CM 300

Three-Channel Electrocardiograph
CM300
Service Manual
Shenzhen Comen Medical Instrument Co., Ltd.

Shenzhen Comen Medical Instruments co., ltd.
Content
Chapter 1 Safety Guidance ........................................................................................................ 1
1.1 Safety Information .................................................................................................... 1
1.1.1 Danger ............................................................................................................... 1
1.1.2 Warnings ........................................................................................................... 2
1.1.3 Cautions ............................................................................................................ 4
1.1.4 Notes ................................................................................................................. 6
1.2 Equipment Symbols .................................................................................................. 6
Chapter 2 Warranty and Service........................................................................................................ 7
2.1 Warranty Terms ......................................................................................................... 7
2.2 What is excluded? ..................................................................................................... 7
2.3 Service Procedure...................................................................................................... 8
2.4 Fill in the Service Claim Form (SCF) ....................................................................... 8
2.5 Send COMEN the SCF and Select a Solution........................................................... 8
2.6 Obtain the RMA Form .............................................................................................. 9
2.7 Send the Parts to COMEN ........................................................................................ 9
2.7.1 Contact Information ........................................................................................ 10
Chapter 3 Principle introduction ..................................................................................................... 11
3.1 CM300 system principle block diagram ................................................................. 11
3.2 CM300 Module Introduction .................................................................................. 11
3.2.1 Main board (2410 core board + CM300 bottom board) .................................. 11
3.2.2 3.2.2CM100_300 ECG Board ......................................................................... 12
3.2.3 R-type transformer: ......................................................................................... 13
3.2.4 LCD Adapter Board ........................................................................................ 13
Chapter 4 Trouble Shooting ............................................................................................................ 14
4.1 Introduction ............................................................................................................. 14
4.2 Part Replacement .................................................................................................... 14
4.3 Checking Software Version ..................................................................................... 14
4.4 Checking Technical Alarms..................................................................................... 14
4.5 Troubleshooting Guide ............................................................................................ 15
4.5.1 4.5.1 Failure to power on with AC supply ...................................................... 15
4.5.2 Failure to power on with battery ..................................................................... 15
4.5.3 4.5.3 White or Black Screen............................................................................ 15
4.5.4 Abnormal screen display ................................................................................. 16
4.5.5 No ECG output from certain lead. .................................................................. 16
4.5.6 ECG disturbance. ............................................................................................ 16
4.5.7 Electromyograhic disturbance ......................................................................... 17
4.5.8 Unstable baseline ............................................................................................ 17
4.5.9 Partial buttons or all buttons failure ................................................................ 18
4.5.10 Print problem. .................................................................................................. 18
Chapter 5 Performance Verification ................................................................................................ 20
5.1 Safety Test ............................................................................................................... 20
5.2 Performance Tests.................................................................................................... 20
5.2.1 ECG Performance test ..................................................................................... 20

5.2.2 Print speed test ................................................................................................ 20
Chapter 6 Disassembling Procedure ............................................................................................... 22
6.1 Disassemble the rear panel ...................................................................................... 22
6.2 Separate the function board in the front panel. ....................................................... 23
6.3 Disassemble the ECG board.................................................................................... 25
6.4 Disassemble the main board.................................................................................... 26
6.5 Disassemble the power unit .................................................................................... 26
6.6 Printer disassembling .............................................................................................. 27
Chapter 7 Software Upgrade ........................................................................................................... 28
7.1 Tools ........................................................................................................................ 28
7.2 Preparation before Upgrade System Software ........................................................ 28
7.3 System Software Upgrade ....................................................................................... 28
Chapter 1 Safety Guidance
1.1 Safety Information
The design of the 3-channel electrocardiograph complies with international standard IEC 60601-1
Medical Electrical Equipment: General Requirements for Safety and IEC 60601-2-25 Particular
Requirements for the Safety of Electrocardiographs etc. The classification of this equipment is
Class І, type CF, which means a higher degree of protection against electric shock and the patient
connection is fully isolated and defibrillation protected.
This equipment is not explosion-proof. Do not use it in the presence of flammable
anesthetics.
This equipment is designed for continuous operation and is ‘ordinary’ (i.e. not drip or
splash-proof).
Classification:
Anti-electric-shock type: Class І with internal power supply
Anti-electric-shock degree: CF
Degree of protection against harmful Ordinary equipment (Sealed equipment without

