COMPACT 9

SERVICE MANUAL
Version 1.1

www.medical-econet.com
 Service Manual of COMPACT 9

Revision History
Edition Date Page Comment

Revision A. 2013-07-24 Initial release

Ver. 1.0 2015-01-21 All Upgrade

Ver. 1.1 2017-01-04 108 Battery changed.

Ver. 1.1 2017-01-04 112, NIBP cuff changed.

114

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Table of Contents
Section 1 General Information .................................................................................................. 5
1-1. Introduction................................................................................................................ 5
1-2. Features of the equipment........................................................................................ 5
1-3. Equipment description .............................................................................................. 6
1-4. System installation ................................................................................................... 13
1-5. Terms of warranty .................................................................................................... 15
1-6. Specification ............................................................................................................ 16
Section 2 Troubleshooting ....................................................................................................... 21
2-1. Introduction.............................................................................................................. 21
2-2. Trouble Shooting Guide .......................................................................................... 22
Section 3 Technical Description.............................................................................................. 37
3-1. Introduction.............................................................................................................. 37
3-2. COMPACT 9 Hardware Overview........................................................................... 37
3-3. Power Supply ........................................................................................................... 38
3-4. Main digital Board ................................................................................................... 40
3-5. Analog1 Board......................................................................................................... 41
3-6. Analog2 Board......................................................................................................... 42
3-7. Analog3 Board......................................................................................................... 43
3-8. Noninvasive Blood Pressure Assembly .................................................................. 43
Section 4 Check Out ............................................................................................................... 44
4-1. Visual Inspection ..................................................................................................... 45
4-2. Cleaning................................................................................................................... 45
4-3. Battery Maintenance .............................................................................................. 46
4-4. Electrical Safety Tests .............................................................................................. 48
4-5. ECG Test ................................................................................................................... 57
4-6. Respiration Test ........................................................................................................ 59
4-7. Temperature Test ..................................................................................................... 60
4-8. Cardiac Output Test (option) .................................................................................. 60
4-9. Invasive Blood Pressure Test (option)..................................................................... 61
4-10. Pulse Oximetry Test for SpO2 Oximeter ................................................................. 62
4-11. Noninvasive Blood Pressure Test ............................................................................ 63
4-12. NIBP Calibration ....................................................................................................... 64
4-13. ECG Calibration ....................................................................................................... 66
4-14. IBP Calibration ......................................................................................................... 66
4-15. End tidal CO2 Test (Option) .................................................................................... 66

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4-16. Battery Test ............................................................................................................... 66

4-17. Graph speed............................................................................................................ 67
4-18. Speaker Test............................................................................................................. 67
4-19. Data Acquisition Test ............................................................................................... 67
4-20. Checkout Procedure Completion.......................................................................... 73
Section 5 Assemblies and Kits ................................................................................................. 74
5-1. Introduction.............................................................................................................. 74
5-2. Replacing Parts ........................................................................................................ 74
Section 6 Disassembly and Reassembly................................................................................. 82
6-1. Introduction.............................................................................................................. 82
6-2. How to Use this Chapter .......................................................................................... 82
6-3. Tools Required ......................................................................................................... 82
6-4. Screws Used ............................................................................................................. 83
6-5. Disassembly ............................................................................................................. 84
6-6. Reassembly............................................................................................................ 107
Section 7 Replaceable Parts List and Accessory................................................................. 108
7-1. Replaceable Part List............................................................................................. 108
7-2. Accessory .............................................................................................................. 116
Section 8 Connector Pin Assignment ................................................................................... 124
8-1. Connector information .......................................................................................... 124
8-2. Harness interfaces ................................................................................................. 126
Section 9 PCB Part disposition ............................................................................................... 135
9-1. Main Digital Board ................................................................................................. 135
9-2. Analog1 Board....................................................................................................... 136
9-3. Analog2 Board-7ch ............................................................................................... 137
9-4. Analog2 Board-12ch ............................................................................................. 138
9-5. Analog3 Board....................................................................................................... 139
9-6. Power Board........................................................................................................... 141
9-7. Key I/F Board ......................................................................................................... 142
9-8. USB/SDcard I/F Board ............................................................................................ 143
9-9. Connector Signal Board........................................................................................ 144
9-10. I/F Board ................................................................................................................. 145
9-11. Analog3 connector Board .................................................................................... 146
9-12. Printer Board........................................................................................................... 147
9-13. Multi-ECG-connector Board ................................................................................. 148
9-14. Connector Board ................................................................................................... 149
9-15. Alarm LED Board .................................................................................................... 150

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Section 1 General Information

1-1. Introduction
This manual tells you how to install, service and repair an COMPACT 9 patient monitor. It
describes the system hardware and software, and tells you how to test the system and
diagnose operating and service problems. It also tells you what upgrade paths are
available and how to follow them.
The features available on the monitor you are installing or servicing depend on which
options have been purchased. If your monitor does not have a described parameter, you
can skip that part of the instruction and move on to the next point.

1-2. Features of the equipment

COMPACT 9 is a small-size multifunctional monitoring equipment for a patient designed to an easy
usage during movement. It features DC power supply (Bridgepower,MW160,DC 18V,2.5A) as well
as installing its handle to the patient’s bed. The equipment also measures major parameters such
as ECG, respiration rate, SpO2, pulse rate, NIBP, IBP, EtCO2, and temperature, displaying them on
a 12.1-inch color LCD screen. It also enables users to check waves and parameters and other vital
signs of a patient via the 58mm thermal printer and monitor the patient by the remote-controlled
alarm system. It also enables to build a central monitoring system by linking devices used for
separate patients so that one can monitor several patients at a time. USB/SDCARD slot is used to
copy the stored trend data or read the patient id using a barcode reader. Space to insert an additional
battery to use if you need to maintain the battery for an extended period of time, an extra battery

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1-3. Equipment description

① Patient monitor system main body(1)

② User’s Manual (1)
③ NIBP Cuff and Hose (1)
④ ECG Lead Cable (1)
⑤ SpO2 Probe ( 1 )
⑥ Thermal Parper roll
⑦ Power Adaptor ( 1 )
⑧ Power cord (1)

▣ Front view

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① Alarm Lamp Handle

② Silence Alarm Key

③ Printer Go/Stop Key

④ NIBP Go/Stop Key

⑤ Function Key

⑥Trim Knob Control Key

⑦Power Key

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▣ Rear view

① Alarm Lamp
② Nurse Call
③ RJ45 LAN Port
④ VGA Output
⑤ DC Power Input Port
⑥Wireless LAN Power
⑦Protective Ground Terminal

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▣ Left side view

PRINTER

USB / SDCARD
SLOT

EXTENSION
BATTERY SLOT

① Printer
② USB/SD Card Slot
③ Extension Battery Slot

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▣ Right side view

CSM
CONNECTOR

ECG
CONNECTOR

NIBP
CONNECTOR

SpO2
CONNECTOR

TEMPERATURE
CONNECTOR

EtCO2
CONNECTOR

IBP
CONNECTOR

C.O.
CONNECTOR

① CSM Connector
② ECG Connector
③ NIBP Connector
④ SpO2 Connector
⑤ Temperature Connector
⑥ EtCO2 Connector
⑦ IBP Connector
⑧ C.O. Coonector

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▣ Key Overlay label

▣ Buttons

Alarm : Change a mode of alarm awareness and display

①
window message.

② Print out the data in a selected form after recording

10sec data or 20sec data and signaling them.

③ Nibp Measurement start/stop

④ Change a view of the graphic display window to initial

main window.

⑥ Device Power On/Off

▣ Indicator Lights

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Show the state of connection with AC adapter and a green

⑦
light indicator when plugging AC adapter into device

A light indicator lets you know that there is battery and

show your current battery charging status. A red light
⑧ indicator lets you know that the battery is charging and
a green light indicator lets you know the batter is fully
charged

▣ Rotary Key

Used when navigating or selecting menu items

⑤ (Same functionalities can be achieved by touching
menu items on the screen)

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1-4. System installation

Installation precautions
When installing COMPACT 9 system, take the following precautions.
- The equipment should be operated within 10∼40℃ temperature and
30∼85％humidity.
- Check the power cord connection and probe should be handled with care.
- Do not plug several power cords in one electric outlet.
- Main unit should be installed on an even, level place.
- Check that the equipment is properly grounded to avoid noise.
- The entire system settings are stored on the internal memory even when system
power is turned off and on again
- Avoid excessive shock or vibration that could result in equipment damage.
- Avoid using in the vicinity of dust and flammable material.

Power Adapter connection

The equipment operates when the power adaptor end connect into the COMPACT 9
power adptor. Replace adapter of the equipment if power is not turned on despite that
power adpator is connected and battery power is in normal condition. Contact service
dept. of Medical ECONET Co., Ltd. if the equipment is not operated after replacing adaptor.

Product information
Manufacture : Bridgepower corp.
Model Name: BPM050S18F02
Input power: 100~240V 1.2A
Output power: 18V ,3.2A

Caution

This equipment must only be connected to a supply mains with protected earth.
Noise or distortion of signals using non-off-the-shelf products rather than adapters supplied by
our company may be caused. Also dangerous to the safety related isolation and protection by
using the adapter supplied by our company in order to give

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Patient cable connection

- Module connection when connecting a 12-channel electrocardiograph to the
equipment: Connect the Patient Cable to the patient cable connection terminal at
the back of the main body and connect the limb electrodes to the terminals of
Patient Cable RL(N), LL(F), RA(R), LA(L), and chest electrodes to the terminals of
Patient Cable V1(C1), V2(C2), V3(C3), V4(C4), V5(C5), and V6(C6).

Recording paper installation

- Printer door open if printer pull cover at the left side of COMPACT 9 is pushed in the right.
Place the recording paper with the signal-recording side up and push back to close.

1-5. General Requirements for a System

After installation or subsequent modification, a system must comply with the requirements
of the system standard IEC/EN 60601-1-1. Compliance is checked by inspection, testing or
analysis, as specified in the IEC/EN 60601-1-1 or in this book.
Medical electrical equipment must comply with the requirements of the general standard
IEC/EN 60601-1, its relevant particular standards and specific national deviations. Non-
medical electrical equipment shall comply with IEC safety standards that are relevant to
that equipment.
Relevant standards for some non-medical electrical equipment may have limits for
equipment leakage currents higher than required by the standard IEC/EN 60601-1-1. These
higher limits are acceptable only outside the patient environment. It is essential to reduce
equipment leakage currents to values specified in IEC 60601-1 when non-medical
electrical equipment is to be used within the patient environment.

This illustration shows a system where both the medical electrical equipment and thenon-
medical electrical equipment are situated at the patient’s bedside.
For any IT equipment (IEC60950) operated in patient vicinity ensure that the equipment
leakage current does not exceed the limits described in IEC 60601-1. Use a separation
device to ensure compliance. After installation of IT equipment in patient vicinity, an

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enclosure leakage current test is required.

1-6. Terms of warranty
- This product is manufactured and passed through strict quality control and
thorough inspection. Compensation standard concerning repair, replacement,
refund of the product complies with “Consumer’s protection law” noticed by
ministry of finance and economy.
- COMPACT 9 is warranted by Medical ECONET Co., Ltd. to be free from defects in
material and workmanship for one year (two years in Europe) from date of purchase.
- Warranty repair or replacement will be made by Medical ECONET Service Center
at no charge for warranty period if properly used under normal condition in
accordance with the instructions for use.
- In the event of a malfunction or failure during warranty period, customer should
inform Medical ECONET Co., Ltd. of the model name, serial number, date of
purchase and explanation of failure of the defective equipment.

