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Manual de Servicio EDAN
Manual de Servicio EDAN
签批信息:
作者 : 陈 艳娟 (chenyanjuan) 2017-08-02 09:40:51
EN 件
审核人 : 程 亮 (chengliang) 2017-08-02 10:59:10
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审核人 : 史 洪华 (shihonghua) 2017-08-02 17:29:28
ID 文
审核人 : 韩 吉灯 (hanjideng) 2017-08-02 09:44:33
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审核人 : 陈 良款 (chenliangkuan) 2017-08-02 15:40:57
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版权©深圳市理邦精密仪器股份有限公司
ED 理 AN
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About this Manual
P/N: 01.54.456004
MPN: 01.54.456004013
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
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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.
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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
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languages.
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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
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not disclose such information to any irrelevant third party.
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The user shall understand that nothing in this manual grants him, expressly or implicitly, any
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EDAN holds the rights to modify, update, and ultimately explain this manual.
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EDAN only considers itself responsible for any effect on safety, reliability and performance of
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The electrical installation of the relevant room complies with national standards, and
EDAN will make available on request circuit diagrams, component part lists, descriptions,
calibration instructions, or other information that will assist service personnel to repair those parts
of the equipment that are designated by EDAN as repairable by service personnel.
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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
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A NOTE provides useful information regarding a function or a procedure.
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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 ............................................................................................................... 5
2.4 Explanation of Symbols on the Monitor ............................................................................. 6
Chapter 3 Installation .................................................................................................................. 10
3.1 Environment Requirements............................................................................................... 10
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3.2 Electrical Requirements .................................................................................................... 10
3.3 Safety Requirements ......................................................................................................... 11
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3.4 Installing the Monitor ........................................................................................................ 11
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3.5 Connecting to AC Power ................................................................................................... 12
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Chapter 4 Test and Maintenance ................................................................................................ 13
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4.1 Routine Test....................................................................................................................... 13
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4.1.1 Visual Inspection ..................................................................................................... 13
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4.2.10 C.O. Functional Test.............................................................................................. 19
4.2.11 AG Functional Test ................................................................................................ 20
4.3 Safety Test ......................................................................................................................... 20
4.3.1 Safety Test Procedures ............................................................................................ 20
4.3.2 Protective Earth Resistance ..................................................................................... 21
4.3.3 Enclosure Leakage Current ..................................................................................... 22
4.3.4 Patient Leakage current ........................................................................................... 23
4.3.5 Patient Leakage Current- Single Fault Condition (S.F.C) Mains on Applied Part . 24
4.4 Maintenance ...................................................................................................................... 25
4.4.1 Cleaning the Monitor and Accessories .................................................................... 25
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4.4.2 Maintaining the Battery........................................................................................... 25
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Chapter 5 Configuration ............................................................................................................. 26
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5.1 Opening User Maintain Menu........................................................................................... 26
5.2 Entering Demo Mode ........................................................................................................ 26
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5.3 Selecting Lead Style .......................................................................................................... 26
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5.4 Changing the Bed No. ....................................................................................................... 27
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5.5 Network Setup ................................................................................................................... 27
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7.7 Technological Alarms ........................................................................................................ 39
Chapter 8 Disassembling the Monitor........................................................................................ 40
8.1 Tools Required .................................................................................................................. 40
8.2 Replacing Fuses ................................................................................................................ 40
8.3 Disassembling the Main Unit ............................................................................................ 41
8.4 Disassembling the Front Housing Assembly .................................................................... 43
8.4.1 Replacing the Touch Screen or Protective Screen .................................................. 43
8.4.2 Replacing the LCD .................................................................................................. 44
8.4.3 Replacing the Switch Board .................................................................................... 45
8.4.4 Replacing the Key Board ........................................................................................ 45
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8.4.5 Replacing the Knob ................................................................................................. 46
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8.4.6 Replacing the Touch Screen Adapter Board ........................................................... 46
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8.4.7 Replacing the Alarm Indicator Board ..................................................................... 47
8.5 Disassembling the Main Frame Assembly ........................................................................ 47
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8.5.1 Replacing the Power Module .................................................................................. 48
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8.5.2 Replacing M3600 Module....................................................................................... 48
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8.5.3 Replacing CO2/IBP Module .................................................................................... 49
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iM70 Patient Monitor Service Manual Warranty and 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
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Direct, indirect or final damage and delay caused by the following situations for which EDAN is
not responsible may void the warranty:
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Groupware is dismounted, stretched or redebugged.
Unauthorized modification or misuse.
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Damage caused by operating beyond the environmental specifications for the medical
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product.
Change or remove original serial number label or Manufacturer symbol.
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Improper use.
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Service Procedure
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Fill in the SCF with detailed information including: Model Name, Serial Number (SN) and
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Problem Phenomena.
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EDAN should not have any obligation to take over the case without this information. The
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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:
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Within Warranty:
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iM70 Patient Monitor Service Manual Warranty and Service
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
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EDAN service department once the SCF is confirmed by service engineer.
(2) The customer is responsible for freight & insurance charges when the equipment
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is shipped to EDAN for service, including custom charges. EDAN is responsible
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for the freight, insurance & custom charges from EDAN to the customer.
