SVM-7500 - EngSM - NIHON KOHDEN

Service Manual
Bedside Monitor
SVM-7501
SVM-7503
SVM-7521
SVM-7523
SVM-7500 Series
0634-901074D
About This Manual
In order to use this product safely and fully understand all its functions, 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.
Accompanying Documentation
The product comes with the following manuals. Refer to the manual depending on your needs.
Operator’s Manual
Describes the operation and settings of the product. Read this manual before use.
Administrator’s Guide
For administrators. Describes how to install the product. Read the Operator’s Manual together with this
guide.
Service Manual (this manual)

For qualified service personnel. Describes information on servicing the product. Only qualified service
personnel can service the bedside monitor.
User’s Guide
Gives supplemental information on the operation of the product.
Copyright Notice
The entire contents of this manual are copyrighted by Shanghai Kohden Medical Electronic Instrument
Corp., hereinafter referred to as “Shanghai Kohden” or “SKC”. All rights are reserved. No part of this
document may be reproduced, stored, or transmitted in any form or by any means (electronic, mechanical,
photocopied, recorded, or otherwise) without the prior written permission of Shanghai Kohden.
This product stores personal patient information. Manage the information appropriately.
Patient names on the screen shots and recording examples in this manual are fictional 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: https://www.nihonkohden.com/
1
Contents
2
GENERAL HANDLING PRECAUTIONS...................... i Assembling............................................................. 4-24
WARRANTY POLICY...................................................ii 3
EMC RELATED CAUTION ................................iii
Conventions Used in this Manual and Instrument.......vi
5 Maintenance Check Sheet
4
Related Documentation...............................................vi Maintenance Check Sheet....................................... 5-2
5
1 General 6 Replaceable Parts List
Introduction............................................................... 1-2 Replaceable Parts List............................................. 6-2 6

General Information on Servicing............................. 1-3
Service Policy and Service Parts............................. 1-5
Composition............................................................. 1-7
Specifications........................................................... 1-8
Panel Description................................................... 1-27
Storage and Transport............................................ 1-30
Hard Keys and Soft Keys....................................... 1-31
Connection and Block Diagram.............................. 1-32
2 Troubleshooting
General..................................................................... 2-2
Troubleshooting........................................................ 2-3
Error Code and History........................................... 2-10
3 Diagnostic Check and Safety

Check
Displaying the DIAGNOSTIC CHECK Screen......... 3-2
Checking on the Home Screen.............................. 3-36
Safety Check.......................................................... 3-53
4 Disassembly and Assembly

Disassembling the Power Supply Unit (PSU)........... 4-2
Disassembling the Speaker...................................... 4-8
Disassembling the USB&LAN Board........................ 4-8
Disassembling the Input Panel Unit......................... 4-9
Disassembling the Valve........................................ 4-13
Disassembling the Rolling Pump............................ 4-14
Disassembling the Main Board............................... 4-16
Disassembling the SW Panel................................. 4-18
Disassembling the ALARM LED Board.................. 4-18
Disassembling the Touch Panel............................. 4-19
Disassembling the LCD.......................................... 4-20
Disassembling the Recorder.................................. 4-21
SVM-7500 Series Service Manual Contents 1

GENERAL HANDLING PRECAUTIONS
This device is intended for use only by qualified medical personnel.
Use only Shanghai Kohden approved products with this device. Use of non-approved products
or in a non-approved manner may affect the performance specifications of the device. This
includes, but is not limited to, batteries, recording paper, pens, extension cables, electrode
leads, input boxes and AC power.
Please read these precautions thoroughly before attempting to operate the instrument.
1. To safely and effectively use the instrument, its operation must be fully understood.
2. When installing or storing the instrument, take the following precautions:

(1) Avoid moisture or contact with water, extreme atmospheric pressure, excessive humidity and temperatures, poorly
ventilated areas, and dust, saline or sulphuric air.
(2) Place the instrument on an even, level floor. Avoid vibration and mechanical shock, even during transport.
(3) Avoid placing in an area where chemicals are stored or where there is danger of gas leakage.
(4) The power line source to be applied to the instrument must correspond in frequency and voltage to product
specifications, and have sufficient current capacity.
(5) Choose a room where a proper grounding facility is available.
3. Before Operation
(1) Check that the instrument is in perfect operating order.
(2) Check that the instrument is grounded properly.
(3) Check that all cords are connected properly.
(4) Pay extra attention when the instrument is combined with other instruments to avoid misdiagnosis or other
problems.
(5) All circuitry used for direct patient connection must be doubly checked.
(6) Check that battery level is acceptable and battery condition is good when using battery-operated models.
4. During Operation
(1) Both the instrument and the patient must receive continual, careful attention.
(2) Turn power off or remove electrodes and/or transducers when necessary to assure the patient's safety.
(3) Avoid direct contact between the instrument housing and the patient.
(4) T
he operator must not touch the patient and the input/output interface of the equipment simultaneously. This may
cause electric shock.
5. To Shutdown After Use

(1) Turn power off with all controls returned to their original positions.
(2) Remove the cords gently; do not use force to remove them.
(3) The mains plug or appliance coupler is intended to be used as an isolation device from the supply mains. Always
make sure that the mains plug or appliance coupler is easy to operate.
(4) Clean the instrument together with all accessories for their next use.
6. The instrument must receive expert, professional attention for maintenance and repairs. When the instrument is
not functioning properly, it should be clearly marked to avoid operation while it is out of order.
7. The instrument must not be altered or modified in any way.
SVM-7500 Series Service Manual i

8. Maintenance and Inspection
(1) The instrument and parts must undergo regular maintenance inspection at least every 6 months.
(2) I f stored for extended periods without being used, make sure prior to operation that the instrument is in perfect
operating condition.
(3) Technical information such as parts list, descriptions, calibration instructions or other information is available for
qualified user technical personnel upon request from your Nihon Kohden representative.
9. When the instrument is used with an electrosurgical instrument, pay careful attention to the application and/or
location of electrodes and/or transducers to avoid possible burn to the patient.
10. When the instrument is used with a defibrillator, make sure that the instrument is protected against defibrillator
discharge. If not, remove patient cables and/or transducers from the instrument to avoid possible damage.
11. Contraindications: None.
12. The electrodes cannot be applied directly on the heart.
WARRANTY POLICY
Shanghai Kohden Medical Electronic Instrument Corp. (SKC) shall warrant its products against all defects in materials and
workmanship for one year from the date of delivery. However, consumable materials such as recording paper, ink, stylus
and battery are excluded from the warranty.
SKC or its authorized agents will repair or replace any products which prove to be defective during the warranty period,
provided these products are used as prescribed by the operating instructions given in the operator's and service manuals.
No other party is authorized to make any warranty or assume liability for SKC's products. SKC will not recognize any other
warranty, either implied or in writing. In addition, service, technical modification or any other product change performed by
someone other than SKC or its authorized agents without prior consent of SKC may be cause for voiding this warranty.
Defective products or parts must be returned to SKC or its authorized agents, along with an explanation of the failure.
Shipping costs must be pre-paid.
This warranty does not apply to products that have been modified, disassembled, reinstalled or repaired without Shanghai
Kohden approval or which have been subjected to neglect or accident, damage due to accident, fire, lightning, vandalism,
water or other casualty, improper installation or application, or on which the original identification marks have been
removed.
ii SVM-7500 Series Service Manual

EMC RELATED CAUTION
This equipment and/or system complies with IEC 60601-1-2 International Standard for electromagnetic
compatibility for medical electrical equipment and/or system. However, an electromagnetic environment
that exceeds the limits or levels stipulated in IEC 60601-1-2, can cause harmful interference to the
equipment and/or system or cause the equipment and/or system to fail to perform its intended function or
degrade its intended performance. Therefore, during the operation of the equipment and/or system, if there
is any undesired deviation from its intended operational performance, you must avoid, identify and resolve
the adverse electromagnetic effect before continuing to use the equipment and/or system.
The following describes some common interference sources and remedial actions:
1. Strong electromagnetic interference from a nearby emitter source such as an authorized radio station
or cellular phone:
Install the equipment and/or system at another location. Keep the emitter source such as cellular
phone away from the equipment and/or system, or turn off the cellular phone.
2. Radio-frequency interference from other equipment through the AC power supply of the equipment
and/or system:
Identify the cause of this interference and if possible remove this interference source. If this is not
possible, use a different power supply.
3. Effect of direct or indirect electrostatic discharge:
Make sure all users and patients in contact with the equipment and/or system are free from direct or
indirect electrostatic energy before using it. A humid room can help lessen this problem.
4. Electromagnetic interference with any radio wave receiver such as radio or television:
If the equipment and/or system interferes with any radio wave receiver, locate the equipment and/or
system as far as possible from the radio wave receiver.
5. Interference of lightning:
When lightning occurs near the location where the equipment and/or system is installed, it may induce
an excessive voltage in the equipment and/or system. In such a case, disconnect the AC power cord
from the equipment and/or system and operate the equipment and/or system by battery power, or use
an uninterruptible power supply.
6. Use with other equipment:
When the equipment and/or system is adjacent to or stacked with other equipment, the equipment
and/or system may affect the other equipment. Before use, check that the equipment and/or system
operates normally with the other equipment.
7. Use of unspecified accessory, transducer and/or cable:
When an unspecified accessory, transducer and/or cable is connected to this equipment and/or
system, it may cause increased electromagnetic emission or decreased electromagnetic immunity.
The specified configuration of this equipment and/or system complies with the electromagnetic
requirements with the specified configuration. Only use this equipment and/or system with the specified
configuration.
SVM-7500 Series Service Manual iii

Caution - continued
8. Use of unspecified configuration:
When the equipment and/or system is used with the unspecified system configuration different than
the configuration of EMC testing, it may cause increased electromagnetic emission or decreased
electromagnetic immunity. Only use this equipment and/or system with the specified configuration.
9. Measurement with excessive sensitivity:
The equipment and/or system is designed to measure bioelectrical signals with a specified sensitivity. If
the equipment and/or system is used with excessive sensitivity, artifact may appear by electromagnetic
interference and this may cause mis-diagnosis. When unexpected artifact appears, inspect the
surrounding electromagnetic conditions and remove this artifact source.
If the above suggested remedial actions do not solve the problem, consult your Nihon Kohden
representative for additional suggestions.
For EMC compliance, refer to "Specification - Electromagnetic Compatibility" in the Reference section.
Note about Waste Electrical and Electronic Equipment (WEEE) directive 2002/96/EC.
For the member states of the European Union only:
The purpose of WEEE directive 2012/19/EU is, as a first priority, the prevention of waste electrical and
electronic equipment (WEEE), and in addition, the reuse, recycling and other forms of recovery of such
wastes so as to reduce the disposal of waste.
Contact your Nihon Kohden representative for disposal at the end of its working life.
In IEC 60601-1-2 Medical Electronic Equipment, Part 1: General Requirements for Safety, 2. Collateral
Standard: Electromagnetic compatibility-Requirements and test. Section 36. 202. 3 Radiated radio-
frequency electromagnetic fields, PATIENT COUPLED EQUIPMENT and/or SYSTEMS applicable
IMMUNITY test methods are under consideration at SC62A/WG13. The 3 V/m IMMUNITY level may be
inappropriate especially when measuring SpO2 because physiological signals can be much smaller than
those induced by a 3 V/m electromagnetic field.
When measuring SpO2, various interference may produce false waveforms which look like pulse
waveforms. SpO2 value and pulse rate may be measured from these false waveforms, causing the alarm to
function improperly.
When installing the monitor, avoid locations where the monitor may receive strong electromagnetic
interference such as radio or TV stations, cellular phone or mobile two-way radios.
iv SVM-7500 Series Service Manual

WARNING
Interaction Between Minute Ventilation Rate-Adaptive Pacemakers and Cardiac Monitoring and Diagnostic
Equipment*
The bioelectric impedance measurement sensor of a minute ventilation rate-adaptive implantable
pacemaker may be affected by cardiac monitoring and diagnostic equipment which is connected to the
same patient. If this occurs, the pacemaker may pace at its maximum rate and give incorrect data to the
monitor or diagnostic equipment. If this occurs, disconnect the monitor or diagnostic equipment from the
patient or change the setting on the pacemaker by referring to the pacemaker’s manual. For more details,
contact your pacemaker representative or Nihon Kohden representative.
* Minute ventilation is sensed in rate-adaptive pacemakers by a technology known as bioelectric impedance measurement (BIM).
Many medical devices in addition to pacemakers use this technology. When one of these devices is used on a patient with an active,
minute ventilation rate-adaptive pacemaker, the pacemaker may erroneously interpret the mixture of BIM signals created in the
patient, resulting in an elevated pacing rate.
SVM-7500 Series Service Manual v

Conventions Used in this Manual and Instrument
Warnings, Cautions and Notes
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 SVM-7500 series come with the following manuals in addition to the Operator’s Manual.
Administrator’s Guide
Describes how to install the bedside monitor. It also explains about the password protected settings on the SYSTEM
SETUP window and SYSTEM CONFIGURATION screens which only an administrator can change.
User’s Guide
Gives supplemental information on the operation of the bedside monitor and describes the features and settings of the
monitoring parameters.
Service Manual
Describes information on servicing the bedside monitor. Only qualified service personnel can service the bedside monitor.
vi SVM-7500 Series Service Manual

1
1
General
Introduction.................................................1-2 Environment....................................................... 1-21

Mechanical Strength........................................... 1-22
General Information on Servicing...............1-3
Electromagnetic Compatibility............................ 1-22
Service Policy and Service Parts...............1-5 Safety Standard.................................................. 1-22
Service Policy....................................................... 1-5 Dimensions and Weight (Approximate).............. 1-22
Patient Safety Checks.......................................... 1-5 Lifetime............................................................... 1-23
Monitor Status on Power Interruption................... 1-6 Electromagnetic Emissions................................ 1-23
Electromagnetic Immunity.................................. 1-24
Composition...............................................1-7
Recommended Separation Distances
Specifications.............................................1-8 between Portable and Mobile RF
Measuring Parameters......................................... 1-8 Communications Equipment.............................. 1-26
Influence on Measuring Accuracy System Composition for EMC Test..................... 1-26

by Electrosurgery, Defibrillation, and
Electrostatic Discharge.................................... 1-8
Panel Description.....................................1-27
Display.................................................................. 1-8 Front Panel......................................................... 1-27
Alarm.................................................................... 1-9 Left Side Panel................................................... 1-28
Alarm Delay Time............................................... 1-10 Right Side Panel................................................. 1-29
ECG (IEC 60601-2-27: 2011)............................. 1-11 Rear Panel......................................................... 1-29
Respiration (Impedance Method)....................... 1-13

Storage and Transport..............................1-30
SpO2 (ISO 80601-2-61: 2011)............................ 1-14
Storage............................................................... 1-30
Noninvasive Blood Pressure (NIBP) (IEC
Transport............................................................ 1-30
80601-2-30: 2009).............................................. 1-16
Invasive Blood Pressure, IBP (SVM- Hard Keys and Soft Keys.........................1-31
7503/7523)......................................................... 1-17 Hard Keys........................................................... 1-31
Temperature (ISO 80601-2-56: 2009)................ 1-18 Soft Keys............................................................ 1-31
CO2 (Mainstream Method) (SVM-7503/7523).... 1-19
Connection and Block Diagram................1-32
Recorder (WS-752P Recorder Module)............. 1-20
Connection Diagram........................................... 1-32
Battery (SB-752P Battery Pack)......................... 1-20
Block Diagram.................................................... 1-36
Power Requirement............................................ 1-21
Clock Accuracy................................................... 1-21
1. GENERAL
Introduction
This service manual provides useful information to qualified service personnel
to understand, troubleshoot, service, maintain and repair the SVM-7500 series
(SVM-7501, SVM-7503, SVM-7521, SVM-7523) Bedside Monitors (referred to
as “the instrument” in this service manual).
The SVM-7501/7521 bedside monitor is installed near a patient and displays

the patient's vital signs such as ECG, NIBP, temperature, SpO2 and respiration,
and generates alarms. The SVM-7503/7523 bedside monitor is installed near a
patient and displays the patient's vital signs such as ECG, NIBP, temperature,
SpO2, respiration, IBP and CO2, and generates alarms.* The monitor is designed
so the operator can directly touch the screen from the operator position.
All replaceable parts or units of this instrument and its optional units are clearly
listed with exploded illustrations to help you locate the parts quickly.
The information in the operator’s manual is primarily for the user. However, it
is important for service personnel to thoroughly read the operator’s manual and
service manual before starting to troubleshoot, service, maintain or repair this
instrument. This is because service personnel need to understand the operation of
the instrument in order to effectively use the information in the service manual.
* Essential performance
1-2 SVM-7500 Series Service Manual

