EDAN iM80 Building instructions

I
About this Manual
P/N: 01.54.455512-10
Release Date: April 2012
© Copyright EDAN INSTRUMENTS, INC. 2012. All rights reserved.
Statement
This manual will help you understand the operation and maintenance of the product better. It is
reminded that the product shall be used strictly complying with this manual. User’s operation
failing to comply with this manual may result in malfunction or accident for which EDAN
INSTRUMENTS, INC. (hereinafter called EDAN) can not be held liable.
EDAN owns the copyrights of this manual. Without prior written consent of EDAN, any
materials contained in this manual shall not be photocopied, reproduced or translated into other
languages.
Materials protected by the copyright law, including but not limited to confidential information
such as technical information and patent information are contained in this manual, the user shall
not disclose such information to any irrelevant third party.
The user shall understand that nothing in this manual grants him, expressly or implicitly, any
right or license to use any of the intellectual properties of EDAN.
EDAN holds the rights to modify, update, and ultimately explain this manual.
Responsibility of the Manufacturer
EDAN only considers itself responsible for any effect on safety, reliability and performance of
the equipment if:
Assembly operations, extensions, re-adjustments, modifications or repairs are carried out by
persons authorized by EDAN, and
The electrical installation of the relevant room complies with national standards, and
The instrument is used in accordance with the instructions for use.
Upon request, EDAN may provide, with compensation, necessary circuit diagrams, and other
information to help qualified technician to maintain and repair some parts, which EDAN may
define as user serviceable.

II
Terms Used in this Manual
This guide is designed to give key concepts on safety precautions.
WARNING
A WARNING label advises against certain actions or situations that could result in personal
injury or death.
CAUTION
A CAUTION label advises against actions or situations that could damage equipment, produce
inaccurate data, or invalidate a procedure.
NOTE
A NOTE provides useful information regarding a function or a procedure.

III
Table of Contents
Chapter 1 Warranty and Service..................................................................................................1
Chapter 2 Safety Guidance ...........................................................................................................4
2.1 Introduction.........................................................................................................................4
2.2 General Information............................................................................................................4
2.3 Safety Precautions...............................................................................................................4
Chapter 3 Installation....................................................................................................................7
3.1 Environment Requirements.................................................................................................7
3.2 Electrical Requirements......................................................................................................7
3.3 Safety Requirements ...........................................................................................................8
3.4 Installing the Monitor..........................................................................................................8
3.5 Connecting to AC Power.....................................................................................................9
Chapter 4 Test and Maintenance................................................................................................10
4.1 Routine Test.......................................................................................................................10
4.1.1 Visual Inspection.....................................................................................................10
4.1.2 Power- on Test.........................................................................................................10
4.1.3 Key Test...................................................................................................................10
4.1.4 Recording Test.........................................................................................................10
4.1.5 Alarm Test...............................................................................................................11
4.2 Performance Test...............................................................................................................11
4.2.1 ECG Performance Test............................................................................................11
4.2.2 SpO2Performance Test ...........................................................................................12
4.2.3 NIBP Performance Test...........................................................................................12
4.2.4 NIBP Leakage Test..................................................................................................13
4.2.5 NIBP Calibration.....................................................................................................13
4.2.6 TEMP Performance Test .........................................................................................14
4.2.7 CO2Performance Test.............................................................................................15
4.2.8 IBP Performance Test..............................................................................................15
4.2.9 C.O. Performance Test ............................................................................................15
4.3 Safety Test.........................................................................................................................16
4.3.1 Safety Test Procedures............................................................................................16
4.3.2 Protective Earth Resistance.....................................................................................17
4.3.3 Enclosure Leakage Current.....................................................................................17
4.3.4 Patient Leakage current...........................................................................................19
4.3.5 Patient Leakage Current- Single Fault Condition (S.F.C) Mains on Applied Part .20
4.4 Maintenance......................................................................................................................21

