GoodKnight® 425ST - Service Manual
GoodKnight® 425ST - Service Manual
GoodKnight® 425ST - Service Manual
GoodKnight® 425ST
SERVICE MANUAL
This document is the property of NELLCOR PURITAN BENNETT, Inc and is distributed on the express condition that
it is neither divulged nor reproduced in part or in full by anyone other than NELLCOR PURITAN BENNETT, Inc with-
out prior written agreement, and no right is granted to divulge or use any information contained in this document.
PREFACE
This manual provides information necessary to service the GoodKnight 425 and the GoodKnight
425ST Respiratory System. This information is intended for use by technicians or personnel quali-
fied to repair and service medical equipment. The information is not exhaustive and may not be ap-
plicable to future models.
DEFINITION OF STATEMENTS
Statements in this manual preceded by the followings words are of special significance.
WARNING
Means there is the possibility of injury or death to yourself or others.
CAUTION
Means there is the possibility of damage to the GK 425/425ST unit or other property.
NOTE
Indicates points of particular interest for more efficient and convenient operation.
REVISION LIST OF
GoodKnight 425 / 425ST Service Manual
Federal law restricts this device for sale by or on the order of a physician.
CONTENTS
PREFACE 2
REVISION LIST 3
A. SPECIFICATIONS I-2
1) Performances I-2
2) Electrical specifications I-2
3) Environmental specifications I-3
4) Physical specifications I-3
5) Pressure stability I-3
6) Dynamic resistance I-4
C. SYMBOLS I-5
C. DISASSEMBLY III-22
I - GENERAL INFORMATION
A. SPECIFICATIONS
1) Performances
GoodKnight 425 and GoodKnight 425ST
Ä Setting restrictions: The maximum duration of the IPAP pressure is limited to 3 sec-
onds. Consequently certain combinations of frequency, rise time and I/E ratio will be
forbidden, especially for low frequency setting.
As well, certain combinations of frequency, rise time and I/E ratio which prevent the
IPAP set pressure to be reached will be forbidden, especially for high frequency setting.
NOTE 1
The display can be in “hPa”. The pressure adjustment range is then between 2.9 hPa
and 24.5 hPa. To select the unit, unplug the device, depress the hidden key and recon-
nect the device, keeping the hidden key depressed until the unit is displayed.
NOTE 2
All the stated performances are for a 6 ft (1.80-meter) patient circuit, recommended by
the manufacturer, fitted with a stopper with a 4 mm diameter leak.
2) Electrical specifications
Power supply
Ä External Power Supply Class II 100-240 VAC 50/60 Hz—13VCC 4A
Goodknight
Ä Consumption 40 VA max.
3) Environmental specifications
Ä Storage / Transport temperature -20° C to 60° C
Ä Storage / Transport humidity up to 95 % (non-condensing)
Ä Operating temperature +5° C to +40° C
Ä Operating humidity between 15 % and 95 % (non-condensing)
Ä Operating relative pressure 700 hPa to 1060 hPa (approximately up to
altitude of 7874 ft -2.400 m)
4) Physical specifications
Ä Width 5.6” (144 mm)
Ä Height 2.9” (79 mm)
Ä Length 7.7” (198 mm)
Ä Weight (without external power module) 1.58 lbs (780 g)
6) Dynamic resistance
The values below were measured from a simulated sinusoidal respiratory signal with a tidal volume
of 500 ml after a warm-up period of 2 hours. These measurements were made with a single unit.
B. USING A HUMIDIFIER
A heating or non-heating humidifier may be used with the GoodKnight 425 / 425ST on the
condition that the following warnings are noted.
WARNING
You are strongly advised to read the manufacturer’s recommendations for the humidi-
fier before use.
WARNING
Using a humidifier can alter the performance of the GoodKnight 425 / 425ST.
WARNING
The GoodKnight 425 / 425ST must always be placed above the humidifier. This position
will minimize the potential for water entering the Cpap device.
Water can damage the device.
C. SYMBOLS
SYMBOLS DEFINITIONS
~ Alternating current
Direct current
Class 2 Equipment
Type B
On / Off
Access to settings
Ramp
RS 232
Input DC voltage 13 V
Patient Output
D. CLEANING INSTRUCTIONS
WARNING
Unplug the unit from all electrical power sources before cleaning. Do not allow
water to enter the unit through any opening.