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1-7. Specification
Display, Resolution 12.1” color TFT, 800 x 600 pixels
Dimension, Weight 322(W) x 250(H) x 224.8(D) mm, Approx. 4.5kg
Parameter ECG, Heart Rate, Respiration Rate, SpO2, Pulse Rate, Systolic BP,
Diastolic BP, Mean BP, 2 x Temperature, 2 x IBP, EtCO2, FiCO2,
Airway Respiration Rate
Trace 6 waveforms : 2*ECG, SpO2, RR or EtCO2, 2*IBP
Sweep speed : 6.25, 12.5, 25, 50 mm/sec
Indicators Categorized alarms (3 priority levels), Visual alarm lamp handle
QRS beep & SpO2 pulse beep, Percent(%) SpO2 pitch tone
Battery status, External power LED, Touch screen, Rotary knob
Interfaces DC input connector : 12 to 18VDC, 2.5A
Defibrillator Sync. Output :
- Signal Level : 0 to 5V pulse
- Pulse width : 100 ± 10 ms
LAN digital output for transferring data, Nurse call system
connection -0.3A at 125VAC – 1A at 24VDC
DC output : 5VDC, 1A Max
USB Barcode Scanner, USB & SD memory data storage
Battery Rechargeable Li-ion battery, 1hours for continuous working
Thermal Printer Speed : 25, 50mm/sec, Paper width : 58mm
(option)
Data Storage 168hours trends, 20cases of 10sec alarm waveform
Language English, French, Spanish, Italian, Germany, Chinese, Russian,
Czech, Bulgarian, Portuguese, Romanian, Hungarian, Turkish,
Polish,Korean
ECG Performance
Lead type 3-lead, 5-lead, 10-lead(option)
Lead Selection 3-lead : I, II, III
5-lead : I, II, III, aVR, aVL, aVF, V
10-lead: I, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6
ECG waveforms 3-lead : 1 channel
5-lead : 2/7 channels
10-lead: 12 channels
Heart Rate Range Adult : 30 – 300 bpm

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Neonate/Pediatric : 30 – 350 bpm

Heart Rate Accuracy ±1bpm or ±1%, whichever is greater

Sweep speed 6.25, 12.5, 25, 50 mm/sec
Filter -Diagnosis : 0.05Hz - 150Hz -Monitoring : 0.5 – 40 Hz
-Moderate: 0.5 – 25Hz -Maximum : 5 – 25 Hz
S-T segment -2.0 to 2.0 mV
detection range
Arrhythmia analysis ASYSTOLE,VTACH,VFIB,BIGEMINY,ACCVENT, COUPLET,IRREGULAR,
PAUSE,PVC,RONT,TRIGEMINY,VBRADY, SHORTRUN
Pacemaker Detection Indicator on waveform display (user selectable)
Mode
Protection Against electrosurgical interference and defibrillation
Respiration Performance
Method Thoracic impedance
Channel selection RA-LA or RA-LL
Measurement range 5 – 120 Breath per minute
Accuracy ±1 Breath per minute
Apnea alarm Yes
SpO2 Performance
Saturation range 0 to 100%
Saturation accuracy 70 to 100% ±2 digits
0 to 69% unspecified
Pulse rate range 30 to 254 bpm
Pulse rate accuracy ±2 bpm
MASIMO SpO2 Performance (Option)
Saturation range 0 ~ 100%
Saturation accuracy 70 to 100 % ( ≤ 2% ; No motion , ≤ 3% ; motion )
50 to 69 % ≤ 3 %
1 to 49 % ≤ 4 %
Pulse rate range 25 to 240 bpm
Pulse rate accuracy ≤ 3 bpm ; No motion , ≤ 5 bpm ; motion
Perfusion Index range 0.02% ~ 20.0%
Perfusion Index 0.1% to 20.0% (± 10% of Perfusion Index)
accuracy

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NIBP Performance
Method Oscillometry with linear deflation
Operation Mode Manual/Automatic/Continuous
Measurement range Adult Pressure : 20 to 260 mmHg
Pediatric Pressure : 20 to 160 mmHg
Neonate Pressure : 20 to 130 mmHg
Accuracy Meets accuracy requirements of ANSI/AAMI SP10:1992 and 2002

Temperature Performance
Measurement range 15 to 45℃ (59 to 113℉)
Accuracy ±1℃
Compatibility YSI Series 400 temperature probes

IBP Performance (Option)

Channels 2
Measurement range -50 to 300mmHg
Accuracy <100mmHg : ±1mmHg
>=100mmHg : ±1% of reading
Pulse rate 0 to 300bpm
measurement range
Zero balancing Range : ±200mmHg
Accuracy : ±1mmHg
Drift : ±1mmHg over 24hours
Transducer 5µV/mmHg
sensitivity
Pulse rate 0 to 300bpm
measurement range
Sidestream CO2 (Option)
Measurement range 0 to 150 mmHg, 0 to 19%
Accuracy 0-40mmHg ±2 mmHg,
41-70mmHg ±5% of reading
71-100mmHg ±8% of reading,
101-150mmHg ±10% of reading
Respiration rate 2 to 150 breath per minute
Respiration accuracy ±1breath per minute

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Mainstream CO2 (Option)

Measurement range 0 to 150 mmHg, 0 to 19%
Accuracy 0-40mmHg ±2 mmHg,
41-70mmHg ±5% of reading
71-100mmHg ±8% of reading,
101-150mmHg ±10% of reading
Respiration rate 0 to 150 breath per minute
Respiration accuracy ±1breath per minute
Anesthetic GAS/O2 - Phasein (Option)
Method Infra-red absorption characteristic
Gas CO2, O2, N2O, Des, Iso, Enf, Hal, Sev
Warm-up time Main stream (IRMA AX+)
Iso accuracy mode: 45s
Full accuracy mode : 60s

Side stream (ISA OR+/ AX+) : <20s

Sample flow rate 50 ± 10 ml/min
(for ISA OR+/AX+)
Measuring Range CO2 : 0 ~ 15 %
N2O: 0 ~ 100%
Hal/Iso/Enf: 0 ~ 8%
Sev: 0~10%
Des: 0 ~ 22%
O2: 0 ~ 100%(ISA OR+/AX+)
Respiratory Rate 0 ~ 150bpm ± 1bpm
C.O. (Optional)
Method Thermodilution Technology
Measuring Range C.O. : 0.1 ~ 20L/min
TB : 23 ~ 45℃
TI : 0 ~ 27℃
Alarm range 23 ~ 45℃
CSM (Optional)
EEG sensitivity ±400µV
Noise < 2µVp-p, < 0.4µV RMS, 1–250 Hz
CMR >140dB

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Input impedance >50MOhm

Sample rate 2000 samples/sec. (14 bits equivalent)
CSI and update 0-100. Filter 6-42 Hz, 1 sec. update
EMG 0-100 logarithmic. Filter 75-85 Hz, 1 sec. update
BS% 0-100%. Filter 2-42 Hz, 1 sec. update
Sensor impedance 0-10kOhm / measurement current 0.01µA
range

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Section 2 Troubleshooting
2-1. Introduction
A list of system error messages and troubleshooting information for common problems
you may encounter while using the monitor and its accessories is given in the manual for
Use. This chapter provides a guide for qualified service personnel for troubleshooting
problems that cannot be resolved by the user.

Caution

If the troubleshooting procedure requires you to disassemble the monitor or

transducers, be certain to follow the disassembly and reassembly procedures
given in Section 5, “Disassembly and Reassembly”.

 Who Should Perform Repairs

Only qualified service personnel should open the monitor housing, remove and
replace components, or make adjustments. If your medical facility does not have
qualified service personnel, contact Medical ECONET’ Response Center or your local
Medical ECONET representative.

Warning
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.

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2-2. Trouble Shooting Guide

Problems
Before starting any detailed troubleshooting, complete a thorough visual inspection of the
following.
 All cable connections secure?
 Devices properly powered?
 Connected to a proper power source?

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Problem Possible Reason Solution

General The output voltage of the Perform “Power Outlet Test” to

The unit is plugged in, but it does power confirm AC power.

not supply is inadequate for the Replace the power supply.

switch to AC from battery power. processor PCB to recognize. Replace the processor/power

management assembly.

Alarm Audio The speaker cable is loose or Restore the cable

Audio does not sound. disconnected. connections.
Go to the Alarm Help Menu The speaker failed Replace the speaker.
and select “Alarm” Listen for The audio circuit on the Replace the Replace the
the three-beep audio. processor PCB failed. processor/power
management assembly.
Waveform Display Patient cables are bad. Perform appropriate sections
The acquisition PCB, DAS of the “Data Acquisition Tests”
Assembly or power supply PCB depending on the waveform
failed. problem.
Optional Printer Graph locations are set With the Trim Knob control,
incorrectly.
No paper comes out, even select MONITOR SETUP. Verify
though that MANUAL, ALARM, and
“Graphing” is displayed. PRINT locations are set
properly.
Paper comes out, but no The paper may be loaded Refer to the Operator
graph data is shown. incorrectly. Manual for correct paper
Print head may be dirty or installation.
defective.
Clean the printhead. Refer
to “Clean the Print Head”
Perform a graph test. If
problem persists, replace the
printer assembly.
Saving Message Writer is busy. When the graph is complete,
Writer is no longer available. the saved graph prints out.
Check the graph locations.
Set the correct graph
locations if necessary.

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Missing segments in the graph Print head may be dirty or Clean the printhead. Refer
data. defective.
to “Clean the Print Head”
Perform a graph test. If
problem persists, replace the
printer assembly.
Optional Alarm Light Indicator Cable may be loose or Restore the connection.
The red or yellow lights do not disconnected. Replace the alarm light
light on boot up of the patient LEDs are burned out. assembly or PCB.

monitor.
Video Display Possible burned-out pixels. Run the display tests in the
There are bars/strips of pixels boot loader.
missing on the display in Replace the display
rows/columns. Or only one assembly.
row/column of pixels on the No display
display is missing or never
turned on. Display may be in standby Press the POWER button. If
The remaining portion of the mode. display still does not appear
display functions properly. Backlight inverted may be within 20 seconds, replace the
defective. display
assembly.
Replace back light inverter.
Network Connector The patient monitor is Connect the network cable
No network connection when connected to a BM Central to the remote station’s internet
a station. The patient monitor’s connector.
network cable is connected to Network Connector is inactive Enable network in boot code.
the when it is connected to the
patient monitor’s Network remote station.
Connector.
Network is disabled in boot
code.

Analog PCB Symptoms

Symptoms relative to patient signal acquisition such as missing parameter text and waveform(s)
may be associated with analog PCB failure. It is important that you are able to distinguish the
difference between the general format of the display, which is generated by the processor PCB,
versus the patient signals and data that is associated

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with these patient signals, a function of data acquisition, which is generated by the analog PCB.

Processor PCB Symptoms

Symptoms with battery operation, network communications, asynchronous communications, NIBP
control, USB communications, analog output, audio/sound generation, and video signals as well as
other display-related problems all may be associated with processor PCB failure. All of these are
functions controlled by microcontroller or
graphics processing circuitry located on the Processor/Power Management PCB.

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1) Power is off

The power is off

Does the
Change the
power input
Yes power input A
cable break
cable
down?

No
A
Does the
Change the
power switch
Yes power switch A
cable short-
cable
circuit?
Normal
Yes Use
No operation

Does the
Change the B
main power No
Yes main power A
connector
connector
break down?

No

Is the fuse Again blown

Yes Change the fuse No
blown? fuse
A

No Yes

Does the main power Repair or

module produce the No change the main A
power properly? power module

Yes
Ask the
manufacturer
about it, then
take action

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2) LCD screen is blank although the power is on

LCD screen is
blank although the
power is on

Does the LCD cable Check the

have a poor condition condition of the
of connection or Yes connection and A
short-circuit? then change if
it's not good A

No

Change the
Broken 34Pin Normal
Yes 34Pin shield A Yes Use
shield cable? operation
cable

No No

Is the LCD
module Change the B
Yes A
unsatisfactory LCD Module
?

No

Ask the
manufacturer
about it, then
take action

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3) LCD Touch is not working properly

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4) Noise in ECG
- Gel is dry
- Electrodes does not stick well to skin

The patient’s skin Yes Apply ECG gel or water to the area
is extremely dry of contact then use the electrode

No

Replace the electrodes

The electrode is Yes
in poor condition (Use CE compatible products)

No

The cable (lead wire) Yes Replace lead wires

is disconnected

No

Repair the ECG B/D

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5) SpO2 malfunction

Connectors of the equipments are in bad condition?

The extension cables Yes

are disconnected Replace extension cables

No

The Finger probe is Yes

in bad condition? Replace the finger probe

No

Repair the ECG B/D

6) Temp malfunction

The probe is Yes

in bad condition? Replace the probe

No

Repair the Temp B/D

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7) NIBP malfunction

Are leaks from the hose Yes

connector of cuff Replace the hose of cuff

No

Repair the NIBP B/D

8) Abnormality in NIBP measurements

The patient moved Yes Make sure the patient stay still
while measuring during diagnosis

No

The measurements Yes

appear lower Loosen the cuff during diagnosis

No

There is a delay Yes

in measuring Tighten the cuff during diagnosis

No

Repair the NIBP B/D

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9) Printer is not working properly

When the printer

is not working
properly
B

Does you Make the paper flat

place on the and place it facing up
No
printer in order to let printer
correctly? cover shut?

Does the
Does the
paper come Change the A
No motor work No
out while motor
properly?
printing?

Yes

Have you
Connet the
connected the A
No motor power
motor power
cable correctly
cable correctly?
Yes Yes A

Is the motor Change the

power cable No motor power A
satisfactory? cable

Normal
Yes Use
operation
Does the Have you
signal come Yes connected Connect the
A
out on the No the TPH No THP power
paper while powor cable cable correctly
printing? correctly
Yes B

Is the TPH
power cable Change the TPH A
Yes No
is power cable
satisfactory?

Yes

Ask the
manufacturer
about it, then
take action

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10) ECG wave does not come out or it's very small

ECG wave does

not come out or
small
B

Is the patient
Reconnect the
cable
No patient cable A
connecter
carefully
correctly?

A
Is the
electrode Cleanse the
connected to electrode with
Yes A
the patient alcohol or water,
cable then it use
correctly? Normal
No Yes Use
operation
Is the
electrode Reconnected the
connected to electrode to the
No A
the patient patient cable
cable properly
correctly? B
Yes

Is the patient
Change the
cable short- Yes A
patient cable
circuited?

No

Control the
Is the ECG
volume by setting
signal adjusted No A
a gain on the
properly?
main board

Yes
Ask the
manufacturer
about it, then take
action

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11) USB memory does not working properly

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12) USB barcode reader does not working properly

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13) Failure in battery recharge

( the battery does not fully recharge in 6 hours or more)

The output voltage of No Replace the adapter

(the battery will not be changed
the adapter is 18V
at the rate lower than 17V)

Yes

The battery voltage Yes

is lower than 5V Replace the battery

No

Repair the power B/D

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Section 3 Technical Description

3-1. Introduction
This chapter gives a brief technical description of the various modules and assemblies to
be found in the COMPACT 9 range of Patient Monitors.
The descriptions given are to block diagram level only. These are presented to assist in the
overall understanding of the operation of the unit and are not intended to assist in the
repair of a module to component level.

