ECG2350 EnglishSM 08SK2.006.00045B
ECG2350 EnglishSM 08SK2.006.00045B
ECG2350 EnglishSM 08SK2.006.00045B
Electrocardiograph
ECG-2350
08SK2.006.00045B
If you have any comments or suggestions on this manual, please contact us at:
www.nihonkohden.com.cn
Copyright Notice
The entire contents of this manual are copyrighted by Shanghai Kohden. All rights are reserved. No part of this
document may be reproduced, stored, or transmitted in any form or by any means (electronic, mechanical, photocopied,
recorded, or otherwise) without the prior written permission of Shanghai Kohden.
Trademark
The mark printed on the SD card that is used in this instrument is a trademark. The company name and model name are
trademarks and registered trademarks of each company.
1
Contents
2
GENERAL HANDLING PRECAUTIONS...................... I
WARRANTY POLICY.................................................. II 4 Disassembly and Assembly 3
EMC RELATED CAUTION......................................... III Before You Begin...................................................... 4-2
Conventions Used in this Manual and Device.............V Connection Diagram................................................. 4-3 4
General Safety Information........................................VI Removing the Handle............................................... 4-5
Removing the Battery............................................... 4-6 5
1 General Removing the Top Case........................................... 4-7
Removing the Main Board........................................ 4-8
Introduction............................................................... 1-2
Removing the Power Board..................................... 4-9
General Information on Servicing............................. 1-3
Removing the Connector Board............................. 4-10
Service Policy and Service Parts............................. 1-5
Removing the Thermal Head.................................. 4-11
Specifications........................................................... 1-6
Removing the Paper Mark Sensor Board............... 4-12
Panel and Parts Descriptions................................. 1-10
Removing the Speaker........................................... 4-13
Composition........................................................... 1-17
Removing the Recorder Assy................................. 4-14
Location.................................................................. 1-18
Removing the LCD Unit.......................................... 4-16
Connector Pin Assignment..................................... 1-19
Removing the Magazine......................................... 4-18
Circuit Diagram....................................................... 1-20
Fuse Locations....................................................... 4-19
Outline of Operation............................................... 1-21
Power..................................................................... 1-22
5 Replaceable Parts List
3 Maintenance
Periodic Replacement Schedule.............................. 3-2
Cleaning the Parts.................................................... 3-3
Setting the Date and Time........................................ 3-5
Saving the System Settings..................................... 3-7
Loading the System Settings.................................... 3-8
System Test.............................................................. 3-9
Adjusting Recording Darkness............................... 3-18
Displaying the Software Version, Model, Internal
Voltage and SD Card Information......................... 3-19
Adjusting the Cue Mark.......................................... 3-20
Setting the Diameter of the Platen Roller............... 3-21
Setting the Mac Address........................................ 3-22
Adjusting the Thermal Head................................... 3-23
Changing the Recording Paper Width (210 mm
to 216 mm)........................................................... 3-25
Maintenance Check Sheet..................................... 3-28
Please read these precautions thoroughly before attempting to operate the instrument.
1. To safely and effectively use the instrument, its operation must be fully understood.
3. Before Operation
(1) Check that the instrument is in perfect operating order.
(2) Check that the instrument is grounded properly.
(3) Check that all cords are connected properly.
(4) Pay extra attention when the instrument is combined with other instruments to avoid misdiagnosis or other
problems.
(5) All circuitry used for direct patient connection must be doubly checked.
(6) Check that battery level is acceptable and battery condition is good when using battery-operated models.
4. During Operation
(1) Both the instrument and the patient must receive continual, careful attention.
(2) Turn power off or remove electrodes and/or transducers when necessary to assure the patient's safety.
(3) Avoid direct contact between the instrument housing and the patient.
(4) The operator should not touch patients and non-medical equipment simultaneously, otherwise may cause electric
shock.
6. The instrument must receive expert, professional attention for maintenance and repairs. When the instrument is
not functioning properly, it should be clearly marked to avoid operation while it is out of order.
9. When the instrument is used with an electrosurgical instrument, pay careful attention to the application and/or
location of electrodes and/or transducers to avoid possible burn to the patient.
10. When the instrument is used with a defibrillator, make sure that the instrument is protected against defibrillator
discharge. If not, remove patient cables and/or transducers from the instrument to avoid possible damage.
WARRANTY POLICY
Shanghai Kohden Corparation (SKC) shall warrant its products against all defects in materials and workmanship for one
year from the date of delivery. However, consumable materials such as recording paper, ink, stylus and battery are excluded
from the warranty.
SKC or its authorized agents will repair or replace any products which prove to be defective during the warranty period,
provided these products are used as prescribed by the operating instructions given in the operator's and service manuals.
No other party is authorized to make any warranty or assume liability for SKC's products. SKC will not recognize any other
warranty, either implied or in writing. In addition, service, technical modification or any other product change performed by
someone other than SKC or its authorized agents without prior consent of SKC may be cause for voiding this warranty.
Defective products or parts must be returned to SKC or its authorized agents, along with an explanation of the failure.
Shipping costs must be pre-paid.
This warranty does not apply to products that have been modified, disassembled, reinstalled or repaired without Shanghai
Kohden approval or which have been subjected to neglect or accident, damage due to accident, fire, lightning, vandalism,
water or other casualty, improper installation or application, or on which the original identification marks have been
removed.
The following describes some common interference sources and remedial actions:
1. Strong electromagnetic interference from a nearby emitter source such as an authorized radio station
or cellular phone:
Install the equipment and/or system at another location. Keep the emitter source such as cellular
phone away from the equipment and/or system, or turn off the cellular phone.
2. Radio-frequency interference from other equipment through the AC power supply of the equipment
and/or system:
Identify the cause of this interference and if possible remove this interference source. If this is not
possible, use a different power supply.
Make sure all users and patients in contact with the equipment and/or system are free from direct or
indirect electrostatic energy before using it. A humid room can help lessen this problem.
4. Electromagnetic interference with any radio wave receiver such as radio or television:
If the equipment and/or system interferes with any radio wave receiver, locate the equipment and/or
system as far as possible from the radio wave receiver.
5. Interference of lightning:
When lightning occurs near the location where the equipment and/or system is installed, it may induce
an excessive voltage in the equipment and/or system. In such a case, disconnect the AC power cord
from the equipment and/or system and operate the equipment and/or system by battery power, or use
an uninterruptible power supply.
When the equipment and/or system is adjacent to or stacked with other equipment, the equipment
and/or system may affect the other equipment. Before use, check that the equipment and/or system
operates normally with the other equipment.
When an unspecified accessory, transducer and/or cable is connected to this equipment and/or
system, it may cause increased electromagnetic emission or decreased electromagnetic immunity.
The specified configuration of this equipment and/or system complies with the electromagnetic
requirements with the specified configuration. Only use this equipment and/or system with the specified
configuration.
When the equipment and/or system is used with the unspecified system configuration different than
the configuration of EMC testing, it may cause increased electromagnetic emission or decreased
electromagnetic immunity. Only use this equipment and/or system with the specified configuration.