2) Air filter
Frequency Inspect the air filter frequently by removing it from the back panel.
Clean at least once a week or more often, if necessary.
How to clean Wash in warm, soapy water. Rinse thoroughly to remove all soap.
Pat dry with towel. Allow to air dry completely before reinstalling.
Replace filter if worn or damaged.
CAUTION
Only the standard air filter can be cleaned. The fine filter supplied as an option and
fitted in addition to the standard air filter, cannot be cleaned. It must be changed.
II - THEORY OF OPERATION
A. General description
1) General design synopsis
Voltage Patient
Patient
Interfac
Main Power
Power AC
AC Reference
Inte rface
Flow
Flow P
nal Module
External Module Flow filtered
C/DC i
AC/DC Flow direct Sensor t
o
t
otection Pressure
Protection
ltering
Filtering
Pressure filtered
Sensor
Temperature Blower
ulation 5V
Regulation Current filtered
5V Current
Current
C
Alarm Current Measurement T
N
Backlight
Motor Reset
Type cycle
le LCD
LCD Module
Respiratory phase
Microcontroler BusyI2CMotor Microcontroler Power
Keypad
ypad C508 C508 Blower
BusyI2CMaster Driver
Master Motor driver
ErrorMotor
al Link
Serial Link Set Change
Slope
Air
OM
ROM RAM Controler of Set-up RTC + Input
4ko
64K 64 ko NVRAM Battery RAM 56 octets
Watchdog
Hidden Key
LCD Display
Information On/Off
Access button or
Parameter settings
Ramp activation or
Parameter settings
3) Description
The general architecture of the device is based on the use of a blower (pressurised air genera-
tor) and two micro-controllers (one for the general functions of the unit and another one for
the motor control).
Some functions are hardware-controlled, some are software-controlled and others are a mix-
ture of hardware and software.
The GoodKnight 425 BiLevel is a BiLevel positive airway pressure device used in the treat-
ment of obstructive sleep apnea or for the titration in the sleep lab of a patient having obstruc-
tive sleep apnea. It is intended to treat OSAS patients who are over 30 kg in weight (66
pounds).
In the BiLevel mode the GoodKnight 425 tracks patient breathing cycles and, in response to
the patient’s inspiratory and expiratory efforts, provides two levels of pressure :
-IPAP : a higher level of pressure for inspiration (a range from EPAP to 25 cmH2O)
-EPAP : a lower pressure for expiration (a range from 3 to IPAP or 20 cmH2O).
-If IPAP is equal EPAP, than the unit operates in CPAP mode.
The GoodKnight 420 Series benefits from a new blower technology that is specifically
designed for this range of Cpap systems. This design provides optimum performances in
terms of size, consumption, noise and stability.
In order to guarantee these optimum performances, some parameters are electronically
tuned during the manufacturing process. These parameters are calculated for each
blower and cannot be duplicated for another one. For this reason it is not possible to
change a blower or an electronic board. In the event of failure, an internal chassis as-
sembly fitted with a factory-set blower and electronic board is available.
5) Temperature Sensor
The stator of the blower is fitted with a temperature sensor which will protect the system
against the overheating of the blower in the eventuality of a problem.
The GoodKnight BiLevel will stop working if the temperature goes above 95°C +/-5°C during
10 seconds.