IV
4.4.1 Cleaning the Monitor and Accessories....................................................................21
4.4.2 Maintaining the Battery...........................................................................................21
Chapter 5 Configuration .............................................................................................................22
5.1 Opening User Maintain Menu...........................................................................................22
5.2 Entering Demo Mode........................................................................................................22
5.3 Selecting Lead Style..........................................................................................................22
5.4 Changing the Bed No........................................................................................................22
5.5 Changing Network Bed No...............................................................................................23
Chapter 6 Principle Introduction ...............................................................................................24
6.1 System Principle Block Diagram......................................................................................24
6.1.1 Main Board .............................................................................................................24
6.1.2 ECG Module ...........................................................................................................25
6.1.3 SpO2Module...........................................................................................................26
6.1.4 Print Controlling Board...........................................................................................26
6.1.5 Power Module.........................................................................................................26
6.1.6 Key Board ...............................................................................................................27
6.1.7 Interface Board (big)...............................................................................................27
6.1.8 Interface Board (small) ...........................................................................................27
6.1.9 LVDS LCD..............................................................................................................27
6.2 Interfaces...........................................................................................................................28
6.2.1 DB9 Interface..........................................................................................................29
6.2.2 RJ45 Interface .........................................................................................................29
6.2.3 USB Interface..........................................................................................................29
6.2.4 DB15 Interface........................................................................................................29
6.2.5 BNC Interface .........................................................................................................29
6.2.6 SD Card Interface....................................................................................................30
6.2.7 Nurse Call Interface ................................................................................................30
Chapter 7 Troubleshooting..........................................................................................................31
7.1 Monitor Booting Failures..................................................................................................31
7.2 Display Failures ................................................................................................................32
7.3 Touch Screen Failures.......................................................................................................32
7.4 Operation Failures.............................................................................................................32
7.5 Recorder Failures..............................................................................................................32
7.6 Network Failures...............................................................................................................33
7.7 Alarm Failures...................................................................................................................33
7.8 Power Board Failures........................................................................................................33
7.9 Data Storage......................................................................................................................34

V
7.10 ECG Monitoring Failures................................................................................................34
7.11 SpO2Monitoring Failures ...............................................................................................35
7.12 NIBP Monitoring Failures...............................................................................................35
7.13 TEMP Monitoring Failures .............................................................................................35
7.14 CO2Monitoring Failures.................................................................................................36
7.15 IBP Monitoring Failures..................................................................................................36
7.16 AG Monitoring Failures..................................................................................................37
7.17 Technological Alarms......................................................................................................37
Chapter 8 Disassembling the Monitor........................................................................................38
8.1 Tools Required ..................................................................................................................38
8.2 Replacing Fuses ................................................................................................................38
8.3 Disassembling the Main Unit............................................................................................39
8.4 Disassembling the Front Housing Assembly ....................................................................41
8.4.1 Replacing the Alarm Indicator Board .....................................................................41
8.4.2 Replacing the Key Board........................................................................................41
8.4.3 Replacing the Power Inverter Board.......................................................................42
8.4.4 Replacing the Knob.................................................................................................42
8.4.5 Replacing the LCD..................................................................................................43
8.4.6 Replacing the Touch Screen....................................................................................44
8.5 Module Bracket Assembly................................................................................................44
8.5.1 Replacing the Main Board ......................................................................................44
8.5.2 Replacing the IBP-C.O. Module.............................................................................46
8.5.3 Replacing the SpO2Module....................................................................................46
8.5.4 Replacing the CO2Module .....................................................................................46
8.5.5 Replacing NIBP Module.........................................................................................47
8.5.6 Replacing the ECG Module....................................................................................48
8.6 Main Bracket Assembly....................................................................................................48
8.6.1 Replacing the Recorder...........................................................................................48
8.6.2 Replacing the Speaker.............................................................................................49
8.6.3 Replacing the Power Module..................................................................................49
8.6.4 Replacing the Fan....................................................................................................50
8.6.5 Replacing the Power Interface Board .....................................................................50
8.6.6 Replacing the Interface Board (big)........................................................................51
Appendix 1 Replaceable Parts ....................................................................................................52

