Defibrillation Monitor S Series

Service Manual

Shenzhen Comen Medical InstrumentsCo., Ltd.

 Defibrillator Monitor S Series Service Manual

Copyright

Shenzhen Comen Medical Instruments Co.,Ltd Version: 1.0

Product Name: Defibrillation Monitor

Model: S8

Statement

Shenzhen Comen Medical Instruments Co., Ltd. (belowComen is the copyright of this

non-publicly published maintenance manual and has the right to treat it as confidential

information. This Service Manual is a reference for the maintenance of Comen products.

Others have no right to disclose the contents of this manual to others.

This Service Manual contains proprietary information protected by copyright law.

Copyright, no part of this Service Manual may be photocopied, copied or translated into

another language without the prior written consent ofComen.

Comen is not liable for errors in the service manual or for incidental or

consequential damages resulting from the actual performance and use of this service

manual.Comen does not provide other parties with a franchise under the patent law.Comen

is not liable for legal consequences resulting from violations of patent law and any

third party rights.

The contents of the maintenance manual can be changed without notice.

Contact

Name: Shenzhen Comen Medical InstrumentsCo., Ltd. After-sales Service Department

Address:10-11F, Building 1A, 1A Building, Feiyada Clock Building, South Ring Road,

Matian Street, Guangming District, Shenzhen, China

Tel:0755-26431236

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 Defibrillator Monitor S Series Service Manual

Fax:0755-26431232

Customer Service Phone:4007009488

Zip Code:518052

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 Defibrillator Monitor S Series Service Manual

Directory
目录
Chapter 1 Safety ................................................................................................................................................ 6
1.1 Safety Information ............................................................................................................................. 6
1.2 Symbol Description ........................................................................................................................ 11
Chapter2 Warranty ......................................................................................................................................... 12
2.1 Warranty Terms.............................................................................................................................. 12
2.2 Exclusion of warranty ....................................................................................................................... 12
2.3 Maintenance procedures ................................................................................................................. 13
2.3.1 Fill in the Customer Complaint Form (SCF) ............................................................................ 14
2.3.2 Submit a customer complaint form and choose a solution ................................................... 14
2.3.3 RMA Form............................................................................................................................... 15
2.3.4 Return ..................................................................................................................................... 15
Chapter 3 Introduction to Principles ............................................................................................................... 17
................................................................................................................................................................. 17
3.1 Overview ......................................................................................................................................... 17
3.1.1 Introduction to Defibrillator ................................................................................................... 17
3.1.2 System Composition ............................................................................................................... 17
3.1.3 system structure diagram....................................................................................................... 19
3.2 Module Introduction ....................................................................................................................... 19
3.2.1 Main control board................................................................................................................. 19
3.2.2 AC power board...................................................................................................................... 22
3.2.3 Keyboard ................................................................................................................................ 22
3.2.4 DC power board .................................................................................................................. 24
3.2.5 Treatment module ................................................................................................................. 26
3.2.6 Side panel ............................................................................................................................... 32
3.2.7 NIBP module ........................................................................................................................... 33
3.2.8 IBP module ............................................................................................................................. 36
3.2.9 ECG Module ............................................................................................................................ 36
3.2.10 SPO2 Module ........................................................................................................................ 37
Chapter 4 Troubleshooting ............................................................................................................................. 41
................................................................................................................................................................. 41
4.1 Introduction ...................................................................................................................................... 41
4.2 Replaceable parts ........................................................................................................................... 41
4.3 Checking the monitor ....................................................................................................................... 41
4.4 Checking the software ...................................................................................................................... 41
4.5 Check the error message prompt ................................................................................................ 42
4.6 Troubleshooting.............................................................................................................................. 42
4.6.1 Electricity failure..................................................................................................................... 42

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 Defibrillator Monitor S Series Service Manual

4.6.2 Display failure ......................................................................................................................... 43

4.6.3 Battery failure......................................................................................................................... 44

4.6.4 SPO2 failure ........................................................................................................................ 45

4.6.5 NIBP failure ........................................................................................................................ 46

4.6.6 TEMP Module failure ....................................................................................................... 47

4.6.7 Key failure........................................................................................................................... 48

4.6.8 Software upgrade failure................................................................................................ 48

4.6.9 Technical alarm information ......................................................................................... 49

4.6.10 Electrode piece cable connection failure ................................................................ 49

4.6.11 Treatment Module failure............................................................................................ 50

Chapter 5 software upgrade ........................................................................................................................... 52