ingress of water: liquid proof)
Disinfection/sterilization method: Refer to the user manual for details
Degree of safety of application in the Equipment not suitable for use in the presence
presence of flammable gas: of flammable gas
Working Mode: Continuous operation
EMC: Group І, Class A
1.1.1 Danger
There are no dangers that refer to the product in general. Specific “Danger” statements may be
given in the respective sections of this manual.
1
1.1.2 Warnings
In order to use the electrocardiograph safely and effectively, avoiding possible dangers caused by
improper operations, please read through the user manual and be sure to be familiar with all
functions of the equipment and proper operation procedures before use.
Please pay more attention to the following warning and caution information.
1.1.2.1 Safety Warnings
WARNING :
♦ The electrocardiograph is provided for the use of qualified physicians or

personnel professionally trained. And they should be familiar with the
contents of this user manual before operation.
♦ Only qualified service engineers can install this equipment. And only
service engineers authorized by our company can open the shell.
♦ Only qualified installation or service engineers can shift the mains shift
switch (100V~115V/220V~240V) according to local mains supply.
♦ The results given by the equipment should be examined with respect to

the overall clinical condition of the patient. And it can not substitute for
regular checking.
WARNING :
♦ EXPLOSION HAZARD-Do not use the electrocardiograph in the

presence of flammable anesthetic mixture with oxygen or other
flammable agents.
♦ SHOCK HAZARD-The power receptacle must be a hospital grade

grounded outlet. Never try to adapt the three-prong plug to fit a
two-slot outlet.
♦ If the integrity of external protective conductor in installation or

arrangement is in doubt, the equipment should be operated from the
built-in rechargeable battery.
♦ Do not use this equipment in the presence of high static electricity or

high voltage equipment which may generate sparks.
♦ This equipment is not designed for internal use and direct cardiac
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application.
WARNING :
♦ Only patient cable and other accessories supplied by our company can
be used. Or else, the performance and electric shock protection can not
be guaranteed.
♦ Be sure that all electrodes have been connected to the patient correctly
before operation.
♦ Be sure that the conductive parts of electrodes and associated

connectors, including neutral electrode, should not contact with earth
or any other conducting objects.
♦ Electrodes with defibrillator protection should be used while

defibrillating.
♦ There is no danger for patients with pacemaker.
♦ Do not touch the patient, bed, table and the equipment while using
defibrillator or pacemaker simultaneously.
♦ In order to avoid burning, please keep the electrode far away from the
radio knife while using electrosurgical equipment simultaneously.
WARNING :
♦ Accessory equipment connected to the analog and digital interfaces

must be certified according to the respective IEC standards (e.g. IEC
60950 for data processing equipment and IEC 60601-1 for medical
equipment). Furthermore all configurations shall comply with the valid
version of the standard IEC 60601-1-1. Therefore anybody, who
connects additional equipment to the signal input connector or output
connector to configure a medical system, must make sure that it
complies with the requirements of the valid version of the system
standard IEC 60601-1-1. If in doubt, consult our technical service
department or your local distributor.
♦ The summation of leakage current should never exceed leakage current

limits while several other units are used at the same time.
♦ The potential equalization conductor can be connected to that of other

equipment when necessary, to make sure that all these equipment are
3
connected with the potential equalization bus bar of the electrical

installation.
1.1.2.2 Battery Care Warnings
WARNING :
♦ Improper operation may cause the battery to be hot, ignited or exploded,

and it may lead to the declination of battery’s capacity. It is necessary to
read the user manual carefully and pay more attention to warning
messages.
♦ Only qualified service engineer authorized by our company can open