3-2. COMPACT 9 Hardware Overview

Fig 3.1 System Block Diagram

 The monitor consists of the following main functional components:

- Power supply
- Main digital Board
- Analog1 Board ( SpO2,IBP1,2 , Temp )
- Analog2 Board ( ECG, RESP )
- Analog3 Board ( C.O, IBP3,4 , CSM )
- Power Board

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- Key Interface Board ( tatical key , Wheel key )

- Thermal Printer board unit
- Noninvasive Blood Pressure unit
- 12 Channel Resting ECG Module( Optional )
- Input / Output Interface Board :
- LAN
- RS232
- USB ( 1channel HOST )

3-3. Power Supply

The power supply is a wide-range input switching unit, with an output of 18V. It is located in
the chassis assembly.
The Power Supply unit contains no user-adjustable components or replaceable items. No
attempt should be made to gain access to the inside of the module. The following
paragraphs are provided for information only and should not be used to aid repairs to the
module itself, which should be replaced on failure.

Warning
Under normal conditions, after switching off the unit all internal
capacitors will discharge to safe levels within ten seconds. Under
fault conditions however, high voltage charges may be held for
much longer and suitable precautions should be taken before
handling a disconnected or removed Power Supply Module.

The COMPACT 9 is connected between the local source of AC mains and the double-
fused IEC mains input connector on the adaptor module, using the supply lead provided.
The unit will operate from AC supplies in the range 100 to 120 volts or 220 to 240 volts without
adjustment. Note however, that the supply input fuses located in the inlet connector should
be rated at 1.5 Ampere for supplies in the range 100 to 120 volts, 0.75 Ampere for 200 to 240
volts.

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Fig 3.2 Block Diagram: Power Supply Part in the Power Board

The various regulated output voltages produced by the Power Supply part are routed to
the Power Board for use on the board and also for distribution to other boards and
assemblies. As shown in Fig 3.2, Four voltage regulator devices are fitted to the power board;
two of these are powered from the +18 V supply, 7.5 V regulator for the printer motor and
printer head. The remaining Voltage provide the +5Vdigi and two +5Vanlog supplies from
the +12V supply.

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3-4. Main digital Board

Fig 3.3 Block Diagram: Main Digital Board

The Main CPU Board controls the monitor’s human interface( LCD touch , input key ..), and
is responsible for the final processing of data from the Bus Master Board. It sends this data to
the 12.1" TFT LCD display, and to the thermal printer unit for recording traces and other
patient data. It also controls the LAN/RS232 interface board. The board contains Nand Flash
which contain all the system software.
The board includes the following sections:

 Microprocessor Section:
- S3C2440 ( ARM9TDMI ) microprocessor.
- Flash containing all system software and a boot program allowing
- Software upgrades via the Service Connector( USB HOST , JTAG ).

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- Flash memory, backed to store short time device and user settings etc.
- A real-time clock, battery-backed and power-fail protected. The processor has
access to all clock registers.
- A watchdog function which monitors the operation of the microprocessor and
restarts the system if it is not served at a constant rate.

 Bus Control Section:

- Address and data bus control chips.
- Board select logic to access all system boards.
- DMA circuits to allow DMA access via the system bus to the Combined
Interface.

 Service Interface: A RS232 serial interface is provided for use during production
and service. Connection is via a DSUB 9pin on the rear cover.
- Serial interface for option and software upgrades and Debugging.
- Settings and configuration via an external computer.

 Printer interface :
- The Parallel( Main Digital CPU to Printer CPU) for the thermal array data.
- A heating timer to control the heating pulse for the thermal array. The voltage
from a thermistor on the thermal array is A/D converted and the CPU programs
the heating timer with a value which compensates the ambient temperature.
- The recorder sensing hardware consists of a reflective light sensor that detects
the black marks on the paper and paper out.
- +7.5V is blocked by capacitor and supplied to the thermal print head.

3-5. Analog1 Board

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Red LED control

Driver
Timing
Circuits/
LEDs IO/DAC
Current
IR control
Driver

ARM7 core
DSP
(algorithm,
I/O processor)

Differ. Gain Offset

ADC
Photodiode AMP Control Control

DAC

Probe Sensor Pulse Oximeter

HOST

DIGITAL B/D PIC16F873A

( ARM9 (AD, I/O ,
Processor ) timer )

3-6. Analog2 Board

H Analog power +/-5v

DC-DC
I Input 5~15V
RA converter
G Digital power 3.3v/1.8v
H
LA
V
Resp Part Host
O Digital
LL L 24bit A/D Signal Patient Monitor
(ADS1256) Processing ECG Data
T
A
ECG Part (TMS320F2811) 7 Channel waveform
V
Heart rate
G
Leadfault detection
RL E
Pacemaker detection
P Isolation Barrier

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3-7. Analog3 Board

3-8. Noninvasive Blood Pressure Assembly

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Section 4 Check Out

Manufacturer Recommendations
These safety tests and checkout procedures provide service personnel with a method to verify
operational and functional performance of the patient monitor. Failure to attain any of the listed
results indicates a potential malfunction of the patient monitor.
The safety tests and checkout procedures are based on the assumption that the tested patient
monitor has known good cables and test equipment. It also requires that the user be familiar with
the operation of all test equipment required for the procedures. For more information concerning
the operation of these components, refer to the respective operator manual(s).

Frequency
Medical ECONET recommends that you perform the checkout procedures:
Upon receipt of the device.
Every 12 months thereafter.
Each time the main enclosure is disassembled or a circuit board is removed, tested, or replaced.

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4-1. Visual Inspection

The patient monitor and its components should be carefully inspected prior to installation,
once every 12 months thereafter and each time the equipment is serviced.
- Carefully inspect the equipment for physical damage to the case, the display screen, and
the keypad. Do not use the patient monitor if damage is determined. Refer damaged
equipment to qualified service personnel.
- Inspect all external connections for loose connectors or frayed cables. Have any
damaged connectors or cables replaced by qualified service personnel.
- Inspect the display face for marks, scratches, or other damage. Physical damage to a flat
panel display glass may pose an implosion hazard. Have the flat panel display replaced by
qualified service personnel if necessary.
Safety labels and inscription on the device are clearly legible.

4-2. Cleaning
Precautions
Use one of the following approved solutions:
- Cidex solution, or
- Sodium hypochlorite bleach (diluted), or
- Mild soap (diluted)
- Lint-free cloth
- Dust Remover (compressed air)
To avoid damage to the equipment surfaces, never use the following cleaning agents:
- organic solvents,
- ammonia-based solutions,
- acetone solution,
- alcohol-based cleaning agents,
- Betadine solution,
- a wax containing a cleaning substance, or
- abrasive cleaning agents.
Clean the Display
Use a soft, clean, lint-free cloth dampened with a glass cleaner to clean the display.

Caution
To avoid getting liquid into connector openings, do not spray
glass cleaning or general cleaning solutions directly onto the
product’s surface.

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Clean the Exterior

Clean the exterior surfaces with a clean, lint-free cloth and one of the cleaning solutions listed in
the table above.
- Wring the excess solution from the cloth. Do not drip any liquid into open vents, switches,
plugs, or connectors.
Dry the surfaces with a clean lint-free cloth.

4-3. Battery Maintenance

How to Charge the Battery
The battery can be charged by methods:
- Outside of a patient monitor by using AC adapter charger.

The battery is charged whenever the patient monitor is connected to an AC power source.
When you store the battery inside of a patient monitor that is connected to an power adapter
source, the battery will selfdischarge to less than 90% of its Full Charge Capacity after
approximately two weeks (depending upon the temperature of the battery). At this time, the
patient monitor will automatically recharge the battery to 100% of its Full Charge Capacity.

How to Condition the Battery

Warning
PATIENT RISK HAZARD — Never condition a battery while the
patient monitor is connected to a patient. Serious injury or death
could result.

Complete the following steps to manually condition the battery using the patient monitor:
1. Remove all batteries from the patient monitor.
2. Insert one battery into Slot of the patient monitor.
3. Disconnect the patient monitor from the AC adaptor power source.
4. Access the patient monitor’s Battery Status window to monitor the
battery’s Charge Level.
5. Allow the battery to discharge to less than a 90% Charge Level.
6. Re-connect the patient monitor to the AC adaptor power source and fully
charge the battery.
7. Disconnect the patient monitor from the AC adaptor power source and allow the patient
monitor to run until it displays the BATTERY LOW message, or until the patient monitor shuts down.

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8. Re-connect the patient monitor to the AC adaptor power source. Allow the battery to fully
charge to complete the conditioning cycle.
How to Store the Battery
- Condition the battery before storing it. Conditioning the battery to 100% capacity
increases the storage shelf-life of the battery.
- Store the battery outside of the patient monitor at a temperature between 20°C to 25°C
(68°F to 77°F).
- When the battery is stored inside a patient monitor that is powered by an AC power
source, the battery cell temperature increases by 10°C to 15°C (18°F to 27°F) above the
room’s ambient temperature. This reduces the life of the battery.
- When the battery is stored inside a patient monitor that is continuously powered by an AC
power source and is not powered by battery on a regular basis, the life of the battery may
be less than 12 months. Medical ECONET recommends that you remove the battery and
store it near the patient monitor until it is needed for transport.
- Re-condition a stored battery every six months to increase the storage shelf-life.
How to Replace the Batteries
1. Open the battery doors on the left side of the patient monitor, along the bottom.
2. Remove the faulty batteries.
3. Replace with a new battery. The patient monitor supports up to two exchangeable lithium-ion
batteries. Install the battery with the connection pins facing down and inserted first.
4. Close the battery covers.
5. Verify that the patient monitor operates correctly.
a. Confirm that the Battery with a battery icon displays in the upper right corner of the patient
monitor.
b. Verify that the Battery LEDS illuminate amber.

Warning
EXPLOSION HAZARD — DO NOT incinerate the battery or store at
high temperatures. Serious injury or death could result.

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4-4. Electrical Safety Tests

General
Electrical safety tests provide a method of determining if potential electrical health hazards to the
patient or operator of the device exist.
Recommendations
Medical ECONET recommends that you perform all safety tests presented in this chapter.
- upon receipt of the device (patient monitor and its associated equipment),
- every twelve months thereafter,
- each time the main enclosure is disassembled or a circuit board is removed, tested,
repaired, or replaced, and
- record the date and results on the paper.

These instructions are intended for every component in the system.

Test Conditions
Electrical safety tests may be performed under normal ambient conditions of temperature,
humidity, and pressure.

Test Equipment
The recommended test equipment required to perform electrical safety tests is listed below.
Item Specification
Leakage Current Tester Equivalent to the circuits shown
Digital Multimeter (DMM) AC volts, ohtm
Ground Bond Tester 0 – 1ohm
ECG Test Body All leads together
SpO2 Test Body %spo2, Pulse rate

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Power Outlet Test

Before starting the tests, the power outlet from which the monitoring device will get electrical
power must be checked. This test checks the condition of the power outlet to ensure correct results
from leakage tests.
A standard power outlet consists of three connections: line, neutral and ground. The figure below
indicates the location of each on a 220 VAC power outlet commonly used in korea. The location
and shape of pins may be different on power outlets used in countries other than korea.

LINE

NEUTRAL

GROUND

For international power outlets, refer to the internal standards agencies of that particular country.
If other than normal polarity and ground is indicated, corrective action must be taken before
proceeding. The results of the following tests will be meaningless unless a properly wired power
outlet is used.
Use this procedure to verify that the AC power outlet that the patient monitor is plugged into is
correctly wired. This is accomplished by performing a:
- voltage measurement between all three connections of the power outlet, and
- ground-to-neutral loop resistance measurement.
1. Use a digital multimeter (DMM) to measure the voltage between the three connections.
a. Select the AC voltage scale on the DMM.
b. Measure the voltage from line to neutral, line to ground, and neutral to ground and make sure
these are correct. With a correctly wired power outlet used in korea, the following readings
should be obtained:
Line to neutral: 220 VAC
Line to ground: 220 VAC
Neutral to ground: < 3 VAC
Readings other than these indicate improper wiring. Have the power outlet checked by an
electrician.
2. Use a DMM to measure the ground-to-neutral loop resistance.

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Caution
DO NOT check the ground-neutral loop resistance unless the
power outlet is correctly wired.

a. Select the milliohms (mΩ) scale on the DMM.

b. Measure resistance across the power cord ground and neutral.
c. Measure from the ground lug on the rear power connector to any exposed metal of the
patient monitor. The resistance between the ground and neutral connections, after the
ohmmeter is nulled, must be less than 100 mΩ. If not, have the power outlet checked by an
electrician.

Power Cord and Plug

Verify the power cord being used with the patient monitor is good. The following are a couple of
things to check for in this regard:
- Failure of the power cord strain relief is very common. Often times users of the equipment
pull on the power cord itself, rather than the power cord plug, to unplug the patient
monitor from a wall
- receptacle. If in doubt, test for continuity through each conductor of the power cord
connector and plug.
- Verify line, neutral, and ground conductors are properly connected to the power cord
plug and are not short-circuited. Rewire and tighten these, or replace the power cord, as
necessary.

