Advanced Pm2000b Monitor SERVICE MANUAL

SERVICE MANUAL
PM2000B SERIES PATIENT MONITOR

Version 1.0
About this Manual
P/N: 01.54.455516
MPN: 01.54.455516012
Release Date: October 2015
© Copyright ADVANCED INSTRUMENTS, INC. 2012-2015. 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. User‘s operation
failing to comply with this manual may result in malfunction or accident for which
ADVANCED INSTRUMENTS, INC. (hereinafter called ADVANCED) cannot be held liable.
ADVANCED owns the copyrights of this manual. Without prior written consent of
ADVANCED, 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 ADVANCED.
ADVANCED holds the rights to modify, update, and ultimately explain this manual.
Responsibility of the Manufacturer

ADVANCED only considers itself responsible for any effect on safety, reliability and
performance of the equipment if:
Assembly operations, extensions, re-adjustments, modifications or repairs are carried out by

persons authorized by ADVANCED, and
The electrical installation of the relevant room complies with national standards, and
The instrument is used in accordance with the instructions for use.
Upon request, ADVANCED may provide, with compensation, necessary circuit diagrams,
and other information to help qualified technician to maintain and repair some parts, which
ADVANCED may define as user serviceable.
I
Terms Used in this Manual
This guide is designed to give key concepts on safety precautions.
WARNING
A WARNING label advises against certain actions or situations that could result in personal
injury or death.
CAUTION
A CAUTION label advises against actions or situations that could damage equipment, produce
inaccurate data, or invalidate a procedure.
NOTE
A NOTE provides useful information regarding a function or a procedure.
II
Table of Contents
Chapter 1 Warranty and Service .................................................................................................. 1
Chapter 2 Safety Guidance ............................................................................................................ 4
2.1 Introduction ......................................................................................................................... 4
2.2 General Information ............................................................................................................ 5
2.3 Safety Precautions ............................................................................................................... 5
2.4 Explanation of Symbols on the Monitor.............................................................................. 6
Chapter 3 Installation .................................................................................................................... 9
3.1 Environment Requirements ................................................................................................. 9
3.2 Electrical Requirements ...................................................................................................... 9
3.3 Safety Requirements.......................................................................................................... 10
3.4 Installing the Monitor ........................................................................................................ 10
3.5 Connecting to AC Power ................................................................................................... 10
Chapter 4 Test and Maintenance................................................................................................. 11
4.1 Routine Test ................................................................................................................................. 11
4.1.1 Visual Inspection ..................................................................................................... 11
4.1.2 Power- on Test .................................................................................................................. 11
4.1.3 Key Test............................................................................................................................. 11
4.1.4 Recording Test .................................................................................................................. 11
4.1.5 Alarm Test ......................................................................................................................... 12
4.2 Functional Tests and Accuracy Tests ........................................................................................ 12
4.2.1 ECG Functional Test........................................................................................................ 12
4.2.2 SpO2 Functional Test ...................................................................................................... 12
4.2.3 NIBP Functional Test ....................................................................................................... 13
4.2.4 NIBP Leakage Test........................................................................................................... 13
4.2.5 NIBP Calibration ..................................................................................................... 14
4.2.6 TEMP Accuracy Test ....................................................................................................... 15
4.2.7 CO2 Functional Test ........................................................................................................ 15
4.2.8 IBP Functional Test .......................................................................................................... 15
4.2.9 C.O. Functional Test ........................................................................................................ 16
4.3 Safety Test .................................................................................................................................... 16
4.3.1 Safety Test Procedures .......................................................................................... 16
4.3.2 Protective Earth Resistance ..................................................................................... 17
4.3.3 Enclosure Leakage Current ..................................................................................... 18
4.3.4 Patient Leakage current ........................................................................................... 19
4.3.5 Patient Leakage Current- Single Fault Condition (S.F.C) Mains on Applied Part . 20
4.4 Maintenance ...................................................................................................................... 22
4.4.1 Cleaning the Monitor and Accessories .................................................................... 22
4.4.2 Maintaining the Battery ........................................................................................... 22
Chapter 5 Principle Introduction ................................................................................................ 23
3
5.1 System Principle Block Diagram....................................................................................... 23
5.1.1 Main Control Board................................................................................................. 23
5.1.2 Parameter Modules .................................................................................................. 24
5.1.3 Key Board and Alarm LED......................................................................................... 24
5.1.4 Display Screen ......................................................................................................... 25
5.1.5 Interface Board ........................................................................................................ 26
5.1.6 Power Module ......................................................................................................... 26
5.2 Interfaces ........................................................................................................................... 27
5.2.1 USB Port ................................................................................................................. 27
5.2.2 Network / Nurse Call Interface ................................................................................ 27
Chapter 6 Troubleshooting .............................................................................................................. 28
6.1 Device Failures .................................................................................................................. 28
6.2 Display Failures................................................................................................................. 29
6.3 Operation, Recording and Networking Failures ................................................................ 29
6.4 Alarm Failures ................................................................................................................... 30
6.5 Parameter Monitoring Failures .......................................................................................... 31
6.6 Data Storage Failures......................................................................................................... 34
6.7 Technological Alarms ........................................................................................................ 34
Chapter 7 Disassembling the Monitor ........................................................................................ 35
7.1 Tools Required................................................................................................................... 35
7.2 Replacing Fuses ................................................................................................................. 35
7.3 Disassembling the Main Unit ............................................................................................ 36
7.4 Disassembling the Front Assembly ................................................................................... 40
7.4.1 Replacing the Protective Screen .............................................................................. 41
7.4.2 Replacing the Key Board......................................................................................... 41
7.4.3 Replacing the Alarm LED ........................................................................................... 41
7.4.4 Replacing the Trim Knob ........................................................................................ 41
7.5 Disassembling the LCD Assembly .................................................................................... 41
7.5.1 Replacing the LCD ...................................................................................................... 42
7.5.2 Replacing the Inverter ............................................................................................. 43
7.6 Disassembling the Main Frame Assembly ........................................................................ 43
7.6.1 Replacing the Main Board ....................................................................................... 44
7.6.2 Replacing the Parameter Modules ........................................................................... 44
7.6.3 Replacing the Battery Interface Board..................................................................... 45
7.6.4 Replacing the Power Module .................................................................................. 45
7.6.5 Replacing the USB Interface Board, Ethernet Interface Board ................................ 46
7.6.6 Replacing ADVANCED EtCO2 Module................................................................. 47
7.7 Disassembling the Rear Housing Assembly ...................................................................... 48
7.7.1 Replacing the Speaker ............................................................................................. 48
7.7.2 Replacing the Fan .................................................................................................... 48
Appendix 1 Renewal Parts........................................................................................................... 49
4
Patient Monitor Service Manual Warranty and Service
Chapter 1 Warranty and Service

Standard Service
ADVANCED provides a one-year-warranty for the warranted products (accessories are

included). The warranty period begins on the date the products are shipped to customers. If a
customer promptly notifies ADVANCED of customer‘s warranty claim here under,
ADVANCED will either repair, adjust or replace (with new or exchange replacement parts)
ADVANCED‘s products. ADVANCED warrants that any service it provides to customers
will be performed by trained individuals in a workmanlike manner.
Limitation of Warranty
Direct, indirect or final damage and delay caused by the following situations for which
ADVANCED is not responsible may void the warranty:
 Groupware is dismounted, stretched or redebugged.

