Edan M3 - Vital Signs Monitor Service Manual
Edan M3 - Vital Signs Monitor Service Manual
Edan M3 - Vital Signs Monitor Service Manual
P/N: 01.54.109399-11
Release Date: November 2011
Copyright EDAN INSTRUMENTS, INC. 2008-2011. All rights reserved.
Statement
This manual will help you understand the operation and maintenance of the product better. It is
reminded that the product shall be used strictly complying with this manual. Users operation
failing to comply with this manual may result in malfunction or accident for which EDAN
INSTRUMENTS, INC. (hereinafter called EDAN) can not be held liable.
EDAN owns the copyrights of this manual. Without prior written consent of EDAN, any
materials contained in this manual shall not be photocopied, reproduced or translated into other
languages.
Materials protected by the copyright law, including but not limited to confidential information
such as technical information and patent information are contained in this manual, the user shall
not disclose such information to any irrelevant third party.
The user shall understand that nothing in this manual grants him, expressly or implicitly, any
right or license to use any of the intellectual properties of EDAN.
EDAN holds the rights to modify, update, and ultimately explain this manual.
II
Table of Contents
Chapter 1 Warranty and Service................................................................................................. 1
1.1 Standard Service................................................................................................................. 1
1.2 Limitation of Warranty ...................................................................................................... 1
1.3 Service Procedure............................................................................................................... 1
1.4 Contact Information ........................................................................................................... 3
Chapter 2 Installation and Safety................................................................................................ 4
2.1 Environment Requirements................................................................................................ 4
2.2 Electrical Requirements ..................................................................................................... 5
2.3 Safety Requirements .......................................................................................................... 5
2.4 Installing the Monitor......................................................................................................... 6
2.4.1 Install the Monitor on a Flat Surface........................................................................ 6
2.4.2 Mount the Monitor on Wall ..................................................................................... 6
2.4.3 Install the Monitor on Pole Clamp ........................................................................... 6
2.4.4 Install the Monitor on Trolley .................................................................................. 6
Chapter 3 Test and Maintenance................................................................................................. 7
3.1 Routine Test ....................................................................................................................... 7
3.1.1 Visual Inspection...................................................................................................... 7
3.1.2 Power- on Test ......................................................................................................... 7
3.1.3 Key Test ................................................................................................................... 7
3.1.4 Recording Test ......................................................................................................... 7
3.1.5 Alarm Test................................................................................................................ 8
3.2 Performance Test ............................................................................................................... 8
3.2.1 SpO2 Performance Test ............................................................................................ 8
3.2.2 NIBP Performance Test ........................................................................................... 8
3.2.3 NIBP Leakage Test .................................................................................................. 8
3.2.4 NIBP Calibration...................................................................................................... 9
3.2.5 TEMP Performance Test........................................................................................ 10
3.3 Safety Test........................................................................................................................ 10
3.3.1 Safety Test Procedures........................................................................................... 10
3.3.2 Protective Earth Resistance.................................................................................... 11
3.3.3 Enclosure Leakage Current .................................................................................... 11
3.3.4 Patient Leakage current.......................................................................................... 12
3.3.5 Patient Leakage Current- Single Fault Condition (S.F.C) Mains on Applied Part 13
3.4.1 Cleaning the Monitor and Accessories .................................................................. 14
3.4.2 Maintaining the Battery.......................................................................................... 15
Chapter 4 System Configuration ............................................................................................... 16
4.1 Enter Factory Maintain .................................................................................................... 16
4.2 Enter Demo Mode ............................................................................................................ 16
III
ii) The customer signs the Declaration Form and sends it back by email or fax. This form is
legally certificated to make sure the customer or end-user will return the defective parts to
EDAN on time. We will, at this option, dispatch the replacement one (s) with confirmed
shipping invoice.
NOTE:
1 Both Return Material Authorization Form and Declaration Form are offered by EDAN
service department once the SCF is confirmed by service engineer.
2 The customer is responsible for freight & insurance charges when the equipment is
shipped to EDAN for service, including custom charges. EDAN is responsible for the
freight, insurance & custom charges from EDAN to the customer.