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Out of Warranty:
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After receiving the RMA form from the service department, the customer sends defective
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parts to EDAN in advance. We will analyze the problems and discuss with the customer about
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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.
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NOTE: The customer is responsible for any freight & insurance charge for the
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returned product.
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Before the shipment of the materials, the customer must obtain an RMA form from our
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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.
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NOTE:
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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.
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iM70 Patient Monitor Service Manual Warranty and Service
Please disassemble the parts with anti-static facility, do not touch the parts with naked hand.
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‟.
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Contact Information
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If you have any question about maintenance, technical specifications or malfunctions of devices,
do not hesitate to contact us.
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EDAN Instruments, Inc.
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TEL: +86-755-26898321, 26899221
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FAX: +86-755-26882223, 26898330
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E-mail: support@edan.com.cn
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iM70 Patient Monitor Service Manual Safety Guidance
2.1 Introduction
This service manual is a reference for periodic preventive maintenance and corrective service
procedures for the iM70 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 of doing so might result in damage to the monitor or personal injury.
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2.2 General Information
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iM70 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:
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Anti-electroshock Type Class I equipment and internal powered equipment
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Anti-electroshock Degree NIBP, SpO2, CO2, AG BF
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Degree of Safety in Presence of Not suitable for use in presence of flammable gases
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Flammable Gases
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iM70 Patient Monitor Service Manual Safety Guidance
WARNING
1 The monitor must be serviced only by authorized and qualified personnel. EDAN does
not assume any responsibility for damage or injury if modifications or repairs are
carried out by unauthorized personnel.
2 Use and replace the substitutive parts provided or recommended by EDAN only.
3 The service personnel must be familiar with the operation of this monitor. Refer to
Patient Monitor User Manual for details.
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4 Perform periodic safety test to ensure patient safety. Safety test should include
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leakage current measurement and insulation testing.
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5 Disconnect the monitor from power before replacing the fuses which are with the
identical specifications.
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6 SHOCK HAZARD – Do not remove the top panel cover during operation or while
power is on. The unit cover must be removed only by authorized service personnel.
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7 SHOCK HAZARD – Do not attempt to connect or disconnect the power cord with wet
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hands. Make sure that your hands are clean and dry before touching the power cord.
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8 Accessory equipment connected to the analog and digital interface must be certified
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according to the respective IEC/ EN standards (e.g. IEC/ EN 60950 for data
processing equipment and IEC/ EN 60601-1 for medical equipment). Furthermore, all
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configurations shall comply with the valid version of the system standard IEC/ EN
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60601-1. Anybody who connects additional equipment to the signal input connector or
signal output connector to configure a medical system must ensure that the system
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complies with the requirements of the valid version of the system standard IEC/ EN
6060-1-1. If you have any question, please consult our technical service department
or your local distributor.
10 Do not directly solder the lead wire and the batter terminal.
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iM70 Patient Monitor Service Manual Safety Guidance
CAUTION
1 The device is designed for continuous operation. Avoid splashing water over the
device.
2 Do not operate the device when it is damp or wet. Avoid using the device immediately
after relocating it from a cold environment to a warm and humid environment. If the
monitor gets damp or liquid pours on the monitor, please contact the service
personnel of EDAN.
3 While the battery is charged, used or stored, keep it away from objects or materials
with static electric charges.
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2.4 Explanation of Symbols on the Monitor
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1
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DEFIBRILLATION-PROOF TYPE CF APPLIED PART
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2 DEFIBRILLATION-PROOF TYPE BF APPLIED PART
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3
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Caution
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(MRI) equipment
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5 Equipotential grounding
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Alternating Current
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iM70 Patient Monitor Service Manual Safety Guidance
SERIAL NUMBER
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9 Network port
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12 NIBP measurement
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13
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Trend
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14 Picture freeze
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15 Graphical recorder
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16 Menu
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17 Video output
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Write data into store
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iM70 Patient Monitor Service Manual Safety Guidance
20 Output
21 CE marking
Date of manufacture
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23
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24 MANUFACTURER
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25 Part Number
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26 General symbol for recovery/recyclable
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27 Disposal method
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28 Operating instructions
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30 Warning
(Background: Yellow; Symbol & outline: black)
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31 Anti-theft lock
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iM70 Patient Monitor Service Manual Safety Guidance
32 Gas inlet
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Ingress Protection IPX1 (Protected against vertically
36
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falling water drops)
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Caution: Federal (U.S.) Law restricts this device to sale by
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37 or on the order of a physician.
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60601-2-49
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NOTE:
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iM70 Patient Monitor Service Manual Installation
Chapter 3 Installation
WARNING
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Atmospheric Pressure 86 kPa ~ 106 kPa
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Storage
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Temperature -20 ºC ~ 55 ºC(-4 ℉~131℉)
Relative Humidity
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15%RH ~ 95%RH (non-condensing)
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Atmospheric Pressure 70 kPa ~ 106 kPa
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NOTE:
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2 Keep the environment clean and keep the device away from corrosive medicine.
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Prevent the device from vibration, high temperature, humidity and exposure to the
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sun.
