SERVICE MANUAL

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Defibrillator
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TEC-8332K/TEC-8342K
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TEC-8352K
TEC-8300 series

First Edition: 05 Apr 2011

Seventh Edition:
on: 11 Mar 2015

0634-900736F
Printed: 2015/04/03
 Service Manual

Defibrillator
TEC-8321K/TEC-8322K
TEC-8332K/TEC-8342K
TEC-8352K
TEC-8300 series
In order to use this product safely and fully understand all its functions, make sure to read this manual before using the
product.

Keep this manual near the instrument or in the reach of the operator and refer to it whenever the operation is unclear.

This product stores personal patient information. Manage and operate the information appropriately
appropriately..

Patient names on the screen shots and recording examples in this manual are ctional and any resemblance to any
person living or dead is purely coincidental.

The contents of this manual are subject to change without notice.

If you have any comments or suggestions on this manual, please contact us at: www.nihonkohden.com

Copyright Notice
The entire contents of this manual are copyrighted by Nihon 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 Nihon Kohden.

Trademark

The mark printed on the SD card that is used in this instrument is a trademark.

Bluetooth® and its logo are trademarks of Bluetooth SIG, Inc.

 1
Contents 2

GENERAL HANDLING PRECAUTIONS

PRECAUTIONS ............................................................................. i 3
WARRANTY
WARRANTY POLICY ..................................................................................
.........................................................................................................
....................... ii
EMC RELA
RELATED
TED CAUTION...........................................................................................
..................................................................................................iii
.......iii 4
Conventions Used in this Manual and Instrument .............................................................. v
Warnings, Cautions and Notes ................................................................................. v 5

Related Documentation ...............................................................................................

.....................................................................................................
...... vi

Section 1 General...........
.......................
........................
.......................
.......................
........................
.......................
.............
.. 1.1
Introduction ......................................................................................................................1.3
Models and Functions ...........................................................................................1.3
Parameters ............................................................................................................1.3
General Information on Servicing ....................................................................................1.4
Service Policy,
Policy, Service Parts and Patient Safety Checks ................................................ 1.6
Service Policy ........................................................................................................1.6
Service Parts .........................................................................................................1.6
Patient Safety Checks ........................................................................................
............................................................................................
.... 1.7
Maintenance Equipments and Tools
Tools ...................................................................... 1.8
Specifications ...............................................................................................
...................................................................................................................
.................... 1.9
Defibrillator ............................................................................................................1.9
Analysis Accuracy................................................................................................1.12
Monitor .................................................................................................................1.13
Alarm Delay Time ................................................................................................1.13
Lead ECG ............................................................................................................1.13
Paddle ECG .......................................................................................
.........................................................................................................
.................. 1.13
External ECG .....................................................................................
.......................................................................................................
.................. 1.13
Recorder ..............................................................................................................1.14
Noninvasive Pacing
Pacing (TEC-8332/TEC-8352 Only) ................................................ 1.14
External Paddle (ND-831V) .................................................................................1.14
ECG .....................................................................................................................1.14
SpO2 ...................................................................................................................1.14
CO2 .....................................................................................................................1.14
NIBP (TEC-8342/TEC-8352 only) .......................................................................1.14
Invasive Blood Pressure ......................................................................................1.15
Temperature.........................................................................................................1.15
Alarm ...................................................................................................................1.15
Battery .................................................................................................................1.16
AC Power Requirements .....................................................................................1.16
Clock Accuracy ....................................................................................................1.16
Environment.........................................................................................................1.16
Dimensions and Weight .......................................................................................1.16
Safety...................................................................................................................1.17
Safety...................................................................................................................1.17
Environment Conditions.......................................................................................1.17
Conditions.......................................................................................1.17
CONTENTS

Electromagnetic Immunity ...................................................................................1.19

Recommended Separation Distances between Portable and Mobile RF
Communications Equipment ................................................................................ 1.22
System Configuration for EMC Test ..................................................................... 1.23
Panel Description ...........................................................................................................1.24
Front Panel ..........................................................................................................1.24
Right Side Panel ..................................................................................................1.25
Left Side Panel ....................................................................................................1.26
Rear Panel ...........................................................................................................1.27
ND-831V External Paddles (Option) .................................................................... 1.28
ND-860V Series Internal Paddles (Option) .......................................................... 1.29
ND-890V Series Internal Paddles (Option) .......................................................... 1.29
Composition ...................................................................................................................1.30
Standard Components .........................................................................................1.30
TEC-8321 ..................................................................................................1.30
TEC-8322 ..................................................................................................1.31
TEC-8332 ..................................................................................................1.32
TEC-8342 ..................................................................................................1.33
TEC-8352 ..................................................................................................1.34
Options ................................................................................................................1.35
Board and Unit Location ................................................................................................1.37

Section 2 Troubleshooting ....................................................................2.1

How to Troubleshoot ........................................................................................................ 2.2
Error Code ....................................................................................................................... 2.3
Defibrillation ........................................................................................................... 2.4
Operation Panel ..................................................................................................... 2.5
Communication ...................................................................................................... 2.6
Data Error .............................................................................................................. 2.7
Pacing (TEC-8332/TEC-8352 Only) ...................................................................... 2.7
12 Lead ECG Measurement (When Using the Optional AC-831V 12 Lead ECG
Unit) ....................................................................................................................... 2.8
Message .......................................................................................................................... 2.9
Defibrillation and Cardioversion ............................................................................. 2.9
AED .....................................................................................................................2.10
Pacing .................................................................................................................. 2.10
Monitoring ............................................................................................................2.11
ECG........................................................................................................... 2.11
SpO2 .........................................................................................................2.12
CO2 ...........................................................................................................2.13
Invasive Blood Pressure ............................................................................ 2.13
NIBP ..........................................................................................................2.13
Temperature ..............................................................................................2.14
System ................................................................................................................. 2.16
General ...................................................................................................... 2.16
Battery .......................................................................................................2.16
 CONTENTS

Troubleshooting.............................................................................................................. 2.18 1
General ................................................................................................................2.18
Defibrillation .........................................................................................................2.19 2
Pacing (TEC-8332/TEC-8352 Only) ....................................................................2.20
Monitoring ............................................................................................................2.20 3
ECG........................................................................................................... 2.20
SpO2 .........................................................................................................2.21 4
CO2 ...........................................................................................................2.22
NIBP ..........................................................................................................2.23 5

Blood Pressure (PRESS) ..........................................................................2.24

Temperature ..............................................................................................2.24
Recording ............................................................................................................2.24
Battery .................................................................................................................2.25
SD Card ...............................................................................................................2.25

Section 3 Disassembly .......................................................................... 3.1

Before You Begin.............................................................................................................. 3.3
Warnings, Cautions and Notes ..............................................................................3.3
Registering Serial Number after Board Replacement ...........................................3.4
Required Tools ....................................................................................................... 3.5
Connection Diagram ........................................................................................................3.6
Removing the External Paddle Holder or Top Cover......................................................3.11
Removing the Optional 12 Lead ECG Unit ....................................................................3.14
Removing the QI-831V AUXOUT Unit and QI-832V Bluetooth® Module .......................3.16
Removing the Front Case ..............................................................................................3.19
Removing the LCD Unit and the LED DRIVER Board ...................................................3.21
Removing the UR-0414 CONTROL Board and the UR-0415 ECG/PACER Board........ 3.23
Removing the HV-831V HV Unit and UR-0418 HV CPU Board ....................................3.26
Note for Assembling the Defibrillator after HV Unit Replacement .......................3.27
Removing the MP Unit ...................................................................................................3.29
Removing the Input Enclosure.............................................................................3.30
Removing the UR-0454 TEMP Board .................................................................. 3.31
Removing the UR-0455 MP Board ......................................................................3.32
Removing the UR-3908 SpO2 Board ...................................................................3.33
Removing the UR-0444 ECG CONN1 Board ......................................................3.33
Removing the UR-0445 ECG CONN2 Board ......................................................3.34
Removing the NIBP Pump ...................................................................................3.34
Removing the Valve ............................................................................................. 3.35
Removing the UR-0431 REC/EXT Board ......................................................................3.36
Removing the Recorder Unit..........................................................................................3.37
Removing the UR-0417 Power Board ............................................................................ 3.39
Removing the KEY/LED Boards ....................................................................................3.42
Removing the Speaker ..................................................................................................3.44
Removing the Paddle Connector ...................................................................................3.45
CONTENTS

Section 4 Maintenance .......................................................................... 4.1

General ............................................................................................................................ 4.4
Periodic Inspection ................................................................................................ 4.4
Daily Inspection ........................................................................................... 4.4
Monthly Inspection ...................................................................................... 4.4
Yearly Inspection ......................................................................................... 4.4
Repair Parts Availability Policy .............................................................................. 4.4
Before Check ................................................................................................................... 4.5
Recording and Saving the Repor ts........................................................................ 4.5
When Using a Loaner Defibrillator ......................................................................... 4.5
Copying the Settings to the Loaner Defibrillator .......................................... 4.5
Checking the Appearance................................................................................................ 4.6
Checking the SB-831V Battery Pack ............................................................................... 4.7
Checking the Defibrillator ................................................................................................. 4.8
Connecting the Checker and Turning the Defibrillator On ..................................... 4.8
Adjusting the Sync Sound ..................................................................................... 4.9
Checking the Recorder .......................................................................................... 4.9
Record/Stop Key ......................................................................................... 4.9
Date and Time Printed on the Recording Paper.......................................... 4.9
Event Key .................................................................................................... 4.9
Recording Quality ........................................................................................ 4.9
Detecting Out of Paper ..............................................................................4.10
Checking the Defibrillation Function in Manual Mode .................................................... 4.11
Checking the Connector Off Detection ................................................................4.11
Checking the Duration of Charging Energy .........................................................4.13
AC Power................................................................................................... 4.13
Battery Power ............................................................................................4.14
Checking the Discharged Waveform.................................................................... 4.15
Checking the Discharged Energy ........................................................................4.19
AC Power................................................................................................... 4.20
Battery Power ............................................................................................4.20
Checking the Discharge for When Using the Disposable Pads ...........................4.21
Checking the Discharge for When Using the Internal Paddles ............................4.22
Checking for Changing the Energy Setting After Charging is Complete .............4.22
Checking Internal Discharge ...............................................................................4.23
Checking the Synchronized Cardioversion ....................................................................4.25
Checking the Synchronized Cardioversion Using the Paddle Lead ..................... 4.25
Checking the Synchronized Cardioversion Using the ECG Lead ........................4.27
Checking in the AED Mode ............................................................................................4.30
Preparation ..........................................................................................................4.30
Checking ECG Analysis in AED Mode, Charge and Discharge ..........................4.30
Checking the Display ...........................................................................................4.32
Checking the Voice Instruction.............................................................................4.32
Checking the Pacing Function .......................................................................................4.33
Preparation ..........................................................................................................4.33
Checking the Pacing in Fixed Mode ....................................................................4.34
Checking the Pacing in Demand Mode ...............................................................4.35
 Conventions Used in this Manual and Instrument

Warnings, Cautions and Notes

Warnings, cautions and notes are used in this manual to alert or signal the reader to specic information.

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.

NOTE
A note provides specific information, in the form of recommendations, prerequirements, alternative methods or
supplemental information.
 Related Documentation

The TEC-8321K, TEC-8322K, TEC-8332K, TEC-8342K and TEC-8352K debrillators come with the following manuals.

Operator’s Manual, Part I General & Defbrillation

Describes general information (including safety information, installation procedure, basic checks and settings,
troubleshooting and specications), debrillation and pacing.

Operator’s Manual, Part II Parameter Monitoring

Describes parameter monitoring.

Administrator’s Guide
Describes settings on the SYSTEM SET UP screen.