1. GENERAL
1
General Information on Servicing
Note the following information when servicing the instrument.
CAUTION
Safety
• There is the possibility that the outside surface of the instrument,
such as the operation keys, could be contaminated by contagious
germs, so disinfect and clean the instrument before servicing it.
When servicing the instrument, wear rubber gloves to protect
yourself from infection.
• There is the possibility that when the lithium battery is broken,
a solvent inside the lithium battery could flow out or a toxic
substance inside it could come out. If the solvent or toxic
substance touches your skin or gets into your eyes or mouth,
immediately wash it with a lot of water and see a physician.
• No modification of this equipment is allowed. When modification
is needed, please contact your Nihon Kohden representative.
Liquid ingress
The instrument is not waterproof, so do not install the instrument
where water or liquid can get into or fall on the instrument. If liquid
accidentally gets into the instrument or the instrument accidentally
drops into liquid, disassemble the instrument, clean it with clean
water and dry it completely. After reassembling, verify that there is
nothing wrong with the patient safety checks and function/
performance checks. If there is something wrong with the instrument,
contact your Nihon Kohden representative for repair.
Environmental safeguards
Depending on the local laws in your community, it may be illegal to
dispose of the lithium battery in the regular waste collection. Check
with your local officials for proper disposal procedures.
Cleaning after use

Wipe the monitor with a soft cloth moistened with alcohol for
disinfection or neutral detergent. After cleaning, dry the monitor
completely.
Disinfection and cleaning

To disinfect the outside surface of the instrument, wipe it with a
non-abrasive cloth moistened with any of the disinfectants listed
below. Do not use any other disinfectants or ultraviolet rays to
disinfect the instrument.
- Ethanol 76.9 % to 81.4 % (by vol. in 15 oC)
- Chlorhexidine gluconate solution: 0.5 %
- Benzalkonium chloride 0.2 %
- Benzethonium chloride solution: 0.2 %
SVM-7500 Series Service Manual 1-3

1. GENERAL
Caution - continued
- Glutaraldehyde solution: 2.0 %

- Alkyldiaminoethylglycine hydrochloride: 0.5 %
- Phtharal 0.55 %
- Phenol 1.56 %
- Isopropyl alcohol 70 % (by vol.)
Transport
• Use the specified shipment container and packing material
to transport the instrument. If necessary, double pack the
instrument. Also, put the instrument into the shipment container
after packing so that the buffer material does not get inside the
instrument.
• When transporting a board or unit of the instrument, be sure
to use a conductive bag on. Never use an aluminum bag to
transport a board or unit which a lithium battery is mounted. Also,
never wrap the board or unit of the instrument with a styrene
foam or plastic bag which generates static electricity.
Handling the instrument

• Because the outside surface of the instrument is made of resin,
the outside surface of the instrument is easily damaged. So
when handling the instrument, remove clutter from around the
instrument and be careful to not damage the instrument or get it
dirty.
• Because most of the boards in the instrument are multilayer
boards with surface mount electrical devices (SMD), a special
tool is required when removing and soldering the electrical
devices. 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.
Maintenance
Turn off the power of the instrument before doing maintenance,
cleaning or disinfecting. Otherwise you may get an electrical shock
or the instrument may malfunction.
Preventing infection
Follow the local laws or regulations to prevent infection.

1. GENERAL
1
Service Policy and Service Parts
Service Policy
Shanghai Kohden's technical service policy for this instrument is to replace the
faulty unit, board or part or damaged mechanical part with a new one. Do not
perform electrical device or component level repair of the multilayer board or
unit. Shanghai Kohden does not support component level repair outside the
factory for the following reasons:
• Most of the boards are multilayer boards with surface mount electrical devices,
so the mounting density of the board is too high.
• A special tool or high degree of repair skill is required to repair the multilayer
boards with surface mount electrical devices.
Only disassemble the instrument or replace a board or unit in an environment

where the instrument is protected against static electricity.
As background knowledge for repair, pay special attention to the following:

• You can reduce the repair time by considering the problem before starting
repair.
• You can clarify the source of most of the troubles using the information from
the error massage and troubleshooting in the “Troubleshooting” section of this
manual.
Patient Safety Checks

Periodic maintenance procedures and diagnostic check procedures are provided
in this manual to ensure that the instrument is operating in accordance with its
design and production specifications. To verify that the instrument is working
in a safe manner with regard to patient safety, patient safety checks should
be performed on the instrument before it is first installed, periodically after
installation, and after any repair is made on the instrument.
For patient safety checks, perform the following checks as described in the
International Electrotechnical Commission’s standard, IEC60601-1: 2012:
• Protective earth resistance check
• Earth leakage current check
• Enclosure leakage current check
• Patient leakage current check
• Withstanding voltage check

1. GENERAL
Monitor Status on Power Interruption
WARNING
Only use the provided power cord. Using other power cords may
result in electrical shock or injury to the patient and operator. To
avoid risk of electric shock, this equipment must only be connected
to a supply mains with protective earth. Connect the provided power
cord to the AC power cord socket on the rear panel of the bedside
monitor and plug the cord into a 3-prong AC socket.
CAUTION
Before connecting or disconnecting instruments, make sure that
each instrument is turned off and the power cord is disconnected
from the AC socket. Otherwise, the patient or operator may receive
electrical shock or injury.
When there is a power failure or sudden power interruption during AC operation,

the monitor operates as follows.
• When a battery pack is installed, the monitor can operate for about 6 hours on
battery power.
• When no battery pack is installed or the battery is discharged, the monitor
turns off. The patient data and settings are stored for about 30 minutes after
power off. If the monitor power is turned off and on within 30 seconds,
monitoring continues.
If there is a power failure or sudden power interruption, immediately connect
the monitor to an emergency power source. It is recommended to always keep a
battery pack in the monitor.

1. GENERAL
1
Composition
SVM-7501/7521
SVM-7501/7521 Bedside Monitor
UR-4303 PSU BOARD
UR-43052 MAIN BOARD (BASIC)
UR-4306 TEMP BOARD
UR-4307 PWR SW BOARD
UR-4308 ALARM BOARD
UR-4309 LAN&USB BOARD

Options
WS-752P RECORDER MODULE
UR-4304 RECORDER CTRL BOARD
RG-750X PAPER DRIVE UNIT
SB-752P BATTERY PACK
SVM-7503/7523
SVM-7503/7523 Bedside Monitor
UR-4303 PSU BOARD
UR-43051 MAIN BOARD (PLUS)
UR-4306 TEMP BOARD
UR-4307 PWR SW BOARD
UR-4308 ALARM BOARD
UR-4309 LAN&USB BOARD

Options
WS-752P RECORDER MODULE
UR-4304 RECORDER CTRL BOARD
RG-750X PAPER DRIVE UNIT
SB-752P BATTERY PACK

1. GENERAL
Specifications
Measuring Parameters
SVM-7501/7521 ECG, respiration in impedance, SpO2, NIBP, temperature
SVM-7503/7523 ECG, respiration in impedance, SpO2, NIBP, temperature, IBP, CO2
Influence on Measuring Accuracy by Electrosurgery, Defibrillation, and Electrostatic Discharge

The bedside monitor returns to the previous operating mode within 10 seconds without loss of any stored data. When per-
forming defibrillation, the filter setting on the bedside monitor must be set to MONITOR on the ECG window to return to
the previous operating mode within 10 seconds without loss of any stored data. Measurement accuracy may be temporarily
decreased while performing electrosurgery or defibrillation. This does not affect patient or equipment safety.
Display
Display size: SVM-7501/7503: 10.4 inch, color TFT type LCD
SVM-7521/7523: 12.1 inch, color TFT type LCD
Resolution: 800 dots × 600 dots
Viewing area: 211 mm × 158 mm for 10.4 inch, 246 mm × 185 mm for 12.1 inch
Waveform display:
SVM-7501/7521: ECG (maximum 2 traces), respiration, SpO2
SVM-7503/7523: ECG (maximum 2 traces), respiration, SpO2, IBP, CO2 pulse wave
Waveform display mode: Non-fade fixed
Maximum number of waveform trace: 6 traces
Sweep speed: 6.25 mm/s, 12.5 mm/s, 25 mm/s or 50 mm/s
Respiration sweep speed: 1.56 mm/s, 6.25 mm/s, 12.5 mm/s or 25 mm/s
Aspect ratio (ECG display sensitivity ratio to sweep speed):

Standard: 0.4 s/mV
Setting range: 0.05 s/mV to 6.4 s/mV
Sweep time (at 25 mm/s sweep speed): 4.8 seconds for 10.4 inch, 5.6 seconds for 12.1 inch
Display delay time:

DIAG and MONITOR mode: ≤ 250 ms
MAXIMUM mode: ≤ 1 second
Waveform display color: 12 colors
Numeric data display:

SVM-7501/7521: Heart rate, VPC rate (per minute), ST level, respiration rate, NIBP (systolic, diastolic,
MAP), SpO2, pulse rate, temperature
SVM-7503/7523: Heart rate, VPC rate (per minute), ST level, respiration rate, NIBP (systolic, diastolic,
MAP), SpO2, pulse rate, temperature, IBP (systolic, diastolic, mean), ETCO2, FiCO2

1. GENERAL
Synchronization mark: Heart rate sync mark, pulse rate sync mark, respiratory sync mark 1
Numeric display color: 12 colors
Recovery time after defibrillation: Less than 10 seconds (in MONITOR mode)
Alarm
Alarm classification: Crisis, Warning, Advisory
Alarm items: Upper/lower limit alarms, arrhythmia alarms, technical alarms

(connector disconnection alarm, noise alarm, electrode off alarm, waveform detecting alarm,
probe off alarm, cuff / hose check alarm, sensor check alarm, low battery alarm)
Alarm indication*: Alarm indicator, highlighted message, alarm sound

Alarm indicator indication:

Crisis: Red blinking, approx. 1.6 Hz (640 ms) duty cycle 50 %
Warning: Yellow blinking: approx. 0.8 Hz (1280 ms), duty cycle 50 %
Advisory: Yellow lighting
Alarm sound:
Crisis: Pips or IEC standard
Warning: Bing bongs or IEC standard
Advisory: Bong for 20 seconds or IEC standard
Alarm silence: 1 minute, 2 minutes or 3 minutes
Alarm suspend: 1 minute, 2 minutes, 3 minutes or OFF
All alarms off: Alarm function is suspended indefinitely. While alarm function is suspended, a message
appears. Alarm function resumes when the [ALL ALARMS OFF] key on the screen is touched.
Alarm reset: When the [ALARM RESET] key is assigned to a function key, it will be displayed on the
screen. While the key is touched, the “ALARM RESET” message appears, the alarm value is
highlighted and the alarm sound is deactivated. The alarm reoccurs when an alarm different
from the reset one occurs, or cause of alarm was eliminated temporarily.
Alarm volume: 45 dB to 85 dB (A) (Requirement of IEC 60601-1-8: 2012) (at 1 m in front of monitor)
Crisis ≥ Warning ≥ Advisory
Alarm reminder: On SYSTEM SETUP screen, when the REMINDER is check, the reminder blinks for about 3
seconds every 3 minutes.

1. GENERAL
Alarm Delay Time

Includes time to output alarm from the network socket on the monitor when con-
nected to the network.
Heart Rate
Time to alarm for tachycardia: Ventricular tachycardia (amplitude 1 mV p-v, heart rate 206 bpm):
at × 1 gain (Test waveform name: aami4a*): 4 seconds to 10 seconds
at × 0.5 gain (Test waveform name: aami4a_h*): 4 seconds to 10 seconds
at × 2 gain (Test waveform name: aami4a_d*): 4 seconds to 10 seconds
Ventricular tachycardia (amplitude 2 mV p-v, heart rate 195 bpm):
at × 1 gain (Test waveform name: aami4b*): 4 seconds to 10 seconds
at × 0.5 gain (Test waveform name: aami4b_h*): 4 seconds to 10 seconds
at × 2 gain (Test waveform name: aami4b_d*): 4 seconds to 10 seconds
* The test waveforms can be download at https://www.physionet.org
Pulse rate Response time of pulse rate meter to change in pulse rate:
PR change from 80 bpm to 120 bpm: ≤ 20 seconds (upper limit: 100 bpm)
PR change from 80 bpm to 40 bpm: ≤ 20 seconds (lower limit: 60 bpm)
ST Approx. 1 second after measurement value reaches alarm threshold

(averaged 15-second data)
Respiration rate Approx. 5 seconds after measurement value reaches alarm threshold
(with 8 respiration intervals)
NIBP Approx. 5 seconds after measurement value becomes stable
IBP (SVM-7503/7523) IBP change from 100 mmHg to 60 mmHg ≤ 15 seconds

(at pulse rate 80 bpm, SYS lower limit: 80 mmHg)
SpO2 Approx. 5 seconds after measurement value reaches alarm threshold
Temperature Approx. 1 second after measurement value reaches alarm threshold

For time delay when using a thermistor probe, refer to the manual for the probe.
CO2 (Mainstream method, SVM-7503/7523)

Approx. 5 seconds after measurement value reaches alarm threshold
(when the next respiration is detected)
Alarm signal delay in central monitor network: ≤ 4 seconds

1. GENERAL
ECG (IEC 60601-2-27: 2011) 1
Leads:
3-electrode cable: I, II, III
5-electrode cable: I, II, III, aVR, aVL, aVF, V
Defibrillation-proof: ECG input protected against 400 Ws/DC 5 kV

IEC 60601-2-27:2011 201.8.5.5 complied
Applied part: Electrode
Electrode offset potential tolerance: ≥ ± 500 mV
Input dynamic range: ≥ ± 5 mV
Internal noise: ≤ 30 μVp-p (Referred to input)
Noise suppression:
RL driving gain: Maximum 40 dB
Maximum voltage: 1.23 Vrms
Common mode rejection ratio: ≥ 95 dB
Frequency response:
DIAG mode: 0.05 Hz to 150 Hz (-3 dB)
MONITOR mode: 0.3 Hz to 40 Hz (-3 dB)
MAXIMUM mode: 1 Hz to 18 Hz (-3 dB)
NOTE: When performing defibrillation, set the <FILTERS> to MONITOR or MAXIMUM. The waveform
recovery may become slow due to electrode polarization when DIAG is set.
Input impedance: ≥ 5 MΩ (at 10 Hz)

≥ 2.5 MΩ (at 0.67 Hz to 40 Hz)
ESU protection: Provided

Recovers within 10 seconds after ESU and acquired data is not lost.
IEC 60601-2-27: 2011 complied
Leads-off sensing: Each lead has own sensing

Active electrode: < 100 nA (DC)
Reference electrode: < 500 nA (DC)
Waveform display:
Display sensitivity: 10 mm/mV ± 5 % (at DIAG mode, 10 Hz, at × 1 sensitivity)
Number of channels: 2 (maximum, with 5 electrodes on home screen)
Sensitivity control: × 1/4, × 1/2, × 1, × 2, × 4, or AUTO
Pacing mark display: Available
Recording sensitivity (when using WS-752P recorder module):

10 mm/mV ± 5 % (same as the display sensitivity)
Heart rate count:

Calculation method: Moving average/Instantaneous beat to beat

1. GENERAL
Patient type (at × 1 sensitivity): Adult: Width: 70 ms to 120 ms

Range of detection amplitude: 0.5 mV to 5 mV, rate: 30 beats/min
to 200 beats/min
Child and neonate: Width: 40 ms to 120 ms
Range of detection amplitude: 0.5 mV to 5 mV, rate: 30 beats/min
to 250 beats/min
Complies with the QRS detection range specified in IEC 60601-2-27: 2011
201.12.1.101.15
Counting range: 0 beat/min, 15 beats/min to 300 beats/min
Counting accuracy*: ± 2 beats/min (0 beat/min, 15 beats/min to 300 beats/min)