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iM70 Patient Monitor Service Manual Installation
CAUTION
1 SHOCK HAZARD – To protect patients and medical staff, the power receptacle must
be well grounded. Never adapt the three-prong plug from the monitor to fit a
two-socket outlet.
2 Do not simultaneously touch the signal input or output connector and the patient.
4 Do not switch on the monitor until all units and accessories have been properly
connected and verified.
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3.4 Installing the Monitor
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- To install the monitor on a flat surface.
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Place the monitor on a flat surface. Make sure the surface does not vibrate, and is free of
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corrosive medicine and dust.
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iM70 Patient Monitor Service Manual Installation
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Power socket
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Security lock
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Power cable
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Disconnecting Connecting
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iM70 Patient Monitor Service Manual Test and Maintenance
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Do not use the monitor if any damage is detected until the monitor is repaired by the service
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personnel of EDAN or professional service personnel of the dealer.
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4.1.2 Power- on Test
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Switch on the monitor after it is connected to the power source and check:
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If the power indicator lights up;
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If the alarm indicators flicker and if the alarm tone is heard;
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If there are bright spots and dark shadows on the LCD screen;
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If the waveforms, fonts and symbols displayed on the LCD screen are normal.
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If any failure is detected, refer to section Monitor Booting Failures and Display Failures for
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details.
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Press the keys on the front panel in turn to check if they work properly. When pressing a key, a
corresponding functional display is supposed to be seen onscreen. Refer to Patient Monitor User
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Manual for details about the key function. The user can move the cursor by turning the trim knob
clockwise or anticlockwise. Also, the user can confirm the operation by pressing the trim knob.
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Check if the recorder can perform recording without problem. Also, check if all the recorded
traces are correct and clear on the paper.
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iM70 Patient Monitor Service Manual Test and Maintenance
NOTE:
Please make sure paper is well loaded and the setting is correct before recording.
Trigger a signal that is higher than the upper limit or lower than the lower limit to activate a
physical alarm. Disconnect one of the accessories from the monitor to activate a technical alarm.
Check if the audible and visible alarms work properly.
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WARNING
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1 Functional tests and accuracy tests must only be carried out by qualified service
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personnel.
2 If function of the monitor is in question, conduct an overall test on the function and
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accuracy of the monitor according to the instructions offered by the manufacturer.
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3 A functional tester, such as ECG simulator, SpO2 simulator, NIBP simulator and IBP
simulator, can only be used to assess the parameter consistency and function but not
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to be used to assess the clinical measurement accuracy.
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A functional check should be performed once possible device malfunction emerges or after
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Procedure:
- HR=30bpm.
4. Check the displayed HR value against the simulator configuration. The value should be
30bpm ±1bpm or ±1% (whichever is greater).
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iM70 Patient Monitor Service Manual Test and Maintenance
Procedure:
1. Connect the monitor and the SpO2 simulator with a SpO2 cable.
- SpO2 = 70%.
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4. Check the displayed SpO2 value against the simulator configuration. The value should be
70% ±2%.
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4.2.3 NIBP Functional Test
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This test checks the function of the NIBP measurement.
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Tools required:
• NIBP simulator;
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• T-fitting;
• Extension tube;
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• Artificial limb.
Procedure:
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2. Switch on the monitor and the simulator. Calibrate the simulator before using it.
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3. Set the patient type on the monitor to adult; set the simulator to the following configuration:
4. Check the displayed values against the simulator configuration. The differences should be
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iM70 Patient Monitor Service Manual Test and Maintenance
This test checks leakage of the airway and the performance of the NIBP system. See Figure 4-1
for details about tools required.
Procedure:
1. Connect the cuff securely with the socket for NIBP air hole.
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5. Select Leakage Test. Then the prompt Leak. Test Running will appear indicating that the
system has started the leakage test.
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Omron module:
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The system will automatically inflate the pneumatic system to 285 mmHg. After 4 minutes, the
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system will automatically open the deflating valve, which marks the completion of a pneumatic
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measurement.
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EDAN module:
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The system will automatically inflate the pneumatic system to about 180 mmHg. After 20
seconds to 40 seconds, if system leakage has detected, the system will automatically open the
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deflating valve to stop the leak test and indicates NIBP Leak. If no system leakage is detected
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when the pneumatic system is inflated to 180 mmHg, the system will perform a deflation to an
approximate value of 40 mmHg and subsequently perform the second phase leak test. After 20
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seconds to 40 seconds, the system will automatically open the deflating valve and provide
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If the alarm information of NIBP Leak appears, it indicates that the airway may have air leaks. In
this case, the user should check for loose connection. After confirming secure connections, the
user should re-perform the leakage test. If the failure prompt still appears, please contact the
manufacturer for repair.
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NOTE:
Manometer test is for checking the measurement accuracy and cannot change the
measurement results.
Tools required:
• T-fitting
• NIBP extension tubes
• Cylinder (200 ml)
• Manometer (Its measurement range should be within the range of 0 to 300 mmHg; its accuracy
should be more precise than the accuracy of ±0.3 mmHg.)
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Procedure:
1. Press the Menu item on the front panel. Access Menu > Maintenance > User Maintain by
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inputting the password ABC.