Out of Warranty:
After receiving the RMA form from the service department, the customer sends defective parts to
EDAN in advance. We will analyze the problems and discuss with the customer about either
repairing or replacing the part (s). Once the maintenance fee is invoiced and paid, we will make
sure to dispatch good part (s) to the confirmed address.
NOTE:
The customer is responsible for any freight & insurance charge for the returned product.
(3) Obtain the RMA Form.
Before the shipment of the materials, the customer must obtain an RMA form from our service
department, in which the RMA number, description of returning parts and shipping instructions
are included. The RMA number should be indicated on the outside of the shipping container.
NOTE:
EDAN should not have any obligation to the end-user or customer who returns the goods
without the notification by EDANs service department. The sender takes full
responsibility for the accounted fee.
(4) Send the Parts to EDAN.
Follow these recommended instructions:
Please disassemble the parts with anti-static facility, do not touch the parts with naked hand.
Please pack the parts safely before return.
Please put the RMA number on the parcel.
Please describe the returned parts as sample of ***** and put the total value on the invoice,
and note on the invoice as sample, no commercial value.
Please confirm the invoice with Edan before shipment.
Please send back the parts after EDANs confirmation.
-2-
-3-
Temperature
Working
+5 C ~ +40 C
-20 C ~ +55 C
Humidity
Working
Altitude
Working
860hPa ~ 1060hPa
700hPa ~ 1060hPa
CAUTION
1 If the monitor is installed in a cabinet, allow at least 2 inches (5 cm) clearance around
the monitor for proper air circulation; allow adequate accessibility for servicing, and
adequate room for visualization and operation.
2 Ensure the monitor is not subjected to any source of strong electromagnetic
interference, such as CT, radio transmitters, mobile phones base stations, etc.
3 Do not install the monitor in a flammable atmosphere where concentrations of
flammable anesthetics or other materials may occur.
4 Keep the environment clean. Avoid vibration. Keep it far from corrosive medicine, dust
area, high-temperature and humid environment.
-4-
Voltage: 100V-240V ~
Frequency: 50Hz/60Hz
Pmax: 70VA
Battery: 14.8 V/4.4 Ah; 14.8 V/2.2 Ah.
NIBP, SpO2
This symbol indicates that the instrument is IEC/EN60601-1 Type BF equipment. The unit
displaying this symbol contains an F-Type isolated (floating) patient applied part providing a high
degree of protection against shock, and is suitable for use during defibrillation.
TEMP
This symbol indicates that the instrument is IEC/EN60601-1 Type CF equipment. The unit
displaying this symbol contains an F-Type isolated (floating) patient applied part providing a high
degree of protection against shock, and is not suitable for use during defibrillation.
CAUTION
1 SHOCK HAZARD- the power receptacle must be a three-wire grounded outlet. A
hospital grade outlet is required. Never adapt the three-prong plug from the monitor to
fit a two-slot outlet. If the outlet has only two slots, make sure that it is replaced with a
three-slot grounded outlet before attempting to operate the monitor.
2 Do not touch signal input or output connector and the patient simultaneously.
3 Equipment and devices that connect to the monitor should form an equipotential body
to ensure effective grounding.
4 Do not switch on the monitor until all cables have been properly connected and verified.
-5-
-6-
-7-
WARNING
Performance tests must only be carried out by qualified service personnel.
If performance of the monitor is in question, conduct an overall performance test
according to the instructions offered by the manufacturer.
A functional check should be performed once possible device malfunction emerges or after
servicing the device.
It is unnecessary to open the device case for functional checks.
Connect the monitor and the SpO2 simulator with a SpO2 cable.
2.
3.
4.
Check for the display on the monitor. A difference within the range of 2% is reasonable.
2.
Switch on the monitor and the simulator. Perform calibration prior to using the simulator.
3.
Set the patient type both on the monitor and in the simulator to adult; respectively set the
systolic pressure and diastolic pressure (mean pressure) to 255/195(215) mmHg. Start a
NIBP measurement.