The equipment and/or system is designed to measure bioelectrical signals with a specified
sensitivity. If the equipment and/or system is used with excessive sensitivity, artifact may appear by
electromagnetic interference and this may cause mis-diagnosis. When unexpected artifact appears,
inspect the surrounding electromagnetic conditions and remove this artifact source.
If the above suggested remedial actions do not solve the problem, consult your Nihon Kohden
representative for additional suggestions.
The CE mark is a protected conformity mark of the European Community. Products with the CE mark comply with
the requirements of the Medical Device Directive 93/42/EEC.
NOTE about Waste Electrical and Electronic Equipment (WEEE) Directive 2002/96/EC
For the member states of the European Union only:
The purpose of WEEE directive 2002/96/EC is, as a first priority, the prevention of waste electrical and
electronic equipment (WEEE), and in addition, the reuse, recycling and other forms of recovery of such
wastes so as to reduce the disposal of waste.
Contact your Nihon Kohden representative for disposal.
WARNING: A warning alerts the user to possible injury or death associated with the
use or misuse of the instrument.
CAUTION: A caution alerts the user to possible injury or problems with the instrument
associated with its use or misuse such as instrument malfunction,
instrument failure, damage to the instrument, or damage to other property.
General
WARNING WARNING
Never use the electrocardiograph in the presence Never use the electrocardiograph in a hyperbaric
of any flammable anesthetic gas or high oxygen chamber. Failure to follow this warning may
concentration oxygen atmosphere. Failure to follow cause explosion or fire.
this warning may cause explosion or fire.
WARNING WARNING
When the electrocardiograph is used with an When performing MRI test, remove all electrodes
electrosurgical unit (ESU), firmly attach the entire and transducers from the patient which are
area of the ESU return plate. Otherwise, the connected to this device. Failure to follow this
current from the ESU flows into the electrodes of warning may cause skin burn on the patient. For
the electrocardiograph, causing electrical burn details, refer to the MRI manual.
where the electrodes are attached. For details,
refer to the ESU manual.
WARNING WARNING
Before defibrillation, remove everything including Before defibrillation, all persons must keep away
electrodes and patches from the patient’s chest. If from the bed and must not touch the patient or any
the defibrillator paddle contacts an object on the equipment or cable connected to the patient.
patient’s chest, the discharged energy may be Failure to follow this warning may cause electrical
insufficient and cause skin burn. shock or injury.
WARNING WARNING
Use only the specified patient cables. Failure to No modification of this equipment is allowed.
follow this warning may cause skin burn where the
electrode is attached and damage the
electrocardiograph due to discharge energy when WARNING
defibrillation is performed. This device is used for diagnosis only. Do NOT use
for monitoring in ICU/CCU or emergency room.
WARNING WARNING
Connect only the specified devices to the Additional equipment connected to the medical
electrocardiograph and follow the specified electrical equipment must comply with the
procedure. Failure to follow this warning may result respective IEC or ISO standards (e.g. IEC60950
in electrical shock or injury to the patient and for data processing equipment). Furthermore all
operator, and cause fire or device malfunction. configurations shall comply with the requirements
for medical electrical systems (see IEC 60601-1-
1or clause 16 of IEC60601-1 3rd, respectively).
WARNING Anybody connecting additional equipment to
When the electrocardiograph is connected to an medical electrical equipment configures a medical
external device, ground all devices to the same system and is therefore responsible that the
one-point ground and use the specified isolation system complies with the requirements for medical
transformer for the external device even when the electrical systems. Attention is drawn to the fact
electrocardiograph is operated on battery pack. that local laws take priority over the above
Otherwise, the patient and operator may receive mentioned requirements. If in doubt, consult your
electrical shock from leakage current from the local representative or the technical service
external device. department.
WARNING WARNING
When several medical devices are used together, Only use the provided power cord. To avoid risk of
ground all devices to the same one-point ground. electric shock, this equipment must only be
Any potential difference between devices may connected to a supply mains with protective earth.
cause electrical shock to the patient and operator.
WARNING WARNING
When the external device does not comply with the Never use a local purchase multiple portable
IEC 60601-1, use a local purchase medical socket outlet. Failure to follow this warning may
isolation transformer unit between the external cause electrical shock to the patient and operator.
device and the wall AC socket.
WARNING CAUTION
Do not use an additional multiple portable socket Before connecting or disconnecting devices, make
outlet or extension cord. The impedance of the sure that each device is turned off and the power
protective earth increases and the patient and cord is disconnected from the AC socket.
operator may receive electrical shock or injury. Otherwise, the patient or operator may receive
electrical shock or injury.
Battery Pack
WARNING WARNING
Never short-circuit the + and – terminals on the If the battery pack is damaged and the substance
battery pack. It may cause overheating and fire. inside the battery pack contacts the eyes or skin,
• Keep the battery pack away from fire. It may wash immediately and thoroughly with water and
explode. see a physician. Never rub your eyes, because you
• Do not damage, disassemble, drop or give may lose your eyesight.
impact to the battery pack.
• Never use the battery pack on unspecified
devices. WARNING
• Never charge the battery pack on unspecified • Do not immerse the battery pack in water. The
devices. battery pack may overheat and rust and the
• Never install the battery pack with the wrong substance inside the battery pack may leak.
polarity. • Do not leave the battery pack unused for more
• Keep the battery pack away from patients and than about one year. The battery pack may
out of the reach of children. leak.
WARNING
Only use the NKB-301V battery pack.
CAUTION CAUTION
Do not expose the battery pack to direct sunlight The battery pack must be replaced by qualified
or leave in a high temperature place. The lifetime service personnel.
of the battery pack may be shortened, the
performance of the battery pack may be degraded
and the battery pack may leak.
CAUTION CAUTION
Do not leave accessories and consumables such Only use Shanghai Kohden specified parts and
as electrodes or electrolyte cream (Cardio Cream) accessories to assure maximum performance from
near the patient or in reach of children. If they are your electrocardiograph. Using unspecified
swallowed, consult a physician immediately. recording paper or electrodes may cause incorrect
ECG recording and accelerate deterioration of the
electrocardiograph.
WARNING WARNING
Additional equipment connected to the medical Connect the electrocardiograph to a network as
electrical equipment must comply with the specified. Otherwise the patient and operator may
respective IEC or ISO standards (e.g. IEC60950 receive electrical shock or injury. To connect the
for data processing equipment). Furthermore all network, contact your Nihon Kohden
configurations shall comply with the requirements representative.
for medical electrical systems (see IEC 60601-1-1
or clause 16 of IEC60601-13rd, respectively).
Anybody connecting additional equipment to
WARNING
Enter the patient information correctly. Otherwise,
medical electrical equipment configures a medical
the ECG data may be lost or mixed up with
system and is therefore responsible that the
another patient’s ECG data. When managing test
system complies with the requirements for medical
data that is only in electronic file, make sure to
electrical systems. Attention is drawn to the fact
enter the patient information. After sending the
that local laws take priority over the above
DICOM data to an external system (such as
mentioned requirements. If in doubt, consult your
PACS, etc.), make sure the ECG data is received
local representative or the technical service
and displayed correctly and the displayed patient
department.
information are consistent with the entered patient
information.