2. Connect the equipment as shown below:
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Manometer
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Tube
NIBP module
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Tube / Patient
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NIBP
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extension
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tube or hose
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5. Wait 10s until the pressure stabilizes. Check the displayed values on the monitor against the
manometer configuration.
6. A tolerance of ±3mmHg is reasonable.
NOTE:
NIBP calibration must be performed by professional personnel authorized by EDAN.
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iM70 Patient Monitor Service Manual Test and Maintenance
Tools required:
• T-fitting
• NIBP extension tubes
• Cylinder (200ml)
• Manometer (Its measurement range should be within the range of 0 to 300mmHg; its accuracy
should be more precise than the accuracy of ±0.3mmHg.)
Procedure:
1. Connect the equipment as shown below:
Manometer
Tube
NIBP module
Tube / Patient
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Cylinder T-fitting monitor
NIBP
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extension
tube or hose
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Figure 4-3 Diagram for NIBP Calibration
2.
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Access Menu > Maintenance > Factory Maintain by inputting the password 998.
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3. Select NIBP Calibration (Xm) from the menu.
4. Select Calibrate Initialization to start calibration.
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5. Adjust the manometer value to 50 mmHg (If different values are required for calibration,
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keep the value of the manometer consistent with the one displayed on the monitor). After the
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6. Adjust the manometer value to 250 mmHg (If different values are required for calibration,
keep the value of the manometer consistent with the one displayed on the monitor). After the
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9. Apply a fixed static pressure on the monitor with the help of the manometer. Check the
displayed values on the monitor against the manometer configuration.
10. A tolerance of ±3 mmHg is reasonable.
Procedure:
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iM70 Patient Monitor Service Manual Test and Maintenance
2. Set the probe type on the monitor to YSI-10K, and respectively connect the probes to
channel T1 and T2 connectors. And then connect the probes with the resistance box.
Procedure:
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2. Access CO2 setup menu, and set the Work Mode to Measure.
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3. Place the nasal cannula below the nose and normally breathe; check if the CO2 measurement
waveforms are available on the monitor.
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4. The displayed CO2 concentration is supposed to be 34 mmHg ~40 mmHg.
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4.2.9 IBP Functional Test
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This test checks the function of the IBP measurement.
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Procedure:
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1. Connect the IBP cable to the connector for channel BP2 on the patient simulator and to the
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3. After completing the zero calibration, configure the simulator as P (static) = 200mmHg.
4. Perform a dynamic pressure test. Set the simulator to the following configuration:
- RADIALART 120/80
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The tolerances for the measurement value provided by the monitor should be ±4 mmHg or
±4%.
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Procedure:
1. Connect the simulator to the C.O. module using the patient cable.
2. Configure the patient simulator as follows:
- Injection temperature: 0 ℃
- Computation Const: 0.542
(Edward‟s Catheter)
- Flow: 5 l/min
3. Check displayed value against the simulator configuration.
4. Expected test result: C.O.= 5+/-1 l/min
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Tools required: the corresponding AG nasal cannula.
Procedure:
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1. Switch on the monitor.
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2. Access AG setup menu, and set the Work Mode to Measure.
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3. Configure the parameter as CO2 (AG), and the waveform shall be displayed in the waveform
area.
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4. Place the nasal cannula below the nose and normally breathe; check if the CO2 measurement
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Use the test procedures outlined here only for verifying safe installation or service of the product.
These tests are not a substitute for local safety testing where it is required for an installation or a
service event.
When performing a safety test, you must use a standard safety analyzer such as Fluke 601Pro
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Series safety analyzer or equivalent, and perform the test according to your local regulations, for
example, in Europe according to IEC/EN60601-1, in USA according to UL60601-1. For the test
setup, please refer to the Instructions for Use of the test equipment used.
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iM70 Patient Monitor Service Manual Test and Maintenance
NOTE:
1 After the system is installed or set up, safety test must be performed according to IEC
60601-1.
4 With devices that are connected to other devices by means of a data cable, this
connection must be disconnected prior to performing the electrical safety check, in
order to avoid incorrect measurements.
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4.3.2 Protective Earth Resistance
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NOTE:
The circuit diagram is based on the Fluke 601Pro series safety analyzer.
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This measures impendence of Protective Earth (PE) terminal to accessible metal part of Device
under test (DUT) which is protectively earthed. A current of 25A is passed for 5s to 10s through
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the protective terminal and each accessible metal part which is protectively earthed.
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NOTE:
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The circuit diagram is based on the Fluke 601Pro series safety Analyzer.
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This measures leakage current of exposed metal parts of Device under test (DUT) and parts of the
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system within the patient environment; normal and reversed polarity using S2 test performed both
in normal condition and single fault conditions.
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Single fault condition (SFC): S1, S3 open (one for each time) and S5 closed, S2, S4 variable.
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Allowable value:
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iM70 Patient Monitor Service Manual Test and Maintenance
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NOTE:
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The circuit diagram is based on the Fluke 601Pro series safety Analyzer.
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This test measure the leakage current flowing between the selected applied part and the mains PE;
the test with normal and reverse polarity, in normal condition and single fault condition.
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Single fault condition (SFC): S1, S3 open (one for each time) and S5 closed, S2, S4 variable.