the battery compartment and replace the battery. And the battery of
same model and specification provided by manufacturer should be
used.
♦ Danger of explosion -- Do not reverse the anode and cathode when

connecting the battery.
♦ Do not heat or splash the battery or throw it into fire or water.
♦ When leakage or foul smell found, stop using the battery immediately. If
your skin or cloth comes into contact with the leakage liquid, cleanse it
with clean water at once. If the leakage liquid splashes into your eyes, do
not wipe them. Irrigate them with clean water first and go to see a
doctor immediately.
♦ When the battery’s useful life is over, contact with the manufacturer or
local distributor for disposal or dispose the battery according to local
regulations.
1.1.3 Cautions
CAUTION :
♦ Avoid liquid splash and excessive temperature. The temperature must

be kept between 5℃ and 40℃ while working. And it should be kept
between -20℃ and 55℃ during transportation and storage.
♦ Do not use the equipment in dusty environment with bad ventilation or

in the presence of corrosive.
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♦ Be sure that there is no intense electromagnetic interference source

around the equipment, such as radio transmitter or mobile phone etc.
Attention: large medical electrical equipment such as electrosurgical
equipment, radiological equipment and magnetic resonance imaging
equipment etc. are likely to bring electromagnetic interference.
CAUTION :
♦ Before use, the equipment, patient cable and electrodes etc. should be
checked. Replacement should be taken if there is any evident
defectiveness or aging symptom which may impair the safety or
performance.
♦ The following safety checks should be performed at least every 24

months by a qualified person who has adequate training, knowledge,
and practical experience to perform these tests.
a) Inspect the equipment and accessories for mechanical and
functional damage.
b) Inspect the safety relevant labels for legibility.
c) Inspect the fuse to verify compliance with rated current and
breaking characteristics.
d) Verify the device functions properly as described in the
instructions for use.
e) Test the protection earth resistance according IEC 601-1/1988:
Limit 0.2 ohm.
f) Test the earth leakage current according IEC 601-1/1988: Limit:
NC 500 uA, SFC 1000uA.
g) Test the patient leakage current according IEC 601-1/1988: Limit:
10 uA (CF).
h) Test the patient leakage current under single fault condition with
mains voltage on the applied part according IEC 601-1/1988:
Limit: 50uA (CF).
The data should be recorded in an equipment log. If the device is not
functioning properly or fails any of the above tests, the device has to be
repaired.
♦ Ruptured fused must only be replaced with the same type and rating as
the original.
♦ The equipment and reusable accessories can be sent back to the

manufacturer for recycling or proper disposal after their useful lives.
5
1.1.3.1 Cleaning & Disinfection Cautions
CAUTION :
♦ Turn off the power before cleaning and disinfection. If mains supply
used, the power cord should be drugged out of the outlet also. And
prevent the detergent from seeping into the equipment.
♦ Do not immerse the unit or patient cable into liquid under any
circumstances.
♦ Do not clean the unit and accessories with abrasive fabric and avoid
scratching the electrodes.
♦ Any remainder of detergent should be removed from the unit and

patient cable after cleaning.
♦ Do not use chloric disinfectant such as chloride and sodium

hypochlorite etc.
♦ Do not use high temperature, autoclaving or radiation sterilization

processes.
1.1.4 Notes
Refer to Operation Manual for detailed operation and other information.
1.2 Equipment Symbols
External output
Potential equalization
External input Mains supply
Equipment or part of CF type Battery indicator

with defibrillator proof
Attention – general warning (see Battery recharging indicator