CAUTION CAUTION
The network must be managed by the network Select an installation location where patient
administrator. Only the network administrator can information cannot be seen or accessed by
change the network settings on the ECG-2350 unauthorized personnel.
electrocardiograph and connect the
electrocardiograph to the network. Incorrect
settings or connection may cause failure of the
network system and device.
Cart
CAUTION CAUTION
Only use the KD105D/KD-105E cart for this • Do not move the cart with the casters locked.
electrocardiograph. If another cart is used, it may The cart may tip over.
tip over or the electrocardiograph may fall off. • When moving the cart, hold the handle only.
CAUTION CAUTION
When moving the cart with patient cable hanger To prevent the cart from tipping over or the
mounted, fold the upper and lower arms together, electrocardiograph falling off the cart:
rotate the arms so that they point toward the • Do not put or hook anything on the handle.
handle and do not protrude beyond the edges of • Do not ride on the cart. Do not lean on the
the cart. handle or put your weight on the cart.
• Periodically check that the casters, handle and
frame are firmly attached and not wobbly.
• Always lock the casters so that the cart does
not move accidentally.
WARNING WARNING
Do not touch the patient while touching any metal Do not connect the tip of the electrode lead to
part of non-medical electrical equipment or an anything other than an electrode. Connect all the
exposed part when a connector or cover is tips to the corresponding electrodes and attach
removed. Failure to follow this warning may cause them to the patient. If unconnected tips or
electrical shock or injury to the patient. electrodes contact an item which is not
equipotential grounded, the patient may receive
electrical shock. Also, noise may superimpose on
WARNING the ECG waveforms and measurement data may
Do not diagnose a patient based on DICOM or be incorrect.
PDF data acquired by the electrocardiograph.
Otherwise, it may cause incorrect judgment.
CAUTION CAUTION
Enter the patient information correctly. Otherwise, Do not use the output signal from the output
the ECG data may be lost or mixed up with connector of the electrocardiograph for a
another patient’s ECG data. synchronization signal on a defibrillator. There is a
time delay between the input signal and output
signal. When using the output signal from the
electrocardiograph for the synchronization signal
on other device, always consider this time delay.
CAUTION CAUTION
The paper cutter in the recording paper container The filter, auto gain and layout of the DICOM or
is sharp. When setting the recording paper, be PDF data which is output from the
careful not to cut your finger. Set the recording electrocardiograph are not entirely consistent with
paper as specified. those on the recording paper.
CAUTION CAUTION
• The automatic ECG interpretation is performed Take care when judging the ECG recording
for acquired ECG waveforms only and does not because the EMG filter may cause distortion of
reflect all conditions of the patient. The results P-waves and QRS-waves depending on the
of the analysis might not correspond to the waveform shape.
judgement of a physician.
• Overall judgement must be performed by the
physician, referring to the analysis result,
clinical findings, and other examination results.
After the physician’s overall judgement, the
analysis results should be signed or initialed by
the physician.
Maintenance
NOTE: The qualified service personnel refer to those
CAUTION who are trained and appointed by Shanghai
Before maintenance, cleaning or disinfection, turn Kohden.
the electrocardiograph power off and disconnect
the power cord from the AC socket. Failure to
follow this instruction may result in electrical shock
and electrocardiograph malfunction.
Introduction
This service manual provides useful information for qualified service personnel
to understand, troubleshoot, service, maintain and repair the ECG-2350
electrocardiograph (hereinafter referred to as "the instrument" or "ECG-2350").
All replaceable parts or units of the instrument and its optional units are clearly
listed with exploded illustration to help you locate the parts quickly.
The information in the operator’s manual is primarily for the user. However, it
is important for service personnel to thoroughly read the operator’s manual and
service manual before starting to troubleshoot, service, maintain or repair the
instrument. This is because service personnel need to understand the operation of
the instrument in order to effectively use the information in the service manual.
1
General Information on Servicing
Note the following information when servicing the instrument.
CAUTION
Safety
• There is the possibility that the outside surface of the instrument,
such as the operation keys, could be contaminated by contagious
germs, so disinfect and clean the instrument before servicing it.
When servicing the instrument, wear rubber gloves to protect
yourself from infection.
• There is the possibility that when the lithium battery is broken,
a solvent inside the lithium battery could flow out or a toxic
substance inside it could come out. If the solvent or toxic
substance touches your skin or gets into your eyes or mouth,
immediately wash it with a lot of water and see a physician.
Liquid ingress
The instrument is not waterproof, so do not install the instrument
where water or liquid can get into or fall on the instrument. If liquid
accidentally gets into the instrument or the instrument accidentally
drops into liquid, disassemble the instrument, clean it with clean
water and dry it completely. After reassembling, verify that there is
nothing wrong with the patient safety checks and function/
performance checks. If there is something wrong with the instrument,
contact your Nihon Kohden representative for repair.
Environmental safeguards
Depending on the local laws in your community, it may be illegal to
dispose of the lithium battery in the regular waste collection. Check
with your local officials for proper disposal procedures.
Caution - continued
Transport
• Use the specified shipment container and packing material
to transport the instrument. If necessary, double pack the
instrument. Also, put the instrument into the shipment container
after packing so that the buffer material does not get inside the
instrument.
• When transporting a board or unit of the instrument, be sure
to use a conductive bag on. Never use an aluminum bag to
transport a board or unit which a lithium battery is mounted. Also,
never use a styrene foam or plastic bag which generates static
electricity to wrap the board or unit of the instrument.
Maintenance
Turn off the power of the instrument before doing maintenance,
cleaning or disinfecting. Otherwise you may get an electrical shock or
the instrument may malfunction.
Preventing infection
Follow the local laws or regulations to prevent infection.
1
Service Policy and Service Parts
Service Policy
Our technical service policy for the instrument is to replace the faulty unit, board
or part or damaged mechanical part with a new one. Do not perform electrical
device or component level repair of the multilayer board or unit. We do not
support component level repair outside the factory for the following reasons:
• Most of the boards are multilayer boards with surface mount electrical devices,
so the mounting density of the board is too high.
• A special tool or high degree of repair skill is required to repair the multilayer
boards with surface mount electrical devices.
Service Parts
NOTE: When ordering parts or accessories from your Nihon Kohden
representative, please quote the code number and part name
which is listed in this service manual, and the name or model of
the unit in which the required part is located. This will help us to
promptly attend to your needs. Always use parts and accessories
recommended or supplied by Shanghai Kohden Corporation to
assure maximum performance from your instrument.
Specifications
ECG Input
Input impedance: ≥ 50 MΩ at 10 Hz
Polarization-proof voltage: ±550 mV
Input protection function: There is a defibrillation-proof function when the following specified patient cable is
connected:
Recovery time: < 5 s
Recorder
Recording mode: Thermal line
Printing density: 200 dpi (8 dots/mm); 320 dots/mm2 (25 mm/s)
Scanning line density: 1 ms
Number of recording channels: 3, 4, 6, 12
Recording speed: 5 mm/s, 10 mm/s, 12.5 mm/s, 25 mm/s, 50 mm/s
Recording speed accuracy: ±5 %
Recording paper width: 210 mm width, 30 m long Z fold
Printed data: ECG waveform, heart rate, lead name, version, date and time, paper speed, sensitivity, 1
filter setting, patient information, measured information, and marks.