Ground (Earth) Integrity

Listed below are two methods for checking the ground (earth) integrity, “Ground Continuity Test”
and “Impedance of Protective Earth Connection.” These tests determine whether the device's
exposed metal and power inlet's earth (ground) connection has a power ground fault condition.

GROUND pin

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Perform the test method below that is required by your Country/Local governing safety
organization.

Ground Continuity Test

Completion of this test is checked by the following steps:
1. Disconnect the device under test from the power outlet.
2. Connect the negative (-) lead of the DMM to the protective earth terminal (ground pin in power
inlet connector) or the protective earth pin in the Mains plug (ground pin in power cord). Refer to
the KOREA 220Vac power cord figure above.
3. Set the DMM to the milliohm (mΩ) range.
4. Connect the positive (+) lead of the DMM to all exposed metal surfaces on the device under
test. If the metal surfaces are anodized or painted, scrape off a small area in a inconspicuous
place for the probe to make contact with the metal.
5. Resistance must read:
- 0.1 ohm or less without power cord
- 0.2 ohms or less with power cord

Impedance of Protective Earth Connection

This test unlike a ground continuity test will also stress the ground system by using special ground
bond testers.
This test normally is only required as a manufacturing production test to receive safety agency
compliance (i.e. IEC 60601-1).
Some country agency's do require this test after field equipment repairs (i.e. Germany's DIN VDE
0751 standards).
Consult your country/local safety agency if in question.
Compliance is checked by the following steps:
1. A current not less than 10A and not exceeding 25A from a current source with a frequency of 50
or 60 Hz with a no-load voltage not exceeding 6 V is passed for at least 5 s through the protective
earth terminal or the protective earth pin in the mains plug and each accessible metal part which
could become live in case of failure in basic insulation.
2. The voltage drop between the parts described is measured and the impedance determined
from the current and voltage drop. It shall not exceed the values indicated.
For equipment without a power supply cord the impedance between the protective earth terminal
and any accessible metal part which is protectively earthed shall not exceed 0.1 ohms
For equipment with a power supply cord the impedance between the protective earth pin in the
mains plug and any accessible metal part which is protectively earthed shall not exceed 0.2 ohms.
When taking this measurement, move the unit's power cord around.

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There should be no fluctuations in resistance.

Ground (Earth) Wire Leakage Current Tests

Perform this test to measure current leakage through the ground (earth) wire of the equipment
during normal operation.
The device under test is to be tested at its normal operating voltage.
1. Configure the leakage tester like the circuit shown below with normal polarity and NEUTRAL
closed.

2. Connect the power cord of the device under test to the power receptacle on the leakage
tester.
3. Apply power to the device under test.
4. Read the current leakage indicated on DMM.
5. Set the polarity switch on the leakage tester to RVS (reverse).
6. Read the current leakage indicated on DMM.
NOTE
If either reading is greater than the appropriate specification below, the device under test fails.
Contact Medical ECONET Technical Support.
- 300 µA (0.3 volts on the DMM), and the device under test is powered from 100-120 V/50-60
Hz
- 300 µA (0.3 volts on the DMM), and the device under test is powered from a centered-
tapped 200-240 V/50-60 Hz, single phase circuit
- 500 µA (0.5 volts on the DMM), and the device under test is powered from a non-center-
tapped, 200-240 V/50-60 Hz, single phase circuit
NOTE
Center-tapped and non-center-tapped supply circuits produce different leakage currents and the
UL and IEC limits are different.
7. Repeat steps 1 through 7 with NEUTRAL open.

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8. Set the power switch of the device under test to OFF.

NOTE
If the reading is greater than the specification below, and the device under test is powered from
100-240 V/50-60 Hz, the device under test fails. Contact Medical ECONET Technical Support.
- 100 microamperes (0.1 volts on the DMM), and the device under test is powered from 100-
240 V/50-60 Hz
11. Set the power switch of the device under test to OFF.

Patient (Source) Leakage Current Test

This procedure only applies to Class I (grounded/earthed) equipment, and measures the leakage
current from the ECG/RESP connector or the SPO2 connector of the device to ground.
1. Configure the leakage tester like the circuit shown below with GND switch OPEN and polarity
switch NORM.

2. Connect an ECG test body to the ECG/RESP connector of the device under test.
3. Set the power switch of the device to ON.
4. Read the leakage current indicated on the DMM.
5. Change the leakage tester polarity switch to the RVS position.
6. Read the leakage current indicated on the DMM.
NOTE
If either reading is greater than 50 µA (0.05 volts on the DMM), the device fails this test. Contact
Medical ECONET Technical Support.
7. Change the GND switch to the Closed position.
8. Read the leakage current indicated on the DMM.
9. Change the leakage current switch to the RVS position.
10. Read the leakage current indicated on the DMM.

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NOTE
If either reading is greater than 10 µA (0.01 volts on the DMM), the device fails this test. Contact
Medical ECONET Technical Support.
11. Set the power switch of the device to OFF.
NOTE
The AAMI and IEC single fault condition (ground open) is 50 µA, whereas the normal condition
(ground closed) is less.
12. Repeat the steps in this procedure using the appropriate MEDICAL ECONET or SPO2 Test Body.
Connect the SPO2 Test Body to the Green SPO2 connector of the device under test.

Patient (Sink) Leakage Current Test (Mains Voltage on the Applied Part)
This procedure only applies to Class I (grounded/earthed) equipment, and measures the leakage
current from a mains voltage source into the ECG/RESP connector.
1. Configure the leakage tester like the circuit shown below with GND switch CLOSED and polarity
switch NORM.

Warning
Shock hazard. The following step causes high voltage at the test
body. Do not touch the test body.

2. Set power switch on the device to ON.

3. Read leakage current indicated on DMM.
4. Change the leakage tester polarity switch to the RVS position.
5. Read the leakage current indicated on the DMM.
NOTE
If either reading is greater than the appropriate specification below, the device under test fails.
Contact Medical ECONET Technical Support.

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- 10 µA (0.01 volts on the DMM) at 120 VAC using the test body.
- 20 µA (0.02 volts on the DMM) at 240 VAC using the test body.
- 50 µA (0.05 volts on the DMM) at 120-240 VAC using the ECG cable.
NOTE
The 10 and 20 µA limits are based on internal design standards. The 50 µA limit is common to all
standards. AAMI ES-1 standard requires using the patient cable.
6. Set the power switch on the device to OFF.
7. Repeat the steps in this procedure using the appropriate MEDICAL ECONET or SPO2 Test Body.
Connect the SPO2 Test Body to the green SPO2 connector of the device under test.

Patient Monitor Power-up Tests

1. Remove the batteries and unplug the patient monitor (or the docking station) from AC power to
turn the patient monitor off.
2. Restore the batteries to the patient monitor and plug the patient monitor (or the docking station)
into AC power to turn the patient monitor on.
3. Verify all of the front panel indicators illuminate on power up.
4. Verify the AC indicator on the patient monitor stays illuminated.
NOTE
If the AC LED stays on, but the screen is blank, the patient monitor is likely in “standby mode”
(battery charging). Press the POWER button to enter the normal mode.
- If the AC indicator is on, continue with the tests.
- If either of the CHARGING STATUS indicators is yellow, wait for the battery(ies) to fully
charge and the indicators to illuminate green. The batteries may take up to four hours to
charge.
- If the battery “fuel gauge” displays the word “ERROR,” the battery may be asleep. Refer to
“Error Messages”.
5. Verify the optional alarm indicator lights both red and amber on power up.
6. Verify an audio “Beep” sounds at the end of Boot up.
7. Test all of the front panel keys and the Trim Knob control. Verify that an audio “Beep” sounds
after each key press.
8. Check battery power for both batteries.
- Unplug the patient monitor (or the docking station) from AC power and open the battery
door. Verify one LED in the battery compartment is on (batteries must have more than 10%
charge).
- Pull that battery out and verify the other LED lights, thus indicating the unit is powered by
the other battery.
Reinstall battery and plug in patient monitor.

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4-5. ECG Test

Equipment
Use the following equipment for these tests:
- patient simulator or an equivalent 12L ECG patient simulator.
- ECG Patient Cable
- ECG Leadwire Set

5 Lead ECG Test

Perform this test if the patient monitor acquires 5 lead ECG data.
1. Set up the patient simulator as follows.
- Heart rate – 80 bpm.
- Heart rate amplitude – 1.0 mV.
- 5-lead ECG patient cable properly attached.
- 2x gain for a simulator.
2. Attach the ECG patient cable and ECG leadwire set to the ECG/RESP connector on the patient
monitor and the leadwire connectors on the top of the patient simulator.
3. Admit the patient simulator to the patient monitor.
4. Observe the following:
- ECG lead II is displayed and is noise-free,
- Heart rate of 80 ±1 bpm is displayed,
- With QRS tones enabled, an audible tone sounds with each RWave (QRS complex).
5. Verify all six ECG leads are available to view and are noise-free.
6. Select PACEMAKER ON and set to ON.
7. Select a pacemaker pulse on the simulator.
8. Observe the following while you view ECG leads I, II, III, aVL, aVF, and AVR:
- a “P” appears above the PVC count indicating pacemaker pulse detection is enabled,
and
- the heart rate still reads 80 ±1 bpm.
9. Disable pacemaker pulse detection on the patient monitor and return the simulator to these
conditions:
- Heart rate – 80 bpm,
- Heart rate amplitude – 1.0 mV,
- 5-lead ECG patient cable properly attached.
10. Select ECG lead II to view in the top trace position on the patient monitor display.
11. Disconnect the RA leadwire from the patient simulator.
12. Observe that:
- an RA FAIL message appears on the display, and

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- lead III automatically displays in place of lead II in the top trace position.
13. Reconnect the RA leadwire to the patient simulator.
14. Inject a 1-millivolt calibration signal using the patient simulator and start a manual graph.
15. Observe that the calibration pulse properly displays and graphs.

16. This completes the 5 Lead ECG test. Leave the ECG patient cable connected to ECG/RESP and
continue to the next steps of these checkout procedures.

12L ECG Test (option)

Perform this test if your patient monitor uses the 12L ECG option.
1. Set up the patient simulator as follows:.
- Heart rate – 80 bpm.
- Heart rate amplitude – 1.0 mV.
- 12L ECG patient cable (5-leads with V leads) properly attached.
- 2x gain for a simulator.
2. Select ECG from the patient monitor menu. Then, select 12 LEAD ECG ANALYSIS.
3. Verify that the patient monitor is displaying 10 noise-free leads.
4. Select 12LD ECG RUN. Wait for the patient monitor to acquire and analyze the data.
5. Select Transmit-Print.
6. Verify the 12SL ECG prints at the print location assigned in the patient monitor’s 12 LEAD ECG
ANALYSIS >12L Print Location.
- If there is no print location is assigned, an error message appears on the bottom of the
patient monitor’s display.
7. Verify the ECG is transmitted to the MUSE Cardiovascular Information System. Verify the ECG
prints out correctly as defined by the MUSE system.
- If no MUSE system is connected, an error message appears on the bottom of the patient
monitor’s display.
8. Delete this test 12L ECG from the MUSE system’s edit list.

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4-6. Respiration Test

1. With the ECG patient cable connected to the ECG/RESP connector of the patient monitor, set
up the patient simulator as follows:
- Respiration (RESP) baseline impedance – 750Ω
- RESP ∆R – 0.5Ω,
- RESP lead select – I & II
- RESP rate (respirations per minute) – 30.
2. Set up the patient monitor as follows:
- RESP waveform – on,
- RESP waveform lead select – lead II (RESP waveform derived from ECG lead II).
3. Observe the following:
- RESP parameter window appears on the patient monitor with a
- reading of 30 ±2 (respirations per minute),
- RESP waveform appears distortion-free on the patient monitor.
4. Change the RESP waveform lead select of the patient monitor to lead I (RESP waveform derived
from ECG lead I), LA at the simulator.
5. Observe the following:
- RESP parameter window appears on the patient monitor with a reading of 30 ±2
(respirations per minute),
- RESP waveform appears distortion-free on the patient monitor.
6. Disconnect the ECG patient cable from the ECG/RESP connector of the patient monitor.
Proceed to the next steps in these checkout procedures.

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4-7. Temperature Test

Equipment
Use the following equipment for these tests:
- 700 Series Temperature Adapter
- Temperature Simulator Cable for use
Procedures
1. Set up the patient simulator for a temperature output of 37°C.
2. Attach the temperature adaptor cable to the TEMP/CO connector of the patient monitor.
3. Set the switch on the temperature adaptor to the 700 position.
4. Attach the temperature simulator cable from the SERIES 700 TEMPERATURE OUTPUT connector of
the patient simulator to the T1 connector of the temperature adaptor.
5. Verify a TEMP parameter window appears on the patient monitor display with a T1 reading of
37.0° ±0.4° C.
6. Move the temperature simulator cable from the T1 connector of the temperature adaptor to the
T2 connector of the temperature adaptor.
7. Verify a T2 reading of 37.0° ±0.4° C in the TEMP parameter window on the patient monitor display.
8. Repeat the above procedure using 700 settings on simulator and cable.
9. Remove the temperature adaptor and temperature simulator cable from the patient monitor
and patient simulator.