accompanying document)
6
Chapter 2 Warranty and Service
2.1 Warranty Terms
COMEN provides an 18 months warranty for the warranted products (main unit) and 3 months
for the accessories. The warranty period begins on the date products are shipped to customer. If
a customer promptly notifies COMEN of customer’s warranty claim hereunder, COMEN will either
repair, adjust or replace (with new or exchange replacement parts) COMEN’s products. COMEN
warrants that any service it provides to customers will be performed by trained individuals in a
workmanlike manner.
2.2 What is excluded?
The warranty does not cover for the situations caused by the following condition:
 Malfunction or damage caused by improper use or man-made failure.
 Malfunction or damage caused by unstable or out-of-range power input.
 Malfunction or damage caused by force majeure such as fire and earthquake.
 Malfunction or damage caused by improper operation or repair by unqualified or unauthorized
service people.
 Malfunction or damage caused by use of parts or accessories not approved by COMEN.
 Malfunction of the instrument or part whose serial number is not legible enough.
 Others not caused by instrument or part itself.
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2.3 Service Procedure
2.4 Fill in the Service Claim Form (SCF)
Fill in the SCF with detailed information including: Model Name, Serial Number (SN) and Problem
Phenomena. COMEN should not have any obligation to take over the case without this
information. The form can be gotten from COMEN’s Service Department.
2.5 Send COMEN the SCF and Select a Solution
Once the service department receives the fully filled SCF, COMEN’s engineer will offer a solution
in three working days. COMEN will follow out the case based on the two conditions below:
 Within Warranty:
There are two options:
1) After receiving the Return Material Authorization (RMA) form from COMEN service
department, customer sends COMEN 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.
2) 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 COMEN on
time. We will, at this option, dispatch the replacement one(s) with confirmed shipping invoice.
8
NOTE:
 Both Return Material Authorization Form and Declaration Form are offered by
COMEN service department once the SCF is confirmed by service engineer.
 The customer is responsible for freight& insurance charges when the equipment is
shipped to COMEN for service, including custom charges. COMEN is responsible for the
freight, insurance & custom charges from COMEN to the customer.
 Out of Warranty:
After receiving the RMA form from the service department, the customer sends defective parts
to COMEN 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.
2.6 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:
 COMEN should not have any obligation to the end-user or customer who returns the
goods without the notification by COMEN’s service department. The sender takes full
responsibility for the accounted fee.
2.7 Send the Parts to COMEN
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 information (such as price in invoice, address and other necessary issues)
with COMEN before shipment.
 Please send back the parts after COMEN’s confirmation.
9
2.7.1 Contact Information
If you have any question about maintenance, technical specifications or malfunctions of devices,
do not hesitate to contact us.
• COMEN International After-Sale Dept.

• Monday to Friday 09:00-18:00 (UTC +08:00)
• E-mail: support@szCOMEN.com
• Tel: + 86 -755- 26431236-333
• Fax: + 86 -755-26431232
Add: Floor8, Block3, 4th Nanyou Industrial,
Nanshan District, 518052 Shenzhen, China
10
Chapter 3 Principle introduction
3.1 CM300 system principle block diagram
AC Input USB device
USB interface COM interface
R-Type
transformer
Battery CM100_300 To
Main board ECG board Patient
Button
board
User
Inverter
Recorder LCD Panel
3.2 CM300 Module Introduction
3.2.1 Main board (2410 core board + CM300 bottom board)
The main board is the heart of the instrument. It consists of bottom board and core board (CPU
board), it implements a series of tasks including CPU system, display processing, printing control,
keyboard signal processing. CPU system receives electrocardiogram signal that collects by ECG
board, and send to recorder after printing control system. CPU system receives also signals from
button board to finish the button board signal process, moreover, signals of lead-fall, paper
detecting, battery management are all processed by main board CPU. The main board also
process print task, CPU system receives order and data from print control system, generate
control signals for stepping motor and printer head to implements waveforms and other
information’s print. CPU system also sends order and data to display waveforms and other
11
information.
PIN ID CON7 CON10 CON11 CON12