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Allowable value:
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Normal condition: 10µA (BF applied part), 10µA (CF applied part)
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(IEC/EN60601-1, UL60601-1)
Single fault condition: 500µA (BF applied part), 50µA (CF applied part)
(IEC/EN60601-1, UL60601-1)
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Leakage Current
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iM70 Patient Monitor Service Manual Test and Maintenance
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Patient Auxiliary Current
AC: <0.1 mA AC: <0.5 mA
BF
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DC: <0.01 mA DC: <0.05 mA
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4.3.5 Patient Leakage Current- Single Fault Condition (S.F.C) Mains on
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Applied Part
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NOTE:
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The following test is based on test with the Fluke 601 pro series safety analyzer. This
device allows applying a 110% mains voltage between the applied part and the device
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PE. When testing with other device, you may need to apply the 110% mains voltage
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manually.
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iM70 Patient Monitor Service Manual Test and Maintenance
NOTE:
The circuit diagram is based on the Fluke 601Pro series safety Analyzer.
This test measure the current flowing between the applied part and the mains PE in response to an
isolate mains voltage (110% of the mains voltage) applied to applied part. This test is performed
with normal and reverse polarity of the mains voltage using S2, and normal and reverse polarity
of the isolate voltage using S4.
Single fault condition: S1, S3, S5 closed, S2, S4, S6 variable.
Allowable value:
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(IEC/EN 60601-1 UL 60601-1)
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4.4 Maintenance 文
For details about basic cleaning and maintenance methods, refer to relevant sections in Patient
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Monitor User Manual. For further technical support, contact service engineers of EDAN.
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Users are responsible for preventive maintenance and periodic inspection for the monitor.
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4.4.1 Cleaning the Monitor and Accessories
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iM70 Patient Monitor Service Manual Configuration
Chapter 5 Configuration
The users have no access to changing the system configuration of the monitor. As a service
engineer, the users need to change the configuration after the monitor is installed and checked.
件
5.2 Entering Demo Mode
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The monitor works in real-time monitoring mode when monitoring a patient. If you want to show
文
the traces and parameters for a demonstration, you need to enter the Demo mode.
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1 Select Menu > Common Function.
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2 Select Demo Mode, and input the password 3045 by using the soft keyboard.
EN
3 Select OK to enter the Demo mode.
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WARNING
ID
forbidden in clinical applications in case medical staff mistake what displays on the
monitor as the waveforms and parameters of the patient, which will affect patient
NF
2 Select AHA or IEC from the list and press the knob to confirm it.
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iM70 Patient Monitor Service Manual Configuration
CAUTION
Make sure the device No. of the monitors in the same system do not overlap.
件
5.5 Network Setup
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文
The monitor is provided with three network connection methods: wired network, wireless
network, and 3G. The IP address in wired network and wireless network can be chosen as static
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and dynamic, and only if in static, it can be set up. To set the device IP:
密
1 Select Menu > Maintenance;
EN
2 Select User Maintain > Network Maintain;
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iM70 Patient Monitor Service Manual Principle Introduction
NELL module
Power input
件
COM6 AG module
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LPT
control board
文 module
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COM4 LCD_LVD interface 5V
USB/ Nurse Call/
密
Knob input VGA/ Defibrillator
Touch
Synchronization/
Key board controller
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screen input
Analog Output
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X5V(9G45) main control board is a main control board integrated with multiple parameters. It
includes digital part and parameter part. The system working principle is shown above.
The main board contains two CPU; one is the main CPU, the other is the extended CPU. SPI is
adopted as the communication mode between the two CPU. With the abundant resources from the
AN
unit, the main CPU can realize extension of the main storage system, networking (10M/ 100M
self-adaptable) and audio output; additionally, it offers two types of display interface (LVDS and
VGA interface). The extended CPU is able to complete the extension of two serial interfaces and
ED
one LPT, to collect and control valve signals of NIBP, and to offer sufficient I/O ports which can
perform the function of keyboard scanning.
Parameter part applying floating ground technology includes parameters such as ECG, SpO2,
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iM70 Patient Monitor Service Manual Principle Introduction
NIBP, RESP and TEMP. This part adopts STM32F103VD to control the front-end analog signals,
collect data, simply process the data and deliver it.
ECG
X5V(9G45) supports 3/ 5 leads ECG. In the mode of 3 leads, three electrodes used are RA, LA
and LL. 3-lead ECG measurement can be realized by controlling conversion of the drive
electrodes.
In the mode of 5 leads, five electrodes in used are RA, LA, LL, RL and V1; four ECG channels
are available; four channels of ECG signal are amplified; and RL is the drive electrode. In the
mode of 5 leads, seven leads (I, II, III, AVR, AVL, AVF and V1) of ECG signal can be collected.
In the mode of 3 leads: RA, LA and LL are available, I/ II/ III are optional and the drive lead alter
件
accordingly.
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In the mode of 5 leads: RA, LA, LL, RL and V1 are available, two channels among I, II, III, AVR,
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AVF, AVL and V1 are optional and the drive lead is RL.