................................................................................................................................................................. 52
5.1 Upgrade Preparation ..................................................................................................................... 52
5.2 System software upgrade .............................................................................................................. 52
Chapter 6 Performance Verification ............................................................................................................... 54
................................................................................................................................................................. 54
6.1 NIBP test ......................................................................................................................................... 54
6.1.1 NIBP Air leak test .................................................................................................................... 54
6.1.2 NIBP Pressure calibration ....................................................................................................... 55
6.2 IBP test ............................................................................................................................................ 56
6.3 ECG test .......................................................................................................................................... 57
6.4 SpO2 test ......................................................................................................................................... 57
6.5 TEMP test........................................................................................................................................ 58

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 Defibrillator Monitor S Series Service Manual

Chapter 1 Safety

1.1 Safety Information

WARNING

● You may be prompted serious consequences, endanger the safety or

adverse events Case. Failure to follow the warning will result in death or

serious personal injury or property damage to the user or patient.

CAUTION

● Indicates a potentially hazardous or unsafe operation that, if not avoided,

could result in minor personal injury, product malfunction, damage, or

property damage, and may result in more serious injury in the future.

PAY ATTENTION TO

● important precautions, provide instructions or explanations to make

better use of this product.

WARNING

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 Defibrillator Monitor S Series Service Manual

● This defibrillator is intended for use in clinical patient care and only allows

trained physicians and nurses to use the defibrillator.

● Before use, the user should check that the instrument and its accessories

are working properly and safely.

● The alarm volume and alarm upper and lower limits should be set for

different patients. When monitoring a patient, do not rely solely on the

audible alarm system to monitor the patient. If the alarm volume is set too

small or completely turned off, the alarm may be invalidated and the

patient's safety may be compromised. The most reliable method of patient

monitoring should be to pay close attention to the actual clinical condition

of the patient.

● This device can only be connected to a power outlet with protective

grounding. If the power socket is not connected to a grounding wire, do

not use the socket and use a rechargeable battery device to supply power.

● Do not open the case of the instrument to avoid possible electric shock

hazards. Any repairs and upgrades to the monitor must be performed by a

service person trained and authorized by Comen.

● When handling packaging materials, they should be disposed of in

accordance with local laws and regulations or the hospital's waste disposal

regulations. Packaging materials must be placed out of reach of children.

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 Defibrillator Monitor S Series Service Manual

● Do not use the instrument in a location where flammable materials such as

anesthesia are placed to prevent an explosion or fire.

● Carefully install the power cord and various accessory cables to avoid

patient entanglement or suffocation, cable entanglement, or electrical

interference.

● Do not use a mobile phone near the monitor. The mobile phone generates

an excessive radiation field and interferes with the monitor's function.

● For patients with pacemakers, the heart rate monitor may pulse

pacemakers during cardiac arrest or arrhythmia. Do not rely solely on the

heart rate monitor alarm. Patients with pacemakers should be closely

monitored. Refer to the monitor's instruction manual for the ability of the

device to suppress the pacemaker.

● During defibrillation, the operator should not touch the patient, the table

and the instrument. Check that the function is normal before using these

cables again.

● The interconnecting device with the monitor should form an equipotential

body (the protective ground is effectively connected).

● When the monitor is shared with the electrosurgical device, the user

(doctor or nurse) should ensure the patient's safety.

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 Defibrillator Monitor S Series Service Manual

● The physiological waveforms, physiological parameters and alarm

information displayed by the monitor are for medical reference only and

cannot be directly used as clinical treatment basis.

● Electromagnetic fields can affect the performance of the instrument, so

the use of other Instrumentsin the vicinity of the instrument must meet

the appropriate EMC requirements. For example, mobile phones, X-rays, or

MRI devices can all be sources of interference because they emit high-

intensity electromagnetic radiation.

● This is not a treatment device.

● After defibrillation, the recovery time of ECG is not more than 10s, and the

recovery time of other parameters is not more than 5s.

● To prevent burns to the patient when the monitor is used with a high

frequency surgical device, avoid any conductive connections between the

sensor and cable and the high frequency surgical device.

CAUTION

● To install or carry the instrument properly to prevent the instrument from

falling, colliding, being subjected to strong oscillations or other

mechanical external forces.

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 Defibrillator Monitor S Series Service Manual

● Before the device is powered on, please confirm that the power supply

used meets the requirements of the instrument's nameplate label or the

power supply voltage and frequency specified in the instruction manual.

● When the instrument and accessories are about to expire, they must be

disposed of in accordance with relevant local laws and regulations or the

hospital's rules and regulations.

● Disposable accessories can only be used once, and repeated use can result

in performance degradation or cross-contamination.

● If the monitor will not be used for a long time, remove the battery and

keep it in a safe place.