External Input/Output
External input: 2 channels, 10 mm/0.5 V, input impedance ≥ 100 kΩ
Signal output: 1 channel, 0.5 V/mV ± 5 %, output impedance ≤ 100 Ω
Power Requirements
Voltage: AC (100 V to 240 V) ± 10 %
Frequency: (50 Hz or 60 Hz) ± 1 Hz
Power input: ≤ 150 VA
Battery pack: 12 V, battery pack operation time: more than 30 minutes
(In case of fully charged: 6-channel recording, input 1 mV 10 Hz sine wave; recording
speed 25 mm/s)
Connector
USB A type USB 1.1 × 2
SD Slot
×1
LAN Port
×1
Environment
Operating environment temperature: 5 oC to 40 oC
Humidity: 25 % to 95 % (noncondensing)
Atmospheric pressure: 800 hPa to 1060 hPa altitude: < 2000 m
Overvoltage category: II
Pollution degree: 2
Transport and storage environment
Temperature: -20 oC to 65 oC
-20 oC to 50 oC (recording paper)
-20 oC to 55 oC (battery pack, within one month)
-20 oC to 35 oC (battery pack, over one month, and within one year)
Humidity: 10 % to 95 %
10 % to 90 % (recording paper)
20 % to 85 % (battery pack, within two months)
45 % to 85 % (battery pack, over two months and within one year)
Atmospheric pressure: 800 hPa to 1060 hPa altitude: < 2000 m
Overvoltage category: II
Pollution degree: 2
Electromagnetic Compatibility
IEC 60601-1-2 3rd edition: 2007 Medical electrical equipment - Part 1-2: General
requirements for basic safety and essential performance Collateral standard:
Electromagnetic compatibility Requirements and tests
Operation Mode 1
Continuous operation
Lifetime
6 years
(Self certified based on our data; only when the specified yearly inspection is
performed.)
Top View
Name Function
1 Handle Carry the electrocardiograph.
2 LCD screen Displays ECG waveforms, patient information, marks and messages.
3 Function keys Correspond to the functions displayed at the bottom of the screen.
Operation Panel 1
1 2 3 4 5 6 7
9
10
11 12 13 14 15
Name Function
1 POWER key/ lamp Turns the electrocardiograph on or off.
NOTE: Press the POWER key for five seconds to turn the power off when
the electrocardiograph system crashes.
3 Battery pack operation lamp During battery pack operation, indicates the remaining battery pack power with the color
and lighting state. Blinking in orange indicates that the battery pack is almost discharged.
4 Battery pack charge lamp Indicates the battery pack charge status. Lit when the battery pack is being charged.
NOTE: After charging is complete, the battery pack charge lamp lights
every several tens of minutes. This is because a small current
is supplied to the battery pack (supplementary recharging) to
prevent self-discharging of the battery pack. Keep the power cord
plugged into the AC socket when the electrocardiograph is not
used.
14 START/STOP key/ lamp Starts/stops recording. During operation, the lamp lights.
WARNING CAUTION
• Connect only the specified device to the Do not use the output signal from the output
electrocardiograph and follow the specified terminal for a synchronization signal on a
procedure. Failure to follow this warning defibrillator. There is a time delay between the
may result in electrical shock or injury to input ECG signal and output ECG signal. When
the patient and operator, and cause fire and using the output signal from the output terminal
device malfunction. for the synchronization signal on other machines,
• When external device doesn’t comply with always consider this time delay.
IEC 60601-1, connect a market-sold medical
isolation transformer between the external
device and AC power socket.
• Follow IEC 60601-1 for connecting the
electrocardiograph to other devices.
• The operator should not touch patients and
the input/output interface of the equipment
simultaneously. This may cause electric shock.
Name Function
1 Patient cable connector Connects the patient cable.
Name Function
1 Paper magazine Contains the recording paper.
(Recording paper container)
2 Paper magazine release button Press down this button to open the paper magazine and set the recording paper.
Rear Panel 1
1 2 3 4 5 6
Name Function
1 AC power cord socket Connects the power cord to supply AC power to the electrocardiograph.
3 EXT-IN 1/CRO-OUT connector Inputs and outputs analog signals from external devices.
4 Equipotential grounding terminal Connect to an external equipotential grounding system by an equipotential grounding
conductor.
5 USB connector Connects a USB bar code scanner or magnetic card reader.
WARNING
The operator should not touch patients and the input/output interface
of the equipment simultaneously. This may cause electric shock.
Patient Cable
Name Function
1 Electrode leads Connect to chest or limb electrodes.
NOTE: The applied part includes the electrodes and those parts of the
patient cable that need to physically contact the PATIENT in
NORMAL USE.
Defibrillation-proof function
Patient cable: BJ-961D,BJ-962D, BJ-902D, BJ-903D, BA-901D, BA-903D are
in compliance with IEC 60601-2-25 standard, waveforms and electrode recovery
time are within 5 seconds.
1
Composition
Key board
Location
Key Board
Main BD
Motor
Power BD
Trans BD
1
Connector Pin Assignment
EXT-IN 1/CRO-OUT
CRO-OUT
EXT-IN 1
GND
EXT-IN 2
NC
EXT-IN 2
GND
CPU
SPI &
ECG Port A/D ISOLATION NFC FLASH
GPIO
Speaker
WEIM FPGA
USB Host USB OTG Thermal
Port 1 as Host Head
5V OCP
ESDRAM SDRAM
USB Host
USB Host
Port 2
Circuit Diagram
PWM
CRO
JTAG JTAG
EXT 1
EXT 2 ADC
MC34704
in out
5V 3.3V
Batt 1.8V
Voltag 1.5V
Main board
Int
Temp
Therma
l Head Motor
Power board Motor
Temp Driver
Battery 5V Linear
10.5 to REG.
AC/BATT AC/DC
AC inlet
SW REG.
1
Outline of Operation
Main Board
CPU: i.MX25 (operating frequency: 400 MHz)
SDRAM: 64 MByte
FLASH: 128 MByte
CPU unit:
• Processes input signals at 500 samples/second (1.25 μV/LSB);
• Controls the LED on paper sensor, mark sensor and key board;
• Controls key array signal;
• Controls LCD menu display;
• Processes EXT external input simulation signal, and outputs CRO simulation
signal through A/D converter;
• Controls RTC clock module;
• Read/write SD card;
• Exchanges data with external instrument through USB and LAN interfaces;
• Control FPGA for data processing.
FPGA unit:
• Controls motor and printing waveform of thermal head;
• Outputs sound signals.
ECG unit:
• Converts external 8-channel simulation signal into digital signal at the rate of
8,000 samples/second through A/D converter;
• Tests the falling-off of electrodes and PM signals.
Power Board
The main function is voltage conversion. Namely, it could convert common
municipal power supply into various DC power sources for the instrument,
including 24 V DC voltage for thermal head and motor, and 5 V/3.3 V DC
voltage for main board through circuit conversion. Also, it’s available to provide
the same voltage by using external battery. In addition, there is a special circuit
for battery charging.
