Manual de Servicio - B3 Comen
Manual de Servicio - B3 Comen
Manual de Servicio - B3 Comen
Service Manual
B3/B6/B8
Neonatal Incubator
Revision History
This manual has a revision number. This revision number changes whenever the manual is
updated due to software or technical specification change. Contents of this manual are subject to
change without prior notice.
Version number: A
Release time: 2019
@ 2012 Factory. All rights reserved.
This manual provides detailed information about the assembling, disassembling, testing and
troubleshooting of the equipment to support effective troubleshooting and repair. It is not
intended to be a comprehensive, in-depth explanation of the product architecture or technical
implementation. Observance of the manual is a prerequisite for proper equipment maintenance
and prevents equipment damage and personnel injury.
This manual is based on the maximum configuration. Therefore, some contents may not apply to
your incubator. If you have any question, please contact our Customer Service Department.
This manual is for biomedical engineers, authorized technicians or service representatives
responsible for troubleshooting, repairing and maintaining the incubator.
Edition: A
Date: 11/2019
Shenzhen Comen Medical Instruments Co., Ltd.
Product Name: Incubator Monitoring System
Models: B3/B6/B8
CE information: CE0197
Registration Address:No.2 of FIYATA Timepiece Building, Nanhuan Avenue, Gongming
Shenzhen Comen Medical Instruments Co., Ltd. (hereinafter referred to as Comen or Comen
Company) owns the copyright of this Service Manual (non-public publication), and has a right to
process it as restricted materials. This Service Manual may serve as references for operation,
maintenance and repair of Comen products. Anybody else has no right to show to people the
contents of the Service Manual.
The Service Manual contains exclusive data under the protection of law of copyright. All rights
reserved. Any individual or organization must not reproduce, amend or translate the any part of
the Service Manual without prior written approval from Comen Company.
Edition number of the Service Manual is subject to upgrade without further notice due to any
changes in software, technical specification or other causes.
The Service Manual is only applicable to the Neonatal monitor system B3/B6/B8 manufactured by
the Comen Company.
II
If the products need to be returned to Comen Company, please follow the following steps:
Acquisition of the right to return the goods:Contact the after-sales department of Comen
Company, tell them the number of the instrument made by Comen; this number was printed on
the equipment nameplate; if this instrument number is not legible, the goods returned shall not
be accepted. Please specify the instrument number and production date, and briefly describe the
reason for returning the goods.
Demo mode:5188
User maintenance: 5188
Factory maintenance:2016
III
Contents
Preface.............................................................................................................................................. II
1. The range of temperature setting should be: air mode is 25℃~39℃, infant mode is 35~
37.5℃(When the temperature is more than 37 ℃, the 37℃ switch should be turned on). ............ 23
2. The time shall not be more than 35min when temperature rises 11℃. ....................................... 23
3.Alarm accuracy and alarm range: Air mode:±1℃ or±2℃ around set value, alarm range23℃~
41℃. Infant mode:±0.5℃ or ±1℃ around set value, alarm range 34℃~38.5℃. ...................... 23
4.7Weight test.......................................................................................................................... 27
4.8Apnea test........................................................................................................................... 28
V
5.1Who Should Perform Repairs ............................................................................................ 35
VI
6.1.2.5 B6/B8 Main bed assembly ................................................................................ 101
VII
Chapter 1 Safety
The product is used in a neonatal or infant care unit to cultivate and monitor neonates or
infants under 2500g at constant temperature and humidity. The product is used for culture. It has
the functions of apnea monitoring, apnea wake-up, temperature monitoring (box temperature and
skin temperature), humidity monitoring in the box, weight measurement, servo oxygen supply and
oxygen concentration monitoring. It is forbidden to use electrodes in areas with inflammation or
ulceration of the skin; it is forbidden to use electrodes in those allergic to conductive media; it is
forbidden to use blood pressure cuffs in areas with inflammation or ulceration of the upper arm
skin; it is forbidden to use blood pressure cuffs in those allergic to rubber materials; it is forbidden
to clamp oxygen saturation probes in the same place for a long time.