Service Manual
Describes information on servicing the debrillator. Only qualied service personnel can service the debrillator.
 1
Section 1 General

Introduction ..........................................................................................................................................................1.3
Models and Functions ...............................................................................................................................1.3
Parameters ................................................................................................................................................1.3
General Information on Servicing ........................................................................................................................1.4
Service Policy, Service Parts and Patient Safety Checks .................................................................................... 1.6
Service Policy ............................................................................................................................................1.6
Service Parts .............................................................................................................................................1.6
Patient Safety Checks ...............................................................................................................................1.7
Maintenance Equipments and Tools.......................................................................................................... 1.8
Specifications ......................................................................................................................................................1.9
Defibrillator ................................................................................................................................................1.9
Analysis Accuracy ...................................................................................................................................1.12
Monitor ....................................................................................................................................................1.13
Alarm Delay Time ....................................................................................................................................1.13
Lead ECG................................................................................................................................................1.13
Paddle ECG ............................................................................................................................................1.13
External ECG ..........................................................................................................................................1.13
Recorder.................................................................................................................................................. 1.14
Noninvasive Pacing (TEC-8332/TEC-8352 Only)....................................................................................1.14
External Paddle (ND-831V) .....................................................................................................................1.14
ECG.........................................................................................................................................................1.14
SpO2 .......................................................................................................................................................1.14
CO2 .........................................................................................................................................................1.14
NIBP (TEC-8342/TEC-8352 only) ...........................................................................................................1.14
Invasive Blood Pressure .......................................................................................................................... 1.15
Temperature ............................................................................................................................................1.15
Alarm .......................................................................................................................................................1.15
Battery .....................................................................................................................................................1.16
AC Power Requirements .........................................................................................................................1.16
Clock Accuracy........................................................................................................................................ 1.16
Environment ............................................................................................................................................1.16
Dimensions and Weight ........................................................................................................................... 1.16
Safety ......................................................................................................................................................1.17
Environment Conditions ..........................................................................................................................1.17
Electromagnetic Compatibility .................................................................................................................1.18
Electromagnetic Emissions .....................................................................................................................1.18
Electromagnetic Immunity .......................................................................................................................1.19
Recommended Separation Distances between Portable and Mobile RF Communications Equipment .. 1.22
System Configuration for EMC Test.........................................................................................................1.23
Panel Description ..............................................................................................................................................1.24
Front Panel ..............................................................................................................................................1.24
 1. GENERAL

1
Introduction

This service manual provides useful information to qualied service personnel

to understand, troubleshoot, service, maintain and r epair this TEC-8300 series
debrillator.

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 this
debrillator. This is because service personnel need t o understand the operation
of the debrillator in order to effectively use the information in the service
manual.

For simplicity, the sufx C/K for the debrillator and its options are omitted in
this manual. There is no difference in operation among models with different
sufxes unless otherwise specied.

Models and Functions

Functions TEC-8321 TEC-8322 TEC-8332 TEC-8342 TEC-8352

n
o External paddles Option Option Option Option Option
ti
a ll
ri Internal paddles Option Option Option Option Option
b
f
e
D Disposable pads Option Option Option Option Option
AED Standard Standard Standard Standard Standard
Pacing — — Standard — Standard
Playing voice Standard Standard Standard Standard Standard
Sound recording Standard Standard Standard Standard Standard
12 lead ECG Option Option Option Option Option
ECG input Option Option Option Option Option
ECG output Option Option Option Option Option
SD card Option Option Option Option Option
Battery pack Option Option Option Option Option
AC/DC module Option Option Option Option Option
®
Bluetooth module Option Option Option Option Option

Parameters

Functions TEC-8321 TEC-8322 TEC-8332 TEC-8342 TEC-8352

ECG monitoring Available Available Available Available Available
SpO2 monitoring Available Available Available Available Available
Temperature monitoring — Available Available Available Available
NIBP measurement — — — Available Available
Multi-parameter (1)* monitoring Available Available Available Available Available
1. GENERAL

General Information on Servicing

Note the following information when servicing the debrillator.

CAUTION
Safety
• There is the possibility that the outside surface of the defibrillator,
such as the operation keys, could be contaminated by contagious
germs, so disinfect and clean the defibrillator before servicing it.
When servicing the defibrillator, 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 eye or mouth,
immediately wash it with a lot of water and see a physician.

Liquid ingress
• The defibrillator is not waterproof, so do not install the defibrillator
where water or liquid can get into or fall on the defibrillator. If
liquid accidentally gets into the defibrillator or the defibrillator
accidentally drops into liquid, disassemble the defibrillator, 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
defibrillator, contact your Nihon Kohden representative to 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.

Disinfection and cleaning

• To disinfect the outside surface of the defibrillator, wipe it with a
non-abrasive cloth moistened with neutral detergent.
 1. GENERAL

Transport
• Use the specified shipment container and packing material to
transport the defibrillator. If necessary, double pack the defibrillator.
Also, put the defibrillator into the shipment container after packing
so that the buffer material does not get into the inside of the
defibrillator.
• When transporting a board or unit of the defibrillator, be sure to use
a conductive bag. Never use an aluminum bag when transporting
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 defibrillator.

Handling the defibrillator

• Because the outside surface of the defibrillator is made of resin,
the outside surface of the defibrillator is easily damaged. So when
handling the defibrillator, remove clutter from around the system
and be careful to not damage the defibrillator or get it dirty.
• Because most of the boards in the defibrillator are multilayer boards
with surface mounted electrical devices (SMD), when removing and
soldering the electrical devices, a special tool is required. To avoid
damaging other electrical components, do not remove and solder
SMD components yourself.

Measuring and test equipment

• Maintain the accuracy of the measuring and test equipment by
checking and calibrating it according to the check and calibration
procedures.

Preventing infection
• Follow the local laws or regulations to prevent infection.
1. GENERAL

Left Side Panel

Illustration above shows the example when the optional ND-831V external
paddles are used.

No. Name
1 SpO2 socket
2 TEMP modular jack
3 MULTI socket
4 NIBP socket
5 ECG socket
 1. GENERAL

Rear Panel 1

2
3

Illustration above shows the example when t he optional ND-831V external

paddles are used.

No. Name
1 External paddle holder (option)
2 Battery slot A connector
3 AC/DC module/battery slot B connector
1. GENERAL

ND-831V External Paddles (Option)

1

No. Name
1 Shock buttons
2 Paddle contact lamp
3 Charge button
 1. GENERAL

TEC-8322 1

TEC-8322
Defibrillator
UR-0414
CONTROL

UR-04151 No PACER

ECG/PACER

UR-04161 No PACER SW
KEY/LED
UR-0452
KEY/LED1

UR-0453
KEY/LED2
UR-0417
POWER

UR-0429 UR-0444
ECG-CONN ECG-CONN1

UR-0445
ECG-CONN2

UR-04302 No NIBP
MP2/TEMP UR-0455
MP2/NIBP
UR-3908
UR-0454
SpO2 board
TEMP

UR-0431
REC/EXT

HV-831V UR-0420
Biphasic HV unit HV SW

UR-0418
HV CPU

WS-831V UR-0419
Recorder unit Motor assy
(WS-252V)
1. GENERAL

TEC-8332

TEC-8332
Defibrillator
UR-0414
CONTROL

UR-0415
ECG/PACER

UR-0416
KEY/LED
UR-0452
KEY/LED1

UR-0453
KEY/LED2

UR-0417
POWER

UR-0429 UR-0444
ECG-CONN ECG-CONN1

UR-0445
ECG-CONN2

UR-04302 No NIBP
MP2/TEMP UR-0455
MP2/NIBP
UR-3908
UR-0454
SpO2 board
TEMP

UR-0431
REC/EXT

HV-831V UR-0420
Biphasic HV unit HV SW

UR-0418
HV CPU

WS-831V UR-0419
Recorder unit Motor assy
(WS-252V)
 1. GENERAL

TEC-8342 1

TEC-8342
Defibrillator
UR-0414
CONTROL

UR-04151 No PACER
ECG/PACER

UR-04161 No PACER SW
KEY/LED
UR-0452
KEY/LED1

UR-0453
KEY/LED2

UR-0417
POWER

UR-0429 UR-0444
ECG-CONN ECG-CONN1

UR-0445
ECG-CONN2

UR-0430 UR-0455
MP2/NIBP/TEMP MP2/NIBP

UR-0454
UR-3908 TEMP
SpO2 board

UR-0431
REC/EXT

HV-831V UR-0420

Biphasic HV unit HV SW

UR-0418
HV CPU

WS-831V UR-0419
Recorder unit Motor assy
(WS-252V)
1. GENERAL

ND-893V QP-551VK
Internal paddle electrode ø35 with SW Defibrillation report software

ND-894V QS-831V
Internal paddle electrode ø45 with SW Upgrade kit

ND-895V YS-003V5
Internal paddle electrode ø55 with SW Upgrade kit

ND-896V YZ-047H4
Internal paddle electrode ø65 with SW Bed rail hook

ND-897V SB-831V
Internal paddle electrode ø75 with SW Battery pack

JC-855V SB-801V
Pad adapter Battery charger

JC-865V KG-831V

Pad adapter Wall mount

P-510 KG-832V

Disposable paddles Wall mount

P-512 DI-831V

Disposable paddles Basket

P-711 KD-831V
Disposable paddles Cart

P-713 YZ-025H0
Disposable paddles Paste holder kit

AX-250V
Test load unit

AX-251V
Test load unit
 1. GENERAL

1
Board and Unit Location

MP/TEMP/NIBP board POWER board

LED DRIVER board
SpO2 board
KEY/LED board

ECG/PACER board POWER

board
CONTROL board

ECG-CONN board

KEY/LED board

POWER board
ECG-CONN board
REC/EXT board

KEY/LED board KEY/LED board

1. GENERAL

TEST
TEST LOAD
LOAD
AUXOUT
AUXOUT unit
unit
BIPH
BIPHAS
ASIC
IC HV un
unit
it BLUETOOTH
BLUETOOTH module
module

AC/DC
AC/DC mod
module
ule

HV CP
CPU
U bo
boar
ard
d

12LE
12LEAD
AD EC
ECG
G un
unit
it

SPEAKER RECORD
RECORDER
ER unit
unit

LCD
LCD un
unit
it
 Section 2 Troubleshoo
roubleshooting
ting
2

How to Troubleshoot
Troubleshoot ........................................................................................
............................................................................................................................................
.................................................... 2.2
Error Code ...........................................................................................................................................................2.3
Defibrillation ..............................................................................................................................................2.4
Operation Panel.........................................................................................................................................2.5
Communication .........................................................................................................................................2.6
Data Error ..................................................................................................................................................2.7
Pacing (TEC-8332/TEC-8352 Only) ..........................................................................................................2.7
12 Lead ECG Measurement (When Using the Optional AC-831V 12 Lead ECG Unit) ............................2.8
Message ..............................................................................................................................................................2.9
Defibrillation and Cardioversion ................................................................................................................2.9
AED .........................................................................................................................................................2.10
Pacing .....................................................................................................................................................2.10
Monitoring ...............................................................................................................................................2.11
ECG ..............................................................................................................................................2.11
SpO2 .............................................................................................................................................2.12
CO2 ...............................................................................................................................................2.13
Invasive
Invasive Blood Pressure ..............................................................................................
................................................................................................................
.................. 2.13
NIBP ..............................................................................................................................................2.13
Temperature ...............................................................................................
..................................................................................................................................
................................... 2.14
System ....................................................................................................................................................2.16
General .........................................................................................................................................2.16
Battery ...........................................................................................................................................2.16
Recording ......................................................................................................................................2.17
Bluetooth .......................................................................................................................................2.17
Troubleshooting .................................................................................................................................................2.18
General....................................................................................................................................................2.18
General....................................................................................................................................................2.18
Defibrillation ............................................................................................................................................2.19
Pacing (TEC-8332/TEC-8352 Only) ........................................................................................................2.20
Monitoring ...............................................................................................................................................2.20
ECG ..............................................................................................................................................2.20
SpO2 .............................................................................................................................................2.21
CO2 ...............................................................................................................................................2.22
NIBP ..............................................................................................................................................2.23
Blood Pressure (PRESS) ..............................................................................................................2.24
Temperature ...............................................................................................
..................................................................................................................................
................................... 2.24
Recording ................................................................................................................................................2.24
Battery .....................................................................................................................................................2.25
SD Card...................................................................................................................................................2.25
Card...................................................................................................................................................2.25
2. TROUBLESHOOTING

How to Troubleshoot

Use this section to locate, identify and solve a problem in the debrillator or an
error message displayed on the screen. The troubleshooting tables in this section
are divided into general problems and displayed error messages.