 Unauthorized modification or misuse.
 Damage caused by operating beyond the environmental specifications for the medical
product.
 Change or remove original serial number label or Manufacturer symbol.
 Improper use.
Service Procedure
(1) Fill in the Service Claim Form (SCF).
Fill in the SCF with detailed information including: Model Name, Serial Number (SN) and
Problem Phenomena.
ADVANCED should not have any obligation to take over the case without this
information. The form can be downloaded at: http://www.ADVANCED.com.cn or obtained
from ADVANCED‘s Service Department.
(2) Send ADVANCED the SCF and Select a Solution.
Once the service department receives the fully filled SCF, ADVANCED‘s engineer will
offer a solution in three working days. ADVANCED will follow out the case based on the
two conditions below:
Within Warranty:
There are two options:
-1-
i) After receiving the Return Material Authorization (RMA) form from ADVANCED
service department, the customer sends ADVANCED the defective parts and informs
about the shipment tracking number. Then we will dispatch new part(s) to your confirmed
address with confirmed shipping invoice.
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
ADVANCED on time. We will, at this option, dispatch the replacement one(s) with
confirmed shipping invoice.
NOTES:
(1) Both Return Material Authorization Form and Declaration Form are offered by
ADVANCED 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 ADVANCED for service, including custom charges. ADVANCED is
responsible for the freight, insurance & custom charges from ADVANCED to the
customer.
Out of Warranty:
After receiving the RMA form from the service department, the customer sends defective
parts to ADVANCED 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:
ADVANCED should not have any obligation to the end-user or customer who returns the
goods without the notification by ADVANCED’s service department. The sender takes full
responsibility for the accounted fee.
-2-
(4) Send the Parts to ADVANCED.
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 ADVANCED before shipment.
 Please send back the parts after ADVANCED‘s confirmation.
-3-
Patient Monitor Service Manual Safety Guidance
Chapter 2 Safety Guidance
2.1 Introduction
This service manual is a reference for periodic preventive maintenance and corrective service
procedures for the PM2000B series patient monitors. It provides information on troubleshooting,
assembly procedures, and instructions for functional testing as well as performance verification.
The manual is intended for use only by technically qualified service personnel.
WARNING
Please follow the instructions exactly in accordance with this manual during service.
Failure to do so might result in damage to the monitor or personal injury.
-4-
2.2 General Information

Patient Monitor (hereinafter called monitor) is designed in accordance with the international
safety requirements in IEC/ EN 60601-1 for medical electrical equipment. Classification
information of this equipment is as follows:
Anti-electroshock Type Class I equipment and internal powered equipment
Anti-electroshock Degree NIBP, SpO2, CO2, AG ,BF ECG

(RESP), TEMP, IBP, C.O. CF
Ingress Protection IPX1
Degree of Safety in Presence of Not suitable for use in presence of flammable gases
Flammable Gases
Working System Continuous operation equipment

EMC Type Group I Class A
2.3 Safety Precautions

To avoid possible injury, please observe the following precautions during the operation of the
instrument.
WARNING
1 The monitor must be serviced only by authorized and qualified personnel.
ADVANCED does not assume any responsibility for damage or injury if
modifications or repairs are carried out by unauthorized personnel.
2 Use and replace the substitutive parts provided or recommended by ADVANCED only.
3 The service personnel must be familiar with the operation of this monitor. Refer to
Patient Monitor User Manual for details.
4 Perform periodic safety test to ensure patient safety. Safety tests should include
leakage current measurement and insulation testing. It is recommended to perform
the safety test every two years. You are responsible for any requirements specific to
your country.
5 Disconnect the monitor from power before replacing the fuses which are with the
identical specifications.
6 SHOCK HAZARD – Do not remove the top panel cover during operation or while
power is on. The unit cover must be removed only by authorized service personnel.
7 Do not remove the battery while AC power is on.
8 Only connect the device with accessories supplied or recommenced by ADVANCED.
-5-
WARNING
9 SHOCK HAZARD – Do not attempt to connect or disconnect the power cord with wet
hands. Make sure that your hands are clean and dry before touching the power cord.
10 Accessory equipment connected to the analog and digital interface must be certified
according to the respective IEC/ EN standards (e.g. IEC/ EN 60950 for data
processing equipment and IEC/ EN 60601-1 for medical equipment). Furthermore, all
configurations shall comply with the valid version of the system standard IEC/ EN
60601-1.Anybody that connects additional equipment to the signal input connector or
signal output connector to configure a medical system must ensure that the system
complies with the requirements of the valid version of the system standard IEC/ EN
6060-1-1. If you have any question, please consult our technical service department
or your local distributor.
11 Do not directly solder the lead wire and the battery terminal.
CAUTION
1 The device is designed for continuous operation. Avoid splashing water over the
device.
2 Do not operate the device when it is damp or wet. Avoid using the device immediately
after relocating it from a cold environment to a warm and humid environment. If the
monitor gets damp or liquid pours on the monitor, please contact the service
personnel of ADVANCED.
3 While the battery is charged, used or stored, keep it away from objects or materials
with static electric charges.
2.4 Explanation of Symbols on the Monitor
DEFIBRILLATION-PROOF TYPE CF APPLIED PART
DEFIBRILLATION-PROOF TYPE BF APPLIED PART
Caution
-6-
Operating instructions
Equipotential grounding
USB (Universal Serial Bus) Connection
Power Supply switch
Gas inlet
DO NOT REUSE
SERIAL NUMBER
CE marking
AUTHORISED REPRESENTATIVE IN THE EUROPEAN

COMMUNITY
Date of manufacture
MANUFACTURER
Part Number
-7-
General symbol for recovery/recyclable
Disposal method
Caution: Federal (U.S.) Law restricts this device to sale by or on

the order of a physician.
Ingress Protection IPX1 (Protected against vertically falling water

drops)
Refer to User manual
( Background: blue; Symbol :white )
Warning
( Background: yellow; Symbol and outline: black )
NOTE:
The service manual is printed in black and white.
-8-
Patient Monitor Service Manual Installation
Chapter 3 Installation
WARNING
Only qualified service engineers should install this equipment.
3.1 Environment Requirements
Temperature
Working 0 C to +40 C(32 ℉~104 ℉)
Transport and Storage -20 C to +55 C(-4 ℉~131 ℉)
Humidity
Working 15%RHto 95%RH (non-condensing)
Transport and Storage 15%RH to 95%RH (non-condensing)
Altitude
Working 86 kPa to 106 kPa
Transport and Storage 70 kPa to 106 kPa
NOTE:
1 Do not install the monitor in close proximity to flammable anesthetics.
2 Keep the environment clean and keep the device away from corrosive medicine.
Prevent the device from vibration, high temperature, humidity and exposure to the
sun.
3.2 Electrical Requirements