This equipment should be maintained by the authorized and qualified engineers. If the
modification and maintenance are not conducted by the personnel authorized by the Our Company,
our company will be not responsible for the safety, reliability and performance of the equipment.
1.1.1.Danger
There are no dangers that refer to the product in general. Specific “Danger” statements may
1.1.2.Warning
Warning
Before using this incubator, read the whole document carefully. An attempt to use
the device without a thorough understanding of how to operate the device may cause
an injury to an infant or the user.
The device can be operated by a person who has received related training with
instructions of qualified medical personnel understanding the risks and advantages
of this type of devices.
This document also provides notes for specific steps.
The device or system must not be placed near other devices or be stacked. If they
must be placed closely or stacked, make sure that they are working properly with
1-1
their current configurations.
Before putting the device into operation, perform the verification procedures
specified in this document. Stop using the device and repair it when the device fails
to pass any part of the verification.
1.1.3.Cautions
Caution
1) To avoid damage to this instrument and guarantee patient safety, please use the accessories
designated in this instruction manual.
2) Please properly install or move this instrument and prevent the instrument from being
damaged due to fall, collision, strong vibration or other external mechanical forces.
3) Before the instrument is switched on, please confirm whether the power supply used meets
the requirements for power supply voltage and frequency designated in the nameplate label
or in the instruction manual of this instrument.
4) When this instrument and its accessories are about to exceed the service life, they must be
5) disposed of according to local relevant laws and regulations or the rules and regulations of
the hospital.
1.1.4.Notes
1-2
Notes
Please install the equipment in a place that is convenient for observation, operation and
maintenance.
This instruction manual introduces the product according to the most complete
configurations. The product you have purchased may not possess some configurations or
functions.
Please place this instruction manual near the instrument for easy and timely reference.
Description Symbol
Symbol on the left side cover of the
bed
humidification stick
tank
indicator light
light
1-3
Symbol of the button for turning
Wind curtain
symbol
bed
(Chinese standard)
Fuse
1-4
Label of the auxiliary power output
O 2 inlet label
label
the handrail
the drawer
Upside symbol
Do not stack
1-5
Symbol for protection from rain
Do notroll
Recycling symbol
Temperature limits
Humidity limits
European Community
1-6
ConformitéEuropéenneCom
93/42/EEC
Equipotential symbol
Protective grounding
or
Consult Instructions for use
1-7
Chapter 2 Warranty and Service
COMENprovides 24 months warranty for the warranted products (main unit) and 6 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.
Details information please refer to COMEN warranty policy.
The warranty does not cover for the situations caused by the following condition:
service people.
♦Malfunction of the instrument or part whose serial number is not legible enough.
3-1
2.3 Service Procedures
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
Once the service department receives the fully filled SCF, our engineer will offer a solution
in three working days. We will follow the case based on the two conditions below:
Within Warranty
After receiving the Return Material Authorization (RMA) form from our service
department, customer sends us the defective parts and informs about the shipment
3-2
tracking number. Then we will dispatch new part(s) to your confirmed address with
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
shipping invoice.
NOTE
Both Return Material Authorization Form and Declaration Form are offered by
The customer is responsible for freight& insurance charges when the equipment is
shipped to COMEN for service, including custom charges. We are responsible for the
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
NOTE
The customer is responsible for any freight& insurance charge for the returned
product.
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 packaging box.
3-3
NOTE
COMEN should not have any obligation to the end-user or customer who returns the
goods without the notification by our service department. The sender takes full
Please describe the returned parts as‘sample of *****’and put the total value on the
Please confirm the information (such as price in invoice, address and other necessary
3-4
Chapter 3 Principle Introduction
J4
B3
J11
J2 J3
#1310
J1
#1403
P10 B11
#822
B10
J4
P P
J3 J10 J7 J18 J9 J5
#1642
#1642
#1822 #1404 2 2
4 4
#871 J1 J2 J3 JR1 P25
#908
P3
B4
P4
P5
P6
P2 JR3 P27
#1643
J10
TB1 #1399 J6 P1 J4 J8 J7 J14 #780 B8
J9
P2 J3 #491 P19
B2
B12
TB1 #1398 J2
J10 B5 J13 #550 B9
J9 J6 #44 P20
J7
#861 #1397
#862
P1
2
B7
P1
P1
P18
P13
P17
P1
P1
P11
P16
P14
P15
No.