1. Determine which troubleshooting table to use. Also refer to “Messages and

Troubleshooting” in Section 8 of the Operator’s Manual Part I.

2. In the “Error Code”, “Message” or “Problem” column, nd the trouble item
that matches the problem or error message.

3. Do the action recommended in the “Action” column. (Do the rst action
recommended in the “Action” column.)

4. If the problem or error message is not solved, do the next action

recommended in the “Action” column. (If this does not solve the problem,
do the next recommended sections.)

NOTE
Before contacting your Nihon Kohden representative for technical
support, please complete a copy of the Maintenance Check Sheet (the
original copy is provided at the end of the Section 4 “Maintenance”),
and if possible, provide additional detailed information on the problem.
Send the complete copy of the Maintenance Check Sheet to your Nihon
Kohden representative. This will allow your Nihon Kohden representative
to provide you with the best support.
 2. TROUBLESHOOTING

Error Code
2

The debrillator displays an error code if it detects an error when the power is
turned on and during operation.

NOTE
• For problems that are not reproducible, call up the SYSTEM SETUP
– 7. DEVICE HISTORY screen and print the MAINTENANCE REPORT.
Refer to the Administrator’s Guide for the detail of this procedure. The
error code will be lost when the power is turned off.
• Always check all the cable connections in the defibrillator before
performing the action recommended in the troubleshooting tables in
this section. This is because a loose cable connection can cause the
defibrillator to display the error code.

An error code is displayed.

ERROR AXXX
ERROR CXXX
ERROR DXXX
ERROR KXXX
ERROR PXXX
ERROR TXXX

Turn off the instrument, then turn on the instrument and do the same operation.

Error AXXX, CXXX, DXXX and

The error code is saved KXXX:
Is the error code No No
in the “MAINTENANCE Perform charge/discharge test.
displayed?
REPORT”? Error PXXX
Perform pacing test.
Error TXXX
Yes Yes
Perform 12L-ECG test.

Is the error code No Instrument is normal.

displayed? But find the cause of the error code.

Yes
Refer to error code
description for detail.
2. TROUBLESHOOTING

Defibrillation

Error Code Meaning Possible Cause Action

A501 During standby mode, the HV capacitor Faulty biphasic HV unit. Replace the biphasic HV unit.
has more than 1 J energy for more than one Faulty HV CPU board. Replace the HV CPU board.
second.
A512 When charging is started, the HV capacitor Faulty biphasic HV unit. Replace the biphasic HV unit.
energy did not reach 1 J within 2 seconds. Faulty HV capacitor. Replace the HV capacitor.
Faulty HV CPU board. Replace the HV CPU board.
A513 The energy does not reach the selected Faulty biphasic HV unit. Replace the biphasic HV unit.
energy within the specied time. Faulty HV capacitor. Replace the HV capacitor.
Faulty HV CPU board. Replace the HV CPU board.
A524 After charging, the capacitor energy Faulty biphasic HV unit. Replace the biphasic HV unit.
decreases the specied value for each Faulty HV capacitor. Replace the HV capacitor.
energy. Faulty HV CPU board. Replace the HV CPU board.
A527 After charging, the capacitor energy is about Faulty biphasic HV unit. Replace the biphasic HV unit.
15% above the selected energy. Faulty HV CPU board. Replace the HV CPU board.
A529 After charging, the actual charged energy is Faulty biphasic HV unit. Replace the biphasic HV unit.
different from the selected energy. Faulty HV CPU board. Replace the HV CPU board.
A552 The switch that controls output from HV Faulty biphasic HV unit. Replace the biphasic HV unit.
unit is faulty. Faulty CONTROL board. Replace the CONTROL board.
Faulty HV CPU board. Replace the HV CPU board.
A556 Internal discharge takes more than 20 Faulty biphasic HV unit. Replace the biphasic HV unit.
seconds to complete. Faulty CONTROL board. Replace the CONTROL board.
Faulty HV CPU board. Replace the HV CPU board.
A566 HV capacitor’s voltage did not reach its Faulty biphasic HV unit. Replace the biphasic HV unit.
target value 20 seconds after adjusted Faulty HV CPU board. Replace the HV CPU board.
internal discharge.
A570 HV monitoring error signal is detected. Faulty biphasic HV unit. Replace the biphasic HV unit.
Faulty CONTROL board. Replace the CONTROL board.
Faulty HV CPU board. Replace the HV CPU board.
A585 The voltage of the HV capacitor exceeds its Faulty biphasic HV unit. Replace the biphasic HV unit.
specied voltage. Faulty CONTROL board. Replace the CONTROL board.
Faulty HV CPU board. Replace the HV CPU board.
A587 When the disposable pad is used, 12.5% Faulty biphasic HV unit. Replace the biphasic HV unit.
or more of the charged energy remains in Faulty CPU board. Replace the CPU board.
the HV capacitor 2 seconds after external Faulty HV CPU board. Replace the HV CPU board.
discharge.
A597 When discharging, the second phase pulse Faulty biphasic HV unit. Replace the biphasic HV unit.
is not output. Faulty CONTROL board. Replace the CONTROL board.
Faulty HV CPU board. Replace the HV CPU board.
 2. TROUBLESHOOTING

Message Description Action

Pacing stopped Pacing stopped because:
(pad disconnected) • The pad adapter is disconnected from the
disposable pads or the debrillator.
• The disposable pads are detached from the
patient.
When none of above occurred, ECG/PACER
board is faulty.
USE DISPOSABLE In FIXED or DEMAND pacing mode, only
PADS disposable pads are available. External paddles
and internal paddles are not available.
• Firmly connect the pads to the pad adapter. 2
Firmly connect the pad adapter to the
paddle connector of the debrillator.
• Attach the disposable pads to the patient.
When none of above solve the problem,
ECG/PACER board is faulty. Replace the
ECG/PACER board.
Use disposable pads in pacing mode.

Monitoring
ECG

Message Description Action

CANNOT ANALYZE Noise interference for more than 30 seconds Remove noise.
and heart rate cannot be counted and
arrhythmia cannot be analyzed.
If the message still appears when cause of
noise is removed:
• ECG/PACER board is faulty. • Replace the ECG/PACER board
• CONTROL board is faulty. • Replace the CONTROL board.
CHECK Ca Ca electrode is detached from the patient. Attach the Ca electrode to the patient.
ELECTRODE
CHECK Cb Cb electrode is detached from the patient. Attach the Cb electrode to the patient.
ELECTRODE
ECG: CHANGE An electrode is deteriorated. Replace the electrode with a new one.
ELECTRODES
ECG: CHANGE PADS The disposable pads are deteriorated. Replace the pads with new ones.
ECG: CHECK CHEST The chest electrode is detached from the Properly attach the electrode to the patient.
ELECTRODES patient. If the electrode cannot be attached rmly,
replace the electrode.
ECG: CHECK The electrode is detached from the patient. Properly attach the electrode to the patient.
ELECTRODES If the electrode cannot be attached rmly,
replace the electrode.
The electrode lead is disconnected from the Connect the electrode lead to the ECG
ECG connection cord. connection cord.
The clip of the lead is not properly attached to Properly attach the clip to the electrode.
the electrode.
Broken electrode lead Replace the electrode lead.
The external ECG cable is disconnected from Connect the external ECG cable.
the debrillator.
ECG: CHECK PADS The disposable pad is detached from the When using the disposable pads, attach the
patient or paddles used for ECG monitoring disposable pads to the patient or replace the
are not placed on the patient properly. disposable pads with the new ones.
When using the paddles, place the paddles on
the patient.
2. TROUBLESHOOTING

Message Description Action

ECG: CONNECT PADS/ When PADDLE lead is selected in the
PADDLES monitor mode, paddles or pad adapter are not
connected to the debrillator.
When the paddles or pads are connected to the
debrillator, CONTROL board is faulty.
CN1204 harness is disconnected or broken.
Paddle connector pin is broken or bent.
F (LL) LEAD OFF LL electrode is detached from the patient.
L (LA) LEAD OFF LA electrode is detached from the patient.
LIMB LEAD OFF Limb electrode is detached from the patient.
R (RA) LEAD OFF RA electrode is detached from the patient.
V1 (C1) LEAD OFF V1 (C1) electrode is detached from the patient.
V2 (C2) LEAD OFF V2 (C2) electrode is detached from the patient.
V3 (C3) LEAD OFF V3 (C3) electrode is detached from the patient.
V4 (C4) LEAD OFF V4 (C4) electrode is detached from the patient.
V5 (C5) LEAD OFF V5 (C5) electrode is detached from the patient.
V6 (C6) LEAD OFF V6 (C6) electrode is detached from the patient.
Connect the paddles or pad adapter to the
debrillator.
Replace the CONTROL board.
Connect the CN1204 harness to the connector
on the board.
Check the continuity of the CN1204 harness.
• Replace the paddles.
• Replace the paddle connector of the
debrillator.
Attach the LL electrode to the patient.
Attach the LA electrode to the patient.
Attach the limb electrode to the patient.
Attach the RA electrode to the patient.
Attach the electrode to the patient.

SpO2

Message Description Action

SpO2: CHECK PROBE The probe is detached from the patient. Check the probe attachment condition and
remove the cause.
The probe is disconnected from the SpO2 Securely connect the probe to the SpO 2
connection cord. connection cord.
When the SpO2 probe is correctly connected: Replace the SpO2 board and/or MP board.
• SpO2 board is faulty.
• MP board is faulty.
SpO2: CHECK PROBE SpO2 probe is deteriorated. Replace the probe with a new one.
SITE
SpO2: CONNECTOR Connector of the SpO2 connection cord is Check the connection of the SpO2 connection
OFF disconnected. cord.
If the SpO2 connection cable is properly If it does not solve the problem:
connected:
• SpO2 board is faulty. • Replace the SpO2 board.
• MP board is faulty. • Replace the MP board.
SpO2: CORD SpO2 probe is disconnected from the Connect the SpO2 probe to the connection
DISCONNECTED connection cable. cable.
SpO2: LIGHT Too much light on the probe. Remove light or cover the probe site with
INTERFERENCE blanket.
SpO2: LOW QUALITY Considerable body movement. When the message is displayed frequently,
SIGNAL The probe is not attached to the patient check the patient condition and, if necessary,
properly. change the attachment site.
SpO2: MODULE ERROR Faulty SpO2 board. Replace the SpO2 board.
SpO2: PROBE ERROR The probe lifetime is expired. Replace the probe with a new one.
Probe discontinuity or short-circuit. Replace the probe with a new one.
Faulty SpO2 connection cord. Replace the SpO2 connection cord with a new
one.
 2. TROUBLESHOOTING

CO2

Message Description Action

2
CO2: APNEA Respiration was not detected for the period
set on the CO 2 SETUP window for CO2 alarm —
settings.
CO2: 2 SENSORS Two CO2 sensors are connected to the Disconnect one of the CO2 sensors.
CONNECTED debrillator.
CO2: CHANGE The CO2 adapter is damaged, deteriorated or Replace the CO2 adapter with a new one.
ADAPTER the cable is broken.
CO2: CHECK SENSOR Insufcient sensor light. Refer to the CO2 sensor kit manual. If
necessary, replace the kit with a new one.
CO2: CONNECTOR OFF The CO2 sensor kit is disconnected from the Connect the CO 2 sensor kit properly. When
debrillator. CO2 monitoring is not necessary, press the
Silence Alarms key to silence the alarm.
The CO2 sensor kit is damaged. Replace the CO2 sensor kit with a new one.
When the CO2 sensor kit is correctly connected Replace the MP board.
and the CO2 sensor kit is not deteriorated, MP
board is faulty.
CO2: SENSOR ERROR CO2 sensor is damaged, deteriorated or cord is Replace the CO2 sensor with a new one.
broken.
When the CO2 sensor kit is not damaged or Replace the MP board.
deteriorated or cord is not broken, MP board is
faulty.