● Defibrillation recovery time of less than 10s

PAY ATTENTION TO

● Install the instrument in a location that is easy to observe, operate, and

maintain.

● This instrument cannot be used at home.

● The instrument is limited to one patient at a time.

● The life of this monitor is 5 years.

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 Defibrillator Monitor S Series Service Manual

1.2 Symbol Description

(1) Instrument Symbol

measuring instrument type

Note!
approval mark and number
2015R124-44

manufacturing measuring
refer to the operation manual instrument license mark and
Guangdong
number
00000700

BF type application part, with

main menu
anti-defibrillation function

CF type application part, with

waterproof level
anti-defibrillation function

open, shutdown Key production date mark

use battery work light sequence number mark

AC power indicator light equipotential symbol

network connection
VGA interface
symbol

multi-function interface USB interface

manufacturer input port

output port

table 1
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 Defibrillator Monitor S Series Service Manual

(2) packaging symbol

up stacking layer limit

fragile goods rainproof

gauge2

Chapter2 Warranty

2.1 Warranty Terms

Comen provides a 24 month (host) warranty or a 6 month (accessory) warranty for all licensed products,
starting with the customer's purchase date. If your product is determined to be defective and promptly
notified to us during the warranty period, Comen will repair the product or replace it with a new product or
accessory.

2.2 Exclusion of warranty

The Comen warranty will not apply to the following:

 Unreasonable use or damage caused by man

 Damage caused by unstable voltage or super normal range voltage

 Damage caused by irresistible factors, such as fires and earthquakes

 Damage caused by unreasonable operation or repair by an unauthorized maintenance organization or

individual

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 Defibrillator Monitor S Series Service Manual

 Damage caused by attachments that are not approved by Comen.

 The product serial number is not clear.

 Other damage caused by the instrument or the component itself.

2.3 Maintenance procedures

Repair request

Instrument collection

No need to Need to be
Instrument
status

Apply for accessories Inspection / repair

Failed
Office maintenance
Product
testing

Return to customer qualified

Return to office/client

figure 1

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 Defibrillator Monitor S Series Service Manual

2.3.1 Fill in the Customer Complaint Form (SCF)

Fill in the customer complaint form in detail: model number, serial number (SN) and problem description.

Without this information, Comen will not be obliged to accept this complaint. Customers can apply for a
complaint form from Comen's after-sales department if needed.

Serial number
(SN) see this
nameplate

Figure 1

2.3.2 Submit a customer complaint form and choose a solution

Once the after-sales department receives the customer complaint form, the engineer will provide the
customer solution within three days. And deal with it according to the following two situations:

 Warranty period:

There are two options:

1) After receiving the Return Authorization Form (RMA) from the After-sales Department, the customer
can return the defective part and inform the delivery number. We will send a new part with the loading
invoice to your address as soon as possible.

2) You can also send the signed statement to us by mail or fax. The statement has the legal effect to ensure
that the customer or the end customer will send the faulty part to Comen in time. In this case, we will
send the replacement parts and loading invoices in a timely manner.

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 Defibrillator Monitor S Series Service Manual

Caution

 Once the customer complaint form has been confirmed, Comen engineers will provide you with
a return authorization and declaration form.

 The customer is responsible for shipping, insurance and customs fees for the shipment of the
product to Comen.

 The warranty period has expired:

After receiving the return authorization form, the customer will send the faulty part to Comen. Our
engineers will analyze the faulty parts and negotiate with the customer to repair or replace the faulty parts.
After the maintenance fee has been paid, we will send out new replacement parts as soon as possible.

Caution

 The customer is responsible for all costs (including freight, insurance and customs fees) during
the transportation process.

2.3.3 RMA Form

Before returning the goods, the customer will receive an RMA Form (Return Authorization Form)
provided by our after-sales department, which includes the RMA number, a brief description of the returned
parts and shipping instructions. When shipping, please indicate the RMA number on the box.

Caution

 In the absence of a notice to the Comen after-sales department, we will not be obligated to process
returns from the terminal or customer. And the shipper is responsible for all possible expenses.

2.3.4 Return

Please follow the steps below

 When disassembling the instrument, use an anti-static requirements. Do not touch the instrument
directly with your hands.

 Pack the parts carefully before shipping.

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 Defibrillator Monitor S Series Service Manual

 Please indicate the RMA number on the package.

 When describing the product, please use the “*** sample” format to reflect the total value on the
invoice and mark “sample, no commercial value”. .

 Before returning, please check with Comen (for example: total amount, address and other necessary
information on the invoice).

 After receiving confirmation from Comen, please return the faulty part.