To LCD adapter To ECG board Main board To recorder
Description
board Power socket
Working voltage 5V 20V（AC）
Data storage, the CPU of the main unit, display circuit, network circuit,
Module Function
recorder circuit and I/O interface.
3.2.2 3.2.2CM100_300 ECG Board
ECG board process the ECG signal gets from ECG cable. It implements signal amplification
including analog circuit, A/D converter and control circuit.
Analog circuit consists of lead signal amplification, channel switch, anti-alias filter, gain control,
lead-off detection. Control circuit is Responsible for coordinating with A/D convertor, channel
switch, gain control circuit and lead-off detection circuit to implement signal acquisition and
lead-off detection, the digital lead signal will then be sent to CPU by high speed photo-coupler.
PIN ID P1
Description ECG board socket, to main board
Working voltage 5V
Module Function Measure ECG data
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3.2.3 R-type transformer:
PIN ID
Description
Working voltage
Module Function Voltage transformation to feed main board
3.2.4 LCD Adapter Board
PIN ID P1 P2 P4
To LCD panel To main board To Membrane
Description
button
Working voltage
Module Function LCD and button signal transmit
13
Chapter 4 Trouble Shooting
4.1 Introduction
In this chapter, electrocardiograph problems are listed along with possible causes and
recommended corrective actions. Refer to the tables to check the electrocardiograph, identify
and eliminate the troubles.
The troubles we list here are frequently arisen difficulties and the actions we recommend can
correct most problems, but not all of them. For more information on troubleshooting, contact
our Customer Service Department.
4.2 Part Replacement
Printed circuit boards (PCBs), major parts and components in the electrocardiograph are
replaceable. Once you isolate a PCB you suspect defective, follow the instructions in 7
Disassembly and repair to replace the PCB with a known good one and check that the trouble
disappears or the patient monitor passes all performance tests. Defective PCB can be sent to us
for repair. If the trouble remains, exchange the replacement PCB with the original suspicious PCB
and continue troubleshooting as directed in this chapter.
To obtain information on replacement parts or order them, refer to 3Principle introduction.
4.3 Checking Software Version
Some troubleshooting may involve software compatibility. Thus it requires you to your
electrocardiograph configuration and software version. For detailed information on version
compatibility, please contact our Customer Service Department.
To view information on the electrocardiograph system software version, select

[Menu]→[Net]→[Software Version ].
4.4 Checking Technical Alarms
Before troubleshooting the electrocardiograph, check for technical alarm messages. If an alarm
14
message is presented, eliminate the technical alarm first.
For detailed information on technical alarm message, possible cause and corrective action refer
to the electrocardiograph’s Operation Manual.
4.5 Troubleshooting Guide
4.5.1 4.5.1 Failure to power on with AC supply
Symptoms Possible Cause Correction Action
AC power supply cable is not Check whether the power supply cable is
connected well. reliably connected
The two fuses defective Remove power supply cable and open the
fuse-boxes then ensure each of them is
good by multi-meter. If not, change new
The electrocardiograph fuses.
fails to start with AC
AC power supply unit defective Switch the multi-meter to AC voltage gear
power.
and test the transformer output. The
reasonable output should be 18V-20V
Main board defective replace a new main board
Keypad defective replace a new keypad
4.5.2 Failure to power on with battery
The electrocardiograph Battery defective. Check the battery voltage is around 14.8V
fails to start with
battery. Main board defective replace a new main board
4.5.3 4.5.3 White or Black Screen
White or Black screen Keypad cable or connect cable is Check the keypad cable or connector cable
15
not connect well. is reliably connected
System failure replace a main board
LCD screen defective replace a LCD screen
4.5.4 Abnormal screen display
LCD adapter board or LCD cable not Check LCD adapter board or LCD cable
connect well connect well
Abnormal screen
LCD adapter board or LCD cable replace a LCD adapter board or LCD cable
display
defective
LCD screen defective replace a new LCD screen
4.5.5 No ECG output from certain lead.
Identical electrode falls off or has re-install the electrode or paste some
no reliable linked with patient body water or conductive ointment at the
contact position
Cable has been broken due to long The cable and electrode of the same
time use or unit aging/clamp model shall be used to replace the old one.
electrodes or chest bulbs lose
No ECG output from
flexibility or weak connection
certain lead.
ECG board and main board cable Check the internal wire between ECG
didn’t connect well. board and main board connect well.
ECG board defective Change the new ECG board
Main board defective Change the new main board
4.5.6 ECG disturbance.
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Identical electrode had no reliable re-install the electrode or paste some

linked with patient body; water or conductive ointment at the
contact position
ECG machine, electrode, metal bed Check ECG machine, electrode, metal bed
or lead cable reliably connected with or lead cable reliably connected with
grounding grounding
Disturb by electric equipments of Check if there is disturb by electric