Operating Voltage: 100 V-240 V ~
Operating Frequency: 50 Hz/60 Hz
Current: 1.0-0.5 A
-9-
Patient Monitor Service Manual Installation
3.3 Safety Requirements

CAUTION
1 SHOCK HAZARD – To protect patients and medical staff, the power receptacle must
be well grounded.
2 Do not simultaneously touch the signal input or output connector and the patient.
3 The monitor and equipment connected to the monitor should be equipotential to
ensure effective grounding.
4 Do not switch on the monitor until all units and accessories have been properly
connected and verified.
3.4 Installing the Monitor

- To install the monitor on a flat surface.
Place the monitor on a flat surface. Make sure the surface does not vibrate and is free of corrosive
medicine and dust.
Patient Monitor on a Flat Surface
- To install the monitor on a roll stand/trolley.

To install the monitor on a roll stand/ trolley, refer to the assembling instruction delivered with
the roll stand/ trolley for details.
3.5 Connecting to AC Power

Apply the power cable offered with the monitor. Plug one end of the power cable to the power
socket of the monitor, and then connect the other end to a grounded 3-prong power output special
for hospital usage.
- 10
-
Patient Monitor Service Manual Test and Maintenance
Chapter 4 Test and Maintenance
4.1 Routine Test

An overall check of the monitor, including safety check and functional check, should be
performed by qualified personnel every 24 months or after service.
4.1.1 Visual Inspection

Before using the monitor:
 Inspect the monitor and accessories for obvious signs of damage.
 Check the external cables, power socket and power cable.
Do not use the monitor if any damage is detected until the monitor is repaired by the service
engineers of ADVANCED or professional service personnel of the dealer.
4.1.2 Power- on Test

Switch on the monitor after it is connected to the power source and check:
 If the power indicator is in green; if the battery indicator lights up (when battery is inserted);
 If the alarm indicators flicker and if the alarm tone is heard;
 If some images and characters are missing;
 If there are bright spots and dark shadows on the LCD screen;
 If the waveforms, fonts and symbols displayed on the LCD screen are normal.
If any failure is detected, refer to section Device Failures and Display Failures for details.
4.1.3 Key Test

Press the keys on the front panel in turn to check if they work properly. When pressing a key, a
corresponding functional display is supposed to be seen onscreen. Refer to Patient Monitor User
Manual for details about the key function. You can move the cursor by turning the trim knob
clockwise or anticlockwise. Also, you can confirm the operation by pressing the trim knob.
4.1.4 Recording Test

Check if the recorder can perform printing without problem. Also, check if all the printed traces
are correct and clear on the paper.
If any failure is detected, refer to section Recorder Failures for details.
- 11
-
NOTE:
Please make sure paper is well loaded and the setting is correct before printing.
4.1.5 Alarm Test

Trigger a signal that is higher than the upper limit or lower than the lower limit to activate a
physical alarm. Disconnect one of the accessories from the monitor to activate a technical alarm.
Check if the audible and visible alarms work properly.
If any failure is detected, refer to section Alarm Failures for defective details.
4.2 Functional Tests and Accuracy Tests
WARNING
1 Functional tests and accuracy tests must only be carried out by qualified service
personnel.
2 If function of the monitor is in question, conduct an overall test on the function and
accuracy of the monitor according to the instructions offered by the manufacturer.
3 A functional tester, such as ECG simulator, SpO2 simulator, NIBP simulator and IBP
simulator, can only be used to assess the parameter consistency and function but not
to be used to assess the clinical measurement accuracy.
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.
4.2.1 ECG Functional Test

This test checks the function of the ECG measurement.
Tools required: ECG simulator.
Procedure:
1. Connect the ECG simulator to the monitor with an ECG cable.
2. Switch on the monitor and the simulator.
3. Set the simulator to the following configuration:
- HR=30 bpm.
4. Check the displayed HR value against the simulator configuration. The value should be 30
bpm ±1 bpm or ±1% (whichever is greater).
4.2.2 SpO2 Functional Test

This test checks the function of the SpO2 measurement.
Tools required: SpO2 simulator.
- 12
-
Procedure:
1. Connect the monitor and the SpO2 simulator with a SpO2 cable.
2. Switch on the monitor and the simulator.
3. Set the simulator to the following configuration:
- SpO2 = 70%.
4. Check the displayed SpO2 value against the simulator configuration. The value should be
70% ±2%.
4.2.3 NIBP Functional Test

This test checks the function of the NIBP measurement.
Tools required:
• NIBP simulator;
• T-fitting;
• Extension tube;
• Artificial limb.
Procedure:
1. Connect the NIBP simulator to the monitor.
2. Switch on the monitor and the simulator. Calibrate the simulator before using it.
3. Set the patient type on the monitor to adult; set the simulator to the following configuration:
- Patient type: adult;
- Systolic pressure=255 mmHg;
- Diastolic pressure=195 mmHg;
- Mean pressure=215 mmHg.
And then start a NIBP measurement.
4. Check the displayed values against the simulator configuration. A tolerance of ±8 mmHg is
reasonable.
4.2.4 NIBP Leakage Test

This test checks leakage of the airway and the performance of the NIBP system. See Figure 4-1
for details about tools required.
Procedure:
1. Connect the cuff securely with the socket for NIBP air hole.
2. Wrap the cuff around the cylinder with an appropriate size.
3. Make sure the patient type has been set to Adult.
4. Access SYSTEM MENU > MAINTAIN > USER MAINTAIN by inputting the password
ABC. Start a leakage test by selecting NIBP MAINTAIN > LEAK TEST.
- 13
-
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.
Figure 4-1 Diagram for NIBP Leakage Test
4.2.5 NIBP Calibration

NIBP calibration must be performed by professional personnel authorized by ADVANCED.
NOTE:
NIBP calibration can influence measurement results. Incorrect operation may influence
measurement accuracy.
Tools required:
• T-fitting;
• NIBP extension tubes;
• Cylinder;
• Manometer.
Procedure:
1. Access SYSTEM MENU > MAINTAIN > USER MAINTAIN by inputting the password ABC.
2. Connect the equipment as shown below:
Manometer
Tube
NIBP module
Tube / Patient
Cylinder T-fitting monitor
NIBP
extension
tube or hose
Figure 4-2 Diagram for NIBP Calibration
- 14
-
3. Select NIBP MAINTAIN > CALIBRATE.