4.
Check for the display on the monitor. A difference within the range of 8mmHg is
reasonable.
-8-
1.
Connect the cuff securely with the socket for NIBP air hole.
2.
3.
Access SYSTEM MENU > MAINTAIN > USER MAINTAIN by inputting the password
ABC. Start a leakage test by selecting NIBP MAINTAIN > LEAK TEST.
The system will automatically inflate the pneumatic system to 180 mmHg. After 20 seconds, the
system will automatically open the deflating valve, which marks the completion of a pneumatic
measurement.
If the prompt of Leak Test OK appears, it indicates that the airway is in good situation and no air
leaks exist. However if the alarm information of NIBP Cuff Leak appears, it indicates that the
airway may have air leaks. In this case, the user should check for loose connection. After
confirming secure connections, the user should re-perform the pneumatic test. If the failure
prompt still appears, please contact the manufacturer for repair.
Manometer
Tube
Tube
Cylinder
NIBP module
/ Patient
monitor
T-fitting
NIBP
extension
tube or hose
-9-
3.
4.
Apply fixed static pressure on the monitor with the help of the manometer. Compare the
displayed values on the monitor with the manometer values.
5.
With devices that are connected to other devices by means of a data cable, this
connection must be disconnected prior to performing the electrical safety check, in
order to avoid incorrect measurements.
- 10 -
NOTE:
The circuit diagram is based on the Fluke 601Pro series safety analyzer.
This measures impendence of Protective Earth (PE) terminal to accessible metal part of Device
under test (DUT) which is protectively earthed. A current of 25A is passed for 5s to 10s through
the protective terminal and each accessible metal part which is protectively earthed.
Allowable value: without mains cable, maximum impendence: 100 mOhms
(IEC 60601-1 and UL60601-1)
NOTE:
The circuit diagram is based on the Fluke 601Pro series safety Analyzer.
- 11 -
This measures leakage current of exposed metal parts of Device under test (DUT) and parts of the
system within the patient environment; normal and reversed polarity using S2 test performed both
in normal condition and single fault conditions.
Normal condition (NC): with S1, S3, S5 closed, S2, S4 variable.
Single fault condition (SFC): S1, S3 open (one for each time) and S5 closed, S2, S4 variable.
Allowable value:
Normal condition: 100A (IEC/EN60601-1)
Single fault condition: 500A (IEC/EN60601-1)
Normal condition: 100A (UL60601-1)
Single fault condition: 300A (UL60601-1)
NOTE:
The circuit diagram is based on the Fluke 601Pro series safety Analyzer.
This test measure the leakage current flowing between the selected applied part and the mains PE;
the test with normal and reverse polarity, in normal condition and single fault condition.
Normal condition (NC): with S1, S3, S5 closed, S2, S4 variable.
Single fault condition (SFC): S1, S3 open (one for each time) and S5 closed, S2, S4 variable.
Allowable value:
Normal condition: 10A (BF applied part), 10A (CF applied part)
- 12 -
(IEC/EN60601-1, UL60601-1)
Single fault condition: 500A (BF applied part), 50A (CF applied part)
(IEC/EN60601-1, UL60601-1)
Leakage Current
Applied
Part
Normal
Condition
Single Fault
Condition
<0.5 mA
<1 mA
<0.1 mA
<0.5 mA
CF
AC: <0.01 mA
DC: <0.01 mA
AC: <0.05 mA
DC: <0.05 mA
BF
AC: <0.1 mA
DC: <0.01 mA
AC: <0.5 mA
DC: <0.05 mA
CF
<0.05 mA
BF
<5 mA
CF
AC: <0.01 mA
DC: <0.01 mA
AC: <0.05 mA
DC: <0.05 mA
BF
AC: <0.1 mA
DC: <0.01 mA
AC: <0.5 mA
DC: <0.05 mA
- 13 -
NOTE:
The circuit diagram is based on the Fluke 601Pro series safety Analyzer.