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 Defibrillator Monitor S Series Service Manual

Chapter 3 Introduction to Principles

3.1 Overview

3.1.1 Introduction to Defibrillator

S-Series defibrillation monitors can monitor ECG, RESP, SpO2, NIBP, Invasive Blood Pressure (IBP), Carbon
Dioxide (CO2), Body Temperature (TEMP), etc. Vital sign parameters. This product is suitable for manual
defibrillation, AED defibrillation, pacing and vital signs monitoring.

3.1.2 System Composition

The defibrillator monitor consists of a host, a battery, a defibrillation electrode plate (defibrillation

external electrode plate, and a defibrillation internal electrode plate) and corresponding functional

accessories. Mainly achieve the following functions:

1. Defibrillation monitor defibrillation release energy accuracy;

2. Pace frequency accuracy;

3. Pace current accuracy;

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 Defibrillator Monitor S Series Service Manual

4. Heart rate detection accuracy;

5. Respiratory measurement accuracy:

6. Body temperature measurement error;

7. Non-invasive blood pressure measurement accuracy:

8. Invasive blood pressure measurement accuracy;

9. Blood oxygen saturation measurement accuracy;

10. Pulse rate measurement accuracy.

CO2 measurement accuracy:

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 Defibrillator Monitor S Series Service Manual

3.1.3 system structure diagram

Figure 3

3.2 Module Introduction

3.2.1 Main control board

The main board is the core of the entire monitor, responsible for processing: input and output
control, data storage and processing, display, system control, communication management and more.

Main control board functional block diagram:

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Defibrillator Monitor S Series Service Manual

Figure 2

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 Defibrillator Monitor S Series Service Manual

J33

J3

J4

J32

P1

J8

J7

Figure 3

socket description working voltage

J3 4pin, connection button board /

J4 22pin, connection button board 5V

J7 4pin, connection alarm light 5V

J8 4pin, connect LCD screen /

J32 16pin, then the printer 18V60pin,

J33 5V,connected to AC-DC power board

5V, 12V, 18V connected to the LCD screen 5V, 12V, 3.3V
P1 (8000F

table 1
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 Defibrillator Monitor S Series Service Manual

3.2.2 AC power board

P1

P2

Figure 6

socket description working voltage

P1 5pin, connect AC power 100-240V AC

supply

P2 6pin, connect AC-DC power 18V

supply board

table 2

3.2.3 Keyboard

The keypad is located in the front of the monitor. Through the MCU processing on the keypad, the
signal can be transmitted to the main board, as well as the display of the power indicator, AC indicator and
charging indicator.

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 Defibrillator Monitor S Series Service Manual

J5

J10

J14
J13 J9
J8

Figure 7

socket description working

voltage

J5 20pin, connection dial board /

J8 4pin, connect main control board /

J9 2pin, connect speaker /

J10 22pin, connect main control board 5V

J13 2pin, printer keypad /

J14 6pin, connected to the shuttle board /

Table 3

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 Defibrillator Monitor S Series Service Manual

3.2.4 DC power board

J8 J4

J9

J7

J6

J3 Figure 8

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 Defibrillator Monitor S Series Service Manual

J15

J1 J14

J12

J2
J13

Figure 9

socket description working voltage

J1 10pin, battery A /

J2 10pin, battery B /

J3 4pin AC switching power 18V

supply

J4 20pin, connected to the 5V, 12V, VBUS

treatment module

J7 60pin, connected to the 3.3V, 5V, 12V, V_PRINT

main control board

J8 16pin, connected 5V, 12V

parameter module

J9 4pin, connected side 5V

panel

J12 20pin, Multi-function 5V

interface

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 Defibrillator Monitor S Series Service Manual

J13 15pin, VGA interface /

J14 16pin, network port /

J15 6pin, USB port 5V

table 4

3.2.5 Treatment module

J1

J2

J13

Figure 10
J4 J8

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 Defibrillator Monitor S Series Service Manual

J12

J25

J26

Figure 11

socket description working voltage

5pin,connection Charging
J1 /
capacitor

4pin,connect the internal

J2 5V
cable

2pin,connect the micro

J4 /
switch

8pin,connect the internal

J8 /
cable

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 Defibrillator Monitor S Series Service Manual

20pin,connect the power

J12 5V, 12V
supply board

6pin,connect the internal

J13 /
cable

J25 2pin,Connect the cooling fan 12V

J26 2pin,connect the cooling fan 12V

table 5

3.2.5.1 Treatment module pacing board

J1

J3

Figure 12

Socket description working

voltage

J3 12pin, docking high voltage board J11 /

J1 22pin, docking high voltage board J9 /

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 Defibrillator Monitor S Series Service Manual