4-8. Cardiac Output Test (option)

Equipment
Use the following equipment for these tests:
- Cardiac Output Simulator
- Cardiac Output Cable Adapter
Cardiac output testing is different depending on the simulator you use.
The Cardiac Output Simulator II is no longer available, but if you already have that simulator, use
the first section to run this test. Otherwise, go to “Test with Marq II or MarqIII Simulator.”

Test with Cardiac Output Simulator II

1. Connect the cardiac output (CO) cable adaptor to the CO connector of the patient monitor.
2. Connect a simulator cable between the CO cable adaptor and the CO simulator.
3. Set the CO simulator to output blood temperature (BT) readings, as found in the following table:
Simulator BT setting Patient Monitor BT reading Range
36.9°C 36.7~37.1°C
37.0°C 36.8~37.2°C
4. Verify a CO parameter window appears on the patient monitor display with correct BT readings

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as shown in the table above.

5. Set the CO simulator to output injectate temperature (IT) readings, as found in the following
table:
Simulator IT setting Patient Monitor IT reading Range
0.0°C –0.3 – +0.3°C
8.0°C 7.7 – 8.3°C
15.0°C 14.7 – 15.3°C
24.0°C 23.7 – 24.3°C
29.6°C 29.3 – 29.9°C

6. Verify correct IT readings appear on the patient monitor display, as shown in the table above.
7. Disconnect the CO cable adaptor from the CO connector of the patient monitor. This completes
the CO tests.

4-9. Invasive Blood Pressure Test (option)

Equipment
Use the following equipment for these tests:
- Blood Pressure Simulator Adapter Cable
- Dual BP cable
The invasive blood pressure (BP) tests provide a method of verification for both BP connectors (BP1,
BP2, BP1/3 and BP2/4) of a patient monitor equipped with this optional function. Follow these steps:
1. Set up the patient simulator as follows:
- Blood pressure (BP) polarity – POS, if required.
- BP output – 0 mmHg.
- BP transducer output – 5 µVolts.
BP Connector Tests
1. Connect the BP simulator cable from the BLOOD PRESSURE 1 -120/80 connector of the patient
simulator to the enabled BPconnectors you will be testing on the patient monitor.
a. To connect to the BP1 or the BP2 connector.
b. To connect to the BP3 or BP4 connectors.
2. Verify the BP parameter window, waveform label, corresponding graticules, and waveform
appear on the patient monitor display, along with a BP waveform requiring zero reference.
3. Press the ZERO ALL (FUNCTION) key on the front panel of the patient monitor to zero-reference
the BP waveform.
4. Change the patient simulator BP output to 200 mmHg (240 if using the Marq II or MarqIII). ECG BLOO D PRESSUR

N 5. Observe a reading of 200/200 (200) ± 4 mmHg (or 240 ± 4 mmHg if using the Marq II or MarqIII) in
the BP parameter window on the patient monitor display.

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6. Change the patient simulator BP output to WAVE or to a 120/80 wave form (simulated BP
waveform).
7. Observe a distortion-free BP waveform and a reading of approximately 120/80 (93) in the BP
parameter window on the patient monitor display.
8. Disconnect the BP simulator cable from the BP connector of the patient monitor.
9. Complete steps for each enabled BP connector.

4-10. Pulse Oximetry Test for SpO2 Oximeter

Equipment
Use the following equipment for these tests:
SpO2 Simulator.
SpO2 Simulator Cable
Fluke Biomedical’s Index2 SpO2 Simulator (or equivalent).
Procedure
1. Set the pulse oximetry (SpO2) simulator power switch to the OFF position.
2. Connect the Nellcor-style SpO2 simulator cable between the SpO2 connector of the patient
monitor and the SpO2 simulator.
3. Set the simulator as follows:
a. Set the MODE to NELLCOR.
b. Set the SpO2% to 99.
c. Set the PRR to 100 beats/min.
d. Turn the power ON.
4. Verify that the following are displayed at the patient monitor:
- A sinusoidal waveform with an SpO2 label.
- An SpO2% reading between 97 – 100% (97 and 102%).
- A PRR reading between 97 and 103 beats per minute (it might be necessary to turn the
SpO2 ON).
5. Test the accuracy of these SPO2% settings.
Accuracy of SpO2 Settings
Simulator Setting Displayed Spo2 Value
99% (Both types) 97 – 100% (97 – 102%)
80.3% (84%) 78 – 82% (81 – 87%)
49.7 (63%) 48 – 52% (61 – 65%)

6. Test the accuracy of these PPR settings:

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Accuracy of PPR Settings

Simulator Setting Displayed PPR Value
70 68-72
100 97-103
160 156-164

7. Return the simulator to these conditions:

- Set the SpO2% to 99.
- Set the PPR to 100 beats/min.
8. Press the NOISE TEST button ON the simulator for 30 seconds.
9. Make sure the patient monitor still displays an SpO2 value between
97 and 100% (97 and 102%), or an interference detection message is displayed.
10. Turn the simulator OFF.
11. Disconnect the simulator cable from the device under test.

NOTE
A functional tester cannot be used to assess the accuracy of a pulse oximeter monitor.
However, it can be used to demonstrate that a particular pulse oximeter monitor
reproduces a calibration curve that has been independently demonstrated to fulfill a
particular accuracy specification.

4-11. Noninvasive Blood Pressure Test

Equipment
Use the following equipment for these tests:
- NIBP cuff coupling
- NIBP hose coupling
- NIBP tee
- NIBP tubing 2 m
- Manometer: mercury, digital
- NIBP tube
- NIBP cuff
- Pipe: PVC

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Procedures
1. Attach the digital manometer, noninvasive blood pressure (NIBP)cuff, tees and tubing, as shown
in the illustration below, to the NIBPconnector of the patient monitor.
2. Set the digital manometer power switch to the on position.
3. Set the digital manometer range switch to 200 mmHg.
Using the Trim Knob control, access the Service Mode menu starting from the Main Menu.
1. Select MORE MENU > SETUP > MAKER SERVICE.
2. Enter password using the Trim Knob control to select the day and month from patient monitor
screen with leading zeros.
3. Select CALIBRATE > NIBP > CHECK CAL.
The text on the menu item changes from CAL OFF to CAL IN PROGRESS.
Verify the readings in the NIBP parameter window on the patient monitor display and readings on
the digital manometer are equal (± 1mmHg) for at least one full minute. If the readings are not
equal for at least one full minute, the NBP circuit requires calibration.
4. Select CAL IN PROGRESS > STOP.
1

The pneumatic control circuit of the patient monitor vents air pressure in the pneumatic circuit of
the patient monitor to atmosphere and causes the NBP cuff to deflate.
5. Remove the NBP test setup apparatus from the patient monitor. The NBP tests are complete.
1

6. It is recommended that the performance be checked every 2 years and after maintenance and
repair, by utilizing the manometer mode.

4-12. NIBP Calibration

The overall accuracy of noninvasive blood pressure (NBP) readings by the patient monitor depend
on the following:
- the zero pressure reading, and
- the voltage span of the NBP sensor in the patient monitor.
This procedure provides a method of verifying these items are accurate and also checks the NBP
pneumatic circuit plumbing for leaks.

Warning
When the NBP cuff is used in this procedure, it must be tightly
wrapped around a rigid cylinder or pipe. DO NOT put the NIBP
cuff around a human arm during the calibration procedures due
to the potential for injury.

Calibration Procedure
Using the Trim Knob control, access the Service Mode menu starting from the Main Menu.

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1. Select MORE MENU-> SETUP-> MAKER SERVICE.

2. Enter password using the Trim Knob control to select the day and month from patient monitor
screen with leading zeros.
3. Select CALIBRATION-> NIBP-> CAL ZERO OFF->START.
4. The text on the menu item changes from Cal Zero Off to Cal Zero In Progress.
When the process is complete, the menu item shows that it is OFF again.
Gain Calibration Test
1. Connect a cuff and manometer to the patient monitor.
2. Turn the digital manometer on and adjust the range switch to 1000mmHg.
3. Select CAL GAIN OFF-> CAL GAIN OFF-> START.
4. The second line of text on the Cal Gain menu item changes from Cal Gain Holding to Cal Gain
Inflating. The patient monitor starts pumping up the pressure bulb or cuff—the audible whirring
sound of the NBP pump motors occurs and an increase in displayed pressures on both the patient
monitor and the manometer can be observed.
5. The pump shuts off at about 250 mmHg, and the pressure drops slowly to about 240 mmHg
before stabilizing. The second line of text on the Cal Gain menu item changes from Inflating back
to Holding. If the pressure continues to drop at a rate of 1 mmHg or more for every five seconds,
there is a leak in the NBP plumbing. If there is a leak in the NBP plumbing, repair it and restart this
calibration procedure.
6. Select ENTER CAL PRESSURE and use the Trim Knob control to select a pressure value that is 1
mmHg lower than the current manometer reading. When the manometer falls to exactly the value
that you selected in the pop-up window, press the Trim Knob control to enter the value.
7. Select CHECK CAL OFF-> START.
8. The text on the menu item changes from Check Cal Off to Check Cal In Progress. Verify the
pressure readings (shown as Cuff in the NIBP parameter box) on the patient monitor and
manometer are equal (± 1mmHg) for AT LEAST one full minute.
9. Select CHECK CAL IN PROGRESS -> STOP. The patient monitor automatically releases pneumatic
pressure in the entire plumbing circuit.
1

10. Unplug the patient monitor from AC power source and remove the test apparatus from the
patient monitor.

ECG or BP Calibration
To complete the ECG or BP calibration, connect a voltmeter to the patient monitor.
1. Attach the analog output cable (pn 2000633-001) to the patient monitor.
2. Connect a 5.5 digit precision voltmeter to the port pin to be calibrated (If ECG: Pin 7 = ECG
signal, Pin 3 = ground. If BP: Pin 6 = BP, Pin 5 = ground.).

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3. Access the patient monitor’s Service Mode

4. Calibrate the ECG or the BP parameters as follows.

4-13. ECG Calibration

Using the Trim Knob control, access the Service Mode menu starting from the Main Menu.
1. Select MORE MENU-> SETUP-> MAKER SERVICE.
2. Enter password using the Trim Knob control to select the day and month from patient monitor
screen with leading zeros.
3. Select CALIBRATION-> CAL ECG.
4. Select CONFIRM ECG CAL to confirm or abort the calibration

4-14. IBP Calibration

Using the Trim Knob control, access the Service Mode menu starting from the Main Menu.
1. Select MORE MENUS-> MONITOR SETUP-> SERVICE MODE.
2. Enter password using the Trim Knob control to select the day and month from patient monitor
screen with leading zeros.
3. Select CALIBRATE-> IBP CAL.
4. Adjust the count for 100mmHg on the meter and press the TrimKnob control.
5. Select CONFIRM iBP CAL to confirm or abort the calibration

4-15. End tidal CO2 Test (Option)

To verify the mainstream end-tidal CO2, refer to the CO2 chapter in the Patient Monitor Operator’s
Manual. This test requires you perform a zero and reference check by using the sample cells
provided on the end-tidal CO2 cable.
For instructions on verifying sidestream end-tidal CO2 and setting the sample line to zero, refer to the
CO2 module operator instructions.

4-16. Battery Test

1. Disconnect the power cord plug from the power outlet.
2. Verify the BATTERY front panel indicator lights. This indicates operation from the patient monitor’s
battery power.
3. Setup the patient simulator as follows:
- ECG heart rate – 80 bpm,
- ECG amplitude – 1.0 mV,
- 5-lead patient cable attached.
4. Observe the following:

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- ECG Lead II is displayed and is noise-free,

- Heart rate of 80 ±1 bpm is displayed,
- With QRS VOLUME enabled, an audible tone sounds with each R-Wave.
5. Verify all six ECG leads are selectable for display on the patient monitor.
6. Connect the power cord plug to the power outlet.
7. Verify the AC front panel indicator lights. This indicates the patient monitor is operating from
power outlet (AC) power.
8. Verify the CHARGING STATUS front panel indicator lights for a few minutes.
- An amber glow indicates the patient monitor battery is charging.
A green glow indicates the patient monitor batteries are fully charged.

4-17. Graph speed

Using the Trim Knob control, access the Graph Setup menu starting from the Main Menu.
1. Select MORE MENU > PRINT SETUP.
2. Select SPEED:25 (default).
3. Verify that all eight speeds work.

4-18. Speaker Test

1. Change the alarm volume of the patient monitor to 100%.
2. Verify the speaker volume of the patient monitor changes accordingly.
3. Return the volume of the patient monitor to the level it was previously set to, before you changed
it for this test.