10-1
B3 051-001106-00 IBT DC brushless motor
driving board/CM_IBT_BLDCDrive_A
board/CM_IBT_Parameter_A
board/CM_IBT_FlankCheck_A
board/CM_IBT_MotorCheck_A
pack
P5 082-000070-00 Three-wayvalve
/PARKER/ 11-13-4-BE-12F88/991-001110-007
P7 010-000072-00 Microswitch/V-152-1C25
10-2
P11 024-000103-00 Heating rod/M14*1.5-Φ10*124.5
10SS6A-B2BB-QPB
P14 / /
P16 / /
qin/40CP08M1(GP)/8R 2W/OD:φ40MM/height:
10.6MM
Ω resistance/TPE03-01(1002)
/APK/REF:A0916-C05
Table.1
10-3
3.2B6/B8 System Principle Block Diagram
J12 J6 J7 P9
J4
B3
J11
J2 J3
#1310
J1
#1403
P31 B16
#822
J29
#860 J1 B10 J4 #1407 P11
J B1 J3 J6 J5 #1405 P12
B11
B12
8
J4 P P
J3 J10 J7 J18 J9 J5
#1642
#1642
#1822 #1404 2 2
#871 J1 J2 J3 JR1 3P25 3
#908
P3
B4
P4
P5
P6
P13
P14
B8
B9
P2 J2 JR3 P27
J10
#1642
#1162
#1155
#1510
#1393
#863
TB1 #1642 J6
J1 P1 J6 J7
J9
P2 J4 J2 #1347 P28
B15
TB1 #1397 J2 B2
B5 J3 #1154 P29
J7
J5 J3 J4 J1 J8 J1 J5 #491 P30
#834 #1397 #1611 J15
#861 B7
#826
#862
P
2
2
P1
P1
P16
P15
P1
P1
P20
P21
/CM_IBT_BLDCDrive_A
10-4
B7 051-000843-01 Main board/CM_9G45_MAINBOARD_A
/CM_IBT_FlankCheck_A
/CM_BQ80/BQ80A_Pedal_Up_A
/CM_BQ80/BQ80A_Pedal_DOWN_A
/PARKER/ 11-13-4-BE-12F88/991-001110-007
P7 010-000072-00 Micro-switch/V-152-1C25
10-5
P16 024-000095-00 Motor/LA38.A2.4-200-1
10SS6A-B2BB-QPB
P20 / /
P21 / /
/10KΩ resistance/TPE03-01(1002)
/APK/REF:A0916-C05
2W/OD:φ40MM/height:10.6MM
series of tasks including input & output control, data storage and processing,
10-6
display processing, system control, communication management, etc.
1 way humidity
input 18V
2-way oxygen
concentration
connector, 5V
Lithium battery port
11.1V 2200mAh
MCU1debug
port 3.3V
acquisition etc.
mainly used as system power supply, one 12V channel is used as relay / DC
brushless motor power supply, and one step-up and output 12V channel is
Electric actuator
interface
Pedal interface,
Heating/humidifying10-8
open circuit/over current signal;
12V / 5V
IBT power driving board functions:
AC power is input to the IBT power driver board through the filter, and then
3.3.3Main board
10-9
Key board Reserved Alarm lamp
connector,5V C31 port port,5V
Communication
Reserved 7
with control test
inch TTL
board (RS232)
screen port
,12V / 5V
Reserved 7
inch touch
Reserved
screen port
WIFI port
3.3V
Touch screen
port
Reserved
12V/5V port
board,5V
10-10
8 inch TTL screen interface
-7V/4.1V/22V/3.3V
10-11
3.3.3.2 B6/B8Main board
WIFI socket
Printer socket
Key board
port 5V
Serial port&network
port signal,etc.