Invasive Blood Pressure

Message Description Action

PRESS: CHECK The blood pressure transducer is disconnected
SENSOR from the invasive blood pressure connection
cord.
Malfunction of the blood pressure transducer.
The invasive blood pressure connection cord is Replace the invasive blood pressure
damaged.
When the transducer is properly connected
and is not faulty, and connection cord is not
damaged, MP board is faulty.
PRESS: CONNECTOR The PRESS connection cord is disconnected
OFF from the debrillator.
The PRESS connection cord is damaged.
When the PRESS connection cord is properly
connected to the debrillator and is not
damaged, MP board is faulty.
PRESS: LABEL More than one invasive blood pressure
ALREADY USED connection cord with the same label are used.
Connect the blood pressure transducer to
the invasive blood pressure connection cord
properly.
Replace the blood pressure transducer with a
new one.
connection cord with a new one.
Replace the MP board.
Connect the PRESS connection cord
properly.
When PRESS monitoring is not necessary,
press the Silence Alarms key to silence the
alarm.
Replace the PRESS connection cord with a
new one.
Replace the MP board.
Set another label.

NIBP

Message Description Action


Battery
Problem
The battery charging lamp or battery
charging completion lamp is blinking.
After starting battery charging, the
charging stops. (Neither battery charging
lamp nor battery charging completion
lamp lights.)
The “REPLACE BATTERY” message
appears.
SD Card
Problem
Data cannot be saved in the SD card.
Possible Cause
The battery temperature is out of
specied range.
Faulty battery pack.
When battery pack replacement does
not solve the problem, POWER board is
faulty.
The battery pack is deteriorated.
Possible Cause
Upgrade kit is inserted instead of an SD
card.
The card is not inserted.
The card is not inserted properly.
A card other than specied card is
inserted.
Memory is full.
The card is write-protected.
The card is not formatted.
The SD card was removed while the
debrillator power was on and the
debrillator was affected by static
electricity.
2. TROUBLESHOOTING
Action 2
Place the debrillator in the place at
the specied range.
Replace the battery pack with a new
one.
Replace the POWER board.
Replace the battery pack with a new
one.
Action
Insert a card for storage.
Insert a specied card.
Properly insert the card.
Insert a specied card.
Use a new card or delete unnecessary
data.
Remove the write-protect.
Format the card in the SYSTEM
SETUP screen.
Turn the control dial to the OFF
position to turn the debrillator off
then turn the debrillator on again.
 Section 3 Disassembly
3

Before You Begin ................................................................................................................................................. 3.3

Warnings, Cautions and Notes ..................................................................................................................3.3
Registering Serial Number after Board Replacement ...............................................................................3.4
Required Tools...........................................................................................................................................3.5
Connection Diagram ............................................................................................................................................3.6
Removing the External Paddle Holder or Top Cover .........................................................................................3.11
Removing the Optional 12 Lead ECG Unit ........................................................................................................3.14
Removing the QI-831V AUXOUT Unit and QI-832V Bluetooth® Module ...........................................................3.16
Removing the Front Case ..................................................................................................................................3.19
Removing the LCD Unit and the LED DRIVER Board....................................................................................... 3.21
Removing the UR-0414 CONTROL Board and the UR-0415 ECG/PACER Board ........................................... 3.23
Removing the HV-831V HV Unit and UR-0418 HV CPU Board ........................................................................3.26
Note for Assembling the Defibrillator after HV Unit Replacement ...........................................................3.27
Removing the MP Unit ....................................................................................................................................... 3.29
Removing the Input Enclosure ................................................................................................................3.30
Removing the UR-0454 TEMP Board .....................................................................................................3.31
Removing the UR-0455 MP Board ..........................................................................................................3.32
Removing the UR-3908 SpO2 Board .......................................................................................................3.33
Removing the UR-0444 ECG CONN1 Board .......................................................................................... 3.33
Removing the UR-0445 ECG CONN2 Board .......................................................................................... 3.34
Removing the NIBP Pump ......................................................................................................................3.34
Removing the Valve................................................................................................................................. 3.35
Removing the UR-0431 REC/EXT Board .......................................................................................................... 3.36
Removing the Recorder Unit .............................................................................................................................3.37
Removing the UR-0417 Power Board ...............................................................................................................3.39
Removing the KEY/LED Boards ........................................................................................................................3.42
Removing the Speaker ......................................................................................................................................3.44
Removing the Paddle Connector .......................................................................................................................3.45
3. DISASSEMBLY

The procedures in this section explain how to remove, replace and install major
components in the debrillator.
 3. DISASSEMBLY

Before You Begin

Warnings, Cautions and Notes 3

WARNING
The HV capacitor can store lethal amounts of
energy. Discharge this capacitor before touching
any high voltage component (HV capacitor,
biphasic HV unit, paddle socket or paddles).
WARNING
Removal and replacement of any components in
the defibrillator should only be done by qualified
service personnel.

WARNING
To avoid the possibility of injury to yourself or
damage to the defibrillator, do not install or
remove any component while the power is on.
When disassembling, make sure that the
defibrillator is off, the AC power cord is
disconnected from the defibrillator and the battery
pack is removed from the defibrillator. There are
several high voltage units inside the defibrillator:
LCD backlight, high voltage capacitor, pacing DC/
DC converter and switching regulator.

CAUTION
To avoid accidental discharge of static electricity
which could damage the components of the
defibrillator, use a grounded wrist strap when
installing or removing any component of the
defibrillator.
CAUTION
Fuses on the main board and AC/DC unit cut off
the power when an abnormality occurs in the
defibrillator. Eliminate the malfunction before
replacing the fuse. Use the correct fuse only.

CAUTION
Use only parts recommended by Nihon Kohden
to assure maximum performance from your
defibrillator.
3. DISASSEMBLY

NOTE
When the ECG/PACER board, CONTROL board or biphasic HV unit is
replaced with a new one, do the following adjustment. Refer to “System
Maintenance Screen – Adjust AD Screen” in Section 4.

ECG/PACER board:
• ECG sensitivity and offset
• Battery voltage and battery current settings
• Paddle contact impedance threshold

Control board:
• ECG sensitivity and offset
• Charge energy, charge time, delivered energy and TTR
• Battery voltage setting
• Paddle contact impedance threshold

Biphasic HV unit:
• Charge energy, charge time, delivered energy and TTR
• Paddle contact impedance threshold

Registering Serial Number after Board Replacement

After replacing the UR-0414 CONTROL board, register the serial number of the
board by the following procedure.

1. While pressing and holding the Silence Alarms key, turn the control dial to
the BASIC CHECK position to display the SYSTEM SETUP screen.

2. Select SYSTEM SETUP with the ITEM ↑ or ITEM ↓ function key and press
the OK function key.

3. Select ID with the ↑ or ↓ function key and enter the serial number with
SELECT ↑ or SELECT ↓ function key.

4. Saving the settings using the procedure described in “Saving the Settings
before Maintenance (Flash Save Procedure)” in Section 4.

5. Turn the control dial to the BASIC CHECK position and conrm the serial
number on the BASIC CHECK screen.

If the serial number is incorrect, clear the settings on the System

Maintenance screen and register the serial number again. To clear the
settings, refer to “Changing the Settings to Factory Default” in Section 5.
 3. DISASSEMBLY

Required Tools
• Anti-static bench mat
• Wrist ground strap
• Screwdriver (insulated type, for M2.6 and M3 screws)
3
• Hex socket driver (for 3 mm spacer bolt and nut)
• Tweezers
 3. DISASSEMBLY

When removing the optional unit, be careful not to pull the cables between
the unit and the debrillator.

3. When mounting the optional QI-832V Bluetooth® module, remove the

Bluetooth® module from the optional unit. If not, skip this step. 3

i) Remove the BH 3 × 8 screw on the board side of the optional unit.

BH 3 × 8 screw

ii) Turn the optional unit and remove two BH

BH 3 × 8 screws which secures
the QI-832V Bluetooth® module to the optional unit and remove the
QI-832V Bluetooth® module from the optional unit.
BH 3 × 8 screws

QI-832V
Bluetooth®
module
3. DISASSEMBLY

4. When using the QI-831V AUXOUT unit, remove the UR-0426 AUXOUT
board from the unit. If not, skip this step.

Remove the PS 3 × 8 screw and hexagonal bolt from the UR-0426

AUXOUT board and remove the board from the unit. When removing the
AUXOUT board, connector part is removed from the AUXOUT unit. Be
careful not to lose the part.

UR-0426 AUXOUT board

When removing the

AUXOUT unit board,
be careful not to lose
this part.

PS 3 × 8 screw Hexagonal bolt

 3. DISASSEMBLY

Removing the Front Case

Before removing the front case, remove the debrillator top cover (or the 3
optional DP-831VK external paddle holder). Refer to “Removing the External
Paddle Holder or Top Cover” in this section.

1. Remove the fourteen BH 3 × 8 screws from the debrillator rear panel and
remove the front case from the debrillator.

Rear BH 3 × 8 screw

Bottom

Top
3. DISASSEMBLY

Right side panel Left side panel

2. Disconnect the two paddle connectors and FFC connector of the keys on the
front panel. Open the front panel carefully so that the connected cables are
not pulled or damaged.
 3. DISASSEMBLY

Removing the LCD Unit and the LED DRIVER Board

Before removing the LCD unit and the LED DRIVER board, remove the 3
following.
• Debrillator top cover (or the optional DP-831VK external paddle holder)
• Front case
For removing these, refer to the corresponding procedures earlier in this section.

1. Remove the four PS 2.6 × 8 screws and two connectors which secures the
LCD to the front panel of the debrillator and remove the LCD from the
debrillator.
LCD

Connector

Connector

PS 2.6 × 8 screws
3. DISASSEMBLY

2. Remove the two PS 3 × 8 screws and a connector from the LED DRIVER
board and remove the LED DRIVER board.
LED DRIVER board

PS 3 × 8 screws
Connector
 3. DISASSEMBLY

Removing the UR-0414 CONTROL Board and the UR-0415

ECG/PACER Board
3

Before removing the CONTROL board and ECG/PACER board, remove the
following.
• Debrillator top cover (or the optional DP-831VK external paddle holder)
• Front case
• LCD unit and LED DRIVER board
For removing these, refer to the corresponding procedures earlier in this section.

1. Remove the eight PS 3 × 8 screws which secure the UR-0414 CONTROL

board and the UR-0415 ECG/PACER board, three connectors on the
UR-0414 CONTROL board and four connectors on the UR-0415 ECG/
PACER board.
ECG/PACER board connector

ECG/PACER board

CONTROL board
connector

: PS 3 × 8 screws

Metal plate Control board

2. Remove the UR-0414 CONTROL board and the UR-0415 ECG/PACER

board with the metal plate from the debrillator.
 3. DISASSEMBLY

2. Peel off the blank label on the rear panel and remove the four BH 3 × 8
screws and remove the HV
HV-831V
-831V HV unit from the debrillator.
Peel the blank panel off.