Converter Board
It is used to convert signals from main board to LCD, loudspeaker and key
board. In addition, there is a LED control circuit, which is used to control the
LED display on key board.
Power
When the POWER key is pressed, the software controls power off to prevent
turning power off during data writing.
If a problem occurs in the system, all the LEDs light and the keys do not work.
Press and hold the POWER key for 5 seconds to turn the power off. When the
power is turned on again, the system information is printed.
NOTE • Normally do not press and hold the POWER key for 5 seconds.
• Pressing and holding the POWER key for 5 seconds turns the
power off even while data is being written. If power is cut off
while data is being written, the file may be damaged and the
electrocardiograph might not operate.
How to Troubleshoot.......................................................2-2
Operation.........................................................................2-5
Recording........................................................................2-6
2. TROUBLESHOOTING
How to Troubleshoot
This section explains how to locate, identify and solve a problem in the
instrument. The troubleshooting tables in this section are divided into general
problems and error messages.
How to Troubleshoot
2 In the “Problem” column, find the trouble item that matches the problem or
error message.
4 If the problem is not solved, do the next action recommended in the “Action”
column. (If this does not solve the problem, do the next recommended
sections.)
5 If none of the actions solve the problem, contact your Nihon Kohden
distributor or representative.
When the POWER lamp is lit but the LCD does not display
No Yes
The voltage between TP20 and
Is the backlight on? TP21 on the main board is 9.6 V. LCD units failure
Yes No
No
Is there a response when
you press the keys? Main board units failure
Yes
No
Yes
Yes No
No
The voltage of main Power board units failure
board TP13 is 3.3 V.
Yes Yes
No
When pulling the recording Does the main board J8 Main board units failure
paper, the waveforms are have 5V power supply?
printed correctly.
Yes Yes
No
Paper mark sensor unit failure
No
Check the CNJ712 of Power board units failure
the main board unit.
Yes
Motor failure
Operation
2
Problem Possible Cause/Criteria Action
Check the connection to J6 on the main
board.
The POWER LED lights but there is no Faulty connections of connectors.
Check the connection to J7 and J2 on
display or backlight on the LCD screen.
inverter board.
Main board failure. Replace the main board.
Damaged power cord. Replace the power cord.
The instrument does not operate during AC Faulty power board. Replace the power board.
power operation. Faulty main board. Replace the main board.
Damaged key board. Replace the key board.
The battery is not charged. Charge the battery.
Faulty F512 on power board. Replace the F512 on the power board.
The instrument does not operate on
Damaged battery. Replace the battery.
battery power.
Faulty connection of the battery connector. Check the voltage of CN511.
Faulty power board. Replace the power board.
Check the connection between J7 on
inverter board and J6 on main board, and
Faulty connections of connectors.
between J4 on inverter board and key
board.
Faulty key board. Replace the key board.
No key or switch operation Faulty main board. Replace the main board.
Press the POWER key for 5 seconds to
turn the power off. When the power is
The electrocardiograph is affected by static
turned on again, the system information
electricity.
is printed. Show the information to Nihon
Kohden representative.
Press the POWER key for 5 seconds to
turn the power off. When the power is
The electrocardiograph is affected by static
The power does not turn off. turned on again, the system information
electricity.
is printed. Show the information to Nihon
Kohden representative.
The electrodes or cables connections Make sure that all electrodes and cables
Only certain electrode lead waveforms are from the patient to the instruments are not connections from the patient to the
displayed on the screen or noise appears on properly connected. instrument are properly connected.
the waveform.
Faulty main board. Replace the main board.
Make sure that the electrodes are properly
Electrodes are not attached to the patient.
No electrode lead waveforms are displayed attached to the patient.
on the screen or noise appears on all
Faulty main board. Replace the main board.
waveforms.
Faulty speaker. Replace the speaker assy.
Confirm that the connector between main
Faulty connection between J2 on inverter
board and inverter board, and that the
board and LCD, and between J2 on
connector between inverter board and LCD
Vertical and horizontal strips appear on the inverter board and J6 on main board.
are normal.
LCD screen at constant intervals.
Faulty main board. Replace the main board.
Faulty LCD unit. Replace the LCD unit.
Check the connection to J5 on the inverter Check that the connection to J5 on inverter
No sound
board. board is normal.
Recording
Problem Possible Cause/Criteria Action
Dirty paper mark sensor. Clean the paper mark sensor.
Damaged key switch. Replace the key board.
No printing when the START/STOP key
Faulty main board. Replace the main board.
is pressed.
Faulty power board. Replace the power board.
Faulty motor. Replace the motor.
Faulty connection between J4 on main
Check the connection to the cable of
board and printing head, and between
printing head.
CNJ411 on power board and printing head.
The recording paper is fed but there is no Faulty thermal head. Replace the thermal head.
printing.
Faulty main board. Replace the main board.
Faulty power board. Replace the power board.
Faulty motor. Replace the motor.
Dirty paper mark sensor. Clean the paper mark sensor.
Faulty connection between J8 on main
Check the connection to sensor.
The paper mark cannot be detected. board and sensor.
Faulty paper mark sensor. Replace the paper mark sensor.
Faulty main board. Replace the main board.
Sometimes the recorder does not print The input protection circuit which protects
Check the electrode attachment to the
and blank recording paper is fed from the the thermal head from strong noise, such as
Patient.
recorder. hum, is rejecting noisy waveforms.
Dirty thermal head. Clean the thermal head.
The recording paper tracks zigzag or to The recording paper is not properly set in Make sure that recording paper is set
one side. the instrument. normally.
Inaccurate or worn out platen roller. Replace the magazine assy.
For inspection and replacement of the above parts, please contact Shanghai
Kohden or its authorized agents.
3
Cleaning the Thermal Head
CAUTION
• Do not clean the thermal head right after recording because the
head is still hot.
• Only use the provided thermal head cleaner pen. Otherwise the
thermal head may be damaged.
To protect the thermal head from abrasion or damage and assure optimum
performance and long service life, clean the surface of the head with the
provided thermal head cleaning pen after every 10 sets of recording paper.
2 Push the paper magazine release button and open the paper magazine.
3 Clean the gray colored part of the thermal head with the thermal head
cleaner pen.
1 Remove the top case. Refer to Removing the Top Case in Section 4.
2 Remove the recorder assy. Refer to Removing the Recorder Assy in Section
4.
6 Use a brush or a piece of cotton moistened with alcohol to clean the gear.
4 Press the [Enter] function key. The <System settings> screen is displayed.
Select “Date/Time settings”. Press the [Enter] function key.
5 Enter the current date and time according to the format displayed.
4 Select “Save system settings”, and press the [OK] function key. The “Save
completed” message will be displayed, which indicates the completion of
saving.
4 Select “Load system settings”, and press the [OK] function key. The “Load
completed” message will be displayed,, which indicates the completion of
loading.
System Test
You can check the system with the system test functions.