4-19. Data Acquisition Test

ECG Functions
1. Connect the Multifunction simulator and appropriate patient cables, to the ECG connector of
the patient monitor. Turn the patient monitor and the patient simulator on.
2. Set the patient monitor to display leads I, II, III, and V simultaneously:
a. From the main menu, select DISPLAY.
b. Make sure the Display menu item shows Individual plus six waveforms. If it shows Full, change it
to Individual.
c. Select ECG VIEW: 7ch from the menu.
d. Set the displayed waveforms for ECG leads:
3. Set the patient simulator to output calibration (cal) pulses at 1.0 mV.
4. Measure the cal pulse ( ) amplitude. These should be (+/–20%):

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- Lead I:0.5 mV
- Lead II:1 mV
- Lead III:0.5 mV
- Lead V:–0.5 mV
5. It may be necessary to run a graph to accurately measure the cal pulses. Perform these steps to
graph all four waveforms.
a. From the main menu, select GRAPH & ALARMS.
b. Select GRAPH CONTROL from the menu.
c. Set the graphed waveforms for the ECG leads:
d. Press the Graph Go/Stop (Print on Dash 5000) front panel
control on the patient monitor to start and stop a manual graph.
e. Compare the printed graph with the sample shown below.

f. Change the patient simulator output from cal pulses to an 80bpm ECG waveform.
The displayed ECG waveforms should be similar to those shown in the figure below.

If this is the case, the ECG functions of the analog2 PCB, as well as communication between the
acquisition and processor PCBs function as designed.
1

ECG Waveforms Display Incorrectly

1. If the calibration pulses are NOT correct, test the patient simulator using a working patient
monitor. If the patient simulator functions as designed, calibrate the acquisition PCB. Refer to “ECG
Tests”
2. If displayed ECG waveforms contain a significant amount of noise, check the ECG patient
cables.

3. Test the patient simulator and ECG patient cables on a working patient monitor to verify the ECG

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signal.
4. If the ECG signal, patient simulator and ECG patient cables are good, the acquisition PCB is
suspect and you need to replace it.

ECG Waveforms Do Not Display At All

1. Test the ECG patient cables on a working patient monitor.
2. Test the patient simulator on a working patient monitor.
3. Swap the acquisition PCB into a working patient monitor. If the symptoms follow the PCB into the
working patient monitor, replace the acquisition PCB.
4. If none of these first three steps provide any results, swap the processor PCB and/or power supply
PCB into a working patient monitor.

Lead Fail Functions

1. With the patient monitor displaying leads I, II, III, and V from the patient simulator, remove the RA
leadwire from the patient simulator.
2. The patient monitor should display a warning of a RA FAIL message.
Lead fail detection functions properly if this is the case. Lead fail detection does not function
properly if this is NOT the case. The analog2 PCB is suspect. Swap the PCB with a working patient
monitor to verify the malfunction.
3. Reattach the RA leadwire to the patient simulator.
Pace Detect Functions
1. With the patient monitor displaying leads I, II, III, and V, set the patient simulator to output a
ventricular pacemaker simulation waveform.
2. Enable the pacemaker detection function of the patient monitor.
a. Select ECG from the display main menu,
b. Select PACEMAKER and set to ON.
3. Verify the heart rate remains at approximately 80 bpm.
4. Select the ventricular pacemaker simulation on the patient simulator.
5. The heart rate number may disappear from the display for a few seconds and return to the
screen shortly thereafter. Verify the heart rate is at approximately 80 bpm. Verify the pacemaker
spikes display at the same amplitude.
6. Disable the pacemaker detection function of the patient monitor.
Verify the displayed pacemaker spikes have a different amplitude than in the previous step.
7. Select the AVS output (A/V sequential pacemaker simulation) on the patient simulator.
8. Verify the displayed pacemaker spikes are at different amplitudes.
9. Enable the pacemaker detection function of the patient monitor once again.
10. Set ECG GAIN to X2.

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11. Verify a stable heart rate display of approximately 80 bpm. Verify the pacemaker spikes are
again at the same amplitude.
12. Disable the pacemaker detection function of the patient monitor.

Pace Detect Functions Do Not Work Properly

If the pacemaker detection test results are not correct, as described above, complete the
following steps.
1. Verify the patient simulator functions correctly by testing it on a working patient monitor.
2. If the simulator is functioning correctly, the analog2 PCB is suspect. Swap a working acquisition
PCB into the patient monitor and perform this test to verify correct operation.

Invasive Blood Pressure Functions (option)

The invasive blood pressure (IBP) test procedure requires the use of the following patient simulator:
Multifunction simulator. If you need to use a different patient simulator, adjust the procedure
steps/readings accordingly.

Setup IBP
Connect the Blood Pressure output of the patient simulator to each enabled IBP patient connector
on the side panel of the patient monitor.
Zero-Reference Enabled BP Input
Properly zero-reference each enabled BP input.
1. Set the patient simulator IBP output to 0 mmHg
2. Press the ZERO ALL (FUNCTION) key on the patient monitor.

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Generate Dynamic IBP Waveforms

1. Set the patient simulator IBP output to a 120/80 Wave.
2. Setup the IBP scales on the patient monitor to best match the waveform output.
3. Repeat steps 1 and 2 for each enabled IBP channel.
Verify Dynamic BP Results
Once the IBP waveforms are setup as described above verify the following:
- Waveforms are noise-free, as shown in the figure below.
- IBP displayed parameters are within tolerance as indicated in the following list:

Generate Static IBP Waveforms

1. Set the patient simulator IBP output to 200 mmHg, static pressure.
2. Verify the IBP channel is working correctly if systolic, diastolic, and mean pressure values for BP
are displaying parameter readings between 194 and 206 mmHg.
3. Repeat steps 1 and 2 for each enabled IBP channel.

IBP Waveforms Do Not Appear Correctly On The Display

1. If the IBP waveforms displayed on the patient monitor appear noisy or distorted (example shown
below), test the Patient simulator and simulator test cables and on a working patient monitor to
determine the source of the problem.
2. If the static pressure test results were inaccurate, test the Patient simulator and simulator test
cables and on a working patient monitor to determine the source of the problem.
3. If the patient simulator and associated test cables are determined to be functioning correctly,
replace the Analog1 Board.

IBP Waveforms Do Not Appear On The Display At All

1. If the IBP parameter labels, readings and associated waveforms do not display on the patient
monitor, verify the patient simulator and associated test cables on a working patient monitor.
2. Inspect the IBP side panel connectors on the patient monitor for bent or broken pins. If any pins
are bent or broken, replace Jack cover assembly.
3. Inspect the dual BP cable connectors on the patient monitor for bent or broken pins. If any pins
are bent or broken, replace the Jack cover assembly.

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Respiration Functions
Connect the Multifunction simulator and appropriate patient cables to the ECG/RESP side panel
connector on the patient monitor.
1. Adjust the patient simulator to output a respiration waveform using the following settings:
- Rate BPM – 30
- Baseline Impedance Ohms – 750,
- ∆R Ohms – 2.0.
2. Enable the respiration function of the patient monitor.
a. Select SETUP from the main menu display on the patient monitor,
b. Select PARAMETERS ON/OFF from the patient monitor setup menu.
c. Turn and push the Trim Knob control to scroll to and select RR in the parameters on/off pop-up
window.
d. Toggle and select ON in the RR line of the parameters on/off popup window.
3. Verify the following:
- Respiration rate is displayed and accurate.
- Respiration waveform is displayed and noise-free.

No Respiration Waveform or Rate Appear on the Display

If the respiration waveform or rate does not appear on the patient monitor display, perform the
following steps to isolate the problem.
1. Vary the baseline impedance on the patient simulator
2. Vary the ∆R on the patient simulator.
3. Test the patient simulator and appropriate patient cables on a working patient monitor to
determine the source of the problem.
4. If none of the previous recommendations corrects the problem, the acquisition PCB is suspect.
Swap the PCB into a working patient monitor to determine the source of the problem and replace
as necessary.

Markers do not Appear on Respiration Waveform; Respiration Rate is Inaccurate

If the markers on the respiration waveform do not appear on the display or the respiration rate
count is inaccurate, try changing the respiration sensitivity level on the patient monitor. Use the Trim
Knob control on the patient monitor to select the following menu options.
1. Scroll to and select RESP (respiration parameter) from the patient monitor main menu,
2. Scroll to and select AMPLITUE from the respiration parameter menu, and
3. Scroll to and select a different Amplitue size (x) from the sensitivity menu

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Respiration Functions Work Properly on Patient Simulator but not on Actual Patient
Refer to the Operator’s Manual for detailed information regarding patient preparation relative to
respiration monitoring functions.
Achieving optimum results for respiration waveforms and accurate respiration rate detection by the
patient monitor requires proper preparation for ECG electrode placement on the patient. Following
is an example of a noisy respiration waveform which is usually due to bad patient preparation.

NOTE
With patients that exhibit excessively high baseline chest
impedance, proper respiration monitoring can be extremely difficult,
if not impossible.
Noninvasive Blood Pressure Functions
Perform the noninvasive blood pressure (NIBP) Checkout Procedure found in the Maintenance
chapter. This procedure determines whether or not the NIBP functions of the patient monitor are
working as designed or whether the patient monitor requires NIBP calibration.
If, after performing the prescribed checkout procedure, it is determined that there are potential
problems that NIBP calibration does not cure, try the following:
1. If calibration is unsuccessful and cannot be properly performed, there could be leaks in the
pneumatic circuit plumbing. The following steps assist you in determining this.
The NIBP cuff and tubing is the easiest area to inspect for leaks and is also the most likely area for
failure in this regard. Closely inspect these items for cracks or leaks. Test the NIBP cuff and
tubing on a working patient monitor to determine the source of the problem.
If the NIBP cuff and tubing are determined to be good after testing them on a working patient
monitor, the leaks are probably internal to the patient monitor. Disassemble the patient monitor
and check inspect all internal tubing and connections in the pneumatic circuit plumbing.
2. If no leaks are found after performing the previous step, the NIBP pump assembly is suspect. Swap
the NIBP pump assembly with one from a working patient monitor and/or replace as necessary.

4-20. Checkout Procedure Completion

This completes all tests associated with the checkout procedures.
1. Discharge the test patient admitted during the “ECG Tests”
2. Set all test equipment power switches to the off position.
3. Unplug the patient monitor (or docking station) from AC power.
4. Remove all test equipment from the patient monitor.

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Section 5 Assemblies and Kits

5-1. Introduction
This section contains additional information for quick identification of assemblies and kit
contents.

5-2. Replacing Parts

1) Digital Board Ass’y (PCB-470-DIG-4)

2) KEY BOARD ASS’Y (PCB-470-KEY-1)

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3) CONNECTOR BOARD ASS’Y (PCB-410-CON-5)

4) POWER BOARD ASS’Y (PCB-400-PWR-10)

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5) ANALOG2 (12CH ECG) BOARD ASS’Y (PCB-460-ECG12-2)

6) ANALOG2 (7CH ECG) BOARD ASS’Y (PCB-460-ECG07-2)

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7) ANALOG1 (SPO2,IBP,TEMP) BOARD ASS’Y (PCB-400-ANA1-C-3)

8) I/F BOARD ASS’Y (PCB-400-IF-7)

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9) NIBP MODULE ASS’Y

10) PRINTER BOARD ASS’Y (PCB-400-PRN-3)

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11) CON SIGNAL BOARD ASS’Y (PCB-410-CON-5)

12) MULT-ECG CONNETOR BOARD ASS’Y (MULTI-ECG-CON)

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13) USB EXT BOARD ASS’Y (PCB470-USB-SD-IF-1)

14) ANA3 CONNETOR BOARD ASS’Y (PCB-470-ANA3-CON-1)

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15) ANALOG3 (C.O. IBP, CSM) BOARD ASS’Y (PCB-470-ANA3-1)

16) CSM BOARD ASS’Y

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Section 6 Disassembly and Reassembly

Warning
•Before attempting to open or disassemble the monitor, disconnect
it from the AC mains supply.
•Energized circuits are accessible with the covers open. Do not work
on the monitor with the covers open and AC power connected.
Only qualified service personnel should open or disassemble the
monitor.

6-1. Introduction
Remember to store all screws and parts in a safe place for later refitting.

6-2. How to Use this Chapter

- The disassembly sections detail the step-by-step procedures you use to access
replaceable parts of the monitor and the transducers.
- All major assemblies are fitted to the chassis assembly.
- The chassis assembly consists of the chassis, the power supply assembly, the main
CPU board, Basic Board ,the sensor sockets, the recorder assembly, the front bezel
assembly including touchscreen display, the speaker, the noninvasive blood
pressure assembly, the SpO2 assembly, the USB, RS232/LAN connector.