Alarm lamp
socket
3.3.4Powersupply module
AC input
100~240V~
2.5-1.25A Output:
Output Convection
+18V 16.6A
10-13
Power supply module functions:
The power supply board convert AC power to DC power, supply and transfer
3.3.5Solid relay
For heating control relay, a software algorithm controls the on and off of this
relay, so that the temperature of the incubator reaches the control temperature.
With UL508 rated overload endurance test certification and 100KA cut-off
10-14
2. Humidification solid state relay.
algorithm controls the on and off of this relay, so that the humidify of the
It is with high inrush current rating, available with zero-cross electric start
With UL508 rated overload endurance test certification and ROHS VDE CE
certification.
Control voltage:3~15VDC
Rated load
voltage:12~280VAC
Control input type:AC input
Rated load current: 5A
3.3.6Other boards
10-15
IBT Incubator temperature adapter board functions:
10-16
Accessory interface board functions:
Weighing port.
Camera port.
B6/B8
10-17
B3
Printer port.
C30/C31 port.
10-18
B6/B8
B3
>37℃ button.
Mute key.
AC in place indicator.
Running indicator.
B6/B8
10-19
3.3.7Servo O2 supply assembly
P/N:082-000648-00
P/N: 082-000177-00
Two-position three-way
Low flow proportional
valve(2 inlet 1 output)
valve, 211mA 57ohm
Pressure regulator
(082-000461-00),
preset output pressure
155±5KPa
P/N: Silencer
082-000008-00 P/N:041-003896-0
10-20
2. B6/B8 servo O2 supply assembly.
Silencer
P/N:
P/N:082-000177-00 041-003896-00
Low flow proportional +041-003897-00
valve, 211mA 57ohm +045-000656-00
10-21
3.3.8Humidification assembly
P/N:010-000054-00
Temperature control switch,
For over-temperature protection
of humidifying components.
P/N:010-000094-00
P/N:024-000103-00
Temperature control
Heating rod
switch,
For judgment low
water level of water
tank.
P/N:010-000072-00
Micro-switch,For water
tank in place detection.
10-22
Chapter 4 Performance Tests
4.1Temperature Test
Requirements:
1. The range of temperature setting should be: air mode is 25℃~39℃, infant
mode is 35~37.5℃(When the temperature is more than 37℃ , the 37℃ switch
2. The time shall not be more than 35min when temperature rises 11℃.
3.Alarm accuracy and alarm range: Air mode:±1℃ or±2℃ around set value,
range 34℃~38.5℃.
Test method:
1.Air mode setting 25℃ ~39℃, temperature can be set within the range; infant
mode setting
2.It shall not be more than 35min when rises 11℃ at any setting temperature.
3.Air mode set to 32℃, test if there is audio, visual and prompt alarm on
30℃and 34℃; infant mode set to 36℃, test if there is audio, visual and prompt
10-23
4.1.2Temperature stability test
Requirements:
Control temperature at 36℃, test at least 1h, the difference between the average
Test method:
upper central place, other 4 points should place at other 4 location points, keep
15min after temperature reaches to 36℃, record each point temperature in 1hour,
10-24
4.2Humidification test
Requirements:
Humidification time should less than 50min (in the condition of indoor
temperature is 25℃±2℃, relative humidity is 40% ±10% ,to reach 36℃ control
humidity).
Test method:
Requirements:
2. Control errors should be±10% when humidity is lower than 85%, and it is not
3. It should alarm with audible and visual when the tank lack of water.
Test method:
10-25
1. Turn on the incubator,and set the humidity to 60% ,75% and 90% in turn, and
read the humidity value on incubator after 20mins, at 60% and 75%, the actual
measured value is not lower than 75% when the set value is 90%.
2. It alarms with audible and visual when an empty water tank is installed.
Requirement:
Test method:
Requirement:
Air mode: the difference between incubator average temperature and control
Test method:
10-26
4.5Air flow velocity control test
Requirement:
The air velocity of upper bed should less than 0.2m/s when normally working.