3.2.5.2 Treatment module main control board

J8
J4

J23
J7

Figure 13

socket description working

voltage

J4 8pin, connecting machine inside /

J7 26pin, docking high voltage Board J8 /

J8 2pin, connected micro switch /

J23 30pin, docking high voltage board J9 /

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 Defibrillator Monitor S Series Service Manual

3.2.5.3 Treatment module ECG board

J3
J2 J7
Figure 14

socket description working

voltage

J2 16pin, docking high voltage board J6 /

J3 6pin, docking high voltage board J7 /

J7 14pin, docking high voltage board J5 /

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 Defibrillator Monitor S Series Service Manual

3.2.5.3 Treatment module high pressure plate

J1

J2

J10

J11
J9

J8
J13

J6 J5

J7
Figure 15

socket description working

voltage

J1 5pin, charging capacitor socket /

J2 4pin, connecting machine inside /

J5 14pin, Treatment ECG socket /

J6 16pin, treatment ECG socket /

J7 8pin, treatment ECG socket /

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 Defibrillator Monitor S Series Service Manual

J8 26pin, treatment main control panel socket /

J9 30pin, treatment main control panel socket /

J10 22pin, treatment pacing plate socket /

J11 12pin, treatment pacing board socket /

J13 6pin, connecting machine inside /

3.2.6 Side panel

Figure 16

socket description working voltage

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 Defibrillator Monitor S Series Service Manual

J1 10pin, SPO2 socket docking /

parameter module

J5 10pin, IBP socket docking /

parameter module

J10 4pin, CO2 Socket docking power 5V

supply

J11 16pin, ECG, TEMP parameter module /

docking socket

table 6

3.2.7 NIBP module

The NIBP module is responsible for blood pressure pumping, pressure detection, and
overvoltage protection.

NIBP module function box Figure:

EEPROM

CPU

COM
NIBP通讯接口
Sensor CUFF

12V LDO POWER

Motor and Air valve

NIBP board

Figure 17

J7
J4 J3 J6

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 Defibrillator Monitor S Series Service Manual

J11

J5
J1

J2

J10

J8

J9
Figure 18

J12

Figure 18

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 Defibrillator Monitor S Series Service Manual

Socket description working voltage

J1 2pin, connecting air pump 12V

J2 4pin, connecting valve 12V

J3 10pin, docking Masimo oximeter 3.3V

J4 10pin, docking Masimo oximeter /

J5 10pin, docking side panel 3.3V

J6 10pin, docking simulation / 3.3V

Digital/Nellcor oximeter

J7 10pin, docking /
analog/digital/Nellcor oximeter

J8 10pin, docking IBP board 5V

J9 10pin, docking IBP board 5V

J10 10pin, docking side panel /

J11 14pin, connecting seven ginseng 5V, 12V

blood pressure board

J12 10pin, connected to ECG board /

table 7

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 Defibrillator Monitor S Series Service Manual

3.2.8 IBP module

J2

J1

Figure19

socket description working voltage

connection IBS socket IBP

J1 5V
socket J8/J9

connection IBS socket IBP

J2 5V
socket J8/J9

table 8

3.2.9 ECG Module

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 Defibrillator Monitor S Series Service Manual

J2

J3

Figure 20

Socket Description Operating Voltage

J2 Connection NIBP Module 6.6V, 5V, 3.3V

J3 Connection Side Panel 5V

table9

3.2.10 SPO2 Module

Three Blood Oxygen Modules: COMEN Blood Oxygen, Masimo Blood Oxygen and Nellcor
Blood Oxygen

The oximeter is mainly used for the collection of blood oxygen signals,
amplification simulation, and conversion and processing of electrical signals.

During the monitoring process, the pulse amplitude of the optical signal also
changes. By calculation, blood oxygen parameters, pulse rate signals and volume waves
can be obtained. This data is then transferred to the main board via a special
communication protocol.

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 Defibrillator Monitor S Series Service Manual

3.2.10.1 COMEN SPO2 Module

J2

J1

Figure 21

serial number description working voltage

J1 2*5pin，SPO2Module 3.3V

Communication Interface

J2 2*4pin，SPO2Module /

Measurement signal input

interface

table 10

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 Defibrillator Monitor S Series Service Manual

3.2.10.2 MASIMO SPO2Module

J1

J2

Figure 22

serial number description working voltage

J1 2*5pin ， SPO2Module 3.3V

Communication Interface

J2 2*5pin ， SPO2Module /
Measurement signal input
interface

table 11

3.2.10.3 NELLCOR SPO2 Module

J1

J2

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 Defibrillator Monitor S Series Service Manual

Figure

serial number description working voltage

J1 2*5pin，SPO2Module 3.3V

Communication Interface

J2 2*4pin ， SPO2Module /
Measurement signal input
interface

table 12

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 Defibrillator Monitor S Series Service Manual

Chapter 4 Troubleshooting

4.1 Introduction

In this chapter, some common faults and troubleshooting methods for defibrillation monitors are
introduced. If your fault is not listed, please contact Comen's after-sales service department.