7) Pneumatic diagram
DC Motor
Nasal mask
Flow
or
Sensor nasal pillows
Electrical system Humidifier
(optional) Pressure sensor
tube
Inlet filter Pressure Sensor
B. ELECTRICAL DIAGRAM
1) General block diagram
1.1.2 Power
Main Supply
Power Serial Link
1.1.3 AC AC
Interface
Serial Link
Protection
and
Filtrage
Regulation
5V
Electronic
Moteur Driver
Blower
Pitot Flow
Pressure
Air tube Sensor
Sensor
Input
Pressure
Sensor
Case
Case GK420
PATIENT
a) Micro-Master
Data
µC MAX691 Memory Software
MASTER SRAM Memory
P51 WDI ROM
64 ko
Reset 64 ko
Reset CS CS
WR WE
RD OE
G
Vcc
A15
A8
AD7 A0-7
AD0 AD0 – 7
D0 – 7
ALE
Multiplexer
b) Micro-Motor
µC Interfaces Motor
MOTOR Bridges
MOSFET
P12/CC0
P13/COUT0
P14/CC1
P15/COUT1
P16/CC2
P17/COUT2
µC
Pressure Filter RC MASTER
Lowpass Follower and
Sensor Fc = 152 Hz MOTOR
Patient
Tube
Flow Filter
P42 Hightpass
µC fc = 7,23 Hz
MASTER
and
MOTOR Flow filtered Filter
P43 Lowpass
fc = 0,17Hz
P45 Direct Flow
5) Temperature measurement
Blower
µC Master
6) Serial Link
µC Interface Connector PC
MASTER RS232 RS232
Tx
P30/RxD
P31/TxD Rx
This section describes how to service the individual subassembly of the GoodKnight 425
and 425ST Cpap System. It includes instructions where applicable, for removal, disassem-
bly, calibration, re-assembly and installation.
WARNING
The GK 425 and 425ST Cpap System is electrically powered. To prevent seri-
ous injury or death, follow standard safety procedures. Ensure that power
has been disconnected from the unit before servicing any component.
WARNING
After a component has been serviced, the unit must be calibrated and the overall
system operation checked according to the “Performance Verification” section,
before the unit is returned to service.
CAUTION
Circuit boards contain complementary metal-oxide semiconductor (CMOS) inte-
grated circuits (ICs) which are static sensitive devices. To prevent IC damage, follow
the standard safety procedures :
-handle circuit boards by edges only,
-wear a grounded wrist strap,
-work on a grounded conductive mat
-store circuit board in a conductive plastic bag.
CAUTION
Allow to warm up for half hour before carrying out the performance verification and/
or the calibration procedure.
A. PERFORMANCE VERIFICATION
1) General information
The performance verification should be carried out for any one of the following reasons:
-Pressure accuracy,
-Flow measurement chain
-Ramp and starting ramp pressure,
-Back-up frequency (425ST only).
2) Frequency
Þ annually,
Þ after repair.
3) Equipment required
· Calibrated pressure meter 0-30 cm H2O (local source),
· Patient tube P/N : M-261000-27,
· Test kit P/N : M-212430-02 (consists of a coupling 22/22 mm and a stopper with a
4 mm diameter leak),
· PC computer with Silverlining software,
· Serial link cable,
· Calibrated leak M-BH0210 and connecting tube M-213530-05.
Coupling
Test Kit
with 4 mm leak
P/N: M-212430-02
(including coupling)
Patient tube M-261000-27
Figure 3-1
b - Verification of the flow measurement chain
Connecting tube
M-213530-05
Figure 3-2
CAUTION
Allow to warm up for half hour before carrying out the performance verification and/
or the calibration procedure.
5-a) Preparation
Control Alt F9
- Enter the password. The password is given to technicians who have been trained by
the manufacturer or a person accredited by the manufacturer.
- After entering the password, press the “Enter” key or click on OK. The following
screen appears :
Menu "Pressure/Pression"
{
Setting cursor
5-b) Pressure Verification and Calibration
-Click on the button "14 cmH2O" and verify that the pressure meter is reading:
14 cmH2O + 0,5 .
Adjust if necessary the offset of the menu "Pressure/Pression" with the setting cursor
until the pressure meter is reading 14cmH2O.
-Click on the button "25 cmH2O" and verify that the pressure meter is reading:
25 cmH2O + 0,5 .
-Click on the button "3 cmH2O" and verify that the pressure meter is reading:
3 cmH2O + 0,5 .
CAUTION
Allow to warm up for half hour (Cpap mode; P=14cmH2O; plug test with 4mm
leak) before carrying out the performance verification and/or the calibration
procedure.