iM80 Patient Monitor Service Manual Warranty and Service
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Chapter 1 Warranty and Service
Standard Service
EDAN provides a one-year-warranty for the warranted products (accessories are included). The
warranty period begins on the date the products are shipped to customers. If a customer promptly
notifies EDAN of customer’s warranty claim hereunder, EDAN will either repair, adjust or
replace (with new or exchange replacement parts) EDAN’s products. EDAN warrants that any
service it provides to customers will be performed by trained individuals in a workmanlike
manner.
Limitation of Warranty
Direct, indirect or final damage and delay caused by the following situations for which EDAN is
not responsible may void the warranty:
Groupware is dismounted, stretched or redebugged.
Unauthorized modification or misuse.
Damage caused by operating beyond the environmental specifications for the medical
product.
Change or remove original serial number label or Manufacturer symbol.
Improper use.
Service Procedure
(1) Fill in the Service Claim Form (SCF).
Fill in the SCF with detailed information including: Model Name, Serial Number (SN) and
Problem Phenomena.
EDAN should not have any obligation to take over the case without this information. The
form can be downloaded at: http://www.edan.com.cn or obtained from EDAN’s Service
Department.
(2) Send EDAN the SCF and Select a Solution.
Once the service department receives the fully filled SCF, EDAN’s engineer will offer a
solution in three working days. EDAN will follow out the case based on the two conditions
below:
Within Warranty:
There are two options:

iM80 Patient Monitor Service Manual Warranty and Service
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i) After receiving the Return Material Authorization (RMA) form from EDAN service
department, the customer sends EDAN the defective parts and informs about the shipment
tracking number. Then we will dispatch new part(s) to your confirmed address with
confirmed shipping invoice.
ii) The customer signs the Declaration Form and sends it back by email or fax. This form is
legally certificated to make sure the customer or end-user will return the defective parts to
EDAN on time. We will, at this option, dispatch the replacement one(s) with confirmed
shipping invoice.
NOTES:
(1) Both Return Material Authorization Form and Declaration Form are offered by
EDAN service department once the SCF is confirmed by service engineer.
(2) The customer is responsible for freight & insurance charges when the equipment
is shipped to EDAN for service, including custom charges. EDAN is responsible
for the freight, insurance & custom charges from EDAN to the customer.
Out of Warranty:
After receiving the RMA form from the service department, the customer sends defective
parts to EDAN in advance. We will analyze the problems and discuss with the customer about
either repairing or replacing the part(s). Once the maintenance fee is invoiced and paid, we
will make sure to dispatch good part(s) to the confirmed address.
NOTE: The customer is responsible for any freight & insurance charge for the
returned product.
(3) Obtain the RMA Form.
Before the shipment of the materials, the customer must obtain an RMA form from our
service department, in which the RMA number, description of returning parts and shipping
instructions are included. The RMA number should be indicated on the outside of the
shipping container.
NOTE:
EDAN should not have any obligation to the end-user or customer who returns the goods
without the notification by EDAN’s service department. The sender takes full
responsibility for the accounted fee.

iM80 Patient Monitor Service Manual Warranty and Service
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(4) Send the Parts to EDAN.
Follow these recommended instructions:
Please disassemble the parts with anti-static facility, do not touch the parts with naked hand.
Please pack the parts safely before return.
Please put the RMA number on the parcel.
Please describe the returned parts as ‘sample of *****’ and put the total value on the invoice,
and note on the invoice as ‘sample, no commercial value’.
Please confirm the invoice with EDAN before shipment.
Please send back the parts after EDAN’s confirmation.
Contact Information
If you have any question about maintenance, technical specifications or malfunctions of devices,
do not hesitate to contact us.
EDAN Instruments, Inc.
TEL: [phone]
FAX: [phone]
E-mail: [email protected]

iM80 Patient Monitor Service Manual Safety Guidance
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Chapter 2 Safety Guidance
2.1 Introduction
This service manual is a reference for periodic preventive maintenance and corrective service
procedures for the iM80 patient monitor. It provides information on troubleshooting, assembly
procedures, and instructions for functional testing as well as performance verification. The
manual is intended for use only by technically qualified service personnel.
WARNING
Please follow the instructions exactly in accordance with this manual during service.
Failure to do so might result in damage to the monitor or personal injury.
2.2 General Information
iM80 Patient Monitor (hereinafter called monitor) is designed in accordance with the
international safety requirements in IEC/ EN 60601-1 for medical electrical equipment.
Classification information of this equipment is as follows:
Anti-electroshock Type Class I equipment and internal powered equipment
Anti-electroshock Degree NIBP, SpO2, CO2, AG BF
ECG, TEMP, IBP, C.O. CF
Ingress Protection IPX1
Degree of Safety in Presence of
Flammable Gases
Not suitable for use in presence of flammable gases
Working System Continuous operation equipment
EMC Type Group 1 Class A
2.3 Safety Precautions
To avoid possible injury, please observe the following precautions during the operation of the
monitor.