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. A tolerance of ±3 mmHg is reasonable.
4.2.6 TEMP Accuracy Test

This test checks the accuracy of the TEMP measurement.
Tools required: resistance box.
Procedure:
1. Switch on the monitor and the resistance box.
2. Set the probe type on the monitor to YSI-10K, and respectively connect the probes to
channel T1 and T2 connectors. And then connect the probes with the resistance box.
3. Set the resistance value to (6017Ω) 37 C in the resistance box.
4. The displayed value should be 37 C ±0.1 C.
4.2.7 CO2 Functional Test

This test checks the function of the CO2 measurement.
Tools required: nasal cannula.
Procedure:
1. Switch on the monitor.
2. Access CO2 setup menu, and set the WORK MODE to MEASURE.
3. Place the nasal cannula below the nose and normally breathe; check if the CO2 measurement
waveforms are available on the monitor.
4. The displayed CO2 concentration is supposed to be 34~40 mmHg.
4.2.8 IBP Functional Test

This test checks the function of the IBP measurement.
Tools required: patient simulator
Procedure:
1. Connect the IBP cable to the connector for channel BP2 on the patient simulator and to the
IBP connector on the monitor.
2. Set the simulator to 0 pressure; perform a zero calibration.
3. After completing the zero calibration, configure the simulator as P (static) = 200 mmHg.
4. Perform a dynamic pressure test. Set the simulator to the following configuration:
- RADIALART 120/80
The tolerances for the measurement value provided by the monitor should be ±4 mmHg or
±4%.
- 15
-
4.2.9 C.O. Functional Test

This test checks the function of the C.O. measurement.
Tools required: patient simulator
Procedure:
1. Connect the simulator to the C.O. module using the patient cable.
2. Configure the patient simulator as follows:
- Injection temperature: 0 C
- Computation Const: 0.542
(Edward‘s Catheter)
- Flow: 5 l/min
3. Check displayed value against the simulator configuration.
4. Expected test result: C.O.= 5+/－1 l/min
4.3 Safety Test
4.3.1 Safety Test Procedures

Use the test procedures outlined here only for verifying safe installation or service of the product.
These tests are not a substitute for local safety testing where it is required for an installation or a
service event.
When performing a safety test, you must use a standard safety analyzer such as Fluke 601Pro
Series safety analyzer or equivalent; perform the test according to your local regulations, for
example, in Europe according to IEC/EN60601-1, in USA according to UL60601-1. For the test
setup, please refer to the Instructions for Use of the test equipment used.
Additional test may be required by your local regulations.
You are recommended to document the result of the safety test.
NOTE:
1 When testing according to IEC 60601-1, system must be tested and not individual
devices.
2 Systems must be handled as devices.
3 A system is a combination of several devices of which at least one is a medical

electrical device which is connected to other devices by functional connections or by
a transportable multiple socket outlet.
4 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.
- 16
-
4.3.2 Protective Earth Resistance
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)
- 17
-
4.3.3 Enclosure Leakage Current
NOTE:
The circuit diagram is based on the Fluke 601Pro series safety Analyzer.
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: 100µA (IEC/EN60601-1)
Single fault condition: 500µA (IEC/EN60601-1)
Normal condition: 100µA (UL60601-1)
Single fault condition: 300µA (UL60601-1)
- 18
-
4.3.4 Patient Leakage current
NOTE:
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: 10µA (BF applied part), 10µA (CF applied part) (IEC/EN60601-
1, UL60601-1)
Single fault condition: 500µA (BF applied part), 50µA (CF applied part) (IEC/EN60601-
1, UL60601-1)
- 19
-
Leakage Current
Applied Normal Single Fault

Part Condition Condition
Earth Leakage Current <0.5 mA <1 mA
Enclosure Leakage Current <0.1 mA <0.5 mA
AC: <0.01 mA AC: <0.05 mA
CF
DC: <0.01 mA DC: <0.05 mA
Patient Leakage Current
AC: <0.1 mA AC: <0.5 mA
BF
DC: <0.01 mA DC: <0.05 mA
Patient Leakage Current (Mains on CF <0.05 mA

Applied Parts) BF <5 mA
AC: <0.01 mA AC: <0.05 mA
CF
DC: <0.01 mA DC: <0.05 mA
Patient Auxiliary Current
AC: <0.1 mA AC: <0.5 mA
BF
DC: <0.01 mA DC: <0.05 mA
4.3.5 Patient Leakage Current- Single Fault Condition (S.F.C) Mains on
Applied Part
NOTE:
The following test is based on test with the Fluke 601 pro series safety analyzer. This
device allows applying a 110% mains voltage between the applied part and the device
PE. When testing with other device, you may need to apply the 110% mains voltage
manually.
- 20
-
NOTE:
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):
5000µA (BF applied part), 50µA (CF applied part)
(IEC/EN 60601-1, UL 60601-1)
- 21
-
4.4 Maintenance
For details about basic cleaning and maintenance methods, refer to relevant sections in Patient
Monitor User Manual. For further technical support, contact service engineers of ADVANCED.
Users are responsible for preventive maintenance and periodic inspection for the monitor.
4.4.1 Cleaning the Monitor and Accessories

Refer to relevant sections in Patient Monitor User Manual for details.
4.4.2 Maintaining the Battery

Refer to relevant sections in Patient Monitor User Manual for details.
- 22
-
Patient Monitor Service Manual Principle Introduction
Chapter 5 Principle Introduction
5.1 System Principle Block Diagram

Here is the system principle block diagram of the monitor:
SpO2 sensor
Fan
Battery
Power control board NIBP and SpO2
AC NIBP module
module module
Battery
Power J25 optional for connection

control
SpO2 module SpO2 sensor
board
IBP sensor
Speaker IBP-C.O.
IBP sensor
board
C.O. sensor
Nurse call/
RJ45
Network interface
interface
board
iM9 Main control board CO2 isolating
CO2 module
board
USB USB interface
port board
AG module
interface AG module
board
ECG lead
ECG module
TEMP sensor
Inverter Key board Trim knob

Recorder
control
board LCD
Recorder Alarm
indicator
Figure 5-1 System Principle Block Diagram
5.1.1 Main Control Board

The main control board, as the core of the monitor, is responsible for system control, system
resource allocation, system management, data processing, document management, display,
recording management, data storage, system diagnosis, malfunction alarm and so on.
The system operation principle is illustrated in the block diagram above (Figure 5-1). The main
CPU, an ARM9 chip, realizes extension of main memory, data input (network, USB), audio
output, and provides display interface, man-machine interface (keyboard, alarm indicator),
physiological parameter module interface.
- 23
-
5.1.2 Parameter Modules

PM2000Bseries patient monitors can be outfitted with several stand-alone physiological
parameter modules such as ECG, RESP, SpO2, NIBP, TEMP, IBP, CO2, C.O. and AG. modules.
The physiological parameter modules perform parameter data collection and calculation. The
main control board logically controls the modules, processes the data from the modules, and
performs display as well as storing functions. How the physiological parameter modules are
connected to the main control board has been illustrated in Figure 4-1.
The monitor can be outfitted with optional parameter modules; meanwhile, several optional
modules are available for some physiological parameters. For the PM2000B series patient
monitors with standard configuration, the SpO2 and NIBP measuring functions are performed by
the same module (hereafter called SpO2 and NIBP module) which can perform data collection for
both SpO2 and NIBP measuring or be used only for NIBP measuring. A stand-alone SpO2 module
(hereafter called SpO2 module) is alternative for SpO2 measuring. Also, a stand-alone NIBP
module (hereafter called NIBP module) can be outfitted for NIBP measuring.
5.1.3 Key Board and Alarm LED