Prepare the unit under testing as show in the figure 3.2 page III-4
Menu "Flow/Débit"
{
Setting cursor
Step #1
-Wait for the “Value” reading on the screen to become stabilized,
-Verify that this “Value” of the menu “Flow/Débit” is reading:
0 l/s (+/- 0.1)
-If not, adjust the Offset with the setting cursor in order to read in the display “Value”
0 l/s +/-0.1, and then store with the button “Storage”.
-If the value read is within specification, go to step #2.
-If the value reading is not within specification, perform the calibration of the
flow sensor described page III-20. Do not go to the step #2
Step #2
-Unblock the calibrated output,
-Wait for the value reading on the screen to become stabilized,
-Check the value reading on the screen in the “Flow/Débit” menu is reading:
1.2 l/s (+/- 0.1)
-If the value reading is within specification, the verification is good.
-If the value reading is not within specification, perform the calibration of the
flow sensor described page III-20.
Click on the button "Test R" (Test of Ramp). The unit is set with a 5 minutes ramp, start pres-
sure 3 cmH2O , end pressure 20 cmH2O.
Verify that the pressure runs from 3 to 20 cmH2O in the time of::
Click on the button "Test F" (Test of Frequency). The unit is set with a frequency of 10 cycles /
min.(IPAP=14; EPAP=8; I/E=1:1.0). Verify that the pressure is switching from EPAP to IPAP
in 10 cycles +/- one cycles per minute.
NOTE
Some verifications can be performed without a computer (section 6 page III-10). In
order to do them you have to select the corresponding settings with the keypad. (refer
to the sections verification of the pressure, the ramp and the back-up frequency in the
following pages).
The verification of the pressure will not be total (maximum pressure in Cpap mode
=20 cmH2O).
NOTE
According to the settings limitation it will not be possible to verify the pressure
higher than 20 cmH2O. The pressure verification for 25 cmH2O can be done only
with the computer and the software Silverlining.
Check the measured value on the pressure meter, the value must be 20 cmH2O ± 0.5
#13-Go to points #2 to #5 and select
EPAP=IPAP= 3 cmH2O. c m H2 O cm H 2O
Check the measured value on the pressure meter, the value must be 3 cmH2O ± 0.5
If one of these two verifications is not within specification, set IPAP=EPAP=14 cmH2O and
go to step #8.
#14-Press on the key opposite to switch off the
units (display the current time). The pressure XX XX
:
verification is ended.
site.
#12-Check that the pressure increases from 3 cmH2O to 20 cmH2O in 5 minutes +/- 20 seconds.
When you select the “Reprogramming device” menu (see page III-6) and you click on
“OK”, the following two operations occur:
When an Er 01 is displayed the device is not able to communicate with the computer.
-The screen remains blank for a few seconds and then returns to normal mode.
1- Follow the same steps as those described on pages III-5 to III-6 (Performance Verifi-
cation).
2- After entering the password (page III-6), click on the “Serial number and meters”
menu and follow the screen instructions.
CAUTION
The serial number must match the one printed on the base of the device.
The manufacturer is not responsible for any fraudulent use that might result from modification
of the serial number.
adjusted.
NOTE
The setting of date can be done only with the software Silverlining.
Personal Notes
B. CALIBRATION PROCEDURE
1) Equipment required
* a calibrated pressure meter
* a calibrated leak M-BH210 and a connection tube M-213530-05,
* a patient circuit M-261000-27,
* a test kit M-212430-02
NOTE
The calibration pressure mode is accessed via the keypad.
CAUTION
Measure the pressure during calibration at the end of a 6 ft (1.80 m) patient circuit
sealed with a stopper fitted with a 4 mm diameter leak (figure 3.1 page III-4).
CAUTION
Allow to warm up for 1/2 hour before performing the pressure calibration
Connect a patient circuit and a pressure meter as shown in figure 3-1 on page III-4
The pressure sensor calibration can be done with a computer and the Technical Menu of the
software Silverlining (procedure described III-7), or with the keypad (procedure described
page III-10).
NOTE
The pressure calibration with the keypad does not allow to verify the pressure higher than
20 cmH2O
The pressure calibration with the keypad does not reboot the unit with the initial settings.
TR4
TR3
3-b) Calibration
CAUTION
Allow to warm up for 1/2 hour with a set pressure of 14cmH2O, unit in Cpap
mode, before carrying out the pressure calibration.