Test method:
1. Place air velocity transducer at upper center 10cm position of 4 areas formed
Requirements:
Test method:
Click “bed tilt”at the lower menu bar of display screen,then click tilt button, the
4.7Weight test
Requirements:
Resolution: 1g.
10-27
Test method:
1. Before weighting, just keep mattress on the scale, operate as the screen display
prompt, place 3 weights(each with 100g) about 10cm on either side of the center
point.
4.8Apnea test
Requirement:
Test method:
Requirement:
Test method:
1. Start the incubator, turn on bed height adjust function button, it is normally up
10-28
and down by click touch screen.
3. When turn off bed height adjust function, touch screen and foot pedal would
4.10ECG test
Tool required:
1. Connect the patient simulator with the ECG module using an ECG cable.
2. Set the patient simulator as follows: ECG sinus rhythm, HR=80 bpm with the
amplitudes 1mV.
3. Check the ECG waves are displayed correctly without noise and the
80 ± 1 bpm.
4. Disconnect each of the leads in turn and observe the corresponding lead off
5. Set that the simulator outputs paced signals and set [PACE] to [ON] on the
monitor’s patient manage interface. Check the pace pulse marks on the
monitor screen.
10-29
4.11NIBP test
Tools required:
Appropriate tubing
Cylinder
2. Connect the NIBP cuff with the NIBP socket on the monitor.
5. The cuff automatically deflates after 20s, which means NIBP leakage test is
completed.
10-30
indicates that the system may have a leakage. In this case, check if all
connections are good and the cuff and tubing have no leakage. Perform the
test again after making sure all connections are good and the cuff and tubing
have no leakage.
1. Raise the pressure in the rigid vessel to 250 mmHg with the balloon pump.
Then, wait for 5 seconds to let the measured values becoming stable.
2. Record the current pressure value and meanwhile use a time counter to count
3. Compare the two values and make sure the difference should not be greater
than 5 mmHg.
Tools required:
T-shape connector
Appropriate tubing
Balloon pump
mmHg)
10-31
2. Before inflation, the reading of the manometer should be 0. If not, open the
balloon pump to let the whole airway open to the atmosphere. Close the
3. Check the manometer values and the monitor values. Both should be
0mmHg.
4. Set [NIBP Pressure] to 150 mmHg in the [NIBP Measurement Circuit]. Raise
150 mmHg. After the pressure value is stabilized, select the[Calibrate] button
to start a calibration.
and raise the pressure to 350 mmHg. After the pressure value is stabilized,
6. Set the patient type to [Neonate] in the [Overpressure Protection Circuit], and
165 mmHg. After the pressure value is stabilized, select [Calibrate] to start a
calibration.
10-32
All calibration results are displayed in the [Calibrate NIBP] menu. If the
calibration fails, check the test system for leakage and perform another
calibration.
4.12SPO2 test
1. Connect SpO2 sensor to the SpO2 connector of the mini unit. Measure SpO2
2. Check the PLETH wave and PR reading on the screen and make sure that the
3. Remove the SpO2 sensor from foot and make sure that an alarm of SpO2
Tools required:
T-shape connector
Tubing
10-33
2. Wait until the CO2 module warm up is finished, and check the airway for
leakage and perform a leakage test as well to make sure the airway has no
leakage.
5. Open the relief valve to vent standard CO2 and make sure that there is an
6. Check the realtime CO2 value is within 6±0.05% in the [zero CO2] menu.
10-34
Chapter5Disassemble the Incubator
should open the monitor housing, remove and replace components or make
adjustments. If your medical facility does not have qualified service personnel,
Cautions
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 with
power applied to the instrument. Failure to adhere to this warning could cause serious
injury or death
Tools required:
Screwdrivers
Cleaning Agent
Tweezer
10-35
Fixed wrench
Inner hexagon
screws;
combination screws;
10-36
4. Remove the battery, unplug battery cable and unscrew 2 PM 3*8MM
combination screws;
10-37
5. Remove the power driving board, unplug 9 cables and unscrew 6 PM
6. Remove power supply board. Make sure 2 red cables connect to upper
10-38
position, and 2 black cables connect to lower position.