ECG disturbance
large power wor 的 king nearby equipments of large power working nearby
Electrode and skin pasted with Switch on the ECG filtering function of the
sufficient conductive ointment. machine
The patient wearing jewelry such as Switch on the ECG filtering function of the
glasses or gems, AC disturbance can machine
not be cleared.
4.5.7 Electromyograhic disturbance
Communication disturbance
Switch on the shift filtering function of the
Electromyograhic The doctor talk to the patient machine to 25Hz or 35Hz, and then the
disturbance during ECG recording process recorded ECG waveforms will reduce a
little bit.
The Electrode clippers on the
arms and legs too tightened
4.5.8 Unstable baseline
electrode installation stable, lead

cable and electrode connected Switch on the shifting filtering function of
properly the machine to 0.1Hz, 0,2Hz or 0.5Hz, the
Unstable baseline
electrode and patient skin clean recorded ECG waveforms will reduce a
electrode and skin pasted with little bit.
sufficient conductive ointment
17
it is due to body movement or

respiration of the involved patient
or mixed an old electrodes with
new electrodes for together use
4.5.9 Partial buttons or all buttons failure
Connector between the control open the upper cover of the machine and
panel and the line board out of re-connect the connector between control
proper connection. panel and line board
Keypad broken Change new keypad

Partial buttons or all
buttons failure
Internal line between membrane Replace the involved membrane buttons.
buttons is broken due to long time
of use.
Main board defective Change the new main board.
4.5.10 Print problem.
Print paper in incorrect position Load print paper in correct position
Check whether the print paper in the right

Inverse putting of paper
position.
Paper type incorrect Change the correct Paper

Waveforms displayed
properly but can’t be
Print head unclean Clean the print head
printed
Print cable didn’t connect well Check the print cable is reliably connected
Printer defective. Change new printer.
Main board defective Change new main board
18
Problem with the print head. Change new print head
Print unclear Printer defective. Change new printer.
Main board defective. Change new main board
Printer is not covered properly Check if printer is covered properly or
or installed with inclined paper. paper installed in right position.
Print paper type incorrect Change the Correct Paper

Print paper jam
Printer in incorrect position Adjust the position of printer
Main board defective. Change new main board.
Print paper type incorrect Change correct print paper type.
Print paper in incorrect position Load print paper in correct position

Print out of paper
Main board defective. Change new main board
19
Chapter 5 Performance Verification
5.1 Safety Test
Safety tests should be performed by qualified personnel every 6 to 12 months, and each time after
service use a standard safety tester to perform safety tests. The tester must comply with IEC/EN
60601-1or the local standards and statutes.
Refer to the accompanying operation instructions of the tester for test procedure details.
5.2 Performance Tests
The performance test should be done once every 12 months or when you suspect the
measurement is incorrect.
5.2.1 ECG Performance test
Patient cables include two parts: main cables which are connected to the electrocardiograph and
the lead wires which are connected to the patient. Lead wires include 6 chest lead wires and
4limbs lead wires, the user can distinguish the chest leads and limb leads from the color of the
lead wires and the label on the connector.
Required Equipment: ECG Simulator
1) Connect the leadcable and electrocardiograph as show below:
2)Connect the leadcable and the simulator as shown below:
3) Switch on the electrocardiograph.
4) Generate the heart rate 40 bpm, 80 bpm, 120 bpm, 160 bpm, 200 bpm and 240 bpm in turn.
5) Check if the HR value displayed on the screen is accurate. Error within 2 bpm is acceptable.
5.2.2 Print speed test
5.2.2.1 Standard request.
Enterprise standard：with 5 kinds of print speed 5mm/s、10mm/s、12.5 mm/s、25mm/s and