3
User Mode
The user mode checks the condition of the electrocardiograph. To display the
user mode <System test> screen, press the POWER key while pressing the
FEED/ MARK key. You can check the items below.
• Demonstration mode
• Recorder test
• Key test
• LCD/LED test
• Electrode Input test
• ECG input and output circuit test
• CRO/EXT1/EXT2 test
• USB test
• Display internal information
• Display model/version information
• LAN Test
• Optional software
Service Mode
The service mode is used for repairing the electrocardiograph and changing the
parts. To display the service mode <System test> screen, press the POWER
key while pressing the FEED/MARK key and AUTO/MANUAL key. The
following items are available.
• Recorder test
• Thermal head test
• Adjust recording darkness
• Key test
• LCD/LED test
• Electrode Input test
• ECG input and output circuit test
• CRO/EXT1/EXT2 test
• USB test
• Display internal information
• Display model/version information
• Adjust cue mark
• Display SD card information
Demonstration Mode
This item displays the demonstration waveform. Select “Demonstration mode”
and press the [OK] function key.
Recorder Test
This item checks the recorder function. Select “Recorder test” and press the
[OK] function key. This test prints the following figures:
• Diagonal line
• Thermal head check pattern
• Paper speed scale
• Paper mark detection mark
1 Select the “Thermal head test” on the <System test> screen and press the
[OK] function key.
3
The recorder prints a continuous series of H’s and X’s.
Key Test
This item checks the functions of the keys.
1 Select “Key test” and press the [OK] function key to start the test.
Press any key other than the POWER key for test. The name of the pressed
key is shown on the screen.
LCD/LED Test
This item checks the LCDs and LEDs.
Select “LCD/LED test” and press the [OK] function key or the START/STOP
key to start the test. In the LED test, the LEDs light up one by one until all are
lit up and then they go out; then it proceeds to the LCD test. In the LCD test, the
screen lights up in the order red – green – blue.
During the LED test, the battery charge lamp only lights if the battery is charged.
The POWER lamp is lit continuously while the power is on. The AC power
lamp is lit when power is taken from AC power. The AC power lamp is directly
controlled by hardware, so this test cannot check it.
LED Test
Check Possible causes and countermeasures
• Check the connections of the connector.
LCD Test
Check Possible causes and countermeasures
• Check the connections of the connector.
During the LCD test, check that • Replace a faulty LCD unit.
nothing is abnormal with the
LCD. • Replace a faulty main board.
• Replace a faulty inverter board.
Input Jig
3
1 Connect the electrode lead to the electrocardiograph.
2 Insert the tip of the electrode lead in the input check jig. If it is a clip type
induction lead, pinch the edge of the input check jig.
3 Select “Electrode Input test” and press the [OK] function key to start the test.
2 Insert the tips of all the electrode leads into the input check jig. If they are
clip type electrode leads, pinch the edge of the testing tool.
3 Select “ECG input and output circuit test” and press the [OK] function key
to start the test.
The electrocardiograph sends a standard signal from the beginning of the
ECG input circuit and prints the waveform.
When all the waveforms are printed, the test is finished and the <System test>
screen is displayed. To cancel the test, press the [Back] function key.
25 mm
Example
Preparation
A locally made check jig is required for the test. To make the check jig, use the 3
two 3.5 diameter monaural jacks and leads and solder the signal line and ground
line of the two jacks with leads as shown below.
Procedure
1 Connect the check jig to the EXT-IN 1/CRO and EXT-IN 2 connector of the
instrument.
2 Select “CRO/EXT 1/EXT 2 test” and press the [OK] function key.
To quit the test, press the [Back] function key. The <System test> screen is
displayed.
Example
USB Test
This item checks the USB devices function.
2 Select “USB test” on the <System test> screen and press the [OK] function
key. The 4 digits of Vender ID and Product ID are displayed and a chime
sounds.
3 Press the [Back] function key to return to the <System test> screen.
To cancel the test, press the [Back] function key. The <System test> screen is
displayed.
When you connect an unspecified USB adapter, the 4 digits of Vender ID and
Product ID are not displayed and an error sounds. Use a specified USB adapter
and test again.
LAN Test
2 Select “LAN Test” on the <System test> screen and press the [Enter]
function key.
3
3 Enter server IP address, and press the [OK] function key.
The test result will be displayed.
1 Display the service mode <System test> screen. Refer to System Test in this
section.
3 Check the impedance value printed on the label that is attached to the
thermal head and press the [Change] function key until the applicable
number from 1 to 8 is displayed. This sets the adjusted value of the print
level for the thermal head.
Displaying the Software Version, Model, Internal Voltage and SD Card Information
3
Displaying the Software Version and Model
1 Display the service mode <System test> screen. Refer to System Test in this
section.
3 The model name and the software version of this electrocardiograph are
displayed on the screen.
4 Press the [Back] function key to return to the <System test> screen.
2 Select “Display internal information” and press the [OK] function key. The
internal voltage is displayed.
3 Press the [Back] function key. The <System test> screen is displayed.
2 Display the service mode <System test> screen. Refer to System Test in this
section.
3 Select “Display SD card information” and press the [OK] function key. The
information of the SD memory card is displayed.
When displaying the information of another card, change the card and press
the [Back] function key.
4 Press the [Back] function key. The <System test> screen is displayed.
1 Display the service mode <System test> screen. Refer to System Test in this
section.
2 Select “Adjust cue mark” on the <System test> screen. Check that the
setting is “0” and press the [Test] function key to execute feeding with a fine
adjustment value of 0.
3 The recording paper is fed and stopped at the mark position. Measure the
difference between the cutter of the upper casing of the frame and the mark
on the recording paper.
4 Push and hold the [Change] function key until it reaches the number
corresponding with the value measured at the previous step. It has a negative
value if the recording paper is sticking out from the cutter and a positive
value if it is inside the unit.
5 After setting the changed value, press the [Test] function key again and
check that the perforated line is aligned with the unit.
1 Display the service mode <System test> screen. Refer to System Test in this
section.
3 Press the [Change] function key. The diameter of the platen roller is set up.
1 Select “Mac address setting” on the <System test> screen and press the
[Enter] function key.
2 Input the password “0506” and press the [OK] function key.
4 Press the [Back] function key. The <System test> screen is displayed.
3
Preparation
1 Remove the battery and top case. Refer to Removing the Battery and
Removing the Top Case in Section 4.
2 Insert the calibration latch, and then screw down the fixing screws.
Thermal head fixing screw
Calibration
2 Print the calibration waveforms at the top and bottom of the recording paper.
The calibration waveforms are printed with any ECG waveforms.
3 Rotate the adjusting screw so that the start position of the up slope of
the waveforms are within 0.5 mm of the vertical lines on the paper. Each
complete turn of the screw moves the waveforms 0.5 mm.
NOTE: After adjusting the start position of the waveforms, check the print
evenness and fading again. If there is any unevenness or fading,
adjust the thermal head again.
(Print out CAL waveforms at the top and bottom of the recording paper)
4 After adjusting the thermal head, tighten the two thermal head fixing screws.
5 Turn the power off, disconnect the power cord from the AC socket and
attach the top case and battery.