10-39
10-40
6. Remove solid state relay, unscrew 2 PM 4*8MM combination screws and
Note that the red cable is connected to No.3 position, it is positive pole, No.4
position is negative pole connecting with black cable. No.&No.2 cable can be
mixed use.
10-41
7. Unscrew 6 screws to remove the electronic box cover.
8.remove 1 screw of IBP signal box detection connection cable, then remove
10-42
5.2.2 Disassembling the data collection box
1.remove sampling box by press these 2 button, then remove the black wire
protection sleeve.
10-43
2.remove 4 screws and 2 O2 sensors.
10-44
3.Remove parameter connection board of box temperature, lower buckle
10-45
5.2.3 Removing the LCD display screen
10-46
4.remove LCD screen connection board.
10-47
5.remove 4 screws to get off LCD display screen assembly.
10-48
6.remove 4 screws to remove the screen rear cover.
10-49
7.Unscrew 4 screws to remove metal plate.
10-50
9.Unscrew 4 screws to remove interface board.
10-51
10.Unscrew 8 screws to remove LCD screen.
10-52
11.Unscrew 5 screws to remove key board, unscrew 2screws to remove alarm
10-53
10-54
5.2.4 Disassembling the bed
10-55
3.Remove X-ray tray.
4. Remove tilt bed plate. One hand press the front white button inward, and
another hand press side button inward to remove tilt bed plate.
10-56
Elastic
Mattress
Transparent
Weighing plate&X-ray
Tilt plate
10-57
5. Remove bed bath.
10-58
7. Remove both side transparent double doors.
10-59
8. Remove 3 screws, then use fingers to drag out the 4 sides plastic covers.
10-60
10-61
5.2.5 Remove humidity assembly
1. Remove 4 cables .
2. Remove the water tank, use fingers to drug this position, then pressing inward
by left thumb&index finger, and right hand hold the tank to drug it down;
10-62
3.Remove filter.
10-63
4.Unscrew 2 screws near the water tank, and 1 nut to get out the humidity
assembly.
10-64
10-65
5.2.6 Remove heating rod
1.Remove fan.
10-66
3.Remove metal plate.Unscrew 2 screws of both side.
10-67
4.Unscrew 8 screws.
5.Unscrew 6 screws.
10-68
10-69
6.Remove the split washer ,then push the metal axis to remove ball head.
10-70
8.Unscrew this 2 screws of both side, then can get out heating rod.
10-71
5.3B3 disassemble
10-72
2.Unscrew 4 PM 3*8MM combination screws to remove power socket support.
3. Unscrew 12 screws to remove electronic box side panel and rear cover.
10-73
4. Remove head ball.
10-74
6. Unscrew 4 screws as below.
7. Drag out the power driving board then remove 7 cables to remove power
driving board.
10-75
8. Drag out the control detection board then remove 4 cables to remove control
detection board.
10-76
9. Unscrew 2 screws to remove battery, and unscrew 2 screws to remove solid
relay.
10-77
5.3.2Disassemble data collection box and display screen
10-78
2.Take off the oxygen battery and unscrew 4 PM 3*6MM screws.
10-79
Humiditydetectionboard
Temp
buckle
buckle
2.Drag out the black protection sleeve and unplug 5 cables to remove parameter
board.
10-80
3.Remove the display screen as below.
10-81
4.Unscrew 4 screws of display screen.
10-82
5.Unscrew 2 screws to remove alarm lamp board;
lamshade
10-83
5.3.3 Remove bed assembly
1.Unscrew 2 screws
2.Remove humidity tank and cotton filter. use fingers to drag this position, then
pressing inward by left thumb&index finger, and right hand hold the tank to drug
it down.
10-84
pressing inward
10-85
4.Unscrew 3 screws near the humidifier assembly to remove humidifier
assembly.
10-86
2.Remove both side 4 screws to remove storage box.
3.Unscrew 4 screws.