This test measure the current flowing between the applied part and the mains PE in response to an
isolate mains voltage (110% of the mains voltage) applied to applied part. This test is performed
with normal and reverse polarity of the mains voltage using S2, and normal and reverse polarity
of the isolate voltage using S4.
Single fault condition: S1, S3, S5 closed, S2, S4, S6 variable.
Allowable value:
Single fault condition (110% mains voltage on applied part):
5000A (BF applied part), 50A (CF applied part)
(IEC/EN 60601-1 UL 60601-1)
3.4 Maintenance
For details about basic cleaning and maintenance methods, refer to relevant sections in M3 Vital
Signs Monitor User Manual. For further technical support, contact service engineers of EDAN.
Users are responsible for preventive maintenance and periodic inspection for the monitor.
- 14 -
- 15 -
System Configuration
System Principle
5.1 Principle
Parameter module is the basic unit to acquire signals for monitoring parameters in the monitor.
The monitoring signals are transmitted to the main control board and subsequently processed by
it. The measurement data and waveforms will be displayed on the LCD. The power link board
can realize power switching and conversion. The whole system structure is shown in the
following figure:
Medical staff
LCD
Key control
board
Recorder
Display
driver board
Network
interface
board
Main control
board
Power supply
NIBP
SpO2
TEMP
Patient
As shown in the figure above, the three parameter modules execute real-time monitoring of NIBP,
SpO2, and TEMP respectively by using cuff and measuring cables. The results will be sent to main
control board for processing and displayed on the LCD. Hereinafter the function details of
parameter monitor will be explained.
- 17 -
System Principle
5.1.1 NIBP
Blood pressure monitors commonly measure arterial pressure, which is produced by the
contraction of the heart and constantly changes over the course of cardiac cycle. Three blood
pressure values, expressed in millimeters of mercury above atmospheric pressure, are obtained.
The systolic pressure is the maximum cycle pressure; which occurs during ventricular contraction.
The diastolic pressure is the minimum cycle pressure, occurring during the ventricles filling
stage between contractions. The means arterial pressure (MAP) is the mean value of the blood
pressure over the cardiac cycle.
The monitor measures non-invasive blood pressure using the oscillometry method. The following
are detailed measurement procedures. Inflate the cuff encircling the upper arm until the pressure
in the cuff blocks the blood flow in the artery of the upper arm. Then deflate the cuff gradually
according to the requirement of certain arithmetic. With the decreasing of the pressure in the cuff,
the artery blood will palpitate with the pulse, which results in palpitation in the cuff. Through the
pressure sensor connected with the inflating pipe of the cuff, a palpitation signal palpitating with
the pulse will be generated. After being filtered by a high-pass filter (about 1Hz), this signal
becomes pulsating signal and is amplified. Then the amplified signal is converted into digital
signal by A/D. After using the singlechip to process this digital signal, we may obtain systolic
pressure, diastolic pressure and mean pressure. Be careful to choose appropriate cuffs for
neonatal, pediatric and adult patients so as to avoid generating measurement error. NIBP module
also has protection circuit to prevent the cuff from being inflated to a very high pressure. The
following are the main operating modes of NIBP.
a.
b.
5.1.2 SpO2
SpO2 is based on the absorption of pulse blood oxygen to red and infrared light by means of
finger sensor and SpO2 measuring unit. The light-electronic transducer in finger sensor converts
the pulse red and infrared light modulated by pulse blood oxygen into electrical signal, the signal
is processed by hardware and software of the unit. The PLETH curve and numeral value of SpO2
will be obtained.
By tracing the pulse waveform in the fingertip, using specified arithmetic and consulting the
clinical data table, we can obtain the SpO2 value. The SpO2 sensor consists of two LEDs and a
photodetector. The two LEDs are respectively red diode and infrared diode, which are lighted on
according to certain time sequence. When the capillary vessel of the fingertip congests repeatedly,
the light of the LED is absorbed by blood vessels and organs and then projected onto the
photodetector. The photodetector can detect the light intensity varying with pulse changes and
- 18 -
System Principle
display the changing light intensity in the form of changing electronic signals. The ratio between
the DC and AC of the two types of signals for light is the proportion of oxygen in the blood. Then
we can calculate correct SpO2 value by using specified arithmetic and also calculate pulse rate
according to the SpO2 waveform.