4.2 Replaceable parts

The main components and components in the monitor PCB are replaceable. If a separate PCB board is
faulty, follow the instructions for “Assemble and Disassemble”, replace it with a brand new PCB board, and
finally check if the monitor's performance is restored. If the problem persists, reinstall the faulty PCB and
continue troubleshooting according to the instructions in this section. You can also send the PCB back to
Comen for repair.

4.3 Checking the monitor

In troubleshooting, some require you to check the hardware version of the monitor and the status of
the instrument.

4.4 Checking the software

In troubleshooting, some require the customer to check the monitor's configuration and software
version.

View the system configuration and software version: After booting the self-test (heep beep), press
Main Menu -> Monitor Maintenance -> Monitor Information to view the system running time, system
software version and hardware version.

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 Defibrillator Monitor S Series Service Manual

Figure 4

4.5 Check the error message prompt

Check the error message prompt area of the monitor before troubleshooting. If there is an error
message, remove the alarm first according to the instruction manual.

4.6 Troubleshooting

4.6.1 Electricity failure

phenomenon reason measure

Check if the dial cable is

Dish is damaged damaged or not connected. Replace
the dial.

The monitor does not The power cable is not Check the connection of the

start connected properly. power cord

battery is low Check battery level

Boot button board is Replace the power button or

damaged keypad

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 Defibrillator Monitor S Series Service Manual

Check the cable from the keypad

to the main control board, and
Poor wiring contact connect the power cable to the main
control board. Check whether the
wiring is damaged.

The keypad is damaged Replace the keypad

AC power module is
Replace the AC power module
damaged

Power board damage Replace the power board

Main board damage Replace the main board

table 1

4.6.2 Display failure

phenomenon reason measure

Check the LCD cable to the main

control board cable, check the power
Poor contact or damage to the board to the main control board
wiring cable, check the button board to the
The monitor works
main control board cable; check the
normally and the display is
wiring and interface for damage.
blank.
Display module damage Replace the display module

main board damage Replace the main board

keyboard damage Replace the keyboard

Check the wiring of the keypad

Broken wiring or poor and the main board; check the LED
The monitor works
normally, the display is contact Screen and main control board
lacking color or the screen is wiring

main board damage Replace the main board

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 Defibrillator Monitor S Series Service Manual

Display module
Replace the display module
damage

Check the wiring of the keypad

Broken wiring or poor
and the main board; check the LED
contact
screen and button board wiring

Display blinks keyboard damage Replace the keyboard

main board damage Replace the main board

Display module
Replace the display module
damage

Check the wiring of the keypad

Broken wiring or poor
and the main board; check the LED
Uneven display contact
screen and button board wiring
brightness
Display module
Replace the display module
damage

table 2

4.6.3 Battery failure

phenomenon reason measure

Reinsert the battery; models with dual

Battery Poor or damaged battery
battery can be charged for another channel;
cannot be and machine connection
replace the battery
charged
Power board damage Replace the power board

Use the universal table to measure the

voltage and observe whether the voltage range is
Battery
normal. For specific voltage values, please consult
cannot be Battery damage
Comen after-sales personnel; reinsert the battery;
powered
models with dual batteries can be exchanged for
another battery channel; replace the battery

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 Defibrillator Monitor S Series Service Manual

Power board damage Replace the power board

table 3

4.6.4 SPO2 failure

phenomen
reason measure
on

SPO2 probe is damaged Replace the SPO2 probe

Check the cable or socket of the

SPO2Module has poor
SPO2Module and the side interface, and
contact with the side
check
interface
New connection
No
Seven ginseng blood Check if the connection between the
SPO2
pressure plate is in poor seven-parameter blood pressure plate
value
contact with SPO2Module and the SPO2Module is normal.

SPO2 Module is
ReplaceSPO2Module
damaged

SPO2Module type is not

Change SPO2 type
set (default analog SPO2)

SPO2 value Probe does not match

Replace the correct type of probe
is incorrect patient type

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The patient's long-term

blood pressure
Measuring SPO2 under normal
measurement or other
conditions
conditions such as shock or

low temperature

SPO2 Moduleis
Replace SPO2 Module
damaged

table 4

4.6.5 NIBP failure

phenomenon reason measure

Blood pressure catheter is not

Check the interface of the catheter
connected well

Check the blood pressure Module and

Uninflatable NIBP Module has poor contact
the air connection at the side interface
with the side panel
and reconnect

NIBP Module is damaged Replace NIBP Module

Check if the patient type is consistent

Repeated
Patient type error with the cuff in the patient type display
inflation (no
area

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blood Accessories leaking Check cuffs, cuffs and connectors

pressure)
The inflation has a numerical value, but

Blood pressure pump leaks the value is very unstable. It can be seen

that the value has a falling condition.