Heart rate display: Heart rate sync mark delay time: ≤ 100 ms to 200 ms (when QRS is detected)
Heart rate display update cycle: Every 3 seconds or when alarm is generated
Tall T-wave rejection capability: Complies with the heights of T-waves from 0 mV to 1.2 mV specified in IEC 60601-2-
27: 2011 201.12.1.101.17
Heart rate averaging: Calculated by using the most recent 4 beats or 12 beats.
Heart rate meter accuracy and response to irregular rhythm:

Ventricular bigeminy (Test waveform name: aami3a*): 80 bpm
Slow alternating ventricular bigeminy (Test waveform name: aami3b*): 60 bpm
Rapid alternating ventricular bigeminy (Test waveform name: aami3c*): 120 bpm
Bidirectional systoles (Test waveform name: aami3d*): 90 bpm
* The test waveforms can be download at http://www.physionet.org
Response time of heart rate meter to change in heart rate:

HR change from 80 bpm to 120 bpm: 7.7 seconds to 10.7 seconds (average 9.2 seconds)
HR change from 80 bpm to 40 bpm: 6.3 seconds to 8.2 seconds (average 7.8 seconds)
Pacemaker pulse detector rejection of fast ECG signals:

Slew rate at which the pacemaker pulse detector responds: 6 V/s to 8 V/s
Pacemaker pulse rejection capability, without overshoot:

Examined by method A of IEC 60601-2-27: 2011 201.12.1.101.13
The pacemaker pulse is prescribed as follows:
Pacemaker pulses: ± 2 mV to ± 700 mV
Width 0.1 ms to 2 ms
Pacemaker pulse rejection capability, with overshoot:

Examined by method B of IEC 60601-2-27: 2011 201.12.1.101.13*
Rejectable overshoot: ± 0.12 mV/100 ms to ± 2 mV/4 ms
(Overshoot amplitudes/time constants)
* The method B prescribes the pacemaker pulse amplitude and width as follows:
Pacemaker pulse: ± 4 mV/2 ms to ± 80 mV/0.1 ms
Heart rate alarm:

Upper limit range: 16 beats/min to 300 beats/min, OFF in 1 beat/min steps
Lower limit range: OFF, 15 beats/min to 299 beats/min in 1 beat/min steps
Alarm items: TACHYCARDIA, BRADYCARDIA

1. GENERAL
Arrhythmia analysis: 1
Analysis method: Multi-template matching method
Number of channels: 1
VPC counting rate: 0 VPC/min to 99 VPCs/min
Arrhythmia message: ASYSTOLE, VF, VT, VPC RUN, TACHYCARDIA, BRADYCARDIA, COUPLET,
EARLY VPC, BIGEMINY, FREQ VPC, VPC
Other messages: NOISE, CHECK ELECTRODES, LEARNING
Arrhythmia alarm: Upper limit range: OFF, 1 VPC/min to 99 VPCs/min
Arrhythmia recall: Number of recall files: 120 hours
Storage time per file: 10 seconds
ST level measurement:
Number of measurement 3 electrodes: 1 channel
channels: 5 electrodes: 2 channels
Measuring range: ± 2.5 mV
ST level alarm: Upper limit range: –1.99 mV to +2.00 mV in 0.01 mV steps, OFF
Lower limit range: OFF, –2.00 mV to +1.99 mV in 0.01 mV steps
Respiration (Impedance Method)

Measuring method: Transthoracic impedance pneumography
Measuring impedance available range: 220 Ω to 4 kΩ
Excitor current: (35 ± 10) μArms at 40 kHz (sine wave)
Internal noise: ≤ 0.2 Ω (Referred to input)
Respiration rate counting range: 0 count/min to 150 counts/min
Respiration rate counting accuracy*: ± 2 counts/min (0 count/min to 150 counts/min)

Frequency response (high frequency cut-off): 3 Hz (≥ 3 dB)
Defibrillation proof: Respiration input protected against 400 Ws/DC 5 kV
Applied part: Electrode
Impedance respiration: ON / OFF
Heart beat rejection: Available
Waveform display: Display sensitivity: 10 mm/Ω ± 25 % (at × 1 sensitivity)

Sensitivity control: × 1/4, × 1/2, × 1, × 2, × 4
Respiration rate display update cycle:
Every 3 seconds or when alarm is generated
Sweep speed: 1.56 mm/s, 6.25 mm/s, 12.5 mm/s or 25 mm/s
Alarm: Upper limit range: 2 counts/min to 150 counts/min in 2 counts/min steps, OFF
Lower limit range: OFF, 0 count/min to 148 counts/min in 2 counts/min steps
Apnea alarm: Setting range: OFF, 5 seconds to 40 seconds in 5-second steps

Displayed message: APNEA

1. GENERAL
SpO2 (ISO 80601-2-61: 2011)

SpO2 display:
Display update cycle: Every 3 seconds or when alarm is generated
Sync tone modulation: Changes tone depending on SpO2 value (Continuous
high tone of "bong" when the value is high, and low tone
when it is low.)
Sweep speed: 6.25 mm/s, 12.5 mm/s, 25 mm/s or 50 mm/s
Waveform sensitivity: × 1/8, × 1/4, × 1/2, × 1, × 2, × 4, × 8 or AUTO
SpO2:
Measuring method: Two wavelength light absorption method
Data delay time: ≤ 10 seconds
Display range: 0 % SpO2 to 100 % SpO2
Declared range: 70 % SpO2 to 100 % SpO2
Applied part: Sensor
Measuring accuracy*1 (rms*2): 80 % SpO2 ≤ % SpO2 ≤ 100 % SpO2: ± 2 % SpO2
70 % SpO2 ≤ % SpO2 < 80 % SpO2: ± 3 % SpO2
Less than 70 % SpO2 is not specified
SpO2 accuracy is guaranteed at surrounding temperature of 18 °C to 40 °C
(64.4 °F to 104 °F)
*1 Essential performance
Accuracy at surrounding temperature: 18 ºC to 40 ºC (64.4 ºF to 104 ºF)
*2 NOTE for SpO2 Accuracy:
• The SpO2 measuring accuracy was tested on OLV-3100 pulse oximeter using the TL-201T, TL-260T,
TL-271T and TL-631T SpO2 probes. The testing was performed during induced hypoxia on healthy
volunteers (Ethnicity: 10 Caucasians, 2 Africans, 1 Asian and 3 Indians), (Skin: 8 light, 4 medium, 4
dark), (Age: 21 to 34), (5 women and 11 men) under the condition of no motion. Arterial blood was
sampled and measured by a CO-oximeter. The difference between SpO2 measured by the SpO2
probe and functional SaO2 measured by a CO-oximeter was calculated using the root mean square
(rms) according to ISO 80601-2-61: 2011. This measurement accuracy figure represents 2/3 of all test
measurements.
• A pulse oximeter tester that generates simulated signals can be used to check the difference from the
design specification, but it cannot be used as a replacement for human signals for testing accuracy.
Alarm
Upper limit range: 51 % SpO2 to 100 % SpO2 in 1 % SpO2 steps, OFF
Lower limit range: OFF, 50 % SpO2 to 99 % SpO2 in 1 % SpO2 steps
Alarm delay time: 10 seconds (0 second to 10 seconds, in 1-second steps)
Pulse rate:
Display range: 30 beats/min to 300 beats/min
Declared range: 30 beats/min to 300 beats/min
Counting accuracy (rms): ± 3 % ± 1 beat/min
Alarm
Upper limit range: When <SYNC SOURCE> is set to ECG:
16 beats/min to 300 beats/min in 1 beat/min steps, OFF
When <SYNC SOURCE> is set to SpO2 or PRESS1:

1. GENERAL
Lower limit range: When <SYNC SOURCE> is set to ECG: 1

OFF, 15 beats/min to 299 beats/min in 1 beat/min steps
When <SYNC SOURCE> is set to SpO2 or PRESS1:
Response time: Selectable from SLOW, NORMAL and FAST.

The following graphs show the response time example when SpO2 changes 0.6
%/s.
Pulse Rate = 70 bpm
SpO2 Reference SpO2 Fast SpO2 Normal SpO2 Slow
100
95
90
SpO2 (%)
85
80
75
70
65
60
0 10 20 30 40 50 60 70 80 90 100 110 120 130 140
Time (seconds)
Pulse Rate = 140 bpm
SpO2 Reference SpO2 Fast SpO2 Normal SpO2 Slow
100
95
90
SpO2 (%)
85
80
75
70
65
60
0 10 20 30 40 50 60 70 80 90 100 110 120 130 140
Time (seconds)
The following graph shows the response time example when pulse rate changes
10 bpm/s.
SpO2 = 97
PR Reference PR
150
140
130
120
PR (bpm)
110
100
90
80
70
60
0 10 20 30 40 50 60 70 80 90 100 110 120
Time (seconds)

1. GENERAL
Noninvasive Blood Pressure (NIBP) (IEC 80601-2-30: 2009)

Measuring method: Oscillometric
Measuring range:
Adult: SYS: 40 mmHg to 280 mmHg
DIA: 10 mmHg to 235 mmHg
MAP: 20 mmHg to 255 mmHg
Child: SYS: 40 mmHg to 280 mmHg
Neonate: SYS: 30 mmHg to 140 mmHg
The maximum error for the measurement of the CUFF pressure ± 3 mmHg (0 mmHg ≤ NIBP ≤ 300 mmHg)
Clinical accuracy for the measurement of blood pressure (ISO 81060-2:2013):

± 5 mmHg (the mean value of the error)
Within 8 mmHg (standard deviation of error)
Measurement accuracy with a simulator* for blood pressure ± 10 mmHg
measurement::
Cuff inflation time:

Adult/Child: ≤ 11 seconds (700 cc)
Neonate: ≤ 7 seconds (70 cc)
Measurement mode: Manual, STAT (≤ 15 minutes), Periodic and SIM
Cuff pressure settings: Manual or Auto
Auto remeasurement: 1 time
Air leakage: ≤ 3 mmHg/min
Initial pressurization value:

Adult/Child: 180 mmHg / 140 mmHg
Neonate: 100 mmHg
Maximum pressure applied to cuff in neonate mode:

150 mmHg
Cuff pressure display range: 0 mmHg to 300 mmHg
Applied part: Cuff
Display items: Systolic (SYS), diastolic (DIA), mean (MAP), cuff pressure
during NIBP measurement, pulse rate
NIBP data display update cycle: Updated every measurement
Measurement completion sound: Generated at measurement completion (depends on the setting:

OFF, NK1 (three long "bee-bee-bee" sounds) and NK2 (two short
"bee-bee" sounds))
Alarm
Upper limit range: 15 mmHg to 260 mmHg in 5 mmHg steps, OFF

1. GENERAL
Lower limit range: OFF, 10 mmHg to 255 mmHg in 5 mmHg steps 1

Safety
Maximum pressurization value cuff inflation limiter:
Adult / Child: 300 mmHg to 330 mmHg
Neonate: 150 mmHg to 165 mmHg
Cuff inflation time limiter: Adult / Child: ≤ 180
Neonate: ≤ 90 seconds
Interval time limiter: ≤ 30 seconds
Power discontinuity: Deflates immediately after power down
Invasive Blood Pressure, IBP (SVM-7503/7523)

Complies with IEC 60601-2-34: 2011 except for clauses 201.11.6.5 and
201.9.7.5.
Compiled transducers: Edwards Lifesciences (Baxter) disposable transducers
Becton Dickinson disposable transducers DX series
5 μV/V/mmHg, bridge resistor: 200 W to 20 kW, defibrillation-proof or the
equivalent
Volume displacement: 0.04 mm3/100 mmHg
Auto zero balancing range: ± 200 mmHg
Auto zero balancing accuracy: ± 1 mmHg
Measuring range: –50 mmHg to 300 mmHg
Measuring accuracy: ± 1 mmHg ± 1 digit (–50 mmHg ≤ IBP < 100 mmHg)
± 1 % ± 1 digit (100 mmHg ≤ IBP ≤ 300 mmHg)
Total measuring accuracy*1: ± 4 % or ± 4 mmHg (whichever is greater)*2

*1 Essential performance
*2 When used with ANSI/AAMI BP-22-1994 compliant equipment
Internal noise: Within ± 1 mmHg
Temperature zero drift: ± 0.1 mmHg/1 °C
Frequency response: DC to 12 Hz or 20 Hz (selectable)
Display items: Systolic (SYS), diastolic (DIA), mean (MEAN)
BP sync sound: Systolic value 20 mmHg to 120 mmHg, changes in 20 steps every 5 mmHg
Transducer warm-up time (for balancing the whole system):

20 seconds for Edwards Lifesciences transducers (Different transducers have
different warm-up times, refer to the operator's manual of each transducer)

1. GENERAL
Alarm:
Upper limit range: 2 mmHg to 300 mmHg in 2 mmHg steps, OFF
Lower limit range: OFF, 0 mmHg to 298 mmHg in 2 mmHg steps
Alarm inactivation: Alarm is inactivated in certain periods when zero balancing is performed.
Pulse rate
Counting range: 0 beat/min, 30 beats/min to 300 beats/min
Display range: 0 beat/min to 300 beats/min
Counting accuracy (rms): ± 2 beats/min (30 beats/min ≤ PR ≤ 300 beats/min)
Alarm: Upper limit range: When SYNC SOURCE is set to ECG:

When SYNC SOURCE is set to PRESS1 or SpO2:
Lower limit range: When SYNC SOURCE is set to ECG:

When SYNC SOURCE is set to PRESS1 or SpO2:
Temperature (ISO 80601-2-56: 2009)

Mode of operation: Direct mode
Thermistor probe: 400 series (YSI)
Applied part: Sensor
Rated output range: 0 °C to 45 °C (32 °F to 113 °F)
Measuring accuracy*: ± 0.2 °C (25 °C ≤ TEMP ≤ 45 °C)

± 0.3 °C ( 0 °C ≤ TEMP < 25 °C)
Internal noise: ≤ 0.014 °C (at 37 °C)
Temperature drift: Within ± 0.005 °C/°C
Lead break detection: Available
Display range: 0 °C to 45 °C (32 °F to 113 °F)
Alarm
Upper limit range: 0.1 °C to 45 °C (33 °F to 113 °F) in 0.1 °C (1 °F) steps, OFF
Lower limit range: OFF, 0.0 °C to 44.9 °C (32 °F to 112 °F) in 0.1 °C (1 °F) steps

1. GENERAL
CO2 (Mainstream Method) (SVM-7503/7523) 1
For the TG-901T4/TG-921T4/TG-971T4/TG-981T4 CO2 sensor kit specifica-

tions, refer to the kit manual.
Displayed CO2*: Values detected by the TG-901T4/TG-921T4/TG-971T4/TG-981T4 CO2 sensor kit
Calculation method
TG-901T4/TG-921T4: Semi-quantitative
TG-971T4/TG-981T4: Quantitative
CO2 measuring range: TG-901T4/TG-921T4: 0 mmHg to 100 mmHg

TG-971T4/TG-981T4: 0 mmHg to 150 mmHg
CO2 measuring accuracy

TG-901T4/TG-921T4: ± 0.4 kPa (0 kPa ≤ CO2 ≤ 1.33 kPa) (± 3 mmHg (0 mmHg ≤ CO2 ≤ 10 mmHg))
± 0.53 kPa (1.33 kPa < CO2 ≤ 5.33 kPa) (± 4 mmHg (10 mmHg < CO2 ≤ 40 mmHg))
± 10 % reading (5.33 kPa < CO2 ≤ 13.3 kPa (40 mmHg < CO2 ≤ 100 mmHg))
(At 1 atmospheric pressure, air inspiration, no condensation)
TG-971T4/TG-981T4: ± 0.27 kPa (0 kPa ≤ CO2 ≤ 5.33 kPa) (± 2 mmHg (0 mmHg ≤ CO2 ≤ 40 mmHg))
(When no condensation)
Applied part: Airway adapter and nasal adapter
Warm-up time: TG-901T4/TG-921T4: 5 seconds