The SpO2 module mainly consists of the following four parts: sensor, signal processing, control
unit of LED driving sequence, singlechip.
5.1.3 TEMP
Two optional modules are available for TEMP measurement. The one is T2 module; the other is
TH module.
Regarding the T2 module, the temperature of human body is first converted into electronic
signals, which are then amplified by amplifier and processed. In this way we can obtain the
TEMP value. The circuit includes proportional amplifier constructed by operational amplifiers.
The temperature passes the thermal sensor, producing pressure signals, which are amplified and
transmitted to A/D converter for further processing.
The TH module works on the principle of infrared radiation. It can quickly take a temperature in
the ear in a non-contact way. The measurement value will be displayed on the LCD of the
thermometer within one second and transmitted to the monitor via communication wire. The
monitor consequently displays and stores the measurement value.
- 19 -
System Principle
Choose one
from
T2 TEMP
and
TH TEMP
J1
Infrared
insulate board
J2
Infrared ear
thermometer
NOTE:
The nurse call board and the network board are optional configurations; they can not be
installed at the same time. If you want to use the nurse call function, you should install the
nurse call board; otherwise you should install the network board.
- 20 -
System Principle
LCD
DBAB
The M3 main control board is installed on the display holder with the font shell assembly. Its
main functions are:
1.
To supply power for the external parameter modules (including NIBP, SpO2 and TEMP
module), and to realize communication between each parameter module via serial interfaces;
2.
3.
To control data traffic between each interface board (including alarm LED board, network
USB board, LED backlight driver patching board ,key control board);
4.
To supply power for the external recorder and realize data traffic between the recorder;
5.
6.
There are different ports on the main control board. The port definitions are illustrated as follows.
- 21 -
5.2.1.1
System Principle
Pin NO.
Power input
5.2.1.2
Definition
+5V
GND
GND
+12V
- 22 -
System Principle
Pin NO.
Power control
5.2.1.3
Definition
MTXD8_POWER
MRXD8_POWER
GND
DISG_CHARGE_POWER
DISG_ACON_POWER
DISG_SWITCH_POWER
GND
NC
NC
10
NC
X2 Module Port
X2 module
Pin NO.
Definition
RS232MRXD0_NIBP&CO2
GND
RS232MTXD0_NIBP&CO2
GND
TRTS2_NIBP&CO2
VCC_5V
VCC_12V
- 23 -
5.2.1.4
System Principle
T2 Module Port
Pin NO.
T2 Module
5.2.1.5
Definition
VCC_5 V
GND
MTXD7_T2
MRXD7_T2
TH Module Port
- 24 -
System Principle
Pin NO.
TH Module
5.2.1.6
Definition
VCC_5 V
GND
MTXD7_T2
MRXD7_T2
Pin NO.
Network module
Definition
RX+
RX-
TX-
TX+
- 25 -
5.2.1.7
System Principle
Pin NO.
USB and Nurse call
Definition
GND
DSIG_DN0_USB
DSIG_DP0_USB
VCC_5V
GND
EXGPIO4_NURSECALL
GND
VCC_12 V
NC
10
NC
- 26 -
5.2.1.8
System Principle
Recorder Port
Pin NO.
Recorder
Definition
DSIG_NSTB_PRINTER
DSIG_PD0_PRINTER
DSIG_PD1_PRINTER
DSIG_PD2_PRINTER
DSIG_PD3_PRINTER
DSIG_PD4_PRINTER
DSIG_PD5_PRINTER
DSIG_PD6_PRINTER
DSIG_PD7_PRINTER
10
DSIG_NACK_PRINTER
11
DSIG_BUSY_PRINTER
12
DSIG_PE_PRINTER
13
DSIG_NEER_PRINTER
14
GND
15
GND
16
VCC_12V
17
VCC_12V
18
VCC_12V
19
VCC_5V
20
GND
- 27 -
5.2.1.9
System Principle
Pin NO.