10-87
3.Disconnect 110 temperature control switch connection cable of both side.
4.Unscrew 2 screws of both side then disconnect heating rod cable in the bottom
of the bed.
10-88
5.Unscrew 4 KM3*6MM screws to remove the motor and motor support.
10-89
10-90
Chapter 6 Parts
Number
assembly
6 Base assembly 1
10-91
6.1.1.1 B3 transparent cover assembly
Number
1 Transparent cover 1
2 Medial plate 2
4 Sampling box 1
10-92
6.1.1.2 B3 Storage box assembly
Number
1 Storage box 1
2 Guide rail 2
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Sequenc Part number Name Quantity
Number
4 Double castor 4
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Sequence Part number Name Quantity
Number
1 Display assembly 1
2 Display support 1
6 Air cavity 1
7 Bed assembly 1
8 Water tank 1
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Sequenc Part number Name Quantity
Number
pre-tightening ring
cover
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9 010-000072-00 Micro Switch 1
lower bracket
silicone
sleeve
sleeve(silk screen)
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Sequenc Part number Name Quantity
Number
3 Base assembly 1
4 Transparent assembly 1
Number
1 Storage box 1
2 Guide rail 2
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6.1.2.2 B6/B8 Transparent cover assembly
Number
1 Transparent cover 1
2 Medial plate 1
4 Sampling box 1
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Sequence Part number Name Quantity
Number
1 Display assembly 1
3 C31 unit 1
4 Printer 1
5 Tray assembly 1
6 Infusion rod 1
7 Column 2
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6.1.2.4 B6/B8 Base assembly
Number
1 Lift cover 1
2 Lift 1
3 Base 1
5 Double caster 4
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Sequence Part number Name Quantity
Number
1 Mattress component 1
4 Air cavity 1
8 Water tank 1
9 Bed assembly 1
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Sequence Part number Name Quantity
Number
cover
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9 010-000072-00 Micro-switch 1
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Chapter7Calibration
After the maintenance of the equipment or the replacement of the components, all the tests in
7.1 Calibration
In the boot state, select [device maintenance ]> input maintenance password
5188,enter [device maintenance interface], click touch screen button, enter the
calibration interface, click the 5 icon " " displayed on the screen for calibration.
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7.1.2Weighing calibration & weigh Infant
An infant must be placed at the center of the bed. Do not place toys or other
objects on the walls. Fasten all leads, intravenous injection hoses, and ventilator
hoses. Tuck the blanket under the mattress but not the weight platform.
(1) Choose Incubator Setup>Weigh Infant in the menu bar. The screen as
operation does not respond, and the prompt is: “please access the scale”.
(2) Tap Start to start a countdown. If no medical personnel operate the device,
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(3) Zero the reading of the electronic scale. The device displays the message
"Please pick up the infant". Lift the infantalong with the hoses and cables
connected to the infant. Make sure that the infant's arms, legs, blanket, and
(4) If no medical personnel operate the device, the screen displays the message
"Please put down the infant". Put the infant back onto the mattress and hold
the cables and hoses connected to the infant with your hands. The electronic
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Attention
If you do not put down the infant after the screen displays the message "Please put
The electronic scale weighs any objects on the weighing platform. Therefore, if you
hold the cables and hoses connected to the infant, the infant's weight displayed
7.1.3O2 calibration
2.Connect O2 supply gas source, make sure the gas pressure is within 280Kpa to
600Kpa.
3.Take off 2 O2 sensors from data collection box, then install to O2 calibration
4.On display screen, click [O2 concentration setting] menu, select [oxygen
concentration calibration switch], confirm that the switch is in the [on] state, and
click to select [probe 1 (or 2) calibration]. At this time, the system calibration is
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performed automatically. The system automatically performs a 21% oxygen
calibration after success. (The two probes must be calibrated separately in order.)
failed] prompt is displayed. At this time, you need to confirm whether the above
Chapter8Software upgrade
8.1 Tools
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USB-stick 8 GB(recommend).