Three small boards, namely, trim knob board, key board and alarm LED board, are included in
the front housing assembly of PM2000B series patient monitors.
The key board is the indispensable part of the device. PM2000B series patient monitors adopt
free-standing key board. The key board works with the trim knob to perform information
communication between the user and the device. The module circuit connected with the key
board includes the trim knob and alarm LED. Six functional keys on the key board are alarm
pause, NIBP, trend graph, freeze, recording and menu. Besides, two LEDs with different colors
are on the board. One LED indicates the status of AC power and the other indicates the status of
battery charging.
The structure of the key board is shown in Figure 5-2. The main MCU of the key board
communicates with the host system via the serial interface, transmitting information of key sets
and trim knob to the host system.
Besides, the switch-on key and two power status LEDs are connected to the host system via
another connector.
The alarm LED, whose signal wires will be simply transferred to the key board, is the LED unit
directly controlled by the main board.
- 24
-
Trim
knob
MCU
6 Function
Encoder
Alarm
LED
LED
keys
Switch
Main board interface Main board interface
Figure 5-2 Key Board Principle Block Diagram
5.1.4 Display Screen

The LCD assembly consists of an LCD screen and an inverter. As shown in Figure 5-3, the
inverter is connected to the main board from which the inverter obtains voltage for brightening
the screen; screen brightness adjustment is control by the main control board and realized by
the inverter. Information displayed on the screen is directly driven by the main board. The main
board receives and processes data from parameter measuring modules before transforming
them into waveforms and digit result and then outputs signals to drive the screen to display
information.
Main control board
J21 J20
LCD
Inverter
screen
Figure 5-3 Display Principle Block Diagram
- 25
-
5.1.5 Interface Board

Network interface (nurse call) and USB interface are available on PM2000B series patient
monitors, which is realized by two interface boards installed in the rear housing assembly.
The network interface board is connected with the main board which controls the relay on the
interface and controls the switch-on-and-off of the outlying nurse call indicator. Ethernet signals,
which are insulated by the transformer on the interface board, are transmitted through the
network interface; consequently, the monitor is able to be networked via network cable.
Main board
interface
Network signals
Network
interface Network cable
board
Main board
interface
Nurse call
Figure 5-4 Network Interface Board Block Diagram
USB signal transformation is realized on the USB interface board which is connected to the main
board via the connector, and a USB port is reserved for external connection.
5.1.6 Power Module

The power module, developed by ADVANCED, mainly consists of the AC-DC converter
module and the power control board. It supplies +12V and +5V AC power for the monitor and
manages the power system, including managing power-on/off, power indicator, battery charging
and so on.
Interface Pin Definition

J1 1 2 3
AC_IN N/A AC_IN
J9 1 2 3 4 5 6
+12V +5V GND GND GND NC

J5 1 2
BAT GND
J4 1 2
POWR_ON/OFF GND
- 26
-
Interface Pin Definition

J2 1 2 3 4
POWR_UP CHARGE RXD TXD
5.2 Interfaces
Interfaces on the rear panel of the monitor include:
 1 USB port
 Network / Nurse call interface
5.2.1 USB Port

Via the USB port, external devices which support USB protocols can be connected to the
monitor.
5.2.2 Network / Nurse Call Interface

This interface enables networking and nurse call functions. Ethernet and nurse call share the same
RJ-45 interface. PIN7 and PIN8 are used for nurse call. When there is alarm, PIN7 and PIN8.
- 27
-
Patient Monitor Service Manual Troubleshooting
Chapter 6 Troubleshooting
ADVANCED supports replacement of PCBs and major subassemblies for this product.
When replacement is needed, follow the procedures described in chapter 7 Disassembling the
Monitor.
6.1 Device Failures

Phenomenon Possible Cause Solution
Fuse damage (if fuse is Replace fuse

available)
No display after
power-on, power
Power damage Replace power board
indicator is not on or fan
does not run
Component short-circuit Locate the short-circuit
component
Main board failure Check if it sounds a tone when

pressing the key. If yes, check
No display after power-on
for display failure
or blank screen during
operation; yet power
Display failure If it does not sound a tone when
indicator lights up and the
pressing the key, there may be
fan runs normally
malfunction in the main board.
Replace the main board
Characters are displayed Error in data Replace the main board,

normally; yet waveforms communication between converter board or parameter
are displayed main board and parameter module based on the error
intermittently module prompts
Operation or Main board or Examine the main board and

measurement function is corresponding component the corresponding components
disabled damage
- 28
-
Instantaneous intensive Check power supply and

interference of network grounding system
Poor performance of Replace power board

power board
The monitor occasionally
shuts down
Poor performance of Replace Main board
Main board
Bad connection of power Replace or repair connectors

supply or main board
6.2 Display Failures

Backlight board defective Replace backlight board

No display is on the
screen after monitor‘s Bad connection of display Repair or replace connecting
powering on while power wires wire
supply is ok; blank screen
when the monitor works Main control board defective Replace main control board
normally
Power board defective Replace the power board
6.3 Operation, Recording and Networking Failures

The key board or rotary encoder Replace the key board or

is damaged rotary encoder
Keys or the rotary encoder is
disabled
Wires of key board are damaged Replace or repair the wires
of the key board
Sound is raucous or there is Speaker or wire defective Replace speaker or wires

no sound
- 29
-
Recorder has no paper or paper Install paper and press

bail is not pressed down down the paper bail
Recorder failure Replace the recorder

Recorder cannot execute
printing operation Driving power of the recorder Replace the power supply
has a failure
Recorder wire defective Replace or repair the wire

of the recorder
Record paper goes out on the Recorder is installed or Adjust the installation of
skew positioned badly recorder
Network cable defective Check and repair network

cable
The monitor cannot be linked
to the network Network bed No. conflicts Change bed No.
Main board defective Replace Main board
6.4 Alarm Failures

The audible alarm is temporarily

Activate the audible alarm
disabled
Inaction of audible alarm
Replace the speaker or the
Speaker or wire failure
wire
Replace the alarm indicator

Alarm indicator stays off Alarm indicator board defective
board
Inaction of audible or visual

Program failure Update the software
alarm
- 30
-
6.5 Parameter Monitoring Failures