Key Control Board
Definition
DSIG_CHARGE_POWER
DSIG_ACON_POWER
DSIG_SWITCH_POWER
GND
MTXD2_KEYBOARD
MRXD2_KEYBOARD
GND
VCC_5V
- 28 -
System Principle
Pin NO.
FPC port of LCD
Definition
VCC_12V
VCC_12V
GND
GND
VCC_5V
VCC_5V
- 29 -
System Principle
Pin NO.
FPC port of LCD
Definition
DSIG_PWM_LCD
VBB_3V3
VBB_3V3
10
GND
11
GND
12
LCD_VD19
13
LCD_VD20
14
GND
15
LCD_VD21
16
LCD_VD22
17
GND
18
LCD_VD23
19
LCD_VD10
20
GND
21
LCD_VD11
22
LCD_VD12
23
GND
24
LCD_VD13
25
LCD_VD14
26
GND
27
LCD_VD15
28
LCD_VD3
29
GND
30
LCD_VD4
31
LCD_VD5
32
GND
33
LCD_VD6
34
LCD_VD7
35
GND
36
LCD_HSYNC
37
LCD_VSYNC
38
GND
39
LCD_VCLK
- 30 -
System Principle
Pin NO.
FPC port of LCD
Definition
40
GND
41
LCD_ENAB
42
GND
43
LCD_PWR
44
GND
45
GND
46
LCD_VD0
47
LCD_VD1
48
LCD_VD2
49
DSIG_LIGHTON_5.6LCD
50
GND
Fan
Power
module
Power control
board
Principle Introduction
This module converts +220 V AC mains power supply or battery power into +5 V and +12 V DC
supplies to power other boards. If AC mains and battery coexist, the former take the priority to
power the system and charge the latter at the same time.
- 31 -
System Principle
AC/DC
Converts high-voltage AC supply into low-voltage DC supply to power subsequent circuits and
charge the battery.
Battery Control Circuit
If AC supply and battery coexist, this circuit controls the output from AC/DC part to charge the
battery. If AC supply is disconnected, this circuit controls the battery to power the subsequent
circuits.
+5 V DC
Convert the DC supply from the previous circuit into stable +5 V DC supply to power other
boards.
+12 V DC
Convert the DC supply from the previous circuit into stable +12 V DC supply to power other
boards.
Power Switch Circuit
Control the working status of +5 V DC and +12 V DC in order to control ON/OFF action of the
monitor.
Voltage Detection Circuit
Detects the output voltage of every part in detection circuit, converts analogue signals to digital
signals and then send them to main control board for processing.
- 32 -
Troubleshooting
Chapter 6 Troubleshooting
In transportation, storage and use of monitor, various factors such as unstable network voltage,
changing environmental temperature, falling-down or impact, component aging may all result in
monitor failures and therefore affect normal application of the device. In failure conditions,
professional personnel with the experience of repairing electronic medical devices should
perform component-level upkeep for the failure classification listed in the table below.
Component-level upkeep means based on analyzing, replacing or trial-operating the component,
we can pinpoint the failure on a certain component of the device, such as power board, main
control board, TFT assembly, measuring cable or parameter module, etc. Repair of only some
components means component-level repair. The repair operation must be conducted by a service
engineer with abundant experience and with the assistance of special equipment and in specific
environment and conditions.
Possible Cause
Solution
After switching on, LCD Fuse damage (If it has fuse Replace fuse
has no display; the power
on)
Replace power board
indicator is off.
Power board damage
Anchor the short-circuited
Component short-circuits.
component.
No display after power-on Main control board failure or Refer to section 6.2 Display
or black screen during display failure.
Failure.
operation,
however,
power indicator lights.
Operation
or Main
control
measurement function is corresponding
disabled.
damage.
Abrupt switching off.
board
or Examine the main control
component board and the corresponding
components.
Moment
intensive Check power supply and
interference of network.
grounding system.
Poor performance of power
board.