6-3. Tools Required

You need the following tools:

① Nipper

② Screwdriver(4mm X 100mm)

③ Screwdriver(6mm X 200mm)

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6-4. Screws Used

The following picture shows the range of screws used in the COMPACT 9:

BH M3X5 BH M3X8 Tapping

BH SEMS M3X5 BH M2X8 Tapping

BH M3X10 BH M3X18 Tapping

BH M3X6 BH M2X4 Tapping

FH M3X6 BH M1.7X3 Tapping

BM M3X8 Metal Support 30mm

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6-5. Disassembly

1) Removing the Battery cover of equipment

2) Removing the rear cover of equipment

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3) Removing the cable of equipment

4) Removing the cable of equipment2

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5) Removing the Printer of equipment

6) Removing the frame of equipment

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7) Removing the printer module of equipment

8) Removing the printer module board of equipment

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9) Removing the thermal module of equipment

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10) Removing the printer gear module of equipment

11) Removing the rear handle case of equipment

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12) Removing the battery frame of equipment

13) Removing the frame box of equipment

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14) Removing the frame rear cover of equipment

15) Removing the speaker of equipment

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16) Removing the analog1 board of equipment

17) Removing the analog2 board of equipment

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18) Removing the power board of equipment

19) Removing the jack cover of equipment

20) Removing the jack cover of equipment

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21) Removing the interface board of equipment

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22) Removing the connector board of equipment

23) Removing the front cover of equipment

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24) Removing the front cover cable of equipment

25) Removing the analog3 board cable of equipment

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26) Removing the digital board cable of equipment

27) Removing the front cover case of equipment

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28) Removing the analog3 bracket of equipment

29) Removing the csm module of equipment

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30) Removing the analog3 board of equipment

31) Removing the front jack cover of equipment

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32) Removing the front jack cover cable of equipment

33) Removing the front jack cover module of equipment

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34) Removing the extra battery of equipment

35) Removing the extra battery case of equipment

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36) Removing the usb_sdcard board of equipment

37) Removing the key and alarm board of equipment

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38) Removing the printer board and digital board cable of equipment

39) Removing the digital board of equipment

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40) Removing the front cover bracket of equipment

41) Removing the key board of equipment

42) Removing the key housing of equipment

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43) Removing the lcd bracket of equipment

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44) Removing the lcd bracket rubber of equipment

38) Removing the lcd module of equipment

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6-6. Reassembly

- Reassemble the reverse way from number 40 to 1.

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Section 7 Replaceable Parts List and Accessory

7-1. Replaceable Part List

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NO Detail parts DESCRIPTION Q’TY

1 470-M-COV-2001A Front-Cover 1
2 470-L-COV-2017A LCD-Window-COMPACT 9 1
3 470-M-COV-2018A ROTARY_KNOB 1
4 TM121SDS01+TSP- LCD ASS’Y (TM121SDS01+TSP) 1
ASSY
5 470-R-CUS -2024A LCD_RUBBER_FIX 1
6 470-M-COV-2012A FRONT_KNOB_KEY_COMPACT 9 1
7 470-M-COV-2012A FRONT_KNOB_KEY_COMPACT 9 1
8 470-M-COV-2022A FRONT_POWER_KEY_COMPACT 9 1
9 PCB-470-KEY-1 PCB KEY BOARD 1
10 470-M-COV-3010A RUBBER_FOOT_COMPACT 9 1
11 470-P-BKT-2022B BKT-LCD-HOLDER-TIANMA 2
12 470-M-COV-2015A USB_COVER_ASSY_COMPACT 9 1
13 PCB-470-ALARM-1 ALARM_LED_BOARD 1
14 PCB-470-USB-SD-IF-1 USB_EXT_BOARD_ASS’Y 1
15 PCB-460-DIGI-4 DIGITAL_BOARD_ASS’Y 1
16 PCB-400-PRN-3 PRINTER_BOARD_ASS’Y 1
17 SCREW TAPPING BH M3X8 11
18 SCREW SEMS M3X5 15
19 SCREW BH M3X5 4
• For spare part ordering, please contact Medical Econet service department

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NO Part Num. DESCRIPTION Q’TY

1 470-M-COV-1001A MIDDLE_Cover_COMPACT 9 1
2 470-L-COV-1010A MIDDLE_JACK_COVER 1
3 470-P-BKT-1016A BATTERY_COVER 1
4 470-P-BKT-1022A BRACKET_ANA3_BOARD_COMPACT 9 1
SE
5 470-P-BKT-1017A EXT_BATTERY_ROOM_BRACKET 1
6 PCB-470-ANA3-CON-1 JACK_CONNECTOR BOARD ASS’Y 1
7 470-CSM-SIGCON-CABLE 4PIN CONNECTOR 1
8 lithium ion Battery (4300mA) 2x3 EXT BATTERY PACK 1
9 CSM Modular PCB CSM MODULE 1
10 PCB-470-ANA3-1 ANA3 BOARD 1
11 470-FPC-20P-FM2MM FPC 20PIN CABLE 1
12 SCREW TAPPING BH M3X8 33
13 SCREW SEMS M3X6 5
14 SCREW BH M3X5 4
• For spare part ordering, please contact Medical Econet service department

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NO Part Num. DESCRIPTION Q’TY

1 470-M-COV-3010 FOOT-RUBBER-COMPACT 9 1
2 470-L-COV-1010A SYSTEM_REAR ASS’Y 1
3 470-P-BKT-1016A SYSTEM_FRONT ASS’Y 1
• For spare part ordering, please contact Medical Econet service department

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NO Part Num. DESCRIPTION Q’TY

15 400-P-BKT-2253A JACK BRACKET 1
16 500-B-ASY-1100A 18P CON ASS’Y 1
17 TEMP CONNECTOR ASS’Y 2
18 SpO2 IBP CONNECTOR ASS’Y 1
19 963006W SCREW(M3X6L, ROUND) 4
20 NIBP CONNECTOR ASS’Y 1
21 500-M-COV-2270A COVER JACK/VIOLET/BM5 1
22 EtCO2 12P CON 1
23 500-B-ASY-1200A CABLE REUUBER 12P ASS’Y 1
24 400-A-BKT-2234A LOWER BRACKET ASS’Y 1
25 400-M-GID-3540A CONNECTOR B/D ASS’Y 1
26 963006RW SCREW(M3X6L, ROUND) 3
27 PCB-400-IF-6 I/F B/D ASS’Y 1
28 963006RW SCREW(M3X6L, ROUND) 4
29 400-P-BKT-2234A PRINTER BRACKET 1
30 400-M-GID-3540A PCB GUIDE 1
31 963006RW SCREW(M3X6L, ROUND) 2

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32 400-P-SHL-3481A SHEILD PLATE 1

33 963006RW SCREW(M3X6L, ROUND) 3
34 PCB-400-ANA1-C-3 ANALOG1 B/D ASS’Y 1
35 PCB-460-ECG07-2 ANALOG2 B/D ASS’Y 1
36 PCB-400-NIBP-001 NIBP B/D ASS’Y 1
37 510-P-PKT-6100A NIBP-BRACKET 1
38 400-L-SPT-4590A SUPPPORT 4
39 9230026W NUT (M3) 4
40 PCB-400-PWR-010 POWER B/D ASS’Y 1
41 963006RW SCREW(M3X6L, ROUND) 4
42 NIBP B/D ASS’Y (SUNTECH) 1
43 400-L-SPT-4550A SUPPORT 4
44 400-P-BKT-2302A COVER BRACKET 1
45 963006RW SCREW(M3X6L, ROUND) 4
46 400-P-BKT-2314A REAR BRACKET 1
47 SPEAKER ASS’Y 1
48 963006RW SCREW(M3X6L, ROUND) 2
49 POL-100-EARTH GND POLE ASS’Y 1
50 963006RW SCREW(M3X6L, ROUND) 10
51 973006RY TAPPING SCREW(3X8L, ROUND) 4
52 400-M-COV-1326A REAR COVER / SKY BLUE / COMPACT 9 1
53 400-M-COV-3371A PROTECT COVER/ SKY BLUE 1
54 400-M-HND-2332A HANDLE-FRONT/ SKY BLUE / COMPACT 9 1
55 400-M-HND-2342A HANDLE-REAR/ SKY BLUE / COMPACT 9 1
56 400-M-HND-2352A HANDLE –HOOK/ SKY BLUE / COMPACT 9 1
57 972612RY TAPPING SCREW(2.6X12L, ROUND) 1
58 400-M-COV-3531A LED COVER(COMPACT 9) –투명 1
59 LED B/D ASS’Y 1
60 972008RW TAPPING SCREW(2X8L, ROUND) 2
61 973008RY TAPPING SCREW(3X8L, ROUND) 2
62 973018BY TAPPING SCREW(3X18L, BIND) 2
63 RUF-22 FOOT (φ22X5) 4
64 963008RW SCREW (M3X8L, ROUND) 4
64 510-P-BKT-3580A BATTERY HOLDER BRACKET-3 1
65 963006RW SCREW(M3X6L, ROUND) 2
66 BATTERY- 3 1
67 510-P-BKT-3570A BATTERY HOLDER BREACKET-6 1
68 400-L-SCR-4400A SCREW 2
69 BATTERY-6 1
70 400-M-COV-2383A BATTERY COVER/ SKY BLUE 1
71 400-L-SCR-4400A SCREW 2
72 400-K-SCR-4400A MARK LABEL 1
73 400-K-LBL-4420B ID LABEL / EN 1
74 400-M-COV-2012A PRINTER FRAME/ WHITE 1
75 PCB-400-PSEN-1 PRINTER SENSOR B/D ASS’Y 1
76 963006RY TAPPING SCREW(2X4L, ROUND) 2
77 MGM-01A MOTOR ASS’Y 1
78 961703RW SCREW(M1.7X3L, ROUND) 2
79 400-M-GER-3020A GEAR (A) 1
80 400-M-GEA-3030A GEAR (B) 1
81 400-L-SFT-4040A SHAFT 1
82 FJ04808R471 TPH ASS’Y (AOI) 1

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83 400-P-SPR-3061A PLATE SPRING 1

84 400-A-ROL-3070A PLATE ROLLER ASS’Y 1
85 400-M-GER-3080A PLATE GEAR 1
86 400-M-COV-2091A PRINTER COVER 1
87 BD-400-PCON-1 PRINTER CONNECTOR B/D ASS’Y 1
88 963006RW SCREW (M3X6L, ROUND) 2
89 510-K-LBL-5100A REAR COVER CAP (φ7.6X2.5) 3
90 510-K-LBL-5110A REAR STICKER (φ 8X0.18) 2
91 963006RW SCREW (M3X6L, ROUND) 2
92 400-M-COV-2610A FRAME COVER/ SKY BLUE / COMPACT 9 1
93 963008RW SCREW (M3X8L , ROUND) 4

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7-2. Accessory
 Basic Accessory
Item Code
Picture Description
(Part No.)

1 152600-024000 Multi ECG 5-Lead Button EN Cable For USA

2 152600-024300 Multi ECG 5-Lead Button EU Cable For Europe

SPO2 extension cable 7 Pin type

3 152600-004002 Caution : If s/n are October 2005 and November 2005,

please check if it is 7 pin or 6 pin.

Adult

4 152600-003400 SpO2 Finger Probe

Reusable type

5 152600-02500 Multi ECG 10-Lead Button EN Cable For USA

6 152600-022401 NIBP extension tube(3M)

Adult NIBP cuff

7 152600-033500
Circumference: 458 * 143 cm

DC Adaptor for PM and FM

8 152600-000600 Input : 100 to 240V~ AC (50-60 Hz), 2.5A

Ouput : +18V, 2.5A

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Thermal paper roll of patient monitor

9 152600-007000 Dimension : 57X15

Continuous use 10 minutes

 Option Accessory

Item Code
Picture Description
(Part No.)

152600-
1 Multi ECG 3-Lead Button EN Cable For USA Option
023900

152600-
2 Multi ECG 3-Lead Button EU Cable For Europe Option
024200

152600-
3 Multi ECG 10-Lead Button EN Cable For USA
025000

152600-
4 Multi ECG 10-Lead Button EU Cable For Europe
025300

Child

152600- SpO2 Finger Probe

5
003500 Reusable type

Option

152600- DS01 - More than 30Kg Adult finger

6
003600 Option

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DS02 - Less than 30Kg Child finger

152600- Disposable type

7
003700 DS02

Option

152600- DS03 - Multi-site for Neonatal feet or Adult finger

8
003800 Option

152600- Infant NIBP cuff

9
033510 Circumference : 9-14.8cm

152600- Child NIBP cuff

10
033520 Circumference : 13.8-21.5cm

152600- Small Adult NIBP cuff

11
033530 Circumference : 20.5-28.5cm

152600- Big Adult NIBP cuff

12
033540 Circumference : 35.5-46cm

152600- Thigh NIBP cuff

13
033550 Circumference : 45-56.5cm

Vet. NIBP cuff

151500-
14 Cuff Size : 210 * 60
056000
Arm Circumference : 8 to 13 Cm

Temperature sensor - E
152600-
15 Surface/Skin type
006800
Option

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Temperature sensor - E
120108-
16 Rectal type
042600
Option

120108-
17 Single line monitoring kit. I-MX9604A Option
044400

Single line cable

120108-
18 I-MX961Z42
042100
Option

Transducer mounting plate

120108-
19 I-MX960
044200
Option

Clamp for transducer bracket

120108-
20 I-MX261
043700
Option

120108-
21 Double line monitoring kit. I-MX9602A Option
044300

Double line cable

120108-
22 I-MX962Z42
042200
Option

Transducer mounting plate

120108- X 2 EA
23
044200 I-MX960

Option

Transducer bracket for two transducer mounting plates

120108-
24 I-MX262
043800
Option

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Clamp for transducer bracket

120108-
25 I-MX261
043700
Option

120108-
26 Single line monitoring kit. I-MX9504T Option
044100

Single line cable

120108-
27 I-MX95114
042000
Option

Modular transducer mounting plate

120108-
28 I-MX800
044000
Option

Pole clamp for mounting a transducer plate

120108-
29 I-MX240
043600
Option

C-Fusor 1000ml Pressure Infusor complete unit

120108- with squeeze bulb and pressure gauge.