BH 3 × 8 screw

NOTE
When assembling the defibrillator, make sure to attach the hook blank
panel to the rear cover so that the four BH 3 × 8 screws are covered.

Note for Assembling the Defibrillator after HV Unit Replacement

The HV unit cable is afxed to the HV unit at the factory. This tape is for
preventing the cable from catching on a screw or other object inside the
debrillator.

Do not remove this tape.

3. DISASSEMBLY

When attaching the screw shown in the picture, be careful not to pinch the cable
under the screw.
 3. DISASSEMBLY

Removing the MP Unit

Before removing the MP unit, remove the followings. 3

• Debrillator top cover (or the optional DP-831VK external paddle
paddle holder)
• Front case
• LCD unit and the LED DRIVER board
• UR-0414 CONTROL board
board and UR-0415 ECG/PACER
ECG/PACER board with metal
board
• HV
HV-831V
-831V HV unit
For removing these, refer to the corresponding procedures earlier in this section.

Remove the six BH 3 × 8 screws which secure the MP unit and remove the MP
unit from the debrillator.

BH 3 × 8 screw

MP unit

When removing the MP unit, pull the unit slightly to the right so that the TEMP
modular jack does not catch on the input enclosure.

TEMP modular jack

3. DISASSEMBLY

Removing the Input Enclosure

1. Remove the connector of the TEMP board.
TEMP board

2. Remove the ve BH 3 × 8 screws and remove the input enclosure from the
unit.

Input enclosure
 3. DISASSEMBLY

Removing the UR-0454 TEMP Board

1. Remove the two PS 3 × 8 screws and remove the TEMP board from the
input enclosure.

3
2. Remove the PS 3 × 8 screw which secures the metal plate to the TEMP
board and remove the metal plate from the TEMP board.

TEMP board

Metal plate

PS 3 × 8 screw
3. DISASSEMBLY

Removing the UR-0455 MP Board

1. Remove the L-shaped joint which is connected to the pump tube and two
connectors on the rear side on the MP board.
L-shaped joint

Connectors MP board

2. Remove the eight PS 3 × 8 screws which secure the UR-0455 MP board and
remove the MP board from the unit.

MP board
 3. DISASSEMBLY

Removing the UR-3908 SpO 2 Board

Remove the four PS 3 × 6 screws which secure the UR-3908 SpO 2 board and
remove the UR-3908 SpO2 board from the UR-0430 MP board.

3
PS 3 × 6
screws

SpO2 board

Removing the UR-0444 ECG CONN1 Board

Remove the three PS 3 × 8 screws and connector which secure the metal board
and UR-0444 ECG CONN1 board and remove the metal board and UR-0444
ECG CONN1 board from the unit.

Connector

ECG CONN 1
board

One PS 3 × 8 screw
is on this side.
3. DISASSEMBLY

Removing the UR-0445 ECG CONN2 Board

1. Remove the two PS 3 × 8 screws which secure the UR-0445 ECG CONN2
board to the unit and remove the UR-0445 ECG CONN2 board from the
unit.

2. Remove the PS 3 × 8 screw from the metal board on the UR-0445 ECG
CONN2 board and remove the metal panel from the ECG CONN2 board.

ECG CONN2
board

PS 3 × 8 screw

Removing the NIBP Pump

Remove the two PS 3 × 8 screws, disconnect the pump tube from the unit and
remove the pump from the unit.

PS 3 × 8 screw

PS 3 × 8 screw
is on this side.

Disconnect the tube.

 3. DISASSEMBLY

Removing the Valve

1. Remove four PS 2 × 4 screws which secure the valve, remove the two PS
3 × 8 screws which secure the valve holder and remove the valve holder
from the unit.
3

2. Disconnect the two tubes connected to the valve and remove the valve from
the unit.
Remove these tubes from the valve.

PS 3 × 8 screw PS 3 × 8 screw

PS 2 × 4 screws Valve holder

3. DISASSEMBLY

Removing the UR-0431 REC/EXT Board

Before removing the REC/EXT board, remove the following.

• Debrillator top cover (or the optional DP-831VK external paddle holder)
• Front case
• LCD unit and LED DRIVER board
• UR-0414 CONTROL board and UR-0415 ECG/PACER board with metal
board
For removing these, refer to the corresponding procedures earlier in this section.

Remove the four PS 3 × 8 screws and two connectors on the UR-0431 REC/EXT
board and remove the UR-0431 REC/EXT board from the debrillator.

REC/EXT board

Connectors

PS 3 × 8 screw
 3. DISASSEMBLY

Removing the Recorder Unit

Before removing the recorder unit, remove the following. 3

• Debrillator top cover (or the optional DP-831VK external paddle holder)
• Front case
• LCD unit and LED DRIVER board
• UR-0414 CONTROL board and UR-0415 ECG/PACER board with metal
board
• HV-831V HV unit
• UR-0431 REC/EXT board
For removing these, refer to the corresponding procedures earlier in this section.

NOTE
Before removing the recorder unit, order a rubber sponge (sponge 46 ×
25 × 3, 6114-906977A).

1. Remove the three PS 3 × 8 screws.

Let this cable slide through
the rubber sponge when
removing the recorder unit.

Replace this rubber

sponge after replacing
the recorder unit.

PS 3 × 8 screw WS-831V recorder unit

3. DISASSEMBLY

2. Remove the WS-831V recorder unit from the debrillator by sliding the unit
towards the right side of the debrillator.

NOTE
After replacing the recorder unit, replace the rubber sponge. Using old
rubber sponge decreases water-proof performance.
 4. MAINTENANCE

Before Check

Recording and Saving the Reports

The data in the internal memory may be lost while checking. Before check,
record the data in the internal memory or save the data in the internal memory to 4

an SD card.

For recording and saving the data in an SD card, refer to the Operator’s Manual
Part I.

When Using a Loaner Defibrillator

The settings on the SETUP windows and SYSTEM SETUP screen can
be changed manually and saved in the debrillator. When using a loaner
debrillator during maintenance, set all the settings on the SETUP windows and
SYSTEM SETUP screen of the loaner debrillator to the same as the settings of
the debrillator which will be checked or repaired.

The energy setting and alarm settings of the AED mode may be customized too.
Make sure that the SETUP settings, energy setting in the AED mode and alarm
settings on the loaner debrillator are correct.

NOTE
If you do not use a loaner defibrillator during maintenance and change
the defibrillator settings during maintenance, make sure to return the
settings after maintenance and turn the defibrillator off. The settings are
applied immediately after changing.

Copying the Settings to the Loaner Defibrillator

1. Insert the SD card into the debrillator which will be checked and save
the settings using “57. Save Settings”on the SYSTEM SETUP screen. For
details, refer to the Administrator’s Guide.

2. Remove the SD card from the debrillator and insert it into the loaner
debrillator. Load the settings from the SD card using “56. Load Settings”
on the SYSTEM SETUP screen. For details, refer to the Administrator’s
Guide.
4. MAINTENANCE

Checking the Appearance

Check the following.

Defbrillator
• The debrillator is not dirty.
• The debrillator is not cracked or damaged.
• No labels are removed or torn.
• No connectors or switches are cracked or loose.
• Blood or chemical on the debrillator is cleaned.

Power Cord
• A specied 3-prong power cord is used.
• The metal parts on the connector are not deformed.
• There are no scratches on the cable and cable cover is not torn.
• Using a tester, check that the protective earth is not broken.

External Paddles
• Resin of the external paddles and electrodes for the adult are not cracked or
broken.
• No scratches or cracks on the curled cable or cable mold.
• Paddle electrodes and the metal plates on the paddle holder are not rusted,
dirty, rotten or damaged.
• Conrm that the shock button on the paddle is not removed when pulling it. If
the button is removed, the button must be replaced.

Accessories
• Cables are not broken, bent abnormally or cut.
• Connectors are not damaged or cracked.
• Pins on the connector are not deformed.
• Screws are not loose.
• Pad adapter is not expired.
The life time of the pad adapter is two years. Replace the pad adapter
immediately if it is expired.
 4. MAINTENANCE

Checking the SB-831V Battery Pack

Appearance
Check the following and if the battery pack is faulty, replace it.
• No damage or crack on the battery pack. 4
• No labels are removed or torn.
• The battery pack is not expired.
The life time of the battery pack is two years. Replace the battery pack
immediately if it is expired.

Calibration
Perform the battery calibration once a month using “2. Battery Calibration” on
the SYSTEM SETUP screen. For details, refer to the Administrator’s Guide.
4. MAINTENANCE

Checking the Defibrillator

Connecting the Checker and Turning the Defibrillator On

For connection, also refer to the AX-103V debrillation analyzer Operator’s
Manual.

1. Connect the AX-103V debrillation analyzer and TEC-8300 series

debrillator using the JC-906P ECG connection cord and the BR-903P
electrode lead.
TEC-8300 series
defibrillator

JC-906P ECG connection cord

BR-903P electrode lead

Simulated ECG is output from the colored

terminals on the AX-103V debrillation analyzer.

C: Chest
F: Left foot
L: Left hand
R: Right hand AX-103V
RF: Right foot defibrillation analyzer

Power switch
2. Turn the debrillation analyzer on. The simulated ECG is output from the
debrillation analyzer.

3. Turn the debrillator control dial to the MONITOR position and conrm that
there no abnormalities such as abnormal sound, smell or excess heat.

4. Set the lead to “II” by pressing the LEAD function key.

Wait for several seconds then conrm the following.

• There are no error messages on the debrillator screen and ECG is
displayed correctly.
• The debrillator screen is not dark.
Lead II
 4. MAINTENANCE

Adjusting the Sync Sound

QRS sync mark 1. After turning the debrillator power on, conrm that there is a sync sound
and QRS sync mark blinks synchronized with the ECG on the screen.

2. On the SYNC SOUND setting on the VOLUME SETUP window, conrm

that the sound volume can be changed. For the volume settings, refer to
4
Operator’s Manual Part I.

Checking the Recorder

Record/Stop Key
Press the Record/Stop key on the front panel to record the waveforms.
Conrm that the ECG is recorded correctly and the recording paper feeds
correctly and is not skewed. To stop recording, press the Record/Stop key on
the front panel again.

Date and Time Printed on the Recording Paper

Conrm that the date and time printed on the recording paper is correct. If not,
correct the date and time setting on the DATE AND TIME SETUP window. For
the settings, refer to Operator’s Manual Part I.

Event Key
On the monitoring screen, press the EVENT key to conrm that waveforms for
12 seconds are recorded.
Record/stop key

For details on recording, refer to Operator’s Manual Part I.

Recording Quality
On the System Setup screen, perform “4. RECORDER TEST” and conrm that
the following.
• There are no missing dots.
• The recorded items are not too pale or too dark.
• The width of one cycle of calibration waveform is in the range of 22.5 to 27.5
mm.

For details on the recorder test, refer to the Administrator’s Guide.

22.5 to 27.5 mm
4. MAINTENANCE

Detecting Out of Paper

1. Removing the recording paper from the recorder and close the recorder
cover.

2. Press the Record/Stop key on the front panel to conrm that the
debrillator operates as follows.

Alarm Operation
Message The “OUT OF PAPER”message is displayed in blue.
Sound There is an alarm sound of “ec” in interval of 20 seconds.
Indicator Lights in blue.

Record/stop key
 4. MAINTENANCE

Checking the Defibrillation Function in Manual Mode

Check the debrillation function in manual mode once a month.