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SpO2
密
By outputting the control pulse via DA, MCU controls red ray and illumination of the infrared
illuminators of the SpO2 sensors. The ray measuring system amplifies the minute measured
EN
signal. Subsequently, the amplified signal is delivered for AD sampling. Measurements of SpO2
保
and PR will be calculated based on the corresponding algorithm. To adapt the difference between
the strong and weak signal, the receiving circuit is outfitted with a program control amplifier. If
ID
the measured signal is weak, the system will enhance the gain; if the measured signal is strong,
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NIBP
理
NIBP module can measure the pressure via the pressure transducer and then convert the pressure
signal into electric signal which is subsequently amplified and delivered to AD; after AD detects
CO
and measures the pressure and pulse wave signal, BP can be calculated based on the related
algorithm.
The pressure protection unit of NIBP will protect the patient when individual malfunction occurs.
Once the pressure protection unit detects that the value of pressure exceeds the normal one, it will
AN
RESP
ED
The respiratory carrier wave of 62.8 kHz will act on the body via the resistance-capacitance
network. The change of celiac impedance during respiration a minute amplitude modulated wave
can be obtained on the front end of the respiratory amplifying circuit. By amplifying,
- 29 -
iM70 Patient Monitor Service Manual Principle Introduction
demodulating and reamplifying the amplitude modulated wave, a real respiratory wave can be
attained. X5V(9G45) supports I and II lead selection which can switch between each other by
the host computer sending instruction.
TEMP
The mode utilizing steady voltage source is adopted to collect the body temperature. Compared
with utilizing constant current source, using steady voltage source is relatively simple. There are
two channels in the TEMP circuit, supporting CY and YSI sensor.
The key board is the indispensable part of the device. At present, free-standing key board is
adopted in iM60 Patient Monitor. The key board works with the knob to perform information
件
communication between the user and the device. The module circuit connected with the key
board includes the knob, alarm indicator, touch screen and iM60 main control board. Six
AL
functional keys on the key board are alarm pause, NIBP, trend graph, freeze, recording and menu.
文
Besides, two LED with different colors are on the board. One LED indicates the status of AC and
the other indicates the status of battery charging.
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密
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Host Programs
保
computer Downloading
ID
Switch
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NF
Watchdog
Touch
理
MCU Screen
6 keys
CO
Knob LED
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- 30 -
iM70 Patient Monitor Service Manual Principle Introduction
Printer
Network VGA USB SD WIFI PS2 interface: port
interface card Nurse Call/
Defibrillator
件
Synchronization/
Analog Output
AL
文
Figure 6-3 Interface Board Diagram
TI
密
The power module is EDAN PS900K. It outputs +12V, +5V, +19V voltage and manages charging.
EN
Interface Pin Definition
保
J1 1 2 3
ID
J9 1 2 3 4 5 6
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J5 1 2
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BAT GND
J4 1 2
POWR_ON/OFF GND
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J2 1 2 3 4
POWR_UP CHARGE RXD TXD
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iM70 Patient Monitor Service Manual Principle Introduction
6.2 Interfaces
件
4
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文
5
TI
密
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保
ID
SD card interface
理
USB port
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Network interface
VGA interface
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iM70 Patient Monitor Service Manual Troubleshooting
Chapter 7 Troubleshooting
EDAN supports replacement of PCB and major subassemblies for this monitor. When
replacement is needed, follow the procedures described in chapter 8 Disassembling the Monitor.
件
power indicator is off; no Keyboard failure. Replace the keyboard.
fuses melt and break.
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Power board failure.
文 Replace the power board.
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Power failure. Replace the power board.
The fuses melt and break
密
during switching. Retry after checking the short
Short circuit of other parts.
circuit source and fixing it.
EN
保
grounded system.
lightning strike.
Abrupt switching off.
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- 33 -
iM70 Patient Monitor Service Manual Troubleshooting
件
Main control board failure. Refer to the principle diagram
and repair the replaced one.
AL
文 Check the LCD connection to
Wrong characters are LCD bad connection. X5V main control board and
TI
displayed onscreen. keyboard.
密
LCD failure. Replace display screen.
EN
7.3 Operation Failures
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pressed.
sections in Patient Monitor
User Manual for details.
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- 34 -
iM70 Patient Monitor Service Manual Troubleshooting
件
7.4 Recorder Failures
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Phenomenon
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Possible Cause Solution
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No paper in the drawer Load paper and close the drawer.
密
Select Manufacturer Maintain.
Press Record but no paper Printer mode is not selected. Turn on the printer mode. If the
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is out. printer is Unicode, select U,
保
otherwise E.
ID
drawer.
理
failure. board.
Gear box/ gear failure. Replace the gear box or the gear.
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- 35 -
iM70 Patient Monitor Service Manual Troubleshooting
件
Phenomenon Possible Cause Solution
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The audible alarm is
Activate the audible alarm.
文
temporarily disabled.
Inaction of audible alarm.
TI
Replace the speaker or the
Speaker or wire failure.
密
wire.
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iM70 Patient Monitor Service Manual Troubleshooting
件
SpO2 sensor failure. Replace the SpO2 sensor.
AL
Bad connection of the
No SpO2 trace or
cable of the SpO2 sensor.
文 Check the connection.
measurements.
Circuit failure of SpO2 on
TI
Replace the main control board.
密
the main control board.