NIBP Module is damaged Replace NIBP Module

Check if the patient type is consistent

Patient type error with the cuff in the patient type display

area

Wrong blood
The cuff is too tight or too loose; the
pressure Blood pressure accessories
cuff is leaking or is damaged; the blood
leak
pressure trachea is leaking

NIBP Module is damaged Replace NIBP Module

table 5

4.6.6 TEMP Module failure

phenomenon reason measure

Please make sure the lead wire is

Lead off
connected.

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The host has no ECG Module's temperature

Replace ECG Module
temperature function is damaged

value display Host display failure Please press 4.6.2 to check and replace

table 6

4.6.7 Key failure

phenomenon reason measure

Check if the connection between the

Connection is damaged or
keypad and the motherboard is
Button does not work bad contact
normal.

Keyboard failure Replace the keyboard

table 7

4.6.8 Software upgrade failure

phenomenon reason measure

main board damage Replace the main board

Program upgrade failed Check the USB flash drive on the

U disk is not inserted
USB

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Download the wrong Please use the correct upgrade

upgrade package package

table 8

4.6.9 Technical alarm information

Please refer to the user's instruction manual.

4.6.10 Electrode piece cable connection failure

phenomenon reason measure

Check if the electrode cable is

Defibrillation (please
connected; check if the inner wire
connect the treatment
Poor contact or is of the high voltage machine is
cable), pacing or AED
damaged connected; check if the treatment
(please insert the
socket is damaged; Replace the
electrode cable)
electrode cable.

table 22

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4.6.11 Treatment Module failure

phenomenon reason measure

Check whether the docking of the

treatment Module and the power

board is well connected; check

Defibrillation Instrument Poor contact or is
whether the power board is
failure damaged
connected to the main control

board; replace the main control

board; Replace the Module.

Check whether the docking plate

Pacemaker Instruments and the high pressure plate are in

malfunction, pacing good condition; check whether

Poor contact or is
abnormal stop or the treatment main control board
damaged
defibrillation/pacing is well connected; Replace the

Instrument failure main control board; Replace

treatment Module

Charging failure or Treating high voltage Replace high voltage board;

charging cancellation board is damaged Replace treatment Module

Poor contact or is Check whether the electrode plate

Timed self-test failed
damaged is homed; check the electrode

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 Defibrillator Monitor S Series Service Manual

cable connection; check the

connection between the

treatment module and the power

board; check the power board and

the main control board; check

whether the high voltage machine

is connected properly; check

whether the charging capacitor is

connected; Replace treatment

Module

Refer to the on-screen

instructions for testing; check if

the electrode plate is homed;

check if the electrode plate cable

The user did not follow
is connected; check if the
the instructions on the
User detection failed connection between the
screen, the contact was
treatment module and the power
bad or damaged
supply board is in place; check the

connection between the power

supply board and the main control

board; Replace Treatment Module

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table 23

Chapter 5 software upgrade

System software upgrade can be achieved through U disk

5.1 Upgrade Preparation

1.Before upgrading, please check the version of the software (for details, please refer to section 4.4).

2.Put the folder on the computer (the folder name is SOFTUPDATE, you can't
change the file name, otherwise you can't complete the upgrade). The whole copy is in the root directory
of the U disk (that is, open the U disk directly)

5.2 System software upgrade

After preparing for the work, perform the following software upgrades:
1) Press the power button and the machine starts:

2) The machine will automatically enter the upgrade interface, please wait for the machine
upgrade to complete:

3) Wait a few minutes to upgrade, the screen appears "system update successed, please
restart", you can reboot.

Caution

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 Please check with Comen after-sales personnel to see if the upgrade software meets your
instrument.

 Do not connect the monitor to the patient during the upgrade.

 The upgrade process will last for 30 seconds - 2 minutes. Please ensure that there is sufficient
battery power or AC power.

 The upgrade of the program can only be operated by professional after-sales personnel.

 Do not remove or insert a USB flash drive while the software is being upgraded.

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Chapter 6 Performance Verification

6.1 NIBP test

6.1.1 NIBP Air leak test

requirements：

 Adult non-invasive blood pressure cuff

 Suitable catheter

 Cylinder

Please follow the steps below to do the performance test:

1) Connect the cuff to the NIBP air vent of the monitor.