To check charging and discharging, the AX-103V debrillation analyzer is 4

necessary. When checking the debrillation function, operate the debrillator on
the AC power. For AC operation, refer to the Operator’s Manual Part I.

When performing “Checking the Duration of Charging Energy” and “Checking

the Discharged Energy” in this section, operate the debrillator on the battery
power.

Checking the Connector Off Detection

Paddle contact lamp
1. When using the external paddles, check the paddle contact. When using the
disposable pads, connect the jigs to the debrillator.

When using the ND-831V external paddles

Put the external paddles on the paddle holder and conrm that the paddle
contact lamp lights in green.
Put the paddles on the paddle holder.

If the paddles contact lamp lights in orange or yellow, clean the paddle
electrodes and the metal plates on the paddle holder.
Paddle electrode
Metal plates for test discharge
4. MAINTENANCE

When using the disposable pads

Using the JC-865V pad adapter and JJ-202V analyzer connection cable*,
connect the debrillator and the AX-103V debrillation analyzer.
* An accessory of the AX-103V debrillation analyzer.

Black Red

JJ-202V
analyzer
connection JC-865V pad adapter
cable

Holder JC-865V pad adapter

JJ-202V
analyzer connection cable JJ-202V
analyzer
connection cable

AX-103V
defibrillation analyzer

2. Turn the debrillator control dial to the MONITOR position and conrm that
the ECG lead is “PADDLE”.

If other lead is selected, set the lead to “PADDLE” by pressing the LEAD
function key.

3. Turn the paddle connector to the left to unlock the connector and remove
the connector from the debrillator. Then conrm that the “CONNECT
PADDLES/PADS” message appears on the screen.

Paddle
connector

Unlock Paddle
position connector lock

NOTE
Hold the paddle connector when removing the paddle/pad adapter
from the defibrillator. Holding the part other than paddle connector
may damage the connector or break the paddle/pad adapter cable.

4. Connect the external paddles or pad adapter removed in step 3 to the

debrillator.
 4. MAINTENANCE

Checking the SB-801V Battery Charger

When using the optional SB-801V battery charger, check the charger every 6
months.
4
The numbers uses in the “Inspection Items” section correspond to the numbers
on the maintenance check sheet at the end of this section. Keep the maintenance
check sheet safely after inspection.

Inspection Items
1. Appearance
Check the following.
• The battery charger is not dirty.
• No damage or crack on the battery charger.
• No label is removed or torn.
• The ventilation hole is not clogged with dust.

2. Power Cord
Check the following.
• The provided 3-prong power cord is used.
• The cable jacket is not dirty, damaged or torn.
• The earth lead is not broken (check this using a test equipment)

3. Power-on
Remove the battery packs from the battery slot, turn the power switch on and
check the following.
• The POWER lamp lights.
• The following lamps light for one second and turn off.
- Battery charging lamp
- Battery charge complete lamp
- ERROR lamp
• The fan rotates for a few seconds then stops.

4. Charging
Check the following.
• When the battery pack is inserted in one of the battery slots:
- The battery charging lamp lights.
- Status indicators on the battery pack blink.
• When another battery pack is inserted to the other battery slot:
- The battery charging lamp lights.
- Status indicators on the battery pack blink.
4. MAINTENANCE

Safety Check
Battery packs are not necessary for safety check.

Safety check is performed while the components are connected. You need
to measure two different currents ( earth leakage current and enclose leakage
current) in both the normal condition and a single-failure condition to make sure
that the allowable value is not exceeded. You also need to record the measured
values.

NOTE
Performing safety inspection requires a special instrument of measuring
leak currents.

Example of measuring earth leakage current

AC wall outlet AC power socket

This instrument

LCC-1101
Leakage current checker

• Make sure that the measured value is within the range below.

Normal condition 500 μA or less

Single-fault condition 1 mA or less

Example of measuring contact leakage current (enclosure leakage current)

AC wall outlet AC power socket This instrument

Exposed metallic portion

LCC-1101
Leakage current checker

• Make sure that the measured value is within the range below.

Normal condition 100 μA or less

Single-fault condition 500 μA or less
 4. MAINTENANCE

System Maintenance Screen

Displaying the System Maintenance Screen

1. Turn the control dial to the OFF position to turn the debrillator off.
4

2. While pressing the Silence Alarms key on the front panel, turn the control
dial to the BASIC CHECK position. Hold the Silence Alarms key until the
SYSTEM SETUP screen appears.

3. On the SYSTEM SETUP screen, while holding the F4 key, press F1 → F3

→ F2 key.

Silence Alarms key

F1 F2 F3 F4 F5 F6

The System Maintenance – Menu screen appears.

System Maintenance – Menu Screen

4. MAINTENANCE

Operation on the System Maintenance – Menu Screen

• To select the item, press the ITEM ↓ or ITEM ↑ function key to move the
cursor and press the OK function key. The selected screen opens.
• To exit the System Maintenance screen, turn the control dial to any position
other than BASIC CHECK.

Saving the Settings before Maintenance (Flash Save Procedure)

Do the following procedure after changing or adjusting any setting in the
Conguration screen and Adjust AD screen to save the changed or adjusted
setting in memory.

CAUTION
Write down the settings or save the settings on the System
Maintenance screen as a bitmap file before changing the settings or
performing “flash save”. Changing settings related to HV, ECG or
battery on the System Maintenance screen might decrease the
performance of the defibrillator.

CAUTION
Do this procedure after any setting in the Configuration screen and
Adjust AD screen is changed or adjusted. The new setting or
adjustment is not applied and saved until the “Flash Save” procedure
is performed. Otherwise, the “D511” error code appears the next time
the power is turned on.

1. In the System Maintenance – Menu screen, select “1. Conguration” with

the ITEM ↓ or ITEM ↑ function key then press the OK function key. The
System Maintenance – Conguration screen appears.
 4. MAINTENANCE

3. Press the → function key. The setting changes from “Off” to “Exec” and the
function keys change as follows:

4. Press the OK key to save the changed or adjusted setting in memory.

To cancel saving, press the CANCEL key. 4

To return to the System Maintenance – Menu screen, press the EXIT key.

Changing the Settings to Factory Default

1. In the System Maintenance – Menu screen, select “1. Conguration” with
the ITEM ↓ or ITEM ↑ function key then press the OK function key. The
System Maintenance – Conguration screen appears.

2. Select “10. Default Setting” with the ITEM ↓ or ITEM ↑ function key.

3. Press the → function key. The setting changes from “Off” to “Exec” and the
function keys change as follows:

4. Press the OK function key to change the settings to factory default.

To cancel, press the CANCEL function key.

To return to the System Maintenance – Menu screen, press the EXIT

function key.
4. MAINTENANCE

About the Menu Items

There are six items in the System Maintenance – Menu screen.

Item Description
Changes the settings in the following items:
1 Conguration Installed Language, Flash Save, Charge Times Clear,
Default Setting, Jack Temp Option
Changes the A/D values for ECG waveform
2 Adjust AD acquisition, biphasic HV unit, battery voltage and
paddle contact impedance threshold.
Checks the operation of the keys, buttons, LEDs,
3 Check Hardware
recorder, memories, sounds, etc.
Displays the count of external discharges and
5 Operation Time
operation time.
6 Version Up You can upgrade the system program and data.
Displays the characters used in this debrillator and
7 Debug mode
checks the ash memory.

System Maintenance Screen Flowchart

Menu 1. Configuration

2. Adjust AD 1. Adjust ECG AD

2. Adjust HV AD

3. Adjust Battery AD

4. Adjust Paddle Contact AD

3. Check Hardware 1. Check Key

2. Check LED

3. Check LCD
4. Check Buzzer

5. Check Voice

6. Check Recorder

8. Check Ecg Frequency

9. Check NIBP
10. Check 12 Lead

11. Examination

12. Check Time Constant

5. Operation Time
13. Check MP
6. Version Up

7. Debug mode 1. Check String

 4. MAINTENANCE

Default Settings
The factory default settings are underlined.

Screen Item Setting

Conguration Installed Language Select the language or country.
Selection list: English, Japanese, American, Chinese, Spanish, French,
German, Italian, Norwegian, Finnish, Other 1 to 5
Flash Save Select “Exec” to save the current settings in the System Maintenance 4
screen in the ash ROM.
Selection list: Off, Exec
Charge Times Clear Deletes the count of external discharges and operation time.
Selection list: Off, Exec
Default Setting Select “Exec” to return all settings including the alarm settings to the
factory default settings. Before doing this operation, write down the
necessary settings for each item or save the setting screen as a bitmap
le.
Selection list: Off, Exec
Jack Temp Option Select whether to enable temperature monitoring using the modular jack.
Selection list: On, Off
Default setting: Off for TEC-8321
On for TEC-8322, TEC-8332, TEC-8342 and TEC-8352
Adjust AD Gain Adjust the A/D value for the ECG sensitivity.
→ Adjust ECG AD Setting range: 0 to 31 in steps of 1
Offset Adjust the A/D value for the ECG offset.
Setting range: –99 to +99 in steps of 1
Adjust AD CHARGE AD Adjust the A/D value to measure the charged energy in the HV capacitor.
→ Adjust HV AD Setting range: –25 to +25 in steps of 1
TTR AD Adjust the A/D value to measure the TTR (transthoracic resistance).
Setting range: –25 to +25 in steps of 1
DELIVERED Adjust the A/D value to measure the delivered energy from the HV
ENERGY capacitor.
Setting range: –25 to +25 in steps of 1
Charge Time (AC) Adjust the energy charging time in AC operation.
Setting range: –25 to +25 in steps of 1
Charge Time (Batt) Adjust the energy charging time in battery operation.
Setting range: –25 to +25 in steps of 1
Adjust AD Auto Adjust Adjust the A/D value of the battery voltage.
→ Adjust Battery AD Slot A Battery Voltage Adjust the A/D value of the voltage that is applied to the battery in
battery slot A.
Setting range: –25 to +25 in steps of 1
Slot B Battery Voltage Adjust the A/D value of the voltage that is applied to the battery in
battery slot B.
Setting range: –25 to +25 in steps of 1
Battery current Adjust the A/D value of the battery current.
Setting range: –50 to +50 in steps of 1
Adjust AD 100 ohm, 200 ohm, Adjust the A/D value to measure the skin-paddle contact impedance for
→ Adjust Paddle 350 ohm 100, 200 and 350 Ω.
Contact AD
4. MAINTENANCE

Configuration Screen
You can set the several default settings for the debrillator.

To select a setting for “1. Installed Language”

1. Press the ITEM ↓ or ITEM ↑ function key to select “1. Installed Language”.

2. Select the setting with the ← or → function key.

For “1. Installed Language”, the setting changes as follows:

English ↔ Japanese ↔ American ↔ Chinese ↔ Spanish ↔ French ↔
German ↔ Italian ↔ Norwegian ↔ Finnish ↔ Other 1 to 5

To save the settings (ash save procedure)

Make sure to perform “ash save” to save the changed setting in memory. Refer
to “Saving the Settings before Maintenance (Flash Save Procedure)” in this
section.

CAUTION
Do this procedure after any setting in the Configuration screen and
Adjust AD screen is changed or adjusted. The new setting or
adjustment is not applied and saved until the “Flash Save” procedure
is performed. Otherwise, the “D511” error code appears the next time
the power is turned on.
 4. MAINTENANCE

Check Recorder Screen

You can check the recorder in the Check Recorder screen. When checking starts,
the following waveforms are printed, then all the text messages which can be
used for recording are printed.

NOTE
If necessary, stop recording when the recorder starts printing text
messages. You can check for missing dots just by checking the
waveforms. Printing all the text messages uses a lot of recording paper.

Check ECG Frequency Screen

You can check the frequency response when acquiring the ECG waveforms
from the external paddles, internal paddles, disposable pads or ECG disposable
electrodes (lead II). The maximum and minimum amplitude are calculated and
displayed on the screen.