Required parts
NOTE: Never put too much force on the tab. The tab may break.
• If the current SN No. corresponding to the Product Screen No. is greater than
or equal to the SN No. in the table below, attach the paper cutter blade as
follows.
Product Screen No. SN No.
ECG-2350-100D 110091
ECG-2350-101D 130043
ECG-2350-102D 100006
3
ECG-2350-103D 150480
ECG-2340C 100229
ECG-2350C 101055
ECG-2320 101661
NOTE: Save the paper spacer and magazine spacers so you can use the
210 mm paper again in the future.
Overview
Item Check Procedure Action
If the outside of the cardiograph or
Check if the outside of the cardiograph and
Dirt input box is dirty, clean it with a cotton
input box is dirty.
moistened with warm water, then dry it.
Loose screws Check if there are any loose screws. If any screw is loose, tighten it.
Check if there are any physically damaged
or bent parts. This includes the pins on
Damaged or bent parts If any part is damaged or bent, replace it.
the connector or socket, key switch on the
operation panel and power switch.
Check if the input box is connected to the If the input box is not connected to the
Cable connection
cardiograph firmly. cardiograph, connect them firmly.
Check if the battery pack is used over one
Battery pack If it is used over one year, replace it.
year.
Operation
Item Check Procedure Action
If the error message does not appear, check
Check if an error message appears on the
Electrode detachment detection the input box with the <System test>
screen when an electrode is detached.
screen – “Electrode Input test”. 3
If the manual recording is not available, do
the following.
• Check the CN cable connection between
Manual recording Check if the manual recording is available. the key board and ECG control board.
• Replace the key board.
• Replace the ECG control board.
If the automatic recording is not available,
do the following.
Check the key response with the <System • Check the CN cable connection between
Key on the operation panel the key board and ECG control board.
test> screen – “Key test”.
• Replace the key board.
• Replace the ECG control board.
Check if an SD memory card has no
If the information is not displayed, replace
SD memory card problem with the <System test> screen –
the SD memory card.
“Display SD card information”.
LCD
Item Check Procedure Action
LCD
Check the display quality with the If the display quality is low, replace the
Display quality
<System test> screen – “LCD/LED test”. LCD.
Check if the color pattern is correct with
If the color pattern is not correct, replace
Color pattern the <System test> screen – “LCD/LED
the LCD.
test”.
Check backlight function with the <System If the backlight function is not correct,
Backlight
test> screen – “LCD/LED test”. replace the inverter board or LCD.
Recorder
Item Check Procedure Action
Recorder
If the thermal head is dirty, clean it with a
Check if the thermal head is dirty.
thermal head cleaner pen. 3
If the paper empty sensor is dirty, clean it
Dirt Check if the paper empty sensor is dirty.
with a cotton swab moistened with alcohol.
If the mark sensor is dirty, clean it with a
Check if the mark sensor is dirty.
cotton swab moistened with alcohol.
If the magazine does not open, check the
Check if the magazine opens by pushing
Magazine magazine release lever attachment and
up the magazine release lever.
correct it.
If paper skews, do the following.
• Set the recording paper so that it aligns
Check that there is no paper skew (after with recording paper guide correctly.
Paper skew 100 cm recoding, paper skews less than 0.5
• Clean the thermal head.
mm per 50 cm).
• Clean the feeding roller.
• Readjust the thermal head position.
If the paper speed is not correct, do the
following.
• Clean the paper feeding roller.
Check if the paper speed is correct with the
Paper speed
<System test> screen – “Recorder test”. • Replace the motor assy.
• Replace the ECG control board.
• Replace the power board.
If the message does not appear, do the
following.
Check that the “Check paper or recorder”
• Clean the paper empty sensor.
Paper empty detection message appears when there is no
recording paper. • Check that the data lines between the
paper mark sensor and the main board
are well connected.
Check if the paper feeding is correct and
If the paper does not stop at the paper
Paper mark detection stops at the paper mark or do the <System
mark, clean the mark sensor.
test> screen – “Recorder test”.
Thermal head
If there is any unevenly or incompletely
printed part, do the following.
Check if there is any unevenly or • Clean the thermal head with a thermal
Print intensity incompletely printed part with the <System head cleaner pen.
test> screen – “Recorder test”.
• Readjust the thermal head attachment.
• Replace the thermal head.
If the baseline width is more than 1 mm,
Check if the baseline width is 1 mm or less do the following.
Baseline width with the <System test> screen – “Recorder
• Replace the thermal head.
test”.
• Replace the ECG control board.
If there are any missing dots, do the
following.
Check if there are any missing dots with • Clean the thermal head with a thermal
Missing dots head cleaner pen.
the <System test> screen – “Recorder test”.
• Readjust the thermal head attachment.
• Replace the thermal head.
Safety
Item Check Procedure Action
Check that a 3-prong power cord which
If the 3-prong power cord is not used,
Power cord has three terminals (hot, neutral and
replace it.
ground) is used.
Check if the power cord or connection If the power cord or connection cable is
Power cord and connection cable
cable is damaged. damaged, replace it.
If the cardiograph is not grounded, use
Check if the cardiograph is grounded to a
the provided ground cable to ground the
Equipotential grounding dedicated equipotential ground terminal in
system to a dedicated equipotential ground
the facility.
terminal.
If the protective earth resistance is out
Check that the protective earth resistance is
Protective earth resistance of range, find the cause and reduce it to
within 0.1 Ω of the prescribed range.
within range.
If the earth leakage current is out of range,
Check that the earth leakage current is
Earth leakage current find the cause and reduce it to within
within 500 μA of the prescribed range.
range.
If the enclosure leakage current is out
Check that the enclosure leakage current is
Enclosure leakage current of range, find the cause and reduce it to
within 100 μA of the prescribed range.
within range.
If the patient leakage current is out of
Check that the patient leakage current is
Patient leakage current range, find the cause and reduce it to
within 10 μA of the prescribed range.
within range.
Check that the electrocardiograph can
withstand the following prescribed
If the electrocardiograph cannot withstand
withstand voltage.
Withstand voltage the prescribed voltage, find the cause and
- (A-a1): 1,500 V AC for one minute fix it.
- (B-d): 1,500 V AC for one minute
Date:
Customer:
Customer Address:
Service Personnel: Service Company:
Instrument Name: Instrument Model:
Instrument Serial Number: Hardware Version:
Software Version:
Connection Diagram........................................................4-3
Fuse Locations..............................................................4-19
4. DISASSEMBLY AND ASSEMBLY
WARNING
• Removal and replacement of any components in the
electrocardiograph should only be done by qualified service
personnel.
• To avoid the possibility of injury to yourself or damage to the
electrocardiograph, do not install or remove any component while
the power is on. When disassembling, make sure that the power is
off (The power lamp and standby lamp do not light), the AC power
cord is disconnected and the battery pack is removed. There are
several high voltage units inside the electrocardiograph: Junction
board, LCD backlight (LCD display) and switching regulator (power
unit).
CAUTION
• To avoid accidental discharge of static electricity which could
damage the components of the electrocardiograph, use a
grounded wrist strap when installing or removing any component.