1.Before software upgrade, please check software version and record it to make
sure you are able torevert back in case the failure of software upgrade.
root directory in USB-Stick, do notchange the folder name or the file name(s) in
1. Decompress the software file COMEN send to you, drag the SOFTUPDATE
file to your 8GB U disk. Make sure the u disk is 32 fat format and there is
2. Check that SOFTUPDATE file with one document named StartupBg.bmp, and
3. Plug in U disk to the incubator USB socket( at the rear of the display screen),
then turn on the machine, it will automatically upgrade, after around 3 mins, it
will show succeed on the screen. That means the SOFTUPDATE program file(4
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into the machine.
5. Turn on the machine, when the screen enter to main interface, please plug in
mainUpdate and then press yes>>Wait about 20s, after that turn off the machine
and remove the U disk. This step is used to insert StartupBg.bmp file.
setup>>Info.
“IBT_CTL_48.hex” to MCU2 chip. The two files are all “.hex” format.
2.Prepare one USB to RS232 cable, the COM port of the cable uses a 232 to 3.3v
Note: USB convert to 232 cable need to install a driver, the driver file is
COMEN.
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4.Upgrade steps.
Connect down load cable to USB port and J4 port of control&detection board.
4.2 Open assist software, click search serial port, it will automatically connect
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4.5 Press machine start key, then click start programming key on assist software,
it will automatically start down load program, after that, program will be inserted
to MCU1 chip.
4.6 Insert program “IBT_CTL_48.hex” to MCU2 chip, down load cable connect
J10, then short connect J6, the same way as insert program to MCU1.
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Chapter9Trouble Shooting
9.1 Introduction
In this chapter, Neonatal incubator problems are listed along with possible causes
and recommended corrective actions. Refer to the tables to check the incubator,
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
After-sale Dept.
Printed circuit boards (PCBs), major parts and components in the patient monitor
are replaceable. Once youisolate a PCB you suspect defective, follow the
good one and check that the trouble disappears or the incubator passes all
performance tests. If the trouble remains, exchange the replacement PCB with
Some troubleshooting tasks may require you to identify the hardware version and
Some troubleshooting tasks may require you to identify the configuration and
White screen, splash screen, color Main control board abnormal 1. Restart the machine
abnormality 2. Return to the manufacturer to
repair the main control board
The connection line of LCD or Check and ensure the LCD is
mainboard is loose connected correctly and reliably
LCD screen problem Return to the manufacturer to
replace LCD screen
Alarm display on the screen, there is The speaker connection is Check and make sure the speaker
light alarm but no sound loose, unconnected or cables are connected correctly and
connected incorrectly reliably
Speaker damage Return to the manufacturer to
repair the speaker
Main control board audio Return to the manufacturer to
circuit damage or flash repair the main control board
memory damage
The alarm is displayed on the screen. Disconnect from the alarm Check the connection line of the
There is a sound alarm but no light lamp alarm lamp
alarm Alarm lamp damaged Return to the manufacturer to
repair alarm lamp board
Key board abnormality Return to the manufacturer to
repair the keypad
Unable to The AC indicator Built-in battery capacity is Plug in and switch on
switch is off insufficient
machine AC indicator light The ship type switch Ensure the ship type switch
is on connection is not connected connection is connected normally
Abnormal mechanical and Return to manufacturer to repair
electrical circuit the control inspection board
Mute button The display screen Key, shuttle failure Return to the manufacturer to
standby, no does not alarm repair the keypad
response to “press the key
press or shuttle board”
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knob The display screen Communication between key 1.Check to make sure
has the alarm board and main control board communication line between the
“keypad failure” has abnormality keypad and main control board is
correct and reliable
2.Return to the factory to repair
the keypad
The touch The backup buzzer Touch screen connection is Check and make sure the touch
screen doesn’t has no alarm, the loose screen connection is normal and
response to screen response to reliable
touch button operations Touch screen failure partly 1.Calibrate the touch screen
failure 2.Return to factory for repairing
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parameter acquisition circuit control inspection board is normal
abnormality 3.Return to the manufacture to
maintain control inspection board.
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