• To change the lead, press the LEAD function key.

The lead changes as follows every time you press the LEAD function key.
ECG1 Paddle → ECG1 II LEAD → ECG2 II LEAD → ECG3 II LEAD →
ECG1 Paddle...
• To change the gain, press SENSITIVITY function key.
The gain changes as follows every time you press the SENSITIVITY function
key.
×1/4 → ×1/2 →×1 → ×2 → ×4 → ×1/4...
• When “II LEAD” is selected, you can change the time constant by pressing the
TIME CONSTANT function key. You can select 0.32 or 3.2.
4. MAINTENANCE

To return to the System Maintenance – Check Hardware screen, press the EXIT
function key.

Check NIBP Screen

Do not add pressure to the NIBP connector (do not give impact to the
debrillator and do not breathe on the connector) on the debrillator when
entering the Check NIBP screen and returning to the Hardware Check screen
from the Check NIBP screen.

Select the item to check with the ITEM ↓ or ITEM ↑ function key then press the
OK function key to start check. Finish the test for each check item within
10 minutes.

Pressure Adjust Screen

This screen is for factory use and is not used for maintenance.

To return to the System Maintenance – Check Hardware – Check NIBP screen,

press the EXIT function key.
 4. MAINTENANCE

Examination Screen
On this screen, you can check the sensitivity for normal circuit sensor and safety
circuit sensor.

Items on the screen

• Cuff Type (NORM)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Type (SAFE)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Press (NORM)
Displays the pressure for normal circuit.
• Cuff Press (SAFE)
Displays the pressure for safety circuit.

Check Procedure
Use a 3.5 m air hose (for adult) and 700 cc dummy cuff to apply pressure.

Air tank Manometer Adult air hose Defibrillator

(700 cc) (3.5 m)

Apply 100 mmHg, 200 mmHg and 300 mmHg and check that the displayed
value is as follows.

Applied pressure Cuff Press (NORM) Cuff Press (SAFE)

100 mmHg ±3 mmHg ±8 mmHg
200 mmHg ±3 mmHg ±8 mmHg
300 mmHg ±3 mmHg ±12 mmHg
4. MAINTENANCE

Safety Device Test Screen

On this screen, we can check the NIBP safety circuit operation.

Items on the screen

• Cuff Type (NORM)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Type (SAFE)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Press (NORM)
Displays the pressure for normal circuit.
• Safety Device Action
Displays the cuff pressure at which the safety circuit operates.
• Safety Device Action
Displays the duration that the safety circuit operates. (For adult cuff, time from
the pressure excesses 300 mmHg).
• Safety Device Status
Displays the status of the safety circuit (inactive or active).

Check Procedure
Use a 3.5 m air hose (for adult) and 700 cc dummy cuff to apply pressure.

Press the START TEST function key and check the following.
• The cuff deates.
• “Safety Device Status” changes to “ACTIVE”.
• “Safety Device Action” is 300 to 330 mmHg.

To return to the System Maintenance – Check Hardware – Check NIBP screen,

press the EXIT function key.
 4. MAINTENANCE

Ination Test Screen

On this screen, we can check the ination time for the NIBP pump.

Items on the screen

• Cuff Type (NORM)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Type (SAFE)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Press (NORM)
Displays the pressure for normal circuit.
• Ination Time
Displays time to increase the pressure to 200 mmHg.

Check Procedure
Use a 3.5 m air hose (for adult) and 700 cc dummy cuff to apply pressure.

Press the START TEST function key to apply 200 mmHg pressure and check that
the ination time is less than 7 seconds.

To return to the System Maintenance – Check Hardware – Check NIBP screen,

press the EXIT function key.
4. MAINTENANCE

Deation Test Screen

This screen is for factory use and is not used for maintenance.

To return to the System Maintenance – Check Hardware – Check NIBP screen,

press the EXIT function key.

Step Deation Test Screen

On this screen, we can check the deation speed.

Items on the screen

• Valve 1 Open (50 ms)
Deation value at the 250 mmHg when valve 1 is open for 50 ms.
• Valve 2 Open (50 ms)
Deation value at the 250 mmHg when valve 2 is open for 50 ms.
• Valve 1 Open (120 ms)
Deation value at the 20 mmHg when valve 1 is open for 120 ms.
• Valve 2 Open (100 ms)
Deation value at the 20 mmHg when valve 2 is open for 100 ms.
Cuff Type (NORM)
 4. MAINTENANCE

• Cuff Type (SAFE)

Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Press (NORM)
Displays the pressure for normal circuit.
• Deation Press
Displays test result. 4

Check Procedure
Use a 3.5 m air hose (for adult) and 250 cc dummy cuff to apply pressure for
“Valve 1 Open (50 ms)” and “Valve 1 Open (120 ms)” tests.

Use a 3.5 m air hose (for adult) and 20 cc dummy cuff to apply pressure for
“Valve 2 Open (50 ms)” and “Valve 2 Open (100 ms)” tests.

1. Select the item to check with the ITEM ↓ or ITEM ↑ function key.

2. Press the START TEST function key.

3. Check that “Deation Press” is as follows.

Valve 1 Open (50 ms) 15 ±8 mmHg

Valve 2 Open (50 ms) 10 ±5 mmHg
Valve 1 Open (120 ms) 5 ±3 mmHg
Valve 2 Open (100 ms) 5 ±3 mmHg

To return to the System Maintenance – Check Hardware – Check NIBP screen,

press the EXIT function key.

Air Leak Test Screen

You can check air leak of the NIBP module.

There are 3 types of tests.

4. MAINTENANCE

• Air Leak Test (Normal)

Applies 300 mmHg pressure using an external instrument and compare the
pressure 30 seconds after test start with the pressure 90 seconds after test start.
• Air Leak Test (Automatic)
Applies 300 mmHg pressure and compare the pressure 60 seconds after test
start with the pressure 120 seconds after test start.

Items on the screen

• Cuff Type (NORM)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Type (SAFE)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Press (NORM)
Displays the pressure for normal circuit.
• Elapsed Time
Elapsed time from test start.
• Air Leak
Displays leak pressure.

Check Procedure
Use a 3.5 m air hose (for adult) and 250 cc dummy cuff to apply pressure.

1. Select “Pressure Hold Test” with the ITEM ↓ or ITEM ↑ function key.

2. Press the START TEST function key.

3. Check that “Air Leak” is 5 mmHg or less.

To return to the System Maintenance – Check Hardware – Check NIBP screen,

press the EXIT function key.

Air Circuit Test Screen

On this screen, you can check clogging of the air circuit in the NIBP module.
4. MAINTENANCE

Version Up Screen
This screen is used to upgrade programs of the debrillator.

Upgrading can be performed when two battery packs are inserted. The battery
packs must have remaining power of 2/3 or more. You can also upgrade the
debrillator when the AC power is supplied and a battery pack with remaining
power of 2/3 is inserted. If the “Cannot upgrade. Remaining battery power
is not enough.” message is displayed on the screen, charge the battery before
upgrading.

When an upgrade kit (SD card) is inserted into the SD card slot, the program
versions of the debrillator and upgrade kit are displayed on the screen.

Upgrade Procedure
1. Select the item to upgrade with the ITEM function key.

2. Press the YES key to install the program. “No” displayed beside the item
changes to “Yes”.

Not to install the selected item, press the NO function key to change “Yes”
beside each item to “No”.

3. Press the EXEC function key to start installation. All programs set to “YES”
are sequentially installed.

To return to the System Maintenance – Menu screen, press the MENU function
key.
 4. MAINTENANCE

Debug Mode Screen

Debug mode screens are for factory use.

Check String Screen

This screen is used to check the text messages used in the debrillator. You
can display the language which is selected in “Installed Language” (System
Maintenance – Menu screen) by pressing the LANGUAGE function key.

• To display the next or previous page, press the ↓ or ↑ function key.

• To jump 5 pages forward or back, press the ↓↓ or ↑↑ function key.
• To return to the System Maintenance – Debug Mode screen, press the EXIT
key.
4. MAINTENANCE

AD Viewer Screen
This screen displays each AD value that the main CPU currently receives.

Displaying the AD
1. Turn the control dial to the MONITOR position to display the monitoring
home screen.

2. On the monitoring home screen, press the Silence Alarms key, MENU
function key and CHILD MODE button at the same time. The AD Viewer
window appears.

Every time you press the Silence Alarms key, MENU function key and
CHILD MODE button at the same time, the AD Viewer window changes as
follows.
AD Viewer → AD Viewer (MP) → AD Viewer (REP) → monitoring home
screen...
 4. MAINTENANCE

Saving the System Maintenance Screens as Bitmap Files

You can save the System Maintenance screens as bitmap les.

To save the screens as bitmap les: 4

1. Turn the debrillator off.

2. Insert an SD card into the SD card slot on the debrillator right side panel.

3. Display the System Maintenance screen to save. Refer to “Displaying the

System Maintenance Screen” in this section.

4. Press the CHILD MODE button on the front panel. The SHOCK button on
the front panel lights.

Wait until the SHOCK button turns off.

5. Turn the debrillator off and remove the SD card from the SD card slot.
4. MAINTENANCE

Maintenance Check Sheet

Issuance No.

For detailed procedures, refer to “Checking the Debrillator” to “Safety Check” in this manual.

Facility name Inspection date Person in charge

Address Delivery date Signature

Model Serial number and revision

Check tools Options/Consumables

Product name Serial number Product name Q’ty Product name Q’ty

Overall judgment Conditions of use

[ ] No error Duration of usage: year(s)
[ ] AED is usable but needs to be repaired soon. Used by:
[ ] AED needs to be repaired immediately.

Number Item Result Action

The debrillator is not dirty.
The debrillator is not cracked or damaged.
1 No labels are removed or torn. (Labels are readable.)
No connectors or switches are cracked or loose.
e Blood or chemical on the debrillator is cleaned.
c
n
a
r A specied 3-prong power cord is used.
a
e
p The metal parts on the connector are not deformed.
p
A 2
There are no scratches on the cable and cable cover is not torn.
Using a tester, check that the protective earth is not broken.
3 When using the external paddles, the paddles are not broken.
Connectors are not damaged or cracked.
4
Pad adapter is not expired.
y
No damage or crack on the battery pack. No labels are removed or torn.
r
tte
k
c
5
a
a
P
The battery pack is not expired.
B
6 The battery pack is calibrated.
7 The debrillator correctly turns on and the display operates correctly.
8 QRS sync sound is normal and can be adjusted.
r Recorder operates correctly.
ot
all Recorded date and time is correct.
ri
b
f Event recording can be perfor med correctly.
e
D 9
There are not missing dots or uneven tone on the recording paper.
Sweep speed of the recording paper is within the specied range.
Out of paper is correctly detected.
 4. MAINTENANCE