EN
Bad connection of the cuff,
保
Bad connection of BP
The cuff fails to be module and NIBP Check the connection inside the monitor.
NF
inflated. connector.
理
cable is damaged.
tube or valve.
- 37 -
iM70 Patient Monitor Service Manual Troubleshooting
No CO2 waveform Poor connection of the CO2 Turn off the monitor and reconnect the
件
module. CO2 module.
AL
damaged.
文
The CO2 waveform The CO2 module is in Change work mode from standby to
TI
is a beeline standby mode measure.
密
The sample line is blocked Draw off the sample line, clear it or
or disconnected replace it to another one.
EN
保
The CO2 waveform Long time no zero Enter Menu > CO2 Setup, and perform
is abnormal, values calibration, the measured Zero Calibration.
ID
The measured CO2 The CO2 module is in Change work mode from standby to
NF
Prompts for CO2 The CO2 sample line is Draw off the CO2 sample line, clear it or
CO
The CO2 measured No zero calibration for a Enter Menu > CO2 Setup, and perform
value has error long time; the measured Zero Calibration.
AN
value is incorrect
The compensatory gas and Enter Menu > CO2 Setup > Other Setup,
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- 38 -
iM70 Patient Monitor Service Manual Troubleshooting
件
The monitor Failure in the PCB of IBP
Check the connection of IBP module and
indicates an IBP module or disconnection of
communication board or change the IBP
AL
communication the IBP module and
module.
failure. communication board
文
Bad connection of GAS Power off, and reconnect GAS module.
No waveform module.
TI
密
GAS module defective. Replace GAS module.
EN
GAS module is in Standby Change Standby mode to Measurement
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mode. mode.
AG waveform is The tube is jammed or not
Power off, and clean or replace the tube.
ID
For details on technological alarms, please refer to relevant section in the user manual.
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- 39 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
2 Switch off the monitor and disconnect it from AC power before disassembling the
monitor.
3 After any repair of the device, perform safety tests prior to use.
件
1 – A cross-head screwdriver
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2 – A flat-head screwdriver
文
3 – A M3 nut driver
TI
密
EN
4 – A pair of pliers
保
ID
3. Pull out the fuse box with a flat-head screwdriver and pry the fuse out with pliers.
AN
ED
- 40 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
4. Replace the old fuse with a new one that is supplied by EDAN or with the same
specifications. (Dimensions: Ф5mm*20mm; model: T3.15AH 250VP)
件
AL
文 Recorder
TI
密
EN
保
ID
邦
1 Disassemble the recorder and CO2 assembly from the main unit with a screwdriver.
2 Unscrew the four screws securing the front and rear housings to unfold the front and rear
AN
assemblies. Pull out the LCD linking wires and key board linking wires to separate the front
and rear housings.
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- 41 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
件
AL
文
3
TI
Unscrew the screws securing the main frame on the bottom and inside the unit with cross
密
head screw driver. Pry the probe bracket with flat head screw driver before pressing the
probe board inward, and the main frame are separated from the back assembly.
EN
保
ID
邦
NF
理
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AN
ED
- 42 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
Switch
Silicone
Touch
Keys
screen
adapter
Silicone Keys board
件
Switch Board
Touch Screen LCD LCD Supporting Bracket
Key Board
AL
Knob Board or Display Protective
Rotary Knob Cover
Front housing
文Screen
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Figure 8-2 Front Shell Structure Block Diagram
密
EN
8.4.1 Replacing the Touch Screen or Protective Screen
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Wires connecting
alarm indicator
ID
Separate the front Unscrew the screws Disconnect Remove the LCD Remove the touch
securing the LCD
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- 43 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
Assemble the touch screen or protective screen in the reversed order. Connect the wires and fix
the main unit. Check whether the sponge around the LCD is damaged. If so, please replace a new
one.
NOTE:
The user can only choose one from the touch screen and protective screen to assemble
in the main unit.
件
board and backlight
drive board
AL
Wires connecting key Touch screen wires
board and touch
文
screen adapter board
TI
密
Wires connecting Wires connecting
board
ID
邦
NF
理
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AN
Separate the front Disconnect the related Remove the related Unscrew the four screws
wires screws securing the LCD
and back assembly supporting bracket
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Assemble the LCD in the reversed order. Connect the wires and fix the main unit.
- 44 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
Wires connecting
key board and
power switch board Screw
件
AL
Separate the front Disconnect the Unscrew the screws securing
and back assembly
文
wires from the
switch board
the switch board with a
cross-head screwdriver
TI
Assemble the switch board in the reversed order. Connect the wires and fix the main unit.
密
Wires connecting
key board and Wires connecting
NF
Wires connecting
key board and
rotary knob PCBA
AN
Separate the front Disconnect the wires from Unscrew the screws securing the key
and back assembly the key board board with a cross-head screwdriver
and remove the key board
ED
Assemble the key board in the reversed order. Connect the wires and fix the main unit.
- 45 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
Screw
Wires connecting
key board and
rotary knob PCBA
件
AL
Separate the front Disconnect the wires Remove the knob Unscrew the screws securing
connecting the knob cover with a pair of the knob with a cross head
and back assembly and the key board
文pliers screw driver
TI
Assemble the knob in the reversed order. Connect the wires and fix the main unit.