2) Wrap the cuff around a suitably sized cylinder.

3) Select [NIBP] in the parameter area, and select [Leakage Detection] in the [NIBP
Settings] menu that pops up.

4) At this time, “leakage detection...” will be displayed below the NIBP parameter area
on the screen, and the table system will start to perform air leak detection.

5) The system is automatically inflated to a pressure of 180 mmHg.

6) After about 20 seconds, the system will automatically open the bleed valve to mark
the completion of the leak measurement.

If there is no prompt information in the NIBP parameter area, the table shows that there
is no air leakage. If “Pump leak...” is displayed, there may be a leak in the gas path. At
this point, the operator should check whether the entire connection is loose. After confirming
that the connection is correct, perform another leak detection. If there is still a fault
indication, please contact the manufacturer for repair.

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Figure 5

6.1.2 NIBP Pressure calibration

requirements：

 T-type interface

 suitable trachea

 ball type air pump

 Metal container: 500 ± 25 ml

 Sphygmomanometer (for reference): use a calibrated pressure gauge with an accuracy

greater than 1mmHg

Please follow the steps below to do the performance test:

1. Connect the monitor, pressure gauge, spherical air pump and metal container
(instead of the cuff) as shown in the figure below。

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Figure 6

2. The pressure gauge reading should be zero before inflation. If it is not zero, open the ball pump valve
so that the entire gas path leads to the atmosphere, and then close the valve after the standard
pressure gauge reads zero.

3. In the [Monitor Maintenance] menu, select [User Maintenance], enter the password and enter the
[User Maintenance] menu, select [NIBP Check], and set the monitor to "Check" mode.。

4. The pressure in the metal container was inflated to 0, 50 and 200 mmHg by a ball type air pump.
The difference between the value of the standard pressure gauge and the pressure indicated by the
monitor should be within 3 mmHg. Otherwise, please contact the Comen service engineer.。

6.2 IBP test

Test requirements：

Invasive blood pressure simulator, IBP accessory.

Please follow the steps below to do the performance test:

1. Connect the invasive pressure simulator and monitor through the accessory, set the
output static pressure of the invasive pressure simulator to 0mmHg (0kPa), change
the current IBP channel pressure name in the monitor to ART and zero, the system
should prompt the school Zero success, and the average pressure value is also shown
as 0 mmHg (0 kPa).

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2. Set the static pressure value of the artificial pressure simulator to 100mmHg, 200mmHg,
dynamic pressure value 120/80mmHg, the pressure display range of the current channel
should be (0~1mmHg, 98~102mmHg, 196~204mmHg, (118~122) / (79 ~ 81) mmHg).

3. Repeat the above steps for IBP channels 2, 3, and 4.

6.3 ECG test

Test requirements:

ECG lead, heart" simulator.

Please follow the steps below to do the performance test:

Use ECG lead and ECG simulator to connect one by one. After the ECG simulator is powered
on, press the “NSR” button of the ECG simulator to observe the HR value of the simulator
screen and the ECG waveform of the monitor. After stabilization, the HR value of the
instrument screen is ±1% or ±1bmp.

6.4 SpO2 test

requirements requirements:

SPO2 probe

Please follow the steps below to do a performance test:

1. Connect the SPO2 probe to the monitor. Set the patient type to adult.

2. Test SPO2 on your finger. (assuming you are in good health)

3. Check the volumetric and pulse rate readings to ensure that the SPO2 value is in the
range of 95%-100%.

4. Remove the SPO2 sensor from your finger and the value and waveform gradually become
zero.

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6.5 TEMP test

requirements requirements:

Constant temperature water bath, standard mercury thermometer with a graduation value of 0.05 °C.

Please follow the steps below to do a performance test:

The standard mercury thermometer with a graduation value of 0.05 ° C and the monitor
body temperature sensor are closely attached together, and the thermostatic water bath
is placed at the same time, and the water temperature of the constant temperature water
bath is adjusted. Compare the measured value of the monitor with the standard thermometer
degree. In order to ensure the reliability of the test, the volume of water is required
to be not less than 2L, the water depth is not less than 10cm, and the water temperature
is uniform after being fully stirred. Using a constant temperature water bath and a
standard thermometer, select the temperature point of 0 ° C, 37 ° C, 50 ° C, the
monitor body temperature probe and thermometer are simultaneously put into the water bath
for testing, the test results should be displayed in the following range: 0 ~ 0.1 ° C,
36.9 ~37.1 ° C, 49.9 ~ 50.1 ° C

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