Poor connection of ECG Use new electrodes to ensure good

electrodes contact
ECG wave is deactivated Activate wave via System Menu
No ECG waveform No square waveform exists Replace ECG/RESP module

during CAL self-test
RL electrode is suspended Connect RL electrode
ECG/RESP module is damaged Replace ECG/RESP module
Electrodes are connected Correctly connect electrodes

incorrectly
There is suspending electrode Remove electrodes that are not

used
ECG waveform is
abnormal or No grounding wire for AC Use 3-wire power
interference exists power
Wrong selection of ECG filter Select appropriate filter mode

mode
ECG/RESP module defective Replace ECG/RESP module
Bad connection of electrodes Use RL-LL electrode, connect to

the correct positions
Patient is moving constantly Keep patient quiet

No RESP waveform or
RESP waveform is deactivated Activate waveform via System
RESP waveform is
Menu
abnormal
RESP wave amplitude is small Adjust wave amplitude in RESP
Menu
ECG/RESP module defective Replace ECG/RESP module
Measuring sensor is poorly Connect TEMP sensor stably

TEMP value is incorrect
connected
- 31
-
HR value is inaccurate; ECG waveform is not good Adjust the connection to make the
Arr. and ST analysis are ECG waveform normal
incorrect
NIBP cuff cannot be Air way is folded or leakage Adjust or repair the air way
inflated. exists
Blood pressure cann ot Cuff becomes loose or patient Keep the patient quiet; bind the
be measured is moving cuff correctly and safely
occasionally
Error of blood pressure Cuff size does not fit the patient Use the cuff of appropriate size
measurement is too
NIBP module defective Replace NIBP module
great.
Sensor or SpO2 module Replace the sensor and confirm the

No SpO2 waveform
defective failure
Strong interference Patient is moving Keep the patient quiet

Exists in SpO2 High level of ambient light Minimize the ambient light
waveform. interference
Coloring agent has been Remove the coloring agent before

SpO2 value is inaccurate
injected into patient body measurement
No CO2 waveform Poor connection of the CO2 Turn off the monitor and
module reconnect the CO2 module
The CO2 module is damaged Replace the CO2 module
The CO2 waveform is a The CO2 module is in Change the STANDBY mode to
beeline STANDBY mode MEASURE mode
The sample line is blocked or Draw off the sample line, clear it
disconnected or replace it to another one.
The CO2 waveform is Long time no zero calibration, Enter the CO2 SETUP, do CO2
abnormal, values are the measured values are calibration by ZERO CAL
incorrect incorrect
- 32
-
The measured CO2 The CO2 module is in Change the STANDBY mode to
values are displayed as STANDBY mode MEASURE mode
―---‖
Prompts for CO2 The CO2 sample line is blocked Draw o f f t h e CO2 sample
catheter is blocked on line, clear it or replace it to
screen another one.
The CO2 measured No zero calibration for a long Enter the CO2 SETUP, do CO2
value has error time; the measured value is calibration by ZERO CAL
incorrect
The compensatory gas and Enter the CO2 SETUP, set

barometric is set incorrectly BAROPRESS and
COMPENSATE items in menu for
compensatory gas and barometric
correctly.
No AG waveform Poor connection of the AG Turn off the monitor and

module reconnect the AG module
The AG module is damaged Replace the AG module
The AG waveform is a The AG module is in Change the STANDBY mode to

beeline STANDBY mode MEASURE mode
The catheter is blocked or Turn off the monitor and clear or

disconnected replace the catheter
Caused by automatic zero The beeline caused by automatic

calibration of module zero calibration is abnormal
- 33
-
AG measured value is Long time no zero calibration, Do zero calibration for AG

incorrect the measured value is module.
incorrect
When using AION 02 module, For using AION 02 module, set the
The AGENT in AG setup menu AGENT in AG setup menu
has not been set
The AG measurement is not in After the 10-minute warm up, the

Full accuracy mode. AG measurement enters Full
accuracy mode.
The IBP waveform is
available, yet IBP The IBP module has not been Zero the IBP module.
measurement value is zeroed or zero drift occurs.
unavailable.
The IBP waveform Bad connection of the IBP Check the connection of IBP cable
appears and disappears cable and sensor and sensor.
time after time.
Check whether the IBP label is
The IBP waveform is An unsuitable selection of the
flat and there is no ruler consistent with the measured site
apparent fluctuation. of the patient; adjust the ruler.
Failure in the PCBA of IBP

Check the connection of IBP
The monitor indicates module or disconnection of the
an IBP communication IBP module and communication board
module and
failure. or change the IBP module.
communication board
6.6 Data Storage Failures

The file format of U disk is

Format the U disk into FAT.
The data in the U disk incorrect; it may be NTFS.
cannot be saved The U disk is not inserted Insert t h e U disk once again or
properly. replace it.
6.7 Technological Alarms

For details on technological alarms, please refer to relevant sections in Patient Monitor User
Manual.
- 34
-
Patient Monitor Service Manual Disassembling the Monitor
Chapter 7 Disassembling the Monitor

WARNING
1 Only qualified service personnel shall open the monitor housing.
2 Switch off the monitor and disconnect it from AC power before disassembling the
device.
3 After any repair of the device, perform safety tests prior to use.
7.1 Tools Required
1 – A cross-head screwdriver
2 – A flat-head screwdriver
3 – A M3 nut driver
4 – A pair of pliers
7.2 Replacing Fuses

To replace the melted fuses,
1) Switch off the monitor and disconnect it from power.
2) The back of the device should face the operator.
3) Press and turn the cartridge anticlockwise with a flat-head screwdriver; take out the fuse
from the released cartridge.
- 35
-
4) Replace the old fuse with a new one that is supplied by ADVANCED or with
the same specifications. (Dimensions: Ф5mm*20mm; model: T3.15AH250VP)
5) Put back the cartridge and turn it clockwise until it is secured.
7.3 Disassembling the Main Unit
Recorder assembly
Front housing assembly LCD assembly Main frame assembly Rear housing assembly
Figure 7-1 Main Unit Structure Block Diagram
As shown in Figure 7-1, the main unit of the monitor consists of the front housing assembly, rear
housing assembly, LCD assembly, main frame assembly and recorder assembly. Some function
modules are optional, such as the recorder. If you have not purchased the recorder, the
corresponding position will be covered by a lid. Prior to disassembly, you should understand the
configuration of your purchased monitor. For the modules not purchased or installed, you can
skip the corresponding steps.
Refer to the table below and follow the steps to disassemble the main unit.
Disassembly Renewal Parts
To get the recorder

Step 1 Recorder
assembly
To get the front Alarm LED, key board, trim knob, screen protective
Step 2 housing assembly film
- 36
-
Disassembly Renewal Parts
To get the LCD LCD screen, inverter, main board, battery board, ECG
Step 3 assembly module, NIBP pump and valve
SpO2 module, NIBP module, SpO2 and NIBP module,

