delay ramp sequence cmH2O) control, PC, modem
Interface (Mask) leak/ Patient interface purge hole 1–6 (1 is the lowest leak Top panel, remote All
type leak rate (intended) value, and 6 is the highest) control, PC, modem
Time for dial-out Clock day/time device phones 7 days/week, 24 hours/day PC, modem All
home health care dealer
Device dial-out Phone number for device to Not applicable PC, modem All
telephone number call home health care dealer
Internal Clock Clock used by device 24-hour clock PC, modem All
73
Appendix G: KnightStar 330 ventilators are warranted against defects in workmanship
Service and materials. The full text of the warranty provides the details. Do not make
any service repairs on this equipment during the stated warranty period. Any
Information unauthorized work immediately voids the warranty. If you need information
or assistance, or if the information in this manual is insufficient, contact
Puritan Bennett at: 800.255.6774 (for North America). Outside the US,
contact your local representative.
74
Appendix H: Puritan Bennett warrants to the owner that the KnightStar 330 ventilator,
Limited exclusive of expendable parts and other accessories, shall be free from
defects in material and workmanship for twelve months from the original
Warranty date of sale. Puritan Bennett’s sole obligation, with respect to any such
defect, is limited to the repair or, at Puritan Bennett’s option, replacement of
the ventilator. Purchaser pays return freight charges.
The warranty does not apply to ventilators that have been partially or
completely disassembled; altered; subjected to misuse, negligence, or
accident; or operated other than in accordance with the instructions provided
by Puritan Bennett. This includes repair by unauthorized personnel.
This warranty represents the exclusive obligation of Puritan Bennett and the
exclusive remedy of the purchaser regarding defects in the ventilator.
75
76
Index M
A Mode 15, 60
A/C mode 3 Modem 26
Adjustment 22 Modes
Alarm 61 A/C 3, 11
CPAP 2, 11
Alarms
I/E PAP 11
High Priority 16, 54
Settings 12
Low Priority 16, 54
Medium Priority 16, 54 O
Altitude 7 Operating 7
Autoclear 15, 60 P
B Patient ID 73
Battery Connector 27 PC 26
C Power Cord 26
Clock 73 R
Connectors 25 Ramp 72
AC Power 26 Remote Control 5, 26
RS-232 26 Repair 25
Control Panel 14 Requirements 7
Buttons 14 Respiratory Rate 67
Alarm Silence 15, 60 RS-232 26
Delay/Ramp 15, 18, 60 S
Down Arrow 15, 60 Sensitivity 22, 72
On/Off 15, 60 Service 25
Settings 15, 60 Setup
Up Arrow 15, 60 Checklist 69
Display 14 Start Pressure 18
Indicators 16 Storage 7
CPAP mode 2 T
D Temperature 7
Delay 70, 72 Troubleshooting 54
Dial Out 73 V
Display 14, 67 Volume 68
E W
Electrical 6 Warranty 75
Environmental 7
H
High Pressure 72
Humidity 7
L
Leak 72
Lockout 15, 60
Low Pressure 72
77
78
Note:
Digits of the device serial number refer to the date of manufacture. For example, May 21, 2001 would be represented as
010521 (Y-50201052122).
This device complies with the requirements of Medical Device Directive 93/42/EEC.
Y-102942-00A Rev.D
Model Y-102942-00
Note:
Digits of the device serial number refer to the date of manufacture. For example, May 21, 2001 would be represented as
010521 (Y-50201052122).
This device complies with the requirements of Medical Device Directive 93/42/EEC.
Y-102942-00A Rev.D
Model Y-102942-00
Phone: +44.1329.224000