30
043900 I-MX4810

Option

120200- CAPNOSTAT 5 CO2 Mainstream Sensor

31
011400 Option

Reusable Adult Airway Adapter

120108- For CAPNOSTAT® 5 CO2 Mainstream Sensor

32
054600 7007-01

(1 per box)Option

Reusable Infant/Neonatal Airway Adapter

120108- For CAPNOSTAT® 5 CO2 Mainstream Sensor

33
054700 7053-01

(1 per box) Option

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120200- LoFlo Sidestream Module

34
011500 Option

LoFlo Sidestream Module Bracket

35 N/A (This material is being provided free of charge for LoFlo

Sidestream Module.) Option

Nasal CO2/O2 Cannula-Adult

120108- For Non-Intubated Patients

36
055300 3469ADU-00

(10 per box) Option

Nasal CO2/O2 Cannula-Infant

120108- For Non-Intubated Patients

37
055900 3469INF-00

(10 per box) Option

Adult CO2 Airway Adapter

120108- For Intubated Patients

38
055600 3473ADU-00

(10 per box)Option

Infant CO2 Airway Adapter

120108- For Intubated Patients

39
055700 3473INF-00

(10 per box) Option

Battery type : Li-ION

151900-
40 (LITHIUM ION) Voltage : 11.1V Capacity : 2200mAh
009001
3 Cell, 1 Line

Battery type : Li-ION

151900-
41 Voltage : 11.1V Capacity : 4800mAh
009400
6 Cell, 1 Line

CABLE:백색
1
2
3.백색(RA) 470-CSM-PAT-CABLE
42 N/A CABLE:녹색
2.녹색(LL
)

3S PLUG 4P
CABLE:흑색
1.흑색(LA)
COMPACT 9 SE CSM Patient Cable

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CSM Modular PCB (Cat no.:CSM014)

43 N/A For direct integration in patient monitors with CSM06

cable

44 N/A CSM Procedure Pack (Box of 25) (Cat no.:EN720S)

COMPACT 9 SE Masimo Module Patient Cable

45 N/A
High performance Low Power Module ,UT (Cat no.:3315)

COMPACT 9 SE Masimo SpO2 Adult Probe

46 N/A
M-LNCS DCI Sensor (Cat no.:1863)

IRMA Ax+ Module (Cat no.:200601)

47 N/A
(CO2,N2O,5 AA, AA ID)

IRMA Airway Adapter (Adult/Pediatric) (Cat no.:106220)

48 N/A
(Box of 25)

IRMA Airway Adapter (Infant) (Cat no.:106260)

49 N/A
(Box of 10)

ISA OR+ Module (Cat no.:800401)

50 N/A
(CO2,O2,N2O,5 AA, AA ID)

51 N/A ISA OR+ 를 COMPACT 9 에 고정 하기 위한 기구물

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Nomoline (Cat no.:108210)

Sampling line with male luer lock connector

52 N/A
Single patient use, Adult/Pediatric/Infant, 2.0m (Box of

25)

Nomoline Adapter (Cat no.:108220)

53 N/A Sampling line with female luer lock connector

Adult/Pediatric/Infant, 0.15m (Box of 25)

Nomo Extension (Cat no.:108240)

54 N/A Sampling line with male luer lock connector, 2.0m (Box

of 25)

T-adapter (Cat no.:108250)

55 N/A Airway adapter with female luer lock connector,

Adult/Pediatric (Box of 25)

Cardiac Output Catheter

56 N/A 774HF75

Swan-Ganz Thermodilution catheter

Cardiac Output introducer Catheter

57 N/A M3L9FHSI

AVA introducer catheter

Cardiac Output Bath Temperature Probe (16591 or

58 N/A
16592)

Cardiac Output Patient Cable

59 N/A
470 ICO-PAT-CABLE

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Section 8 Connector Pin Assignment

8-1. Connector information
1) RS-232
The 9-way D-type connector is the RS-232 interface connector. The pin connections are
given in Table below.

Pin No. Connection Details

1 NC

2 RXD-Input

3 TXD-Output

4 NC

5 Ground-Isolated 0V reference

6 NC

7 NC

8 NC

9 NC

2) VGA
The 15-way D-type connector is the D-SUB interface connector. The pin connections are
given in Table below.

Pin No. Connection Details

1 RED

2 GREEN

3 BLUE

4,9,11 NC

5,6,7,8,10 Ground-Isolated 0V reference

12 CRT_SCL

13 HRTC

14 VRTC

15 CRT_SDA

3) USB
The 6-way A-type connector is a USB interface connector. The pin connections are given
in Table below.

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Pin No. Connection Details

1 Supply voltage positive

2 Data interface D-

3 Data interface D+

4 Ground-Isolated 0V reference

5 Shield GND 0V reference

6 Shield GND 0V reference

4) SD Card
The 13-way connector is the SD card interface connector. The pin connections are given
in Table below.

Pin No. Connection Details

1 Data signal 3

2 Input and output command

3 Supply voltage negative

4 Supply voltage positive

5 Clock signal

6 Supply voltage negative

7 Data signal 0

8 Data signal 1

9 Data signal 2

10 Write protect

11 SD card data signal

12 Ground-Isolated 0V reference

13 Ground-Isolated 0V reference

4) LAN
The 12-way connector is the LAN interface connector. The pin connections are given in
Table below.

Pin No. Connection Details

1 NC

2 Data interface D+

3 Ground-Isolated 0V reference

4 Data interface D-

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5 Data interface D-

6 Ground-Isolated 0V reference

7 Data interface D+

8 NC

9 NC

10 NC

11 Shield GND 0V reference

12 Shield GND 0V reference

8-2. Harness interfaces

- Pin connection details are given in the following tables for all the connectors fitted to all
boards.
1) COMPACT 9 ECG FFC (MECG-FFC)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 1 Ground-Isolated 0V reference

2 2 LA CARRIER

3 3 LL CARRIER

4 4 RA CARRIER

5 5 RA MEA

6 6 LA MEA

7 7 LL MEA

8 8 RA ECG

9 9 LA ECG

10 10 LL ECG

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11 11 V1 ECG

12 12 RL ECG

13 13 V2 ECG

14 14 V3 ECG

15 15 V4 ECG

16 16 V5 ECG

17 17 V6 ECG

18 18 CABLE DETECTION

19 19 Ground-Isolated 0V reference

20 20 Ground-Isolated 0V reference

2) COMPACT 9 EtCO2 CABLE (ETCO2-SIG-CABLE)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 1 Ground

2 2 NC

3 3 Ground

4 4 5VCC

5 5 ETCO2 Tx

6 6 ETCO2 Rx

7 7 CO2 RESET

8 8 NC

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3) COMPACT 9 WIRELSS LAN POWER CABLE (500-P-HRN-09)

Pin No. Connection Details

1 Ground-Isolated 0V reference

2 Voltatge supply 5Vdc

4) COMPACT 9 NURSE CALL CABLE (500-P-HRN-08)

Pin No. Connection Details

1 Ground-Isolated 0V reference

2 Nursecall information signal

5) COMPACT 9 DIGITAL BD PWR CABLE (Digi-PWR-Cable-12P)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 12 Ground-Isolated 0V reference

2 11 Ground-Isolated 0V reference

3 10 Ground-Isolated 0V reference

4 9 Voltatge supply 5Vdc

5 8 Voltatge supply 5Vdc

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6 7 Voltatge supply 5Vdc

7 6 Voltatge supply 7.5Vdc

8 5 Voltatge supply 7.5Vdc

9 4 Voltatge supply 7.5Vdc

10 3 Voltatge supply 18Vdc (Adapter power)

11 2 Voltatge supply 3.3Vdc (Main digital Power)

12 1 Voltatge supply 18Vdc (Adapter power)

6) COMPACT 9 DIGITAL BD LCD BACKLIGHT PWR CABLE (LCD-INV-Cable-4P-2P)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 1 Ground

2 NC

3 NC

4 2 12VCC

7) COMPACT 9 DIGITAL DATA CABLE (FFC-Digi-36P)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 1 VALVE ON2

2 2 POWER ON SIGNAL0

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3 3 POWER ON SIGNAL1

4 4 Voltage SW signal

5 5 VALVE ON0

6 6 VALVE ON1

7 7 MOTOR ON

8 8 RxD0

9 9 TxD0

10 10 L RxD-

11 11 L RxD+

12 12 L TxD-

13 13 L TxD+

14 14 PORT0

15 15 PORT1

16 16 PORT2

17 17 PORT3

18 18 Defibrillation sync signal

19 19 Audio Clock Signal

20 20 Speak data signal

21 21 Speak clock signal

22 22 Timer output 0

23 23 RxA

24 24 TxA

25 25 RxB

26 26 TxB

27 27 RxD1

28 28 TxD1

29 29 PORT4

30 30 RxD2

31 31 TxD2

32 32 RxC

33 33 TxC

34 34 RxD

35 35 TxD

36 36 N.C.

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8) COMPACT 9 DIGITAL KEY CABLE (FFC-Key-14P)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 14 Voltatge supply 3.3Vdc (Main digital Power)

2 13 Voltatge supply 18Vdc (Adapter power)

3 12 Voltatge INPUT Signal

4 11 Voltatge SW Signal

5 10 PHASE A signal

6 9 PHASE B signal

7 8 Rotary SW signal

8 7 Switch 0 signal

9 6 Switch 1 signal

10 5 Switch 2 signal

11 4 Switch 3 signal

12 3 AC led control signal

13 2 Battery led control signal

14 1 Ground-Isolated 0V reference

9) COMPACT 9 DIGITAL USB I/F CABLE (USB-BD-Cable-4P)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 1 Voltatge supply 5Vdc (Main digital Power)

2 2 USB D- SIGNAL

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3 3 USB D+ SIGNAL

4 4 Ground-Isolated 0V reference

10) COMPACT 9 DIGITAL ALARM LAMP SIGNAL CABLE (ALM-LED-Cable-8P)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 8 Voltatge supply 5Vdc

2 7 Voltatge supply 5Vdc

3 6 Voltatge supply 5Vdc

4 5 Yellow LAMP Control Signal

5 4 Red LAMP Control signal

6 3 Green LAMP Control signal

7 2 Ground-Isolated 0V reference

8 1 Ground-Isolated 0V reference

11) COMPACT 9 DIGITAL ALARM LAMP SIGNAL CABLE (ALM-LED-Cable-8P)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 8 Voltatge supply 5Vdc

2 7 Voltatge supply 5Vdc

3 6 Voltatge supply 5Vdc

4 5 Yellow LAMP Control Signal

5 4 Red LAMP Control signal

6 3 Green LAMP Control signal

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7 2 Ground-Isolated 0V reference

8 1 Ground-Isolated 0V reference

12) COMPACT 9 POWER SIGNAL CABLE (COMPACT 9-PWR-Cable-6P-3P-1B)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 3 Voltatge supply 18Vdc

2 NC

3 1 Ground-Isolated 0V reference

4 3 Ground-Isolated 0V reference

5 1 BAT Voltage supply

6 2 Battery Exist signal

13) COMPACT 9 POWER SIGNAL CABLE (470-EXT-BAT-Cable)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

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1 3 Battery Voltatge supply

2 2 Battery Ground

3 1 Battery Exist signal

14) COMPACT 9 ANALOG3 POWER SIGNAL CABLE (470-ANA3-PWR-Cable)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 NC

2 NC

3 2 Voltatge supply 5Vdc

4 1 Ground-Isolated 0V reference

15) COMPACT 9 ANALOG3 COM SIGNAL CABLE (470- ANA3-COM-Cable)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 6 Voltatge supply 3.3Vdc

2 5 RxA

3 4 TxA

4 3 RxB

5 2 TxB

6 1 Ground-Isolated 0V reference

16) COMPACT 9 CSM COM SIGNAL CABLE (470-CSM-SIGCON-Cable)

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Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 1 Black lead

2 2 GREEN lead

3 3 White lead

4 NC

17) COMPACT 9 MASIMO COM SIGNAL CABLE (470-MASSPO2-COM-Cable)

Basic Board
SMPS
Connector Connection details
Connector Pin
Pin

1 5 Voltatge supply 5.0Vdc

2 4 Voltatge supply 3.3Vdc

3 3 RxB

4 2 TxA

5 1 Ground-Isolated 0V reference

Section 9 PCB Part disposition

9-1. Main Digital Board (PCB-470-DIG-4)

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9-2. Analog1 Board(PCB-400-ANA1-C-3)

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17) Analog2 Board-7ch (PCB-460-ECG07-2)

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9-3. Analog2 Board-12ch (PCB-460-ECG12-2)

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9-4. Analog3 Board (PCB-470-ANA3-1)

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9-5. Power Board (PCB-400-PWR-10)

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9-6. Key I/F Board (PCB-470-KEY-1)

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9-7. USB/SDcard I/F Board

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9-8. Connector Signal Board(PCB-410-CON-5)

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9-9. I/F Board (PCB-400-IF-7)

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9-10. Analog3 connector Board (PCB-470-ANA3-CON-1)

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9-11. Printer Board(PCB-400-PRN-3)

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9-12. Multi-ECG-connector Board (MULTI-ECG-CON)

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9-13. Connector Board(PCB-410-CON-5)

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9-14. Alarm LED Board (PCB-470-ALARMLED-1)

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