Separate the main
CO2 isolated power converter board, IBP-C.O.
Step 4 frame and rear
module, power module, USB converter board, network
housing
interface board, speaker, fan
Procedure:
Step 1: Remove the screws inside the recorder with a screwdriver; the recorder assembly will be
disassembled from the main unit. Disconnect the wires linking the recorder, and the recorder
assembly is totally separated from the monitor.
2-M3*6 Cross recessed

round head screws
Step 2: Remove the screws securing the front and rear housings as well as the bottom panel; the
front and rear assemblies are unfolded. Disconnect the wires linking the front and rear housing,
namely, the key board wires, and the front housing assembly is totally separated from the rear
housing assembly.
- 37
-
2- φ 3*12 Cross recessed

tapping screws
round head screws
Key board wires
Step 3: Remove the screws securing the screen holder with a cross-head screwdriver and
disconnect the wires linking the screen assembly and main board so that the screen holder is
separated from the main unit and rear housing. And the LCD assembly is get.

round head screws
2-M3*6 Cross recessed round

head spring screws
- 38
-
Step 4: Remove the screws securing the main frame on the bottom panel and inside the unit, and
the main frame assembly is separated. To totally disassemble the main frame from the rear
housing assembly, disconnect the wires linking the speaker, the fan and the sensor board and
remove the NIBP tube.
(1) Remove the screws
3 ‐ φ 3X12 Tapping
screws + washer
4-M4*10 Cross φ 3*8 Cross recessed

recessed round head tapping screws
screws
(2) Disconnect the wires; separate the main frame and rear housing
As shown below, disconnect the wires linking the main frame and rear housing; the main frame
and rear housing assembly are separated.
NOTE:
1 After disconnecting the wires linking the speaker and the ones linking the fan, the
main frame can be pulled out. To separate the main frame from the rear housing,
there is no need to completely remove the wires linking the sensor board and main
frame unless it is necessary, since the sensor board and especially the NIBP tube
are relatively hard to disassemble and assemble.
2 The wire linking the speaker is the one that is threaded through the hole on the main
frame and connected to the main board in the front of the main frame.
3 The two IBP sensor wires should be connected to the board in order as illustrated.
- 39
-
4 In the illustration below, the demonstrated SpO2 sensor wire is for monitor outfitted
with SpO2 module. For monitor outfitted with SpO2 and NIBP module which is
installed in the front of the main frame, the SpO2 sensor wire, as the NIBP tube,
should be threaded through the main frame and connected to the front.
J3- J2- SpO2 sensor wire (for

monitor with SpO2 module)
IBP2 IBP1
Tube
C.O.
CO2
Fan wire
Speaker wire
7.4 Disassembling the Front Assembly
Alarm LED
2 ‐ φ 3*8 Cross recessed

tapping screws
6 ‐ φ 3*8 Cross recessed

Key board tapping screws
Trim knob
Figure 7-2 Front Assembly Diagram
- 40
-
7.4.1 Replacing the Protective Screen
Disassemble the main unit following Remove the Take the protective screen
instructions in the section 7.3 and get protective screen out after removing the
the front housing assembly outwards double-side tape on it
Assemble the protective screen in the reversed order; connect the wires and assemble the main
unit. Refer to 7.3 Disassembling the Main Unit for details.
7.4.2 Replacing the Key Board
Disassemble the main unit following Remove the screws securing Replace the
instructions in the section 7.3 and get the key board with a cross- key board
the front housing assembly head screwdriver
Assemble the key board in the reversed order; connect the wires and assemble the main unit.
Refer to 7.3 Disassembling the Main Unit for details.
7.4.3 Replacing the Alarm LED
Disassemble the main unit following Remove the screws securing Replace the
instructions in the section 7.3 and get the alarm LED with a alarm LED
the front housing assembly cross-head screwdriver
Assemble the alarm LED in the reversed order; connect the wires and assemble the main unit.
Refer to 7.3 Disassembling the Main Unit for details
7.4.4 Replacing the Trim Knob
Disassemble the main unit following Remove the cap Unscrew

instructions in the section 7.3 and get from the trim anticlockwise the nut
knob with a pair securing the trim
the front housing assembly of pliers
knob with the pliers
Assemble the trim knob in the reversed order; connect the wires and assemble the main unit.
7.5 Disassembling the LCD Assembly

Below are the LCD assemblies for iM9, iM9A, M9 and M9A patient monitors. Different screen
and inverter are used for the two models of monitors.
- 41
-
12.1-inch Screen for PM2000BPatient Monitor:
4-M3*6 Cross recessed round head

spring screws
2-M3*6 Cross recessed round head screws
10.4-inch Screen for iM9A&M9A Patient Monitor

spring screws

screws
7.5.1 Replacing the LCD
Disassemble the main unit following Remove the screws securing Replace
instructions in the section 7.3 and get the LCD assembly and the LCD
the screen holder assembly disconnect the wires
Assemble the LCD in the reversed order; connect the wires and assemble the main unit. Refer to
7.3 Disassembling the Main Unit for details.
- 42
-
7.5.2 Replacing the Inverter
Disassemble the main unit following Disconnect the wires linking Replace the
instructions in the section 7.3 and get the inverter and remove the inverter
the screen holder assembly screws securing the inverter
Assemble the inverter in the reversed order; connect the wires and assemble the main unit. Refer
to 7.3 Disassembling the Main Unit for details.
7.6 Disassembling the Main Frame Assembly

The illustration below manifests how the wires are connected and how the main parts are
installed in the main frame.
4-M3*6 Round head screws
Figure 7-3
NOTE:
To avoid wrong connection, note down relation between the wires and the corresponding
connectors during disassembly.
- 43
-
7.6.1 Replacing the Main Board
Disassemble the LCD Disconnect the Remove the screws Replace the main
assembly following wires on the main on the main board board
instructions in the section board with a cross-head
7.3 screwdriver
Assemble the main board in the reversed order; connect the wires and assemble the main unit.
7.6.2 Replacing the Parameter Modules

Refer to Figure 7-3 to learn how the parameter modules are installed. To replace the ECG module,
you only need to remove the LCD assembly. To replace other modules, you need to separate the
main frame assembly from the main unit.
Disassemble the main frame Disconnect the Release the modules Replace the
following instructions in the wires linking the with a cross-head modules
section 7.3 module sensor and screwdriver
main board
Assemble the parameter modules in the reversed order; connect the wires and assemble the main
unit. Refer to 7.3 Disassembling the Main Unit for details.
NOTE:
The specifications of the screws are as follows:
For SpO2 module: 4-M3*6 round head screws
For NIBP module/ SpO2 and NIBP module: 4-M3*6 cross recessed semi-round screws
For ECG module: 4-M3*6 round head screws
For C.O.-IBP module: 3-M3*6 cross recessed round head screws
For CO2 isolating power converter board: 4-M3*6 cross recessed round head screws
- 44
-
7.6.3 Replacing the Battery Interface Board