- 33 -
main
Replace
or
connectors.
control
repair
Troubleshooting
Possible Cause
Solution
improper
Possible Cause
Solution
Buttons or the rotary Malfunction in the key set on the Replace the key set or key control
knob is disabled.
key control board.
board.
Sound of speaker is Malfunction in the audio Replace the key control board.
raucous or there is no
subassembly of the key Replace
the
speaker
or
sound.
control board.
connecting wire.
Malfunction in the speaker or
connecting wire.
- 34 -
Troubleshooting
Possible Cause
Solution
Paper is jammed.
connection
the
recording
control
network.
Possible Cause
Solution
- 35 -
Troubleshooting
Possible Cause
Solution
alarm
Possible Cause
is
Audio
alarm
temporarily disabled.
Speaker
connecting
failure.
and
wire
Solution
is
its
has
Program failure
Possible Cause
Solution
board
- 36 -
has
Troubleshooting
Blood pressure can not Cuff becomes loose or patient is Keep the patient quiet, bind the
be
measured moving.
cuff correctly and safely.
occasionally.
Great error in NIBP Cuff size does not fit the Use the cuff of appropriate
measurement.
patient.
size.
X2
module
performance.
has
Sensor or
damaged.
X2
module
in
- 37 -
Switch off the monitor and remove the AC power cable before disassembling the
monitor.
After any repair of the monitor, perform safety tests before using the monitor again.
A flat-head screwdriver
An M3 nut driver
A pair of pliers
- 38 -
4) Remove the old fuse. Take out a new fuse supplied by EDAN or of the same specification:
Size: 5mm20mm; Model: T1.6AL 250V.
5) Place the new fuse in the fuse socket. Press and screw it clockwise back in position.
- 39 -
Remove the four screws in rear panel with screwdriver to separate the front housing and rear
housing.
- 40 -
2.
Take apart the front housing and rear housing at the joint, and disconnect the linking wires in
order to separate the two parts.
- 41 -
Socket for wire linking PS900K and M3 main board power source
To separate the rear cover, firstly, you should overturn the monitor and remove the fuses as
described in section 7.2 Replacing Fuses. Then remove the three screws for securing the
main frame and rear housing.
- 42 -
M36 cross
recessed
countersunk
head screws
Fuses
2.
Remove the four screws in the main frame and one screw for grounding. Then carefully take
out the main frame.
M36
cross
recessed pan
head screws
- 43 -
M36
cross
recessed pan
head screws
- 44 -
Screws
- 45 -
Block
Wire linking
T2 module
and
main
control
board
Block
5. Remove the four screws on the T2 module; and then separate the module from the monitor.
Screws
- 46 -
Screws
Block
5. Remove the five screws on the module; and then separate the module from the monitor.
- 47 -
Screws
- 48 -
Screws
- 49 -
Screws
Cross
recessed
pan head screws
- 51 -
Speaker
- 52 -
3. After taking off the flat cable for LCD screen, remove the six screws for securing the module,
and then remove the main control board.
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M36
cross
recessed screws
- 54 -
6-3X8
recessed
screws
cross
tapping
- 55 -
3-3X8
cross
recessed
tapping
screws
- 56 -
4-3X8 cross
recessed pan
head tapping
screws
4. Remove the four screws and take out the LCD holder.
4-3X6 cross
recessed
screws
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6. Release the snap-fit of the flat cable, and separate the driver board and the LCD.
Snap-fit
- 58 -
- 59 -
Renewal Parts
Parts
Part Number
21.21.064169
02.03.451187-10
02.03.112196
02.03.112198
12.03.112200-11
11.58.029016
Deflating valve
11.58.40301-13
Pump
11.58.40302
02.01.118001
Speaker
01.14.038010
12.03.220040-10
02.02.100343
12.03.109553-10
12.02.451199-10
12.02.451201-10
01.16.045044-11
01.03.036268-10
Recorder assembly
22.04.240405
02.01.110112
22.01.210442
21.21.064168
21.21.064167
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Specifications
Appendix I Specifications
Please refer to M3 Vital Signs Monitor User Manual for more information.
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