TG-971T4/TG-981T4: 10 seconds
Response time
TG-901T4: 160 ms (typical) for steps from 10 % to 90 %
TG-921T4/TG-971T4: 120 ms (typical) for steps from 10 % to 90 %
TG-981T4: ˂ 60 ms for steps from 10% to 90%
Respiration rate counting range

TG-901T4/TG-921T4: 3 counts/min to 150 counts/min
TG-971T4/TG-981T4: 0 count/min to 150 counts/min
Respiration rate counting accuracy

TG-901T4/TG-921T4: ± 10 % (3 counts/min to 150 counts/min)
TG-971T4/TG-981T4: ± 1 count/min
CO2 value display update cycle: Every 3 seconds or when alarm is generated
CO2 alarm:
Upper limit: CO2 (I): 1 mmHg to 99 mmHg in 1 mmHg steps, OFF
0.1 kPa to 13.0 kPa in 0.1 kPa steps, OFF
ETCO2 2 mmHg to 99 mmHg in 1 mmHg steps, OFF
0.2 kPa to 13.0 kPa in 0.1 kPa steps, OFF
Lower limit: ETCO2: OFF, 1 mmHg to 98 mmHg in 1 mmHg steps

OFF, 0.1 kPa to 12.9 kPa in 0.1 kPa steps
Respiration rate alarm:

1. GENERAL
Upper limit range: 2 counts/min to 150 counts/min in 2 counts/min steps, OFF

Lower limit range: OFF, 0 count/min to 148 counts/min in 2 counts/min steps
Apnea time: OFF, 5 seconds to 40 seconds in 5-second steps

Displayed message: APNEA
Total system response time: 1 second
Recorder (WS-752P Recorder Module)

Recording method: Thermal array recording
Number of channels: 3 (maximum)
Recording width: ≥ 46 mm
Paper speed: 12.5 mm/s, 25 mm/s, 50 mm/s
Recording density:
Amplitude direction: 8 dots/mm
Feeding direction: 40 dots/mm (≤ 25 mm/s)
20 dots/mm (50 mm/s)
Recording paper: RQW50-2SK
Battery (SB-752P Battery Pack)

Type of battery: Rechargeable Li-ion
Number of batteries: 1
Battery lifetime: 1 year
Battery operation time: 6 hours

(new battery, fully charged, no options are used, and operated in normal temperature)
Power off delay time: 5 minutes
DC voltage: 7.2 V
Charging current: 2240 mA
Charging time
90% charge: 3 hours
Full charge: 4 hours
Charging time may be longer at high temperatures.
Battery status indication: Battery lamps on the front panel, screen message and alarm sound, alarm indicator
Operating environment
Charging temperature: 6 °C to 59 °C (43 °F to 138 °F)
Discharging temperature: Below 70°C (158 °F)
Humidity: 15 % RH to 95 % RH (noncondensing)

1. GENERAL
Atmospheric pressure: 700 hPa to 1060 hPa 1

Transport and storage environment: When the battery pack is stored more than 6 months, charge and discharge or charge the
battery once every 6 months.
Temperature: Less than 1 month with 80 % recoverable capacity: –20 oC to +45 oC (–4 oF to +113 oF)
Less than 6 months with 80 % recoverable capacity: –20 oC to +40 oC (–4 oF to +104 oF)
Less than 1 year with 80 % recoverable capacity: -20 oC to 35 oC (-4 oF to 95 oF)
Atmospheric pressure: 700 hPa to 1060 hPa
Power Requirement
Line voltage:
AC: AC (100 V to 240 V) ± 10 %
DC (SB-752P): 7.2 V
Line frequency: (50 Hz or 60 Hz) ± 2 %
Power consumption: AC 95 VA
Clock Accuracy
At operating temperature 25 °C: Approx. ± 3 minutes 30 s/month maximum
At storage temperature –20 °C to +60 °C: Approx. ± 6 minutes/month maximum
Environment
Operating environment:
Temperature: 10 °C to 40 °C (50 °F to 104 °F)
Transport and storage environment:

Temperature: –20 °C to +65 °C (–4 °F to +149 °F)
–15 °C to +55 °C (Recording paper)
Humidity: 10 % RH to 95 % RH

1. GENERAL
Mechanical Strength
Mechanical strength: Indoor portable type
Electromagnetic Compatibility
IEC 60601-1-2: 2014
Safety Standard
Safety standard: IEC 60601-1: 2012
IEC 60601-1-2: 2014
IEC 60601-1-6: 2010
IEC 60601-1-8: 2012
IEC 60601-2-27: 2011
IEC 80601-2-30: 2009
IEC 60601-2-34: 2011*
IEC 60601-2-49: 2011
ISO 80601-2-56: 2009
ISO 80601-2-61: 2011
ISO 80601-2-55: 2011*
* For SVM-7503/7523.
Type of protection against electrical shock:

CLASS I EQUIPMENT (AC Powered)
Internally Powered EQUIPMENT (BATTERY Powered)
Degree of protection against electrical shock

Defibrillation-proof type CF applied part: ECG, Respiration (Impedance), IBP, Temperature, SpO2, CO2, NIBP
Degree of protection against harmful ingress of water:

IPX1 (Protected against vertically dripping water)
Degree of safety of application in the presence of FLAMMABLE ANAESTHETIC MIXTURE WITH AIR, OR WITH OXYGEN
OR NITROUS OXIDE:
Equipment not suitable for use in the presence of FLAMMABLE
ANAESTHETIC MIXTURE WITH AIR, OR WITH OXYGEN OR NITROUS
OXIDE
Mode of operation: CONTINUOUS OPERATION
Dimensions and Weight (Approximate)

SVM-7500 series bedside monitor Dimension: W × H × D: 330 mm × 274 mm × 156 mm (excluding protruding parts)
Weight: 4 kg
WS-752P recorder module Dimension: W × H × D: 86 mm × 87 mm × 64 mm (excluding protruding parts)

Weight: 0.35 kg

1. GENERAL
Lifetime 1
6 years
(Self certified based on our data; only when the specified yearly inspection is
performed.)
Electromagnetic Emissions
The SVM-7500 series bedside monitor essential performance in EMC standard
satisfies the following criteria.
This Model SVM-7500 series bedside monitor is intended for use in the
electromagnetic environment specified below.
The customer or the user of the SVM-7500 series bedside monitor should assure
that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance

Conducted and radiated RF Group 1 The SVM-7500 series bedside monitor uses RF energy only for its internal
EMISSIONS function. Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
CISPR 11
RF emissions Class B The SVM-7500 series bedside monitor is suitable for use in all
establishments, including domestic establishments and those directly
CISPR 11
connected to the public low-voltage power supply network that supplies
Harmonic distortion Class A buildings used for domestic purposes.
IEC 61000-3-2
Voltage fluctuations and Complies
flicker
IEC 61000-3-3
NOTE: The EMISSIONS characteristics of this equipment make it

suitable for use in industrial areas and hospitals (CISPR 11 class
A). If it is used in a residential environment (for which CISPR
11 class B is normally required) this equipment might not offer
adequate protection to radio-frequency communication services.
The user might need to take mitigation measures, such as
relocating or re-orienting the equipment.

1. GENERAL
Electromagnetic Immunity
The SVM-7500 series bedside monitor essential performances in EMC standard
satisfies the following criteria.
This Model SVM-7500 series bedside monitor is intended for use in the
electromagnetic environment specified below.
The customer or the user of the SVM-7500 series bedside monitor should assure
that it is used in such an environment.
Phenomenon
IMMUNITY TEST
Basic EMC Compliance levels Electromagnetic environment - guidance
LEVELS
standard
ELECTROSTATIC ± 8 kV contact ± 8 kV contact Floors should be wood, concrete or ceramic tiles.
DISCHARGE If floors are covered with synthetic material, the
± 2 kV, ± 4 kV, ± 8 kV, ± ± 2 kV, ± 4 kV, ± 8 kV, ±
relative humidity should be at least 30%.
IEC 61000-4-2 15 kV air 15 kV* air
± 2 kV for power supply ± 2 kV for power supply Mains power quality should be that of a typical
Electrical fast
lines lines commercial or hospital environment.
transient/burst
± 1 kV for input/output ± 1 kV for input/output
IEC 61000-4-4
lines lines
Surge ± 1 kV Line-to-line ± 1 kV differential mode Mains power quality should be that of a typical
commercial or hospital environment.
IEC 61000-4-5 ± 2 kV Line-to-ground ± 2 kV common mode
Voltage dips < 0% UT Mains power quality should be that of a typical
0 % UT; 0.5 cycle commercial or hospital environment.
IEC 61000-4-11 0.5 cycles
At 0°, 45°, 90°, 135°, If the user of the SVM-7500 series requires
180°, 225°, 270°, 315° 0°, 45°, 90°, 135°, 180°,
continued operation during power mains
225°, 270°, 315°
interruptions, it is recommended that the SVM-
7500 series be powered from an uninterruptible
0 % UT; power supply or a battery.
0% UT
1 cycle
1 cycle
and
and
70 % UT;
70% UT
25/30 cycles
25/30 cycles
Single-phase: at 0°
Single-phase 0°
Voltage interruptions 0 % UT; < 0% UT
IEC 61000-4-11 250/300 cycle 250/300 cycles
Power frequency 30 A/m 30 A/m Power frequency magnetic fields should be at
levels characteristic of a typical location in a
(50/60 Hz)
typical commercial or hospital environment.
Magnetic field
IEC 61000-4-8
NOTE: UT is the AC mains voltage prior to application of the test level.

*Immediately after electrostatic discharge, temperature value and CO2/Respiration waveform are sometimes disappears temporarily.
Portable and mobile RF communications
equipment should be used no closer to any part
of the SVM-7500 series including cables than the
Conducted disturbances 3 Vrms recommended separation distance calculated from
induced by RF fields 3 Vrms the equation applicable to the frequency of the
IEC 61000-4-6 150 kHz to 80 MHz transmitter.
Recommended separation distance
_
d = 1.2√P

1. GENERAL
Phenomenon 1
IMMUNITY TEST
Basic EMC Compliance levels Electromagnetic environment - guidance
LEVELS
standard _
Radiated RF EM fields 3 V/m 3 V/m d = 1.2√P 80 MHz to 800 MHz
_
IEC 61000-4-3 80 MHz to 2.7 GHz d = 2.3√P 800 MHz to 2.5 GHz
where P is the maximum output power rating
of the transmitter in watts (W) according
to the transmitter manufacturer and d is the
recommended separation distance in meters (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey*a,
should be less than the compliance level in each
frequency range*b.
Interference may occur in the vicinity of
equipment marked with the following symbol:
NOTE • At 80 MHz and 800 MHz, the higher frequency range applies.
• These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios,
a
amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered.
If the measured field strength in the location in which the SVM-7500 series bedside monitor is used exceeds the applicable
RF compliance level above, the SVM-7500 series bedside monitor should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocating the SVM-7500 series bedside
monitor.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

1. GENERAL
Recommended Separation Distances between Portable and Mobile RF Communications Equipment

The SVM-7500 series bedside monitor is intended for use in an electromagnetic
environment in which radiated RF disturbances are controlled. The customer
or the user of the SVM-7500 series bedside monitor can help prevent
electromagnetic interference by maintaining a minimum distance between
portable and mobile RF communications equipment (transmitters) and the SVM-
7500 series bedside monitor as recommended below, according to the maximum
output power of the communications.
Rated maximum output Separation distance according to frequency of transmitter (m)
power of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
_ _ _
(W) d = 1.2√ P d = 1.2√ P d = 2.3√ P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be
estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
NOTE • At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
• These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
WARNING
Portable RF communications equipment (including peripherals such as antenna cables and external
antennas) should be used no closer than 30 cm (12 inches) to any part of the SVM-7500, including cables
specified by the manufacturer. Otherwise, degradaion of the performance of this equipment could result.
System Composition for EMC Test

The SVM-7500 series bedside monitor has been tested to comply with
IEC 60601-1-2: 2014 with the following composition. If any part which is
not specified by Shanghai Kohden is used, it may not comply with EMC
specifications.
Units Cable length
SVM-7500 series bedside monitor —
BJ-753P ECG patient cable 3.5 m
TL-651S finger probe 3.0 m
YN-721S air hose for neonate 3.0 m
YP-821S disposable cuff for neonate 0.2 m
401J thermistor probe for adult 3.5 m
TG-971T4 sensor kit 3.5 m
JP-752P IBP connection cord 3.5 m
DX-100 monitoring kit —
SB-752P battery pack —
Network cable 10 m
Power cord GB 2.5 m
Grounding lead 4m
WS-752P recorder module —

1. GENERAL
1
Panel Description
Front Panel
1 Touch screen 2 Alarm indicator
3 Power key
4 Power lamp
6 Battery lamp
5 AC power lamp
1 Touch screen
Displays monitoring data. Touching a key or data on the screen changes the
displayed screen and settings.
2 Alarm indicator
Red or yellow lamp blinks, or yellow lamp lights according to the alarm
settings. Green lamp blinks in synchronization with the patient’s QRS or
pulse.
3 Power key
Press to turn the monitor power on. When turning the monitor power off, press
and hold for more than one second.
4 Power lamp
Lights when the monitor power is turned on.
5 AC power lamp
Lights when the power cord is connected between the AC SOURCE socket
and AC outlet.
6 Battery lamp
Indicates the battery status of the battery pack.

1. GENERAL
Left Side Panel

2 ECG/RESP socket
1 Handle
3 TEMP sockets
4 CO2 socket* 6 PRESS sockets*
5 NIBP socket
7 SpO2 socket*
1 Handle
For carrying the monitor.
2 ECG/RESP socket
Connects to the ECG PATIENT CABLE.
3 TEMP sockets
Connects to the temperature probe cables.
4 CO2 socket*
For SVM-7503 and SVM-7523. Connects to the CO2 connection cord.
5 NIBP socket
Connects to the air hose.
6 PRESS sockets*
For SVM-7503 and SVM-7523. Connects to the IBP connection cord.
7 SpO2 socket*
Connects to the SpO2 connection cord.
* When inserting the CO2, PRESS or SpO2 connector, make sure the color of the
connector sleeve matches the color of the socket.

1. GENERAL
Right Side Panel 1
1 Recorder module holder
1 Recorder module holder

For mounting a recorder module.
Rear Panel
5 Battery
1 Network socket pack
holder
4 AC power source socket

3 Equipotential grounding terminal
2 USB socket
1 Network socket
Connects to monitor network system by a network cable
(When a central monitor is connected or HL7 is set on the SYSTEM CONFIG
window.)
2 USB socket
For USB memory.
3 Equipotential grounding terminal
For an equipotential grounding lead.
4 AC POWER SOURCE socket
For the AC power cord.
5 Battery pack holder
For installing a battery pack.

1. GENERAL
Storage and Transport

Follow these procedures when storing or transporting the instrument.
Storage
Before storing the instrument for a long time, perform the following steps:
NOTE for Storage and Handling of Battery Pack

When use of the battery pack is not required for more than one month, fully
charge the battery pack and disconnect the battery pack cable from the
instrument before storage.
1 Disconnect the power cord from the instrument.
2 Cover the instrument with a dust cover.
3 If possible, store the instrument in its original shipping container.
4 Make sure the storage place meets the following storage conditions for the
duration of the storage.
Storage temperature: −20 °C to +65 °C (−4 °F to +149 °F)
Storage humidity: 10 % RH to 95 % RH
Transport
To transport the instrument, perform the following steps:
1 Disconnect the power cord from the instrument.
2 Cover the instrument with a dust cover.
3 If possible, transport the instrument in its original shipping container. The

following transport conditions are required.
Transport temperature: −20 °C to +65 °C (−4 °F to +149 °F)
Transport humidity: 10 % RH to 95 % RH

1. GENERAL
1
Hard Keys and Soft Keys
Hard Keys
The instrument has no hard keys.
Soft Keys
When the [MENU] key is pressed or the screen is touched, the screen displays
several keys which have different functions depending on the screen display.
For example, when the HR numeric display is touched, the ECG setting screen
appears and several keys such as ST ALARM, ARRHYTH ALARM, FILTER,
etc. are displayed.