Wires linking the
head screws
battery board
Remove the LCD Disconnect the wire Release the board Replace the
assembly following linking the battery with a cross-head battery interface
instructions in the interface board and screwdriver board
section 7.3 the main board
Assemble the battery interface board in the reversed order; connect the wires and assemble the
main unit. Refer to 7.3 Disassembling the Main Unit for details.
7.6.4 Replacing the Power Module
Disassemble the main unit Disconnect the Remove the screws Replace the
securing the power power module
following instructions in wire connecting
the section 7.3 and get the the power module module with a cross-
head screwdriver
main frame assembly
Assemble the power module in the reversed order; connect the wires and assemble the main unit.
NOTE:
The specifications of the screws are: 4-M3*7 cross recessed pan head screws with flat
washers and spring washers.
- 45
-
7.6.5 Replacing the USB Interface Board, Ethernet Interface Board

countersunk screws
Nurse call
Network
interface

head screws
Disassemble the main unit Remove the Disconnect the Remove the
following instructions in screws securing corresponding corresponding
the section 7.3 and get the the rear panel wires of the screws securing the
main frame assembly assembly interface board which needs
to be replaced
Assemble the boards in the reversed order; connect the wires and assemble the main unit. Refer
- 46
-
7.6.6 Replacing ADVANCED EtCO2 Module
M3X6 screws
Connecting the gas

inlet
1
Connecting exhausted Wire for connecting
gas inlet water trap test board
2
Connecting the gas
inlet
Disassemble the main Remove the Remove the Remove ADVANCED

unit following tubes connecting EtCO2
instructions in the wires screws
section 7.3
Assemble the ADVANCED EtCO2 module in the reversed order; connect the wires and tubes,
and fix the screws. Refer to 7.3 Disassembling the Main Unit for details.
- 47
-
7.7 Disassembling the Rear Housing Assembly

The rear housing assembly is shown below. To replace the fan and speaker, separate the main
frame and the rear housing, and remove the screws circled in the following illustration.
2 ‐ φ 3*8 Cross
recessed cutting
screws
Speaker
Fan 4-M3X25 Cross recessed
countersunk screws plus
M3 nuts
2‐φ 3*6 Round head
tapping screws
Sensor
bracket
7.7.1 Replacing the Speaker
Disassemble the main unit following Remove the screws Replace the
instructions in the section 7.3 and get securing the speaker with speaker
the rear housing assembly a cross-head screwdriver
Assemble the speaker in the reversed order; connect the wires and assemble the main unit. Refer
7.7.2 Replacing the Fan
Disassemble the main unit Remove the screws securing Remove the screws and
following instructions in the the fan assembly with a nuts securing the fan
section 7.3 and get the rear cross-head screwdriver with a cross-head
housing assembly screwdriver
Assemble the fan assembly in the reversed order; connect the wires and assemble the main unit.
- 48
-
Patient Monitor Service Manual Renewal Parts
Appendix 1 Renewal Parts

WARNING
Only connect the renewal parts supplied by ADVANCED to the monitor.
Parts Part Number
Lithium-Ion Button Cell 21.21.064169

PM2000B Main Control Board (without CO2) 12.03.220062
PM2000B Main Control Board (with CO2) 12.03.220061
Power Assembly 12.01.17720
X2 SpO2 and NIBP Module Assembly 22.01.210444
3-5-Lead ECG Module 02.04.100952
3-5-12-Lead ECG Module 02.03.109092
A8 SpO2 Module 02.03.109040
NELL-1 SpO2 Assembly 02.03.109040
M3600 NIBP Module 02.08.102094
IBP-C.O. Module 12.03.33864
CO2 Isolating Power Converter Board 12.02.114575
Speaker 01.14.38007
Fan 01.58.47066
Battery Interface Board 12.02.16988
USB Interface Board 02.02.100516
Network Interface Board 02.02.100437
12.1-inch LCD 01.16.002468
10.4-inch LCD 01.16.045133
Single LED Inverter—10.4-inch LCD Assembly 12.02.100405
Double LED Inverter—12.1-inch LCD Assembly 12.08.30102
Key Board 12.03.30034
Trim Knob Board 12.02.30161
Alarm LED 12.02.30035
Lithium-Ion Battery 11.21.064116
Fuse 21.21.064172
- 49
-

Advanced Pm2000b Monitor SERVICE MANUAL

Uploaded by

Copyright:

Available Formats

Advanced Pm2000b Monitor SERVICE MANUAL

Uploaded by

Document Information

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Advanced Pm2000b Monitor SERVICE MANUAL

Uploaded by

Copyright:

Available Formats

What is the purpose of this manual?

What is the purpose of this manual?

What safety precautions are discussed in the manual?

What safety precautions are discussed in the manual?

SERVICE MANUAL

PM2000B SERIES PATIENT MONITOR

Release Date: October 2015

© Copyright ADVANCED INSTRUMENTS, INC. 2012-2015. All rights reserved.

Responsibility of the Manufacturer

Assembly operations, extensions, re-adjustments, modifications or repairs are carried out by

The instrument is used in accordance with the instructions for use.

A NOTE provides useful information regarding a function or a procedure.

Chapter 1 Warranty and Service

ADVANCED provides a one-year-warranty for the warranted products (accessories are

 Groupware is dismounted, stretched or redebugged.

(1) Fill in the Service Claim Form (SCF).

(2) Send ADVANCED the SCF and Select a Solution.

There are two options:

(3) Obtain the RMA Form.

(4) Send the Parts to ADVANCED.

Follow these recommended instructions:

 Please pack the parts safely before return.

 Please put the RMA number on the parcel.

 Please confirm the invoice with ADVANCED before shipment.

 Please send back the parts after ADVANCED‘s confirmation.

Chapter 2 Safety Guidance

2.2 General Information

Anti-electroshock Type Class I equipment and internal powered equipment

Anti-electroshock Degree NIBP, SpO2, CO2, AG ,BF ECG

Ingress Protection IPX1

Working System Continuous operation equipment

2.3 Safety Precautions

2.4 Explanation of Symbols on the Monitor

DEFIBRILLATION-PROOF TYPE CF APPLIED PART

DEFIBRILLATION-PROOF TYPE BF APPLIED PART

USB (Universal Serial Bus) Connection

Power Supply switch

AUTHORISED REPRESENTATIVE IN THE EUROPEAN

General symbol for recovery/recyclable

Caution: Federal (U.S.) Law restricts this device to sale by or on

Ingress Protection IPX1 (Protected against vertically falling water

Refer to User manual

( Background: blue; Symbol :white )

The service manual is printed in black and white.

3.1 Environment Requirements

Working 0 C to +40 C(32 ℉~104 ℉)

Transport and Storage -20 C to +55 C(-4 ℉~131 ℉)

Working 15%RHto 95%RH (non-condensing)

Transport and Storage 15%RH to 95%RH (non-condensing)

Working 86 kPa to 106 kPa

Transport and Storage 70 kPa to 106 kPa

3.2 Electrical Requirements

3.3 Safety Requirements

3.4 Installing the Monitor

Patient Monitor on a Flat Surface

- To install the monitor on a roll stand/trolley.

3.5 Connecting to AC Power

Chapter 4 Test and Maintenance

4.1 Routine Test

4.1.1 Visual Inspection