• Use only parts recommended by Shanghai Kohden to assure
maximum performance from your electrocardiograph.
Required Tools
• Anti-static bench mat
• Wrist ground strap
• Phillips screwdriver (insulated type, for M3 and M4 screws)
• Hexagon socket driver (for 3 mm spacer bolt and nut)
• Torque wrench (for 4 mm hexagon socket head bolt)
• Allen wrench
• Tweezers
Connection Diagram
NK Code No. of
Index Connector No. NK Code No. Description
Connected component
2 Screw off two screws (BH x 8) on the handle, and take off the handle.
3 While pressing the lock buttons of the battery cable connector, disconnect
the cable and remove the battery.
NOTE: Do not disconnect the connector by pulling the cables, because
this may damage the connector.
Lock button
Battery
1 Connect the battery cable to the electrocardiograph connector and put the
battery in the battery box.
NOTE: If you cannot connect the battery cable, confirm the direction of
the cable and connect it again.
1 Turn the electrocardiograph power off and disconnect the power cord from
the AC outlet.
2 Turn over the electrocardiograph and remove the handle and battery. Refer to
Removing the Handle and Removing the Battery in this section. 4
3 Remove the two screws (BH4 × 8) indicated by (1) and the four screws
(BH4 ×8) indicated by (2).
(1) (2)
(1) (2)
(2)
(2)
4 Turn over the electrocardiograph again. Carefully remove the cable that
connects the top case and bottom case, and the handle fixing piece.
Connecting line
1 Remove the battery and top case. Refer to Removing the Battery and
Removing the Top Case.
2 Remove the three screws indicated by (1) to remove the shielding cover.
3 Disconnect the paper mark sensor line and thermal printing signal line from
the main board.
4 Remove the three screws indicated by (2), raise the main board lightly to
loose the connector between it and the power board at the bottom, and then
take off the main board.
(1) (1)
(1)
(2)
(2)
(2)
NOTE: Do not rotate the main board, since this will possibly damage the
connector between the main board and power board.
1 Remove the battery, top case and the main board. Refer to Removing the
Battery, Removing the Top Case and Removing the Main Board.
2 Remove the four screws indicated by (1), and remove the ground leads.
4
3 Disconnect the motor data line and thermal head power cord connected with
the power board.
(1)
1 Remove the battery and top case. Refer to Removing the Battery and
Removing the Top Case.
3 Remove the four screws indicated by (1) and take off the connector board.
(1)
(1) (1)
(1)
1 Remove the battery and top case. Refer to Removing the Battery and
Removing the Top Case.
4
2 Remove the two head springs.
3 Remove the two screws indicated by (1) that are holding the thermal head.
(1)
(1)
(2)
head
NOTE: When replacing the thermal head, the following adjustments are
required. Refer to Adjusting Recording Darkness and Adjusting
the Cue Mark in Section 3.
1 Remove the battery, top case and the thermal head. Refer to Removing the
Battery, Removing the Top Case and Replacing the Thermal Head.
2 Remove the screws that hold the paper mark sensor board.
Edge
3 Remove the cable from the edge holder and the paper mark sensor board.
1 Remove the battery and top case. Refer to Removing the Battery and
Removing the Top Case.
2 Turn over the top case, and remove the two screws from the speaker bracket.
4
3 Pull off the speaker connector from the inverter board, and take off the
speaker.
NOTE: When attaching the speaker and speaker bracket, fit them into the
guide of the top case.
1 Remove the battery and top case. Refer to Removing the Battery and
Removing the Top Case.
2 Remove the screws and the cable from the main shield.
3 Remove the earth connection screws and cable from the power board.
4 Remove the paper mark sensor board line, thermal head and motor cable
from the main board and power board.
5 Remove four screws (BH3 x 6) from recorder assy, and take off it.
BH3 x 6
1 Remove the battery, top case and inverter board. Refer to Removing the
Battery, Removing the Top Case and Removing the Inverter Board.
2 Remove the two screws indicated by (1) and take off the sheet metal.
(1)
(1)
(2)
(2)
1 Open the magazine, slide it in the direction of the arrow and create a space
between the E-ring and the rib.
2 Insert the tweezers into the space, slide the E-ring in the direction of the
arrow and remove the magazine.
Fuse Locations
F112
F111
401
E
114
122 e 5
301
101 B e
a 121
113
b c 302
112 120
102 111 303
119
a 110
103 118 304
104
105
117 305
116 b
106
124
306
108
107 109 307
115
123
308
309
310
C
311
201
202
3
225
312 d
226 204
D 227 223 203
224 205
228 222
229
230 313 c
231 221
220 206
219
217 314
216
215 214 218
213 212
211 315
210 316
d 207
209 319 317
208 318
401
E
114
122 e
301
101 B 5
e
a 121
113
b c 302
112 120
102 111 303
119
a 110
103 118 304
104
105
117 305
116 b
106
124
306
108
107 109 307
115
123
308
309
310
C
311
201
202
3
225
312 d
226 204
D 227 223 203
224 205
228 222
229
230 313 c
231 221
220 206
219
217 314
216
215 214 218
213 212
211 315
210 316
d 207
209 319 317
208 318
Sales
USA NIHON KOHDEN UK LTD
NIHON KOHDEN AMERICA, INC. Trident Court 118, 1 Oakcroft Road
15353 Barranca Parkway, Irvine, CA 92618, U.S.A. Chessington, Surrey KT9 1BD, UK
Toll-free +1-800-325-0283 Phone +44 20-8391-6800
Phone +1 949-580-1555 Fax +44 20-8391-6809
Fax +1 949-580-1550
Asia
Europe SHANGHAI KOHDEN MEDICAL ELECTRONIC
European Representative INSTRUMENT CORP.
NIHON KOHDEN EUROPE GmbH 567 Huancheng Bei Road, Shanghai Comprehensive
Raiffeisenstrasse 10 Industrial Development Zone, Shanghai China, 201401
D-61191 Rosbach, Germany Phone +86 (21) 62700909
Phone +49 6003-827-0 Fax +86 (21) 62709739
Fax +49 6003-827-599
NIHON KOHDEN SINGAPORE PTE LTD
NIHON KOHDEN DEUTSCHLAND GmbH 1 Maritime Square, #10-34 HarbourFront Centre
Raiffeisenstrasse 10 Singapore 099253
D-61191 Rosbach, Germany Phone +65 6376-2210
Phone: +49 6003-827-0 Fax +65 6376-2264
Fax: +49 6003-827-599
NIHON KOHDEN INDIA PVT. LTD.
NIHON KOHDEN ITALIA S.r.l. 308, Tower A, Spazedge, Sector 47, Sohna Road
Via FratelliBronzetti 28 Gurgaon-122 002 Haryana, India
24124 Bergamo, Italy Toll-free +91 1800-103-8182
Phone +39 035-219543 Phone +91 124-493-1000
Fax +39 035-232546 Fax +91 124-493-1029
The model and serial number of your instrument are identified on the rear or bottom of the unit.
Write the model and serial number in the spaces provided below. Whenever you call your representative concerning this
instrument, mention these two pieces of information for quick and accurate service.
Your Representative