1-32
1. GENERAL
ALARM Board 10.4 inch LCD

Touch Screen
UR-4308
PWR SW Board
UR-4307 TEMP Board
UR-4306
Connection Diagram
LVDS Back Light Power
ECG/RESP
INPUT
SpO2
INPUT
MAIN Board (BASIC) NIBP

UR-43052 INPUT
(ECG/RESP/SpO2/NIBP/TEMP)
Connection and Block Diagram
SVM-7501 Connection Diagram
Speaker Battery
LAN&USB Board PSU Board Pump Valve SB-752P
UR-4309 UR-4303 (OPTION)
Recorder CTRL Board
UR-4304
WS-752P
(OPTION)
SVM-7500 Series Service Manual

Touch Screen
UR-4308
PWR SW Board
UR-4307 TEMP Board
UR-4306

ECG/RESP
INPUT
SpO2
INPUT
MAIN Board (PLUS) NIBP

UR-43051 INPUT
(ECG/RESP/SpO2/NIBP/TEMP/IBP/CO2)
IBP
INPUT
CO2
INPUT
Speaker Battery
Recorder CTRL Board
UR-4304
WS-752P
(OPTION)
1-33
1. GENERAL
1
1-34
1. GENERAL

Touch Screen
UR-4308
PWR SW Board
UR-4307 TEMP Board
UR-4306
ECG/RESP
INPUT
SpO2
INPUT
MAIN Board (BASIC) NIBP

UR-43052 INPUT
(ECG/RESP/SpO2/NIBP/TEMP)
Speaker Battery
Recorder CTRL Board
UR-4304
WS-752P
(OPTION)

Touch Screen
UR-4308
PWR SW Board
UR-4307 TEMP Board
UR-4306

ECG/RESP
INPUT
SpO2
INPUT
MAIN Board (PLUS) NIBP

UR-43051 INPUT
(ECG/RESP/SpO2/NIBP/TEMP/IBP/CO2)
IBP
INPUT
CO2
INPUT
Speaker Battery
Recorder CTRL Board
UR-4304
WS-752P
(OPTION)
1-35
1. GENERAL
1
1-36
 
  


 


1. GENERAL

  

 
   

 
 
   
 
    

 
  

Block Diagram



 

 




 
 
 

  
  
 
 



   

 
 




 
   



  


 
   

 


   







  
 
 

 
 

 
   

  
 





LVDS
  
 
 T 




  
  
 
 
 
SVM-7501/7521 Block Diagram
 

 


 




 
   

 
  
 
 

 
 
 
 


   

  
   





 

 
 
 

 
  


 



  

 
   

 
 
   
 
    

 
  



  

 

 




 
 
 

  
  

 
  


 

   

 
 




 
   



  


 
   
 


   







  
 
 

 
 

 
   

  
 





LVDS
  
 
 T 




  
  
 
 
 
SVM-7503/7523 Block Diagram
 

 


 




 
   

 
  
 
 

 
 
 
 


   

  
   





 

 
 
 
1-37
1. GENERAL
1
2
2
Troubleshooting
General............................................................................2-2
Troubleshooting...............................................................2-3
Power.............................................................................................2-3
Display............................................................................................2-3
Alarm Indicator...............................................................................2-4
Sound.............................................................................................2-4
Key Operation................................................................................2-4
Recording.......................................................................................2-5
USB Memory..................................................................................2-5
ECG................................................................................................2-6
Respiration (Impedance Method)...................................................2-7
CO2 (SVM-7503/7523)...................................................................2-8
Mainstream Method.................................................................. 2-8
Temperature (TEMP)......................................................................2-8
Non-Invasive Blood Pressure (NIBP).............................................2-9
Invasive Blood Pressure, IBP (SVM-7503/7523)...........................2-9
SpO2 ..............................................................................................2-9
Error Code and History..................................................2-10

Error Code List.............................................................................2-10
2. TROUBLESHOOTING
General
Use the troubleshooting tables to locate, identify, and solve a problem in the
instrument. The problems are divided into general problem areas. Each category
has its own troubleshooting table for fast and easy troubleshooting.
If these sections do not solve the problem, contact your Nihon Kohden
representative.
NOTE: Before contacting your Nihon Kohden representative for technical

support, please provide additional detailed information on the
problem. This will allow your Nihon Kohden representative to
provide you with the best support.
How to use the troubleshooting table
1 Determine which troubleshooting table to use.
2 In the “Problem” column, find the trouble item that matches the problem or
error message.
3 Do the action recommended in the “Action” column.
4 If the problem is not solved, do the action for the next possible cause or
criteria.
5 If none of the actions solve the problem, contact your Nihon Kohden
distributor or representative.

2. TROUBLESHOOTING
Troubleshooting
2
Power
Problem Possible Cause/Criteria Action
When the AC power lamp lights: Replace the Power SW board or Main
board with a new one.
Failure in the Power SW board or Main board.
When the AC power lamp does not light:

• Failure in the AC line voltage or power cord. Check the AC line voltage.
The instrument does not turn on in Replace the power cord.
AC power operation. Replace the PSU board.
• Poor contact at either connector of the cable Check the cable between the PSU board
between the PSU board and Main board or and Main board or replace the cable.
failure in the cable.
• Failure in the PSU board. Replace the PSU board.

The rechargeable battery is weak. Charge the battery.
The instrument does not turn on in Battery failure or lifetime of the battery is expired. Replace the battery with a new one.
battery operation. Poor contact at the connector of the battery cable. Check the connector or replace the battery.
Failure in the Main board. Replace the Main board with a new one.
Battery lifetime is expired. Replace the battery.
Memory effect in the battery. Fully discharge and charge the battery for
Battery operation time is shorter
2 or 3 times. If the problem is still there,
than expected.
replace the battery.
Failure in the charging circuit. Replace the Main board.
Display
When the AC power lamp does not light:
• The power cord is loosely connected. Check that the power cord is firmly
connected.
• Failure in the PSU board. Replace the PSU board.
When the AC power lamp lights but the power Replace the Main board.
Nothing is displayed. lamp does not light: Failure in the Main board.
When the AC power lamp and power lamp light:
• Failure in the Main board. Replace the Main board.
• Failure in the LCD unit. Replace the LCD unit.
• Failure in the LCD BL LED cable. (for SVM- Replace the LCD BL LED cable. (for
7521/7523) SVM-7521/7523)
Failure in the LVDS cable. Replace the LVDS cable.
Abnormal screen is displayed. Failure in the LCD unit. Replace the LCD unit.
Failure in the Main board. Replace the Main board.
Failure in the LVDS cable. Replace the LVDS cable.
Blank white screen

2. TROUBLESHOOTING
Alarm Indicator
When no LED lights when using the “ALARM” Replace the Main board.
function on the MANUAL CHECK screen:
Failure in the Main board.
LEDs do not light. When some specific LEDs do not light when Replace the Alarm board.
using the “ALARM” function on the MANUAL
CHECK screen: Failure in the alarm board or
Main board.
Sound
No sound or small volume Failure in the speaker. Replace the speaker.
even if you increase the sound
volume in the ALARM or SYNC
SOUND VOLUME window of the Failure in the Main board. Replace the Main board.
DISPLAY/SOUND window.
Sound is distorted even if you hear Failure in the speaker. Replace the speaker.
various sounds by using “SOUND”
function on the MANUAL CHECK There is a foreign object around the speaker. Remove the foreign object.
screen.
Key Operation
The workable area for a key does
not match the key display on the
screen.
• The mark appears under • Foreign object between the touchscreen and Remove the foreign object.
your finger when you press a front panel.
position on the screen by using
“TOUCH KEY” function on • The edge protection rubber is not properly Remove the rubber from the touchscreen
the MANUAL CHECK screen. attached to the touchscreen. and reattach it to the touchscreen properly.
When you release the finger from
the screen, the mark returns to
• Failure in the touchscreen. Replace the touchscreen.
a particular position. In other
words, the particular position is
always pressed.
• The mark appears under your • The touchscreen is not calibrated after Calibrate the touchscreen.
finger when you press a position replacement.
on the screen by using “TOUCH
KEY” function on the MANUAL • Failure in the touchscreen. Replace the touchscreen.
CHECK screen. When you
release the finger from the • Failure in the Main board. Replace the Main board.
screen, the mark stays around the
position but it is always out of
the acceptable range.

2. TROUBLESHOOTING
Recording
2
Wrong position of the recording paper in the Load the paper into the magazine properly.
magazine.
The heat-sensitive side of the paper is not facing Load the paper into the magazine properly.
the thermal array head.
When the recorder door is firmly closed but the Replace the RG-750X paper drive unit.
“CLOSE PAPER MAGAZINE” message and icon
Nothing is recorded on the paper are still displayed: Failure in the mechanical parts
but the model number, WS-752P, is of the recorder module.
displayed on the INFO page of the When the paper is properly set into the Clean the paper sensor with a cotton swab.
SYSTEM SETUP window. magazine and recorder door is firmly closed Refer to SVM-7500 series operator’s
but the “INSERT REC PAPER” message is still manual.
displayed: Paper sensor is dirty or failure in the Replace the RG-750X paper drive unit or
sensor or related circuit of the recorder. Recorder CTRL board
Waveforms and numeric data can be recorded Replace the RG-750X paper drive unit or
on the paper when you pull out the paper after Recorder CTRL board.
touching the [RECORD] key on the screen.
Nothing is recorded on the paper Failure in the Recorder CTRL board. Replace the Recorder CTRL board.
and the model number, WS-752P, is Failure in the Main board. Replace the Main board.
not displayed on the INFO page of
the SYSTEM SETUP window. Failure in the recorder connection cable. Replace the recorder connection cable
Some garbled numeric data Failure in the Recorder CTRL board. Replace the Recorder CTRL board.
recorded on the paper. Failure in the Main board. Replace the Main board.
The platen roller or gears are dusty or damaged. Clean the platen roller and gears. If the
Waveforms and numeric data problem is still there, replace the RG-
recorded on the paper are distorted 750X paper drive unit.
because the paper speed is unstable. The rotation of the motor is unstable. Replace the RG-750X paper drive unit or
Main board.
Dirt on the thermal array head. Clean the thermal array head.
The thermal array head is improperly attached. Remove the thermal array head and
Waveforms and grid recorded on reattach it properly.
the paper have a faint part. The recorder door is not firmly closed. Close the recorder door firmly.
Failure in the thermal array head. Replace the RG-750X paper drive unit.
Failure in the Recorder CTRL board. Replace the Recorder CTRL board
USB Memory
The USB memory is not inserted properly. Remove and insert the USB memory into the
slot.
USB error is displayed. Failure in the USB memory. Replace the USB memory.
Failure in the LAN&USB board. Replace the LAN&USB board.

2. TROUBLESHOOTING
ECG
When “Check electrode” is displayed, there are the
following possible causes.
• Failure in the path from patient to ECG input socket. Replace the electrodes.
• The electrode peels or the gel of the electrode is dry. Replace the electrodes.
• Contact impedance between the electrode and the skin Perform the skin preparation before
is high. attaching the electrode.
ECG waveform does not • The instrument is not properly grounded. Ground the instrument properly.
appear on the screen.
• The patient cable is not firmly connected. Firmly connect the patient cable.
• Failure in the patient cable. Replace the patient cable.
• The number of electrodes is wrongly set on the Select [3] in the setting of the number of
instrument. electrodes.
• If none of the above problems are found but “Check Replace the ECG internal cable or Main
electrode” is still displayed after you short-circuit all the board.
electrode lead wires: Failure in the ECG internal cable
or Main board.
When “NOISE” is displayed, there are the following

possible causes.
• Failure in the path from patient to ECG input socket. Replace the electrodes.
• The electrode peels or the gel of the electrode is dry. Replace the electrodes.
• Baseline drift or EMG on the ECG due to body Attach new electrodes to different
movement. positions so that the affection of body
movement is reduced.
• Contact impedance between the electrode and the skin Perform the skin preparation before
is high. attaching the electrode.
• The instrument is not properly grounded. Ground the instrument properly.
• If none of the above problems are found and “NOISE” Replace the ECG internal cable or Main
is still displayed after you short-circuit all the electrode board.
lead wires: Failure in the ECG internal cable or Main
board.
Heart rate cannot be counted
correctly. Heart rate is not accurate.
• The patient has a pacemaker but pacing detection is set Set the pacing detection to ON.
to OFF.
• The patient’s condition changed and the current ECG Perform “Learning ECG.”
template is different from the previous ECG reference
template.
• When electrosurgical unit (ESU) is used: High Reduce the high frequency noise by
frequency noise on the ECG waveform. changing the positions of electrodes
and return plate. Refer to “Use with
an Electrosurgical Unit” in “ECG
Monitoring” section of the user’s guide.
• When the pacing mark appears on the ECG frequently:
- The instrument is not properly grounded. Ground the instrument properly.
- The electric blanket is not shielded. Use a shield cover.
• If none of the above problems are found and the Replace the ECG internal cable or Main
baseline is unstable after you short-circuit all the board.
electrode lead wires: Failure in the ECG internal cable
or Main board.

2. TROUBLESHOOTING
Respiration (Impedance Method)

2
“RESP OFF” message is displayed on the screen. Set the IMPEDANCE MEASUREMENT
This means that the impedance method respiration to ON in the RESP window.
measurement is set to OFF.
“- - -” is displayed instead of the respiration rate
(RR).
• The electrode peels or the gel of the electrode Replace the electrodes.
is dry.
• The maker of the electrodes is not Shanghai Use Shanghai Kohden electrodes.
Impedance method respiration Kohden.
waveform does not appear.
• Contact impedance between the electrode and Perform the skin preparation before
the skin is high. attaching the electrodes to the patient.
• Patient cable is not properly connected. Properly connect the patient cable.
• The patient cable has a break. Replace the patient cable.
baseline is still unstable after you short-circuit board.
all the electrode lead wires: Failure in the ECG
internal cable or Main board.
When the respiration rate on the screen is different
from the respiration rate manually counted, there
are the following possible causes.
• The electrode peels or the gel of the electrode Replace the electrodes.
is dry.
• The maker of the electrodes is not Shanghai Use Shanghai Kohden electrodes.
Kohden.
• Contact impedance between the electrode and Perform the skin preparation before
the skin is high. attaching the electrodes to the patient.
• The patient cable is not properly connected. Properly connect the patient cable.
• The patient cable has a break. Replace the patient cable.
• The baseline drifts due to body movement Change the positions of the two electrodes
Respiration rate cannot be counted or a waveform that is synchronous with the for the respiration pickup so there is less
correctly. heartbeat is mixed in the respiration waveform. effect.
Set the “NOISE REDUCTION ON
IMPEDANCE RESP” in the System Setup
window to ON.
• When an electrosurgical unit (ESU) is used, Reduce the high frequency noise by
high frequency noise is on the respiration changing the positions of electrodes
waveform. and return plate. Refer to “Use with
an Electrosurgical Unit” in “ECG
Monitoring” section of the user’s guide.
baseline is still unstable after you short-circuit board.
all the electrode lead wires: Failure in the ECG
internal cable or Main board.