Number Item Result Action

10 Connector of is correctly detected.
11 Charging time is within 5 seconds.
Debrillation is performed correctly.
12
The waveform of the discharged energy is biphasic.
Discharged energy when using the external paddles is correct (write the measured value
below): 4
AC operation
2 J: J 3J J 5J J
7 J: J 10 J J 15 J J
)l 13 —
a 20 J: J 30 J J 50 J J
u
n 70 J: J 100 J J 150 J J
a
M
( 200 J: J 270 J J
n
o it Battery operation
a ll
ri 270 J J
b
f Discharged energy when using the disposable pads is correct (write the measured value
e
D
14 below): —
270 J J
Discharged energy when using the internal paddles is correct (write the measured value
below):
AC operation
15 —
2 J: J 3J J 5J J
7 J: J 10 J J 15 J J
20 J: J 30 J J 50 J J
16 The charged energy can be changed.
17 Internal discharge is correctly performed.
c 18 The synchronized cardioversion using the paddle lead is correctly performed.
n
y
S 19 The synchronized cardioversion using the ECG lead is correctly performed.
VF is correctly detected.
20 Charging automatically starts when VF is detected.
D
E Debrillation is performed correctly.
A
21 Messages and illustrations are correctly displayed.
22 The debrillator correctly generates voice instructions.
23 Fixed pacing can be performed correctly.
g
n
i
c
a
24 Demand pacing can be performed correctly.
P
25 Pacing output is correct.
Heart rate accuracy is correctly displayed and QRS sync tone is correctly generated.
26 Sensitivity of ECG wave is correct.
Heart rate alarm and ECG connector off alarm are correctly generated.
Zero calibration accuracy for IBP is conrmed.
27 Display accuracy for IBP is conrmed.
IBP connector off alarm is correctly generated.
Display accuracy for the respiration rate and CO 2 value is conrmed.
g 28 CO2 connector off alarm is correctly generated.
n
ri Measurement accuracy of the CO 2 sensor kit is conrmed.
oti
n
o Display accuracy for the SpO2 value and pulse rate is conrmed and QRS sync tone is
M
29 correctly generated.
SpO2 upper/lower limit and SpO2 connector off alarm are correctly generated.
NIBP cuff is correctly detected.
30 NIBP measurement is correctly performed and NIBP display is correct.
NIBP measurement can be manually stopped corrrectly.
Display accuracy for temperature is conrmed.
31 Temperature connector off alarm is correctly generated.
4. MAINTENANCE

Number Item Result Action

d
a
e 12 lead ECG is displayed correctly.
l 32
2 Lead off alarm is generated correctly.
1
Normal condition µA
Earth leakage current
Single-fault condition µA
k Contact leakage current Normal condition µA
c
e
h (Enclosure leakage current) Single-fault condition µA
C
y
t
e
f Patient leakage current I Normal condition µA
a
S (Type BF applied part) Single-fault condition µA
Patient leakage current I Normal condition µA
(Type CF applied part) Single-fault condition µA
r e gr a h C yr ett a B V108- BS

Number Item Result Action

The battery charger is not dirty.
No part is broken or rattles.
1
No label is removed or torn.
n The ventilation hole is not clogged with dust.
o
it
c
e The provided 3-prong power cord is used.
p
s
nI 2 The cable jacket is not dirty, damaged or torn.
The earth lead of the power cord is not broken.
3 The operation at power-on is correct.
4 The battery packs are charged normally.
Normal condition µA
y
Earth leakage current
t k Single-fault condition µA
e c
f e
a h
S c Contactleakage current Normal condition µA
(Enclosure leakage current) Single-fault condition µA
Comments
Section 5 Replaceable Parts List

When ordering parts or accessories from your nearest Nihon Kohden Corporation
representative, please quote the code number and part name which are listed in
this service manual, and the name or model of the unit in which the required
 5. REPLACEABLE PARTS
PARTS LIST

8
3
5
X
9
3 V
J
8
4

8
4

5 6
4 4
1
5
7
3 W

4
4
I I

1
4

7 a
4

3
4
5. REPLACEABLE PARTS
PARTS LIST

No. Code No. Q’ty Description

1 6113-913614B 1 Operation SW 3
2 6114-919508A 1 Operation SW 2
3 6114-917608B 2 Operation SW 1
4 6114-917591B 1 CHARGE SW 8300
5 6124-905335B 1 SHOCK SW 8300
6 6122-901067B 1 Front bezel 8300
7 6114-918251B 1 NVI lter 8300
8 6123-903963A 1 LCD lter 8300
9 6113-914195B 1 Energy selector 8300
10 6114-907334 1 Drip proof sheet MIC-2
11 551805 1 D spring 6601
12 674949 1 O ring P-9 (red)
13 6114-907593A 1 MIC holder (2500)
14 6114-909555A 1 Sound lter
15 6111-903424B 1 Front case 8300
16 6123-904383 1 OP panel 8300K
17 6123-904409A 1 Def OP panel (8321K)
17’ 6123-904392A 1 Def OP panel (8332K)
18 6123-904276A 1 Pace blank panel
18’ 6123-904374A 1 Pace OP panel (8332K)
19 6124-906272A 1 Def caution panel (8321K)
20 6124-906263A 1 Def instruction panel (8321K)
21 6124-906156A 1 Slot sign panel
22 6123-904294A 1 ACDC instruction panel
23 6123-904285A 1 Bat instruction panel
24 6124-905897 1 REC guidance panel (8300)
25 6124-906138A 1 Hook blank panel
26 6113-913445B 1 Insulation sheet main
27 6114-917484A 1 SD card cover 8300
28 6111-903433B 1 Bottom case 8300
29 367835 2 Flat rubber feet CK-17
30 6114-920141 2 Front foot TEC
31 6111-903415B 1 Rear case 8300
32 6114-919936 1 Drip proof packing 2
33 6114-919927 1 Drip proof packing 1
34 6113-915586A 1 Option cover 8300 (BLANK)
35 6113-913534B 2 Bottom holder plate
36 6114-918242B 1 Insulation sheet MP
37 6113-913258B 1 Tube main 8300
38 6113-913249B 1 Tube sensor 8300
39 6114-920025 1 Pump packing
40 6114-916939B 1 TEMP cap
41 6114-916921B 1 TEMP jack packing
41’ 6114-919517A 1 TEMP blank packing
42 6113-913213B 1 Input packing
43 6112-906892B 1 Input enclosure
44 531337 1 L-shaped joint
45 6114-923111 1 Silicon tube
46 662329A 1 Valve
 5. REPLACEABLE PARTS
PARTS LIST

No. Code No. Q’ty Description

49 6114-124992A 1 AUX connector part
50 6114-900671 1 DSI CN packing
51 6111-903451B 1 Input frame
52 6123-904204 1 TEC-8321 input panel
52’ 6123-904213 1 TEC-8332 input panel
52’’ 6123-904222A 1 TEC-8352 input panel
53 6111-903861A 1 Paddle cup dispo
54 541576 2 O ring P-3 (silicon) 5
55 6114-124377A 2 Electrode plate
56 6114-035802A 8 Paddle lock packing
57 6114-069677A 8 Paddle lock spring K-718
58 6111-903442B 1 Paddle cup outer
59 6113-913472B 1 Option cover 8300
60 6114-917582B 1 Option packing
61 6124-906129 1 AUX panel (8300)
62 6113-913463B 1 Power PCB holder
63 6114-916886B 2 Power co
connector packing
64 6114-916877A 2 Power connector holder
65 6114-910214 4 Battery spring 1 (2100)
66 6114-919401A 2 Battery lock plate
67 6114-906977A 1 Sponge 46×25×3
A UR-0414 1 CONTROL board
B UR-0415 1 ECG/PACER board (for TEC-8332/8352)
B’ UR-04151 1 ECG/PACER board (for TEC-8321/8322/8342)
C UR-0416 1 KEY/LED board (for TEC-8332/8352)
C’ UR-04161 1 KEY/LED board (for TEC-8321/8322/8342)
D UR-0417 1 POWER board
E HV-831V 1 Biphasic HV
F UR-0418 1 HV CPU board
G UR-0426 1 AUXOUT board
H UR-0428 1 12L-ECG board
I UR-0429 1 ECG-CONN board
J UR-0430 1 MP2/TEMP/NIBP board (for TEC-8342/8352)
J’ UR-04301 1 MP1 board (for TEC-8321)
J’’ UR-04302 1 MP2/TEMP board (for TEC-8322/8332)
K UR-0431 1 REC/EXT board
L UR-3908 1 SpO2 board
M UR-0315 1 Test load
O WS-831V 1 Recorder unit
P 9000-009732 1 Paddle connector (HCV14A-R-NKD)
Q 9000-004746 1 LCD NL8060BC21-11C
R 9000-004737 1 104PW03F LED DRIVER board
S 671097A 1 Speaker TL-C40U0811
T 671088 1 CSA122 DF13-2S-1.25C(S80)
U 909251A 1 CSA123 microphone assy KUC2133-010930
V 532149B 1 Rolling pump P22D-0003R
W 923119 1 TDS-2XV05B-701
X 515542C 1 N-NIBP-R (red) delivery specication 2120B
Y 9000-008484 1 FI-S20S(W65) Triple Line
 Manufacturer
NIHON KOHDEN CORPORATION NIHON KOHDEN ITALIA S.r.l.
1-31-4 Nishiochiai, Shinjuku- ku Tokyo 161-8560, Japan Via Fratelli Bronzetti 28, 24124 Bergamo, Italy
Phone +81 3-5996-8036 Phone +39 035-219543
Fax +81 3-5996-8100 Fax +39 035-232546

NIHON KOHDEN UK LTD

North and South America Trident Court 118, 1 Oakcroft Road
Chessington, Surrey KT9 1BD, UK
Phone +44 20-8391-6800
NIHON KOHDEN AMERICA, INC. Fax +44 20-8391-6809
15353 Barranca Parkway, Irvine, CA 92618, U.S.A.
Toll-free +1-800-325-
+1-800-325-0283
0283
Phone +1 949-580-1555 Asia
Fax +1 949-580-1550

NIHON KOHDEN LATIN AMERICA S.A.S SHANGHAI KOHDEN

Carrera 16 No.93A-36 Of. 802. Bogota D.C., Colombia MEDICAL ELECTRONIC INSTRUMENT CORP.
Phone
Phon e + 57 1-300-1742 567 Huancheng Bei Road
Fax +57 1-300-1825 Shanghai Comprehensive Industrial Development Zone
Shanghai 201401, China
NIHON KOHDEN DO BRASIL LTDA. Phone +86 21-5743-6998
Rua Gomes de Carvalho Fax +86 21-5743-6939
1507-Bloco A 9 andar-cjto 91A Vila Olimpia
CEP 04547-005 Sao Paulo-SP. Brasil NIHON KOHDEN SINGAPORE PTE LTD
Phone
Phone + 55 11- 3841
3841-- 9943 1 Maritime Square, #10-34
#10 -34 HarbourFront Centre
Fax +55 11-3044-0463 Singapore 099253
Phone +65 6376-2210
Fax +65 6376
6376 -2264
Europe
NIHON KOHDEN INDIA PVT. LTD.
308, Tower A, Spazedge, Sector 47, Sohna Road
European Representative
Gurgaon-122 002 Haryana, India
NIHON KOHDEN EUROPE GmbH Toll-free +91 1800-103-8182
Raiffeisenstrasse 10, D-61191
Raiffeisenstrasse D -61191 Rosbach, Germany Phone +91
+91 124-493-1000
Phone +49 6003-827-0 Fax +91
+91 124-493-1029
Fax +49 6003-827-599
NIHON KOHDEN MIDDLE EAST FZE
NIHON KOHDEN FRANCE SARL P.O.Box 261516, JAFZA View 19
8, rue Francois Delage, 94 230 Cachan, France Room 308 Jebel Ali Free Zone, Dubai, U.A.E
Phone +33 1-49-08-05-50 Phone +971
+971 4-884-0080
4- 884-0080
Fax
Fa x +33 1-49-08- 93-32 Fax +971
+971 4- 880-0122

NIHON KOHDEN IBERICA S.L. NIHON KOHDEN KOREA, INC.

C/Ulises 75A, E-28043 Madrid, Spain 5F Miso Bldg.
Phone +34 91-7-161080 890-47 Daechi-dong, Gangnam-gu, Seoul, 135-280 Korea
Fax +34 91-3-004676 Phone +82 2-3273-2310
Fax +82 2-3273-2352

Contact information is accurate as of Jan 2015. Visit www.nihonkohden.com

www.nihonkohden.com for the latest information.

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.

Model Serial Number

Your Representative
Representati ve