密
8.4.6 Replacing the Touch Screen Adapter Board
EN
保
ID
邦
Screw
NF
adapter board
AN
Separate the front Disconnect the wires from the Unscrew the screws securing the
touch screen adapter board touch screen adapter board with a
and back assembly
cross head screw driver
ED
Assemble the touch screen adapter board in the reversed order. Connect the wires and fix the
main unit.
- 46 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
件
AL
Separate the front Disconnect the wires connecting Unscrew the screws securing the
and back assembly
文
key board and the alarm indicator alarm indicator board with a cross
head screw driver
TI
Assemble the alarm indicator board in the reversed order. Connect the wires and fix the main
密
unit.
EN
8.5 Disassembling the Main Frame Assembly
保
Power board
ID
邦
NF
理
Battery board
CO
Main board
Air pump assembly
Advanced
parameter Interface board
AN
modules
Main frame
ED
G2 assembly
Wires connecting
Wires connecting main board and
main board and power control board
power control board
Wires connecting
power module and
battery interface board
Screw
件
AL
Separate the front Disconnect the wires Unscrew the screws securing Replace power
and back assembly from power module
文 the power module module
TI
Assemble the power module in the reversed order. Connect the wires and fix the main unit.
密
Separate the front Unscrew the screws securing Remove module wires Replace M3600
and back assembly and air tube
ED
Assemble the module in the reversed order. Connect the wires and fix the main unit.
- 48 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
Screw
CO2 probe Wires connecting
interface wires main board and
C02 power board
件
AL
Separate the front
文
Disconnect the wires Unscrew the screws Replace CO2/IBP
and back assembly from CO2/IBP module securing the module module
TI
密
Assemble CO2/IBP module in the reversed order. Connect the wires and fix the main unit.
EN
保
ID
邦
NF
理
CO
AN
ED
- 49 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
CO2 probe
interface wires
Wires connecting
main board and
C02 power board
C.O. wires
Wires
connecting X5
main board and
C2 (IBP module)
件
IBP wires
AL
文 Screw
TI
密
EN
保
Power wires
Interface
ID
board wires
邦
Air tube
Interface
CO
board print
signal wires
AN
Separate front and Separate the main frame Disconnect wires Remove main Replace main
ED
back assembly and the main board from main board board board
Assemble the main board in the reversed order. Connect the wires and fix the main unit.
- 50 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
件
Pump&valve wires Air tube
AL
文
Air inflation pump
TI
密
EN
保
Safety valve
ID
邦
Measurement valve
NF
理
CO
Cut strap to
Separate the front Remove Remove linking Remove pump replace pump
and back assembly parameter module wires and air tube &valve assembly
assembly Remove screws
to replace valve
AN
Assemble the pump&valve assembly in the reversed order. Connect the wires and fix the main
unit.
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- 51 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
AC power
input wires
件
Screw
AL
文
TI
密
M3 nut
EN
保
ID
Battery spring
邦
NF
理
Separate the front Disconnect the Unscrew the screws Remove the
and back assembly wires from battery securing the battery battery spring
CO
Replace battery
interface board
AN
Assemble the battery interface board in the reversed order. Connect the wires and fix the main
unit.
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- 52 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
Screw
件
AL
文
TI
Power wires
密
EN
Wires connecting
main board and
保
interface board
Wires connecting printer
ID
interface board
NF
Screw
理
CO
AN
Separate the front Remove the battery Disconnect the wires Unscrew the screws securing
and back assembly assembly from interface board the interface board
ED
Assemble the interface board in the reversed order. Connect the wires and fix the main unit.
- 53 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
件
Separate the front Disconnect the wires Pinch the lock, and Replace Wi-Fi module
and back assembly from WIFI module remove Wi-Fi module
AL
文
Assemble the Wi-Fi module in the reversed order. Connect the wires and fix the main unit.
TI
密
EN
保
ID
邦
NF
理
CO
Assemble the recorder in the reversed order. Connect the wires and secure the screws.
ED
- 54 -
iM70 Patient Monitor Service Manual Disassembling the Monitor
Screw
Exhaust pipe
件
AL
文 Wires
connecting the
Inlet pipe
ID
邦
NF
理
Wires connecting
EDAN EtCO2 module
and cup
AN
Separate the front Unscrew the screws securing Remove module wires Replace EDAN
ED
and back assembly EDAN EtCO2 module and air tube EtCO2 module
Assemble the module in the reversed order. Connect the wires and the air tube. Fix the main unit.
- 55 -
iM70 Patient Monitor Service Manual Replaceable Parts
件
8.4.5 Knob Board 02.02.451577
AL
8.4.6 Touch Screen Adapter Board 02.02.451063
8.4.7
文
Alarm Indicator Board 02.02.451579
TI
8.5.1 PS900Q Power Assembly 02.01.210066
密
8.5.2 M3600 NIBP Module 02.08.102094
CO2 Commutator 02.02.114575
EN
8.5.3
保
Pump 01.58.472008
邦
NOTE:
The part name may vary depending on context, but the part number is constant.
- 56 -
ED 理
AN 邦
CO 保
NF 密
ID 文
EN 件
TI
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