1-Replace the test kit with the calibrated output (figure 3.2 page III-4) and block
the output
2-With the mouse, click on the setting cursor of the menu “Flow/Débit” and adjust
the Offset to 0,
3-Store with the button “Storage”,
4-Place TR4 in a medium position,
5-Adjust TR3 for a Value/Valeur reading of 0 l/s +/-0.05 (Value of Flow in the
“Flow/Débit” menu),
6-Leave the calibrated output free and adjust TR4 for a Value/Valeur reading of:
1.2 l/s +/-0.05,
7-Block again the calibrated output and verify that the value reading is:
0 l/s +/-0.05.
If not, repeat the process from the step #5.
Menu "Flow/Débit"
{
Setting Cursor
C. DISASSEMBLY
Material :
A Torx T10 screwdriver,
A grounded wrist strap,
A grounded conductive mat.
WARNING
The GK 425/425ST BiLevel System is electrically powered. To prevent serious
injury or death, follow standard safety procedures. Ensure that power has
been disconnected from the unit before servicing any component.
CAUTION
After replacing the chassis assembly, enter the serial number and the hour meter value in the device
memory if necessary
Top Bottom
Housing Housing
Inlet baffle
foam
D. TROUBLESHOOTING GUIDE
The device does not The ramp is activated. -Check that the ramp indicator is dis-
produce the correct played. Press the ramp button to cancel the
pressure. function.
-Call your Technical Support
The air output of the The air input filters may be -Clean or replace the filters accordingly.
device is too hot. dirty. Move away any bed linen or clothing from
the GK425/425ST.
The air input is obstructed. -Turn the room thermostat down. Make
The room temperature is sure that the GK425/425ST is not near any
too high. source of heat.
-Remove the tube from under the covers.
-Call your Technical Support
The GK425/GK425ST Check that the external -Check the connection of the external
does not switch on (no power supply module is cor- power supply module to the mains plug.
display). rectly connected.
No mains supply. -Use another appliance (e.g.: lamp, radio,
etc) to check that there is an AC current
supply at the plug.
-Call your Technical Support
The device does not Excessive electromagnetic -Keep device away from all sources of dis-
work correctly and ap- disturbance turbance, such as mobile phones, halogen
pears to be suffering lights...
interference -Call your Technical Support
Er=0XX is displayed The device has detected an -Refer to the “Error Messages” section on
(xx =error code). operating fault. page III-26.
-Call your Technical Support
In 02 is displayed. Excess pressure (higher -Check the connection of the small pressure
than 28 cmH2O) has been point hose. Check that the tube is not
detected by the device for pinched or blocked.
more than 10 seconds.
-Call your Technical Support
In 03 is displayed. There is a drop in power. -Check the connection between the external
power module, the power cable and the de-
vice.
-Check the external battery if used.
E. ERROR MESSAGES
We recommend that you send a copy of the completed forms to your local Factory Service.
Return number This is the official Return Goods Authorization (RGA) or your own re-
turn number if RGA does not exist.
Failure description Describe the failure in a few words or state “Routine Service” if this is
the case.
Servicing done Describe in a few words what you have done in the service.
Report number Enter here your report number if not the same as the return number.
Personal Notes
IV - SPARE PARTS
Part # Description
M-314530-00 Top Housing equipped 425 International
M-314530-01 Top Housing equipped 425ST International
M-314530-02 Top Housing equipped 425 USA
M-314530-03 Top Housing equipped 425ST USA
M-313940-01 Bottom housing 425 / 425ST
M-314560-00 Internal frame assembly 425 (equipped with blower and electronic board
factory set). Inlet baffle foam not included.
M-314560-01 Internal frame assembly 425ST (equipped with blower and electronic
board factory set). Inlet baffle foam not included.
SERIAL # CUSTOMER
RETURN # REPORTING #
Failure
Servicing Done
CALIBRATION
Pressure sensor
Flow sensor
Adjustment with TR3: Value: l/s (Offset =0, calibrated output blocked)
Adjustment with TR4: Value: l/s (Offset =0, calibrated output free)
Observations
145FDS002.0
GoodKnight 425 / 425ST Service Manual