2. TROUBLESHOOTING
CO2 (SVM-7503/7523)
Mainstream Method
CO2 is mixed in the inspiration. (TG-901T4 / Refer to the CO2 section.
TG-921T4 only)
The measurement is performed where Consider the atmospheric pressure when
atmospheric pressure is low, such as at high making evaluations.
altitude. (TG-901T4 / TG-921T4 only)
The measured value is low. Zero calibration is not performed. (TG-971T4 / Calibrate the CO2 sensor.
TG-981T4 only)
A Jackson Rees respiration circuit or Mapleson Cannot measure correctly.
D respiration circuit is connected to the patient.
(TG-971T4/TG-981T4 only)
The airway adapter/nasal adapter is dirty. Replace the adapter with a new one.
Anesthetic gas is used. Set the correct inspired gas composition.
The measured value is high.
N2O: 2 L/min, sevoflurane: 1 % Refer to “Changing the CO2 Settings”.
Oscillation. Check the respirator and remove the cause.
Doing suction with a suction catheter in the Do not let the suction catheter in the airway
airway adapter. adapter.
The measured value is inaccurate.
The airway adapter/nasal adapter is dirty. Replace the adapter with a new one.
The respiration rate of the patient is very high or Cannot measure correctly.
respiration is irregular.
Oscillation. Check the respirator and remove the cause.
The respiration waveform does not
appear. The airway adapter/nasal adapter is Connect the adapter to the CO2 sensor kit.
disconnected from the CO2 sensor kit.
CO2 sensor or CO2 adapter is faulty. (TG-901T4 Replace the CO2 sensor or CO2 adapter with
/ TG-921T4 only) a new one.
The red LED on the CO2 adapter
blinks. Apnea for longer than 20 seconds. (TG-901T4 / The red LED blinks when apnea is longer
TG-921T4 only) than 20 seconds regardless of the alarm
setting on the monitor.
Less than three respirations are detected. The measured value is displayed after three
or more respirations are detected.
After respiration detection, respiration is not The measured value is displayed after
detected for 40 seconds or more. The time respiration is detected.
depends on the APNEA setting.
The measured value is displayed as Zero calibration is performed. (TG-971T4/TG- After zero calibration, the measured value
“---”.
981T4 only) is displayed as “---”. The measured value
is displayed after three or more respirations
are detected.
High frequency oscillatory ventilation (HFOV) ETCO2 value and respiration rate cannot be
is being performed. measured during HFOV.
Temperature (TEMP)
When another working temperature probe is Replace the temperature probe.
connected to the input jack and the temperature
value appears: Failure in the probe.
Cannot be measured. When another working temperature probe is Replace the TEMP board or Main board.
connected to the input jack but the temperature
value does not appear: Failure in the TEMP board
or Main board.

2. TROUBLESHOOTING
Non-Invasive Blood Pressure (NIBP)

2
When “SAFETY CIRCUIT RUNNING” message Before starting the measurement after 30
is displayed, the cuff inflation is disabled for 30 seconds, check that there is no blockage
seconds. in the cuff and air hose and no excessive
The cuff can not inflate. pressure to the patient.
When you touch the NIBP [Start/Stop] key but Replace the pump or Main board.
there is no sound of the pump: Failure in the
pump or pump drive circuit.
When you touch the NIBP [Start/Stop] key and Replace the cuff or air hose.
there is sound of the pump but the pressure does Check each component of the pneumatic
not reach the target pressure, the cuff or air hose circuit and replace it if necessary.
has air leak or there is a failure in the pneumatic Replace the valve or Main board.
circuit, valve or valve drive circuit.
The cuff can inflate. When remeasurement starts after step deflation Attach the cuff to the patient properly.
and finally “MEAS TIMEOUT” appears: The cuff Find any cause which can give vibration or
is not properly attached to the patient, vibration or pressure to the cuff or air hose, and remove
external pressure is applied to the cuff or air hose, the cause.
or failure in the oscillation signal amplification Replace the Main board.
circuit of the Main board.
Invasive Blood Pressure, IBP (SVM-7503/7523)

Air bubbles remain in the circuit. Remove the air bubbles.
An extra tube is connected in the circuit. Remove the extra tube.
The position of the blood pressure transducer is Check the position of the blood pressure
The acquired blood pressure inappropriate. transducer.
value is different from the
estimated value. A blood pressure transducer with different Check the blood pressure transducer.
sensitivity is used.
Other causes. Perform zero balance adjustment again.
The measurement is out of range. Check the measuring condition.
The blood pressure transducer is damaged. Replace the blood pressure transducer with a
No invasive blood pressure value new one.
appears on the screen.
Failure in the IBP internal cable. Replace the IBP internal cable.
SpO2
When “MODULE ERROR” is displayed on the screen: Replace the Main board.
Failure in the Main board.
When “CONNECTOR OFF” or “CHECK PROBE” is Replace the SpO2 connection cord, SpO2
displayed on the screen: Failure in the SpO2 connection probe, SpO2 internal cable or Main board.
cord, SpO2 probe, SpO2 internal cable or Main board.
When “WEAK PULSE” or “CANNOT DETECT Replace the SpO2 connection cord or probe.
PULSE” is displayed: failure in the SpO2 connection
Cannot be measured. cord or SpO2 probe.
When the message is still there after the connection cord Solve the problem. Refer to “Screen
and probe are replaced with new ones, connect an AX- Messages” section in the operator’s manual.
410G vital sign simulator or AX-300T SpO2 simulator Replace the SpO2 internal cable or Main
to the SpO2 socket instead. If there is no message, the board.
instrument and accessories have no problem. If there is
still one of the two messages, there is a failure is in the
SpO2 internal cable or Main board.

2. TROUBLESHOOTING
Error Code and History
The error history records the results of the self tests which are automatically
executed when the power is turned on, and the errors which are detected while
the instrument is in operation. The error history shows the history of past
failures. The error history is deleted only if the system is initialized. The error
history may contain the following error codes.
Error Code List

Details Error Descriptions
1 **** ZERO DIVIDE **** Error of division by zero (divided by zero).
2 **** UNDEFINED INSTRUCTION **** An undefined instruction was given.
3 **** PREFETCH ABORT **** An unauthorized instruction was fetched.
4 **** DATA ABORT/WP ERROR **** An unauthorized address was accessed.
5 **** SYSTEM ERROR **** A system error occurred (SYSTEM_ERROR in the large classification occurred).
6 **** WATCHDOG ERROR **** An interruption by the watchdog timer occurred.
7 **** UNKNOWN ERROR **** A system shutdown occurred due to causes other than the above.

3
Displaying the DIAGNOSTIC CHECK
Diagnostic Check
and Safety Check
Checking on the Home Screen................3-36

3
Screen........................................................3-2 Displaying the Home screen.............................. 3-36

Displaying the MANUAL CHECK Screen............. 3-3 Check Items on the Home Screen..................... 3-36
Check Items on the MANUAL CHECK Screen..... 3-4 Checking the Date and Time.............................. 3-37
Checking the NAND............................................. 3-6 Checking the ECG.............................................. 3-38
Checking the FRAM............................................. 3-7 Checking the Respiration................................... 3-40
Checking the Touch Key Operation...................... 3-8 Checking the SpO2 Value................................... 3-41
Calibrating the Touch Panel.............................3-9 Checking the Temperature................................. 3-43
Checking the RAM............................................. 3-10
Checking the IBP (SVM-7503/7523 only)........... 3-44
Checking the Sound Output............................... 3-11
Checking the CO2 Value (SVM-7503/7523
Checking the Alarm Indicator............................. 3-12 only).................................................................... 3-46
Checking the Backlighting.................................. 3-13 Checking Other Essential Performance of
Checking the WS-752P Recorder Module......... 3-14 the Monitor.....................................................3-52
Checking the GRAPHIC DRAW......................... 3-16 Safety Check............................................3-53
Checking the IMAGE DRAW.............................. 3-17
Checking the NIBP............................................. 3-18
Preparation (Equipment Connection)............. 3-18
Checking the Pressure Measurement
Accuracy (1. CALIBRATION)......................... 3-19
Zero Calibration (2. ZERO CALIBRATION)... 3-21
Checking the Safety Circuit (3. SAFETY
CHECK).........................................................3-22
Checking the Pressurization Speed (4.
INFLATION SPEED)...................................... 3-26
Checking the Held Pressure (5.
PRESSURE HOLD).......................................3-29
Checking the Operation of the Solenoid
Valve (6. STEP DEFLATION)......................... 3-31
Checking the Operation of the Air Circuit
(8. AIR CIRCUIT)...........................................3-34
Checking the Essential Performance.............3-35
3. DIAGNOSTIC CHECK AND SAFETY CHECK
Displaying the DIAGNOSTIC CHECK Screen

Use this screen to view the error history or perform manual check or system
setup and initialization.
CAUTION
This procedure interrupts all monitoring. Only change these settings
before or after monitoring.
1 Turn off the instrument.
2 Press the [POWER] key for about 5 seconds until the DIAGNOSTIC
CHECK screen is displayed.
xx.xx.xx.xx xx.xx.xx.xx xx.xx.xx.xx

xxxxxxxx xxxxxxxx xxxxxxxx
xx.xx xx.xx.xx
xxxxxxxx xxxxxxxx
3 To exit the DIAGNOSTIC CHECK screen and return to the home screen,
touch the [RETURN] key.
You can also open the DIAGNOSTIC CHECK screen by checking the <RUN
SYSTEM CONFIGURATION AT NEXT POWER ON.> check box on the
SYSTEM CONFIG table on the SYSTEM SETUP window. The DIAGNOSTIC
CHECK window appears when the instrument is turned on again after turning it
off.

Displaying the MANUAL CHECK Screen

1 Touch the [MANUAL CHECK] key. The password dialog box appears.
xx.xx.xx.xx x xx.xx
xxxxxxxx xxxxxxxx
xx.xx
xxxxxxxx
2 Enter the password with the number keys and touch the [ENT] key. The
default password is “1234”.
The MANUAL CHECK screen appears.
3 To exit the MANUAL CHECK screen and return to the DIAGNOSTIC

CHECK screen, touch the [RETURN] key.

Check Items on the MANUAL CHECK Screen

You can check the following items on the MANUAL CHECK screen.
NAND check
Check the NAND in the instrument and confirm that there is no problem on the
main board.
FRAM check
Check the FRAM in the instrument and confirm that there is no problem on the
main board.
TOUCH KEYS check

Check that the touch key works correctly.
RAM check
Check the RAM in the instrument and confirm that there is no problem on the
main board.
SOUND check
Check the alarm, sync and key click sounds. Also, confirm the status of power,
amplifier and sound volume.
ALARM INDICATOR check

Check the alarm indicator.
BACKLIGHT check
Check the display brightness.
GRAPHIC DRAW check

Check that LCD displays properly with no missing pixels.
IMAGE DRAW check

Check the images in the instrument.
IBP check (SVM-7503/7523 only)

Factory use only.

TEMP check
Factory use only.
DPU AD TEST check

Factory use only.
3
ECG check
Factory use only.
EPU AD TEST check

Factory use only.
NIBP check
Check the accuracy of NIBP measurement such as pressure sensor, zero
calibration, inflation speed, pressure hold, step deflation, air circuit.
NPU VER check

Check the version of NPU.
WS RECORDER check
Check that WS-752P recorder module works correctly.
RTC check
Check and set the RTC.

Checking the NAND

Check the NAND FLASH in the instrument to make sure that the main board is
not defective.
1 On the MANUAL CHECK screen, touch the [NAND] key to display the
NAND CHECK screen.
2 Touch the [START] key and make sure that no error indication appears.
3 Touch the [STOP] key to stop checking the NAND.
4 Touch the [RETURN] key to return to the MANUAL CHECK screen.

Checking the FRAM

Check the FRAM in the instrument to make sure that the main board is not
defective.
1 On the MANUAL CHECK screen, touch the [FRAM] key to display the 3
FRAM CHECK screen.
2 The FRAM is checked automatically. On the FRAM CHECK screen, check

that the PASS COUNT value increments from 0000 in steps of 1. Make sure
that no error indication appears.
When there is no error indication and the count is increased from 0000 to
0001, it is the end of the check.

Checking the Touch Key Operation

Check that the touch key position is correct.
1 On the MANUAL CHECK screen, touch the [TOUCH KEYS] key to

display the confirmation screen for touch keys.
2 Touch somewhere on the screen and check that the “@” confirmation mark
moves to the touched position.
If the touched position does not match the “@” confirmation mark, perform
the procedure explained in “Calibrating the Touch Panel” on the next page.
3 Press the [POWER] key to return to the MANUAL CHECK screen.

Calibrating the Touch Panel

Calibrate the touch screen if the pressed position and the activated position do
not match.
1 Turn the monitor power off.

3
2 Press [POWER] key for about 5 seconds until DIAGNOSTIC CHECK
screen is display.
Or, check the “RUN SYSTEM CONFIGURATION AT NEXT POWER
ON.” box in SYSTEM - MAINTENANCE - SYSTEM CONFIG window,
then turn the monitor power off. And then turn on the monitor.
3 Press [POWER] key twice. The TOUCHPANEL CALIBRATION screen

appears.
4 Touch the @ mark at the upper left corner of the screen for 2 seconds. When
the mark is correctly touched, another mark appears in the lower right corner
of the screen. Touch the mark for 2 seconds.
When the marks are touched correctly, the “TOUCHPANEL
CALIBRATION SUCCEEDED” message appears, then the DIAGNOSTIC
CHECK screen appears.

Checking the RAM

Check the RAM in the instrument to make sure that the main board is not
defective.
1 On the MANUAL CHECK screen, touch the [RAM] key to display the CPU
RAM CHECK screen.
2 The RAM is checked automatically. On the CPU RAM CHECK screen,

check that the PASS COUNT value increments from 00000 in steps of 1.
This takes about 30 seconds. Make sure that no error indication appears.
When there is no error indication and the count is increased from 00000 to
00001, it is the end of the check.

Checking the Sound Output

Generate the alarm sound, synchronous sound and key sound to check the status
of the sound source and the amplifier. Also, check the sound volume.
1 On the MANUAL CHECK screen, touch the [SOUND] key to display the 3
SOUND CHECK screen.
2 Check the sound output.

i) Select the type of sound to be checked.
ii) Check that the volume of the selected sound changes when you slide the
volume setting bar vertically or touch the [up] and [dn] keys.
Volume setting bar
ii
MUTE
Touch the [MUTE] key to
silence the sound for a while.

Checking the Alarm Indicator

This item checks the function of the alarm indicator on the top of the monitor.
Check that the indicator lights according to the screen indication.
1 On the MANUAL CHECK screen, touch the [ALARM INDICATOR] key to

display the INDICATOR CHECK screen.
2 The RED, YELLOW and GREEN indicators on the screen are highlighted in
order. Check that the highlighted color also appears on the alarm indicator on
top of the monitor.
If the color does not light, the connection cable is loose or disconnected or
the Main board or indicator board is faulty. If the indicator lights partially,
the indicator board is faulty.

Checking the Backlighting

Check the display’s brightness adjustment function.
1 On the MANUAL CHECK screen, touch the [BACKLIGHT] key to display

the BACKLIGHT CHECK screen. 3
2 Check that the screen brightness changes by sliding the brightness

adjustment bar vertically.

Checking the WS-752P Recorder Module

This item checks whether the WS-752P record module works well.
1 On the MANUAL CHECK screen, touch the [WS RECORDER] key to enter
recorder check screen.
2 Touch the [SELF TEST 1] key to perform test recording, then confirm
“SYSTEM CHECK OK” is recorded on the recording paper.
xx.xx
XX . XX . XX
Confirm that "SYSTEM CHECK OK" is displayed on

the recording paper.

3 Touch the [SELF TEST 7] key to perform test recording. Continue to record
for more than 10 cm, then confirm the recording is recorded well with no
missing pixels.
xx.xx
4 Touch the [RETURN] key to return to MANUAL CHECK screen.

Checking the GRAPHIC DRAW

This item checks the screen color. Check that the LCD displays properly with no
missing pixels.
1 On the MANUAL CHECK screen, touch the [GRAPHIC DRAW] key to test
the graphic draw function.
2 Touch anywhere on the screen. The following will be shown in order. Check
that there are no missing pixels.
● ALL OVER WHITE WINDOW PLANE
● ALL OVER BLACK WINDOW PLANE
● ALL OVER RED WINDOW PLANE
● ALL OVER GREEN WINDOW PLANE
● ALL OVER BLUE WINDOW PLANE
● ALL OVER YELLOW WINDOW PLANE
● ALL OVER PURPLE WINDOW PLANE
● ALL OVER SKY BLUE WINDOW PLANE
● FULL COLOR
● REGIST COLOR
3 Press the [POWER] key to return to the MANUAL CHECK screen.

Checking the IMAGE DRAW

This item checks the images in the instrument.
1 On the MANUAL CHECK screen, touch the [IMAGE DRAW] key to test
the image draw function. 3
2 On the IMAGE DRAW screen, all the images can be shown.

Current image Current image index Total images count
Go to the image whose

Previous image index is current index -10.
Go to the image whose

Next image index is current index +10.