20
50mm/s，error limit±2%.
5.2.2.2 Test method
a）Set the sensitivity of electrocardiograph as 10 mm/mv，print speed 25mm/s, AC filter 50Hz，

EMG filter off,low-pass filter 150Hz，drift filter 0.05Hz，manual model.Switch on the ST light of the
detector，press S+SU,keep the indicator of detector“3”lit，Change the output value 20μ V、10Hz
to 0.5mV、10Hz.
b）Enter a triangular-wave signal of frequency of 25Hz±1%、0.5mVp-p，set the print speed as

25mm/s ，after paper advanced 1s,measure by square master.
5 Groups continuous sequence（each group with 10 cycles），the distance of each sequence on
the print paper is 10±0.5mm，the distance of 50 cycles on the print paper should be 50±2.5mm.
c）Set the print speed as 5mm/s,and set the signal frequency as 5Hz±1%，repeated test.
d）Set the print speed as10mm/s,and set the signal frequency as 10Hz±1%，repeated test.
e) Set the print speed as 12.5mm/s,and set the signal frequency as 12.5Hz±1%，repeated test.
f) Set the print speed as 50mm/s,turn off the AC filter,and set the signal frequency as 50Hz±1%，
repeated test.
21
Chapter 6 Disassembling Procedure
The following section describes the disassembly and reassembly procedures for the monitor and
its components
Who Should Perform Repairs.
Only qualified service personnel (biomedical engineers or technicians) should open the monitor
housing, remove and replace components or make adjustments. If your medical facility does not
have qualified service personnel, contact COMEN or your local COMEN representative.
Caution High-Voltage – Voltages dangerous to life are present in the instrument when it
is connected to the mains power supply. Do not perform any disassembly procedures (other
than server removal) with power applied to the instrument. Failure to adhere to this warning
could cause serious injury r death.
Tools required
 Small flat head screwdriver
 Needle Nose Pliers
 ESD mat and wrist strap
 Cleaning Agent
6.1 Disassemble the rear panel
1. First unscrew all screws in the back panel of the monitor below
22
Battery
compartment
Caution: remove the battery first in order to operate in safe situation
6.2 Separate the function board in the front panel.
1. Open the paper cover and upper cover.
23
2. Unscrew the screw labeling in the figure.
3. Unplug the cables carefully.
24
3. Then unplug indicate cable, LCD transmit board LCD FFC ribbon cable and next you should
unscrew all screws then remove these board.
6.3 Disassemble the ECG board
1.After separating the front and back panel ,finding the back panel including four parts
(printer ,power unit ,ECG board ,main board )
2. Separating ECG board (unplug the four PA3x8 screws.
AC power unit Mainboard
ECG board
printer
25
6.4 Disassemble the main board
1. Unscrew five PA3x8 screws and then unplug the printer ribbon cable carefully. Last do not forgot
to unplug the power cable and monitoring cable)
6.5 Disassemble the power unit
1. Separate the power main board (unplug the grounding cable and AC power cable .Then
unscrew four screws)
26
6.6 Printer disassembling
1. Unscrew all screws in the printer support below. Then remove the printer support.
27
Chapter 7 Software Upgrade
The system software is able to be upgraded with the USB disk through USB interface on monitor.
7.1 Tools
The following tools are required during the software upgrade:

 USB disk 2GB
 USB adapter cable (For C30 software upgrade only)
7.2 Preparation before Upgrade System Software
1. Before software upgrade, please check software version and take it down to make sure you are
able to revert back in case the failure of software upgrade.
2. Take a USB disk, the size of the USB disk should be 2GB or less, format it to “FAT” format
before software upgrade;
4. Unzip the package file that got from COMEN and copy the folder * to the root path on USB
disk, do not change the folder name or the file name(s) in the folder unless you are informed by
COMEN to have the necessary change.
* Generally the folder name should be “COMENSOFT”, “CMC90_BigHost” (for C90 only)
or “CMC70_BigHost” (for C70 only);
4. Turn off the monitor before software upgrade.
7.3 System Software Upgrade
After the preparation work’s done, please plug USB disk on the USB interface of the monitor, and
then turn on the monitor, the monitor will then detect the upgrade package, software upgrade will
be automatically done, the display will then show “System is updating” and “System update
success!” to indicate the status during software upgrade process.
After the display shows “System update success!”, please unplug the USB disk and restart monitor
to check the new software.
NOTE
 Make sure you have confirmed with COMEN Customer Service Department the
software package is fit for the software upgrade for the monitor you are currently
operating on.
28
 Disconnect the patient monitor from patient before software upgrade;

 Make sure the battery capacity is enough or plug on AC power while doing the software
upgrade process, it takes around 2-10 minutes during the whole upgrade;
 Program upgrade should be performed by qualified service personnel only.
Do not unplug the USB disk during the software upgrade process.
29

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Three-Channel Electrocardiograph

Shenzhen Comen Medical Instrument Co., Ltd.

5.2.1 ECG Performance test ..................................................................................... 20

Chapter 1 Safety Guidance

1.1 Safety Information

Degree of protection against harmful Ordinary equipment (Sealed equipment without

Working Mode: Continuous operation

EMC: Group І, Class A

1.1.2.1 Safety Warnings

♦ The electrocardiograph is provided for the use of qualified physicians or

♦ The results given by the equipment should be examined with respect to

♦ EXPLOSION HAZARD-Do not use the electrocardiograph in the

♦ SHOCK HAZARD-The power receptacle must be a hospital grade

♦ If the integrity of external protective conductor in installation or

♦ Do not use this equipment in the presence of high static electricity or

♦ Be sure that the conductive parts of electrodes and associated

♦ Electrodes with defibrillator protection should be used while

♦ There is no danger for patients with pacemaker.

♦ Accessory equipment connected to the analog and digital interfaces

♦ The summation of leakage current should never exceed leakage current

♦ The potential equalization conductor can be connected to that of other

connected with the potential equalization bus bar of the electrical

1.1.2.2 Battery Care Warnings

♦ Improper operation may cause the battery to be hot, ignited or exploded,

♦ Only qualified service engineer authorized by our company can open

♦ Danger of explosion -- Do not reverse the anode and cathode when

♦ Do not heat or splash the battery or throw it into fire or water.

♦ Avoid liquid splash and excessive temperature. The temperature must

♦ Do not use the equipment in dusty environment with bad ventilation or

♦ Be sure that there is no intense electromagnetic interference source

♦ The following safety checks should be performed at least every 24

♦ The equipment and reusable accessories can be sent back to the

1.1.3.1 Cleaning & Disinfection Cautions

♦ Any remainder of detergent should be removed from the unit and

♦ Do not use chloric disinfectant such as chloride and sodium

♦ Do not use high temperature, autoclaving or radiation sterilization

Refer to Operation Manual for detailed operation and other information.

1.2 Equipment Symbols

External input Mains supply

Equipment or part of CF type Battery indicator

Attention – general warning (see Battery recharging indicator

Chapter 2 Warranty and Service

2.1 Warranty Terms

2.2 What is excluded?

2.3 Service Procedure

2.4 Fill in the Service Claim Form (SCF)

2.5 Send COMEN the SCF and Select a Solution

2.6 Obtain the RMA Form

2.7 Send the Parts to COMEN

Follow these recommended instructions:

2.7.1 Contact Information

• COMEN International After-Sale Dept.

Chapter 3 Principle introduction

3.1 CM300 system principle block diagram

AC Input USB device

USB interface COM interface

Recorder LCD Panel

3.2 CM300 Module Introduction

3.2.1 Main board (2410 core board + CM300 bottom board)

PIN ID CON7 CON10 CON11 CON12

3.2.2 3.2.2CM100_300 ECG Board

3.2.3 R-type transformer:

3.2.4 LCD Adapter Board