Checking the NIBP

Check the NIBP for measurement accuracy and other factors. This manual
explains a method of verification with a manometer.
Preparation (Equipment Connection)

Before checking the NIBP, connect the following parts (1) to (4) to a manometer
as shown below. In the following procedure, the term “manometer” refers to
what is connected with the (1) to (4) parts.
Part Name Code Number Q’ty
(1) Silicon tube 4 (diameter) L150 6114-110213 6
(2) SMM-02 air joint (male) 531524 3
(3) SMF-02 air joint (female) 538624 1
(4) T-type coupling F-3145-85 551396 2
(1) (2) (3) (1) (4) (1)
(2) (1) (2)

(1) (1)
(4)
The following parts are used or changed depending on the check item. Prepare
the parts before starting the check. The connection diagram and the instructions
for use are explained in each section.
Part Name Type/Code Number Q’ty
Adult/child air hose (3 m) YN-701S -- 1
Neonate air hose (3 m) YN-721S -- 1
Clamp Purchase locally 1
Luer fitting (male) for neonate air hose 930272 1
Air tank 70 cc (dummy cuff) 626262 1

Checking the Pressure Measurement Accuracy (1. CALIBRATION)

A manometer is used to check the pressure measurement accuracy.
1 Connect the instrument, adult air hose (3 m), a manometer, and a 700 cc air
tank as shown below.
3
Air tank Manometer Adult air hose (3 m) Bedside monitor

(700 cc)
2 Turn on the manometer.
3 On the MANUAL CHECK screen, touch the [NIBP] key to display the
NIBP CHECK screen.
4 The zero calibration is automatically performed when the NIBP CHECK

screen is displayed. Check that the CUFF PRESSURE becomes 0 and OK is
displayed.

5 Run the check.

i) On the NIBP CHECK screen, touch the [1-1. CALIBRATION] and
[START] key.
Touching the [STOP] key stops the check.
ii) Using a rubber bulb, apply pressure until the value shown on the
manometer reaches a value between 0 and 300 mmHg. Check that the
value shown on the manometer and the values shown in the screen’s
SENSOR 1 and SENSOR 2 meet the requirement of the tables below.
Check the values shown in <SENSOR 1> and <SENSOR 2>
<SENSOR 1>
Indication of the Manometer
Indication of <SENSOR 1>
(Pressurized Value)
Value of the manometer ± 3 mmHg
0 to 300 mmHg (If the reading is 0 mmHg, then it is always at
0 mmHg.)
<SENSOR 2>
Indication of the Manometer
Indication of <SENSOR 2>
(Pressurized Value)
Value of the manometer –2 to +3 mmHg
0 to 15 mmHg (If the reading is 0 mmHg, then it is always at
0 mmHg.)
16 to 200 mmHg Value of the manometer ± 8 mmHg
201 to 300 mmHg Value of the manometer ± 12 mmHg
6 When the check is completed, touch the [2-1. ZERO CALIBRATION] key
to perform the procedure explained in the next section “Zero Calibration (2.
ZERO CALIBRATION)”.

Zero Calibration (2. ZERO CALIBRATION)
1 On the NIBP CHECK screen, check that <2-1. ZERO CALIBRATION> is

highlighted.
2 Run the zero calibration.

3
i) Check that the air tank is completely exhausted and touch the [START]
key.
ii) Check that the <CUFF PRESSURE> value reaches 0 and that the OK
appears.
Check that <2-1. ZERO CALIBRATION> is highlighted.
Check that the <CUFF PRESSURE> value reaches 0

and that the OK appears.
3 Touch the [3-1. OVER PRESS 1] key to perform the procedure explained in
the next section “Checking the Safety Circuit (3. SAFETY CHECK)”.

Checking the Safety Circuit (3. SAFETY CHECK)

Using a manometer, check the operation of each safety circuit in adult/child
mode and in neonatal mode.
1 On the NIBP CHECK screen, check that <3-1. OVER PRESS 1> is
highlighted.
2 Run the check in adult/child mode.

Checking in Adult/Child Mode
i) Touch the [START] key to start the check procedure in <3-1. OVER
PRESS 1>. ADULT is displayed in <3. SAFETY CHECK>.
ii) Apply pressure quickly from the rubber bulb until the <CUFF
PRESSURE> value reaches 300 mmHg.
iii) Once the <CUFF PRESSURE> value reaches 300 mmHg, apply pressure
slowly from the rubber bulb.
iv) During pressurization, the pressure limiter (safety circuit) works to release
the pressure. Check that the OK appears when the value shown in <3-1.
OVER PRESS 1> is between 300 and 330 mmHg.
While the pressure limiter is working (the pressure is being released), the
“SAFETY CIRCUIT ON” message is highlighted at the bottom right of the
screen.
The pressurized value is displayed.
Select ADULT
This is the pressurized value measured

when the pressure limiter (safety circuit)
is working. Check that OK appears when
the displayed value is between 300 and 330
mmHg.
While the pressure limiter is working (the pressure is

being released), the “SAFETY CIRCUIT ON” message
is highlighted.

v) Touch the [3-2. OVER PRESS 2] key.
vi) Touch the [START] key to start the check procedure in <3-2. OVER
PRESS 2>.
vii) Apply pressure quickly from the rubber bulb until the <CUFF
viii) Once the <CUFF PRESSURE> value reaches 300 mmHg, apply pressure
slowly from the rubber bulb and keep the value for a while in the range
from 300 to 310 mmHg.
ix) While this value is continued, the pressure limiter (safety circuit) works
to release the pressure. Check that OK appears when the value shown in
<3-2. OVER PRESS 2> is between 0 second and 15 seconds.
“SAFETY CIRCUIT ON” message is highlighted at the bottom right of the
screen.
The elapsed time, which is measured until the pressure limiter

(safety circuit) starts operating, is displayed. Check that OK
appears when the displayed value is between 0 and 15 s
While the pressure limiter is working (the pressure

is being released), the “SAFETY CIRCUIT ON”
message is highlighted.

3 When the check in adult/child mode is completed, touch the [3-1. OVER
PRESS 1] key.
4 Run the check in neonatal mode.

Checking in Neonatal Mode
i) Using a neonatal air hose (3 m), reconnect between the instrument and the
manometer. Before connecting a neonatal air hose (3 m), change the CPC
SMM-02 air joint to a VRS 306 luer fitting (male).
Change the CPC SMM-02 air joint to a VRS 306 luer fitting (male)
before connecting a neonatal air hose (3 m).
Air tank Manometer Reconnect by using a Bedside monitor

(700 cc) neonatal air hose (3 m)
ii) Touch the [START] key to start the check procedure in <3-1. OVER
PRESS 1>. Check that NEO is displayed in <3. SAFETY CHECK>.
iii) Apply pressure quickly from the rubber bulb until the <CUFF
iv) Once the <CUFF PRESSURE> value reaches 150 mmHg, apply pressure
slowly from the rubber bulb.
v) During pressurization, the pressure limiter (safety circuit) works to release
the pressure. Check that OK appears when the value of <3-1. OVER
PRESS 1> is between 150 mmHg and 165 mmHg.

“SAFETY CIRCUIT ON” message is highlighted at the bottom right of
the screen.
This is the pressurized value measured when

the pressure limiter (safety circuit) is working.
Check that OK appears when the displayed
value is between 150 mmHg and 165 mmHg.
3
Select NEO
While the pressure limiter is

The pressurized value is displayed. working (the pressure is being
released), the “SAFETY CIRCUIT
ON” message is highlighted.
5 When the check in neonatal mode is completed, touch the [4-1. ADULT]
key to perform the procedure explained in the next section “Checking the
Pressurization Speed (4. INFLATION SPEED)”.

Checking the Pressurization Speed (4. INFLATION SPEED)

Check the pressurization speed in adult/child mode and in neonatal mode.
1 After the check in neonatal mode is run in the previous “Checking the
Safety Circuit (3. SAFETY CHECK)” section, use an adult air hose (3 m) to
reconnect between the instrument and the manometer. Before connecting an
adult air hose (3 m), change the VRS 306 luer fitting (male) to a CPC SMM-
02 air joint.
2 Clamp the silicon tube which connects the manometer and the rubber bulb
with a clip.
NOTE: Connecting a rubber bulb lets a small amount of air leak out
during pressurization. As shown, therefore, use a clip to firmly
clamp the silicon tube connecting the manometer and the rubber
bulb. Alternatively, you can remove the manometer and connect
the air tank directly to the adult air hose (3 m).
Change the VRS 306 luer fitting (male) to a CPC SMM-02
air joint before connecting an adult air hose (3 m).
Use a clip to clamp the tube.
Bedside monitor
Air tank Manometer Reconnect by using an
(700 cc) adult air hose (3 m).
3 Run the check in adult/child mode.

Checking in Adult/Child Mode
i) On the NIBP CHECK screen, check that <4-1. ADULT> is highlighted.
ii) Touch the [START] key to start the check procedure in <4-1. ADULT>.

iii) Automatic pressurization starts. Pressurization continues until the

<CUFF PRESSURE> value reaches 200 mmHg, and it is followed by
air evacuation. Check that OK appears when the value displayed in <4-1.
ADULT> is between 0 second and 11 seconds.
Check that <4-1. ADULT> is highlighted.

3

The pressurization time, which is measured
until the <CUFF PRESSURE> value reaches
200 mmHg, is displayed. Check that OK
appears when the displayed value is between 0
and 11 seconds.
4 When the check in adult/child mode is completed, touch the [SELECT

NEXT] key to highlight <4-2. NEONATAL>.
5 Run the check in neonatal mode.

Checking in Neonatal Mode
i) Replace the air tank with a 70 cc tank.
Change a CPC SMM-02 air joint to the VRS

306 luer fitting (male) before connecting an
neonatal air hose (3 m).
Air tank Bedside monitor

Manometer Reconnect by using an
(70 cc) neonatal air hose (3 m).

ii) Touch the [START] key to start the check procedure in <4-2.
NEONATAL>.
iii) Automatic pressurization is started. Pressurization continues until the
<CUFF PRESSURE> value reaches 200 mmHg, and it is followed by
air evacuation. Check that OK appears when the value displayed in <4-2.
NEONATAL> is between 0 and 7 seconds.
The pressurization time, which is measured

until the <CUFF PRESSURE> value reaches
200 mmHg, is displayed. Check that OK
appears when the displayed value is between
0 and 7 seconds.
6 When the check in neonatal mode is completed, touch the [SELECT NEXT]
key to perform the procedure explained in the next section “Checking the
Held Pressure (5. PRESSURE HOLD)”.

Checking the Held Pressure (5. PRESSURE HOLD)

Check the held pressure.
1 After you have performed the check in neonatal mode according to the
previous section “Checking the Pressurization Speed (4. INFLATION
SPEED)”, use an adult air hose (3 m) to reconnect between the instrument 3
and the manometer and remove the clip from the silicon tube connecting the
manometer and the rubber bulb. Also, replace the air tank with a 250 cc tank.
Before connecting an adult air hose (3 m), change the VRS 306 luer fitting
(male) to a CPC SMM-02 air joint.
NOTE: Using an adult air hose (1.5 m) and a neonatal air hose prevents
you from making accurate inspection in the following items.
Change the VRS 306 luer fitting (male) to a CPC SMM-02
air joint before connecting an adult air hose (3 m).
Air tank Manometer Reconnect by using an Bedside monitor

(250 cc) adult air hose (3 m).
2 Run the check.

i) On the NIBP CHECK screen, check that <5-1. PRESSURE HOLD> is
highlighted and touch the [START] key. The [START] key is replaced
with the [MEASURE START] key.
Check that <5-1. PRESSURE HOLD> is highlighted.
Changed to MEASURE START.
ii) Apply pressure from the rubber bulb until the <CUFF PRESSURE> value
reaches 250 mmHg.

iii) When the <CUFF PRESSURE> value reaches 250 mmHg, use a clip to
clamp the silicon tube connecting the manometer and the rubber bulb,
thus stopping the pressurization.
bulb.
Bedside monitor
Air tank Manometer Adult air hose (3 m)
(250 cc)
iv) Touch the [MEASURE START] key to start the test.

v) The “CUFF PRESSURE” values of 10 second and 20 second later (10sec
and 20sec) and the difference (Diff) between them are automatically
measured. Check that the Diff value does not exceed 5 mmHg and OK
appears.
10sec, 20sec
These are the pressurized values measured in 10 seconds and
20 seconds after the [MEASURE START] key is touched.

Diff
This displays the difference between the 10sec and
20sec items. Check that OK appears and that the
measured value does not exceed 5 mmHg.
3 When the check is completed, touch the 6-1. V1 250 mmHg key to perform
the procedure explained in the next section “Checking the Operation of the
Solenoid Valve (6. STEP DEFLATION)”.

Checking the Operation of the Solenoid Valve (6. STEP DEFLATION)

Check the operation of the quick exhaust valve (V1) and the slow exhaust valve
(V2). 3
1 Reconfirm that the following components are connected as shown: the
instrument, an adult air hose (3 m), a manometer, and an air tank.
NOTE
• Using an adult air hose (1.5 m) and a neonatal air hose
prevents you from making accurate inspection.
• Change the capacity of the air tank depending on the check
items.
Air tank Manometer Adult air hose (3 m) Bedside monitor

V1: 250 cc
V2: 70 cc
2 Repeat steps i) to v) to check all of the following items: <6-1. V1 250

mmHg>, <6-2. V2 250 mmHg>, <6-3. V1 20 mmHg>, and <6-4. V2 20
mmHg>.
i) On the NIBP CHECK screen, check that the check items are highlighted
and touch the [START] key. The [START] key is replaced with the
[MEASURE START] key.
Check that the check item is highlighted.

Changes to the [MEASURE START] key.
ii) Apply pressure from the rubber bulb until the <CUFF PRESSURE> value
reaches the value shown below. (For details about the pressurized value,
refer to the table below.)
<CUFF PRESSURE>
Item Name Air Tank Capacity
Value
6-1.V1 250 mmHg 250 cc
250 mmHg
6-2.V2 250 mmHg 70 cc
6-3.V1 20 mmHg 250 cc
20 mmHg
6-4.V2 20 mmHg 70 cc
iii) When the <CUFF PRESSURE> value reaches 250 mmHg, use a clip to
clamp the silicon tube connecting the manometer and the rubber bulb,
thus stopping the pressurization.
bulb.
Bedside monitor
Air tank Manometer Adult air hose (3 m)
(250 cc)
iv) Touch the [MEASURE START] key to start the test.

v) Check that OK appears when the measured value shown in each item
meets the requirement of the table below.
<CUFF PRESSURE>
Item Name Air Tank Capacity
Value
6-1.V1 250 mmHg 250 cc 7 mmHg to 23 mmHg
6-2.V2 250 mmHg 70 cc 5 mmHg to 15 mmHg 3
6-3.V1 20 mmHg 250 cc
2 mmHg to 8 mmHg
6-4.V2 20 mmHg 70 cc
Check that the measured value of

each item and OK appear.
vi) Touch the [6-2. V2 250 mmHg], [6-3 V1 20 mmHg] or [6-4. V2 20

mmHg] key to select the check item.
3 Once the check ranging from <6-1. V1 250 mmHg> to <6-4. V2 20 mmHg>
is completed, touch the [8-1. AIR CIRCUIT] key to perform the procedure
shown in the next section “Checking the Operation of the Circuit (8. AIR
CIRCUIT)”.

Checking the Operation of the Air Circuit (8. AIR CIRCUIT)

Check the operation of the air circuit.
1 Remove the air hose from the NIBP socket.
2 Run the check.

i) On the NIBP CHECK screen, check that <8-1. AIR CIRCUIT> is
highlighted and touch the [START] key. Automatic check starts.
ii) When the check is completed, check that the measured value and the OK
appear in <8. AIR CIRCUIT>.
Check that <8. AIR CIRCUIT> is highlighted.
Check that the measured value and the OK appear.

Checking the Essential Performance

Check the following essential performance according to the method(s) which is/
are stipulated in IEC 80601-2-30:2009.
Requirement Subclause
Electrosurgery interference recovery 202.6.2.101 3
Limits of the error of the manometer, 201.12.1.102
201.11.8.102
or generation of a TECHNICAL ALARM CONDITION 201.12.1.101

Limits of the change in the error of the BLOOD 201.12.1.107
PRESSURE DETERMINATION and low and high
201.12.3.101
BLOOD PRESSURE PHYSIOLOGICAL ALARM
CONDITIONS (if provided),
or generation of a TECHNICAL ALARM CONDITION 201.11.8.102

201.12.1.101

Checking on the Home Screen

Check the operation of the instrument on the home screen. Checking on the
home screen requires you to change the system setup, alarm, and other settings.
Before changing the system setup, alarm, and other settings, write down the
current settings because they must be reset after maintenance.
Displaying the Home screen

Check the operation on the home screen referring to the following sections.
Refer to this section to display the home screen after checking on the MANUAL
CHECK screen, and go to the particular section for the specific check procedure.
1 On the MANUAL CHECK screen, touch the [RETURN] key to return to the
DIAGNOSTIC CHECK screen.
2 On the DIAGNOSTIC CHECK screen, touch the [RETURN] key to display

the home screen.
Check Items on the Home Screen

You can check the following items on the home screen.
Date and time

Check that the date and time is correct.
ECG check
• Heart rate accuracy and sync sound
• ECG sensitivity
• HR/RR and electrode-off alarm detection
RESP check
• Respiration count accuracy
• Respiration count alarm detection
SpO2 check
• SpO2 value and pulse rate accuracy
• SpO2 value and connector-off alarm detection

IBP check
• Accuracy of zero calibration
• Accuracy of blood pressure
• Connector-off detection
3
Temperature check
• Temperature accuracy
Set the temperature output from the AX-410G vital sign simulator and make
sure that the temperature shown on the instrument is within the accuracy range
shown in the table below.
AX-410G settings Indication on the instrument
25 °C 24.8 to 25.2 °C
37 °C 36.8 to 37.2 °C
44 °C 43.8 to 44.2 °C
• Connector-off detection check

Make sure that the connector-off is detected. While inputting the temperature
signal on the AX-410G vital sign simulator, remove the temperature cable plug
from the TEMP socket and make sure that you see a “CONNECTOR OFF”
message on the screen.
CO2 check
• Respiration rate and CO2 value accuracy
• Connector-off detection
Checking the battery

If the battery pack (SB-752P) is installed in the instrument, check that the battery
pack works correctly.
Checking the Date and Time

Check that the date and time settings on the instrument are correct.
1 Touch the [MENU] key to display the MENU window. You can also touch
the MENU function key to display the MENU window if the function key is
registered.
2 Touch the [DATE] key on the MENU window to display the DATE window.
Alternatively, you can touch the clock at the top right of the home screen to
display the DATE window.
3 Check that the date and time on the DATE window are correct.
If the displayed date and time are not correct, reset them.
4 Touch the [HOME] key to return to the home screen. Or, use the following
operations to return to the home screen.
● Touching the waveform display area
● Touching the HOME function key (Only when the function key is
registered.)

Checking the ECG

Connect the AX-410G vital sign simulator to the instrument, and check the
accuracy of the heart rate as well as the amplitude of ECGs in each lead.
Additionally, check whether the alarm works normally. To obtain stable
measurement accuracy, perform the accuracy check every six months.
After the check, return the current settings to your own settings.
Preparations
Connect the AX-410G* vital sign simulator to the instrument with the BJ-
753P/755P ECG patient cable.
* Ca lead is connected to V1.
AX-410G BJ-753P/755P Bedside monitor

ECG patient cable
Setting
Set the following items on the instrument.
ECG window Setting
Sensitivity x1
Lead II
Filter DIAG
Electrode 5
SYNC source ECG
Checking the Accuracy of the Heart Rate and the

Generation of Sync Sound
Set the output from AX-410G as the following table, and confirm whether the
heart rate displayed on the screen is in the range as shown in the table, and check
whether the SYNC sound is synchronized with QRS.
Setting of AX-410G Display of the bedside monitor
HR 20 18 beats/min ~ 22 beats/min

Checking the Detection of the Heart Rate and Electrode-

Off Alarms
Confirm whether the heart rate upper limit and lower limit alarm performance is
normal.
1 Set the following items on the bedside monitor. 3

ECG window Setting
HR/PR alarm Lower limit: 70
Lead II
2 Set the heart rate output from AX-410G to "HR 60", and check whether the
bedside monitor operates as follows.
Alarm Operation of the bedside monitor
Display of heart rate The value is highlighted
When “ARRHYTHMIA ANALYSIS” is ON:
Display of message
BRADYCARDIA
Alarm sound When “ARRHYTHMIA ANALYSIS” is OFF: HR alarm
Electrode There is a sound depending on the setting
Alarm indicator The indicator blinks or lights depending on the setting

Defibrillator protection 201.8.5.5.1
Interruption of the power supply / SUPPLY MAINS to ME
201.11.8
EQUIPMENT
Protection against depletion of battery 201.11.8.101
ESSENTIAL PERFORMANCE of ME EQUIPMENT 201.12.1.101
Electrosurgery interference 202.6.2.101
Time to alarm for heart rate ALARM CONDITIONS 208.6.6.2.103
TECHNICAL ALARM CONDITIONS indicating inoperable ME
208.6.6.2.104
EQUIPMENT

Checking the Respiration

Connect the AX-410G vital sign simulator to the instrument and check the
accuracy of the respiration rate. Also, check that the alarm works normally.
To obtain stable measurement accuracy, perform the accuracy check every six
months.
Preparation
Connect the AX-410G vital sign simulator to the instrument with the BJ-
753P/755P ECG patient cable.
AX-410G BJ-753P/755P Bedside monitor

ECG patient cable
Checking the Accuracy of the Respiration Rate

Check the accuracy of the respiration rate.
1 Set the following items on bedside monitor.

RESP/CO2 window Setting
Lead of impedence repiration R-F
Sensitivity x1
2 Set the heart rate output from AX-410G to "HR 60", and check whether
the respiration rate displayed on the bedside monitor is in the range of 18
minutes ~ 22 minutes.
The respiration rate output from AX-410G is 20 minutes.
Checking the Detection of Alarms for the Respiration

Rate
Confirm whether the respiration rate upper limit and lower limit alarm
performance is normal.
1 Set the following item on the bedside monitor.

RESP/CO2 window Setting
RR alarm Lower limit: 30
2 Set the heart rate output from AX-410G to "HR 60", and check whether the
bedside monitor operates as follows.
Alarm Operation of the bedside monitor
Display of respiration rate The value is highlighted
Display of message “RESP (IMP) alarm” message is displayed
Alarm sound There is a sound depending on the setting
Electrode There is a sound depending on the setting
Alarm indicator The indicator blinks or lights depending on the setting

Checking the SpO2 Value

Connect the AX-410G vital sign simulator to the instrument to check the SpO2
value and the accuracy of the pulse rate. Also, check that the alarm is generated
normally. To obtain stable measurement accuracy, perform the accuracy check
every six months. 3
Preparation
Connect the AX-410G vital sign simulator to the instrument with the JL-701P
SpO2 connection cable.
AX-410G JL-701P Bedside monitor

SpO2 connection cord
Checking the Accuracy of the SpO2 Value and the Pulse Rate
1 Set the bedside monitor as follows.

Setting screen Setting value
Sound Sync tone SpO2
2 Set the SpO2 values on the AX-410G vital sign simulator as shown in the
following table and check that the SpO2 value and the pulse rate (SpO2-PR)
displayed on the instrument are within the accuracy shown in the table. Also,
check that there is a sound synchronous with the pulse wave.
Settings on AX-410G Display on the bedside monitor
97 % SpO2 95 % SpO2 ~ 99 % SpO2
SpO2 80 % SpO2 78 % SpO2 ~ 82 % SpO2
70 % SpO2 66 % SpO2 ~74 % SpO2
SpO2-PR 60 bpm* 57 bpm ~ 63 bpm
* The pulse rate (SpO2-PR) generated from the AX-410G vital sign
simulator is fixed at 60 bpm. No setting is required.


are stipulated in ISO 80601-2-61:2011.
For PULSE OXIMETER EQUIPMENT provided with an
ALARM SYSTEM that includes the capability to detect a
PHYSIOLOGICAL ALARM CONDITION: SpO2 ACCURACYa,
PULSE RATE ACCURACY and limit ALARM CONDITIONS
201.12.1.101
201.12.1.104
208.6.1.2.101
or generation of a TECHNICAL ALARM CONDITION 201.11.8.101.1

201.12.4
201.13.101
For PULSE OXIMETER EQUIPMENT not provided with
an ALARM SYSTEM that includes the capability to detect a
PHYSIOLOGICAL ALARM CONDITION: SpO2 ACCURACYa
and PULSE RATE ACCURACY 201.12.1.101
201.12.1.104
or indication of abnormal operation 201.12.4

201.13.101
a Subclause 202.6.2.1.7 indicates methods of evaluating SpO2 ACCURACY and
PULSE RATE ACCURACY as acceptance criteria following specific tests required
by this standard.

Checking the Temperature

Connect the AX-410G vital sign simulator to the instrument and check the
accuracy of the temperature with the TEMP socket. After the check, return the
setting to your setting used at your facility.
3
Preparations
Connect the AX-410G vital sign simulator to the instrument.
To the TEMP socket

Use the SVM connector cable assembly.
AX-410G SVM connector cable Bedside monitor

assembly
Check the Accuracy of the Temperature

Set the temperature output from the AX-410G vital sign simulator and make sure
that the temperature shown on the instrument is within the accuracy range shown
in the table below.
Setting on the AX-410G Indication on the Bedside Monitor
25 °C 24.8 °C to 25.2 °C
37 °C 36.8 °C to 37.2 °C
44 °C 43.8 °C to 44.2 °C
Checking the Sensor-Off Detection

Make sure that the sensor-off is detected. While the temperature signal from the
AX-410G vital sign simulator is being input, remove the temperature cable plug
from the TEMP socket. Make sure that instrument operates as follows.
Alarm Operation of the Bedside Monitor
Message display The “CONNECTOR OFF” message appears.
Alarm sound The caution alarm sound is heard.
The alarm indicator lights in the color specified
Alarm indicator
for the caution alarm.

are stipulated in ISO 80601-2-56:2009.
Accuracy of the CLINICAL THERMOMETER or at least 201.101.2
one of the following:
– generation of a TECHNICAL ALARM CONDITION; 201.12.1.101
– not providing an OUTPUT TEMPERATURE; 201.4.101
– marking the ambient temperature operating range.

Checking the IBP (SVM-7503/7523 only)

Connect the AX-410G vital sign simulator to the instrument to check zero
calibration and the accuracy of the blood pressure value. To obtain stable
measurement accuracy, perform the accuracy check every six months.
Preparation
Using SVM connector cable assembly to connect the AX-410G vital sign
simulator to the instrument.
SVM connector cable

assembly
AX-410G Bedside monitor
Checking the Accuracy of Zero Calibration
1 Set the AX-410G vital sign simulator to “CAL 0 mmHg.”
2 Touch [PRESS] → [ZERO CALIBRATION] key. Touch the [ZERO CAL]

key to perform zero calibration. Check that the blood pressure displayed
after calibration is within the range of –2 mmHg to 2 mmHg. Or, touch the
ZERO CAL function key to perform zero calibration if the function key is
registered.
Checking the Accuracy of the Blood Pressure Value

Check the accuracy of the blood pressure value. After performing the zero
calibration, set the blood pressure value produced from the AX-410G vital sign
simulator in the following way and check that the blood pressure value displayed
on the instrument meets the requirement of the table below.
Setting of AX-410G Displayed value on bedside monitor
10 mmHg 8 mmHg ~ 12 mmHg

Checking the Detection of an Connector-Off Alarm

Check that the connector-off alarm is normally generated. While the blood
pressure signal is being entered from the AX-410G vital sign simulator, remove
the connector for the blood pressure cable from the instrument and check that the
instrument works in the following way.
Alarm Operation of the Bedside Monitor
3
Message display The “CONNECTOR OFF” message appears.
Alarm sound The caution alarm sound is heard.
The alarm indicator lights in the color specified for
Alarm indicator
the caution alarm.

Accuracy of pressure measurements 201.12.1.101
Delays to or from a DISTRIBUTED ALARM SYSTEM 208.6.4.2
PHYSIOLOGICAL ALARM CONDITIONS, ALARM LIMITS
208.6.6.2.101
and delay time of physiological ALARM SIGNALS
Detection of TRANSDUCER and TRANSDUCER cable fault 208.6.6.2.102
Detection of disconnected catheter 208.6.6.2.103

Checking the CO2 Value (SVM-7503/7523 only)

If the CO2 measurement involves significant error, use the gas for sensitivity
calibration to check the accuracy. To obtain stable measurement accuracy,
perform the accuracy check regularly every six months.
Preparations
Only use the gas cylinder for sensitivity calibration and flow regulator specified
by Nihon Kohden to check the accuracy. Also, prepare a CO2 sensor kit and
airway adapter.
<Gas cylinder for sensitivity calibration> <Flow regulator>
CO2 5 % sensitivity gas A-4 PR-150
CAUTION
Follow the CAUTION label on the CO2 gas cylinder.
NOTE:
• The gas cylinder for sensitivity calibration and flow regulator
specified by Shanghai Kohden must be purchased locally. Use
CO2 cylinders with the following specifications.
Manufacturer: Nellcor Puritan Bennett, Scott Medical Products
division of Air Liquide Healthcare, or equivalent
Outlet fitting: CGA 600
Gas component: 5 % CO2, 21 % O2 and N2 mix
Expiration: 3 years after the gas is packed in the cylinder
Accuracy: ± 0.03 % absolute
If the above CO2 cylinders are not available in your country, find highly
compressed disposable gas cylinders with the same specifications
from other manufacturers.
• The gas cylinder for sensitivity calibration has its expiration

date. Using the gas cylinder whose expiration date has been
reached would not guarantee the accuracy of calibration. Check
the expiration date (EXP. DATE) on the gas cylinder.
• Only use the PR-150 in which the pressure meter has a full
scale of 700 psi. Using a non-specified flow regulator might
damage the pressure meter.
• To dispose of calibration gas after use, ask the manufacturer for
instructions.

Checking the Accuracy of the TG-901T4 / 921T4
1 Rotate the flow regulator to attach it firmly to the top of the gas cylinder for
sensitivity calibration.
2 Connect the CO2 sensor kit to the CO2 socket.
3 Connect the airway adapter to the CO2 sensor.

Airway adapter
CO2 sensor
Align the
marks

4 Let the CO2 gas flow.

Turn the knob of the flow regulator counterclockwise by about a half turn to
let the CO2 gas flow. Turn the knob slowly.
Pressure meter Knob

Turn the knob
counterclockwise to open.
Slip joint
Connect and disconnect

the sensor to form the
expiratory phase and the
inspiratory phase. (When
disconnected, strongly shake
the CO2 sensor so that no
CO2 gas remains in the
airway adapter.)
5 Form the expiratory and inspiratory phases and display the value of the CO2
partial pressure (preparation).
i) Connect the slip joint and the airway adapter (expiratory phase).
ii) Disconnect the airway adapter from the slip joint section (inspiratory
phase).
iii) Repeat steps i) and ii) three times to display the value of the CO2 partial
pressure.
6 Check the accuracy.

i) Connect the slip joint and the air adapter (expiratory phase).
Check that the value of the CO2 partial pressure displayed on the screen is
between 34 mmHg and 42 mmHg. (See the “Supplementary” information
on the next page.)
ii) Disconnect the air adapter from the slip joint section (inspiratory phase).
Check that 0 mmHg is shown in the CO2 display area on the instrument.
iii) Repeat steps i) and ii) to check the accuracy.
NOTE: Measuring the CO2 value in the TG-901T4 / 921T4 is based
on the inspiratory compensation method; therefore, the CO2
condensation in inspiratory mode should be calibrated to 0
mmHg. After the CO2 gas equivalent to expiratory air is made
to flow and the airway adapter is removed from the slip joint,
strongly shake the CO2 sensor so that no CO2 gas remains
(that is, the CO2 gas in the airway adapter shows a reading of 0
mmHg), with the result that the existing CO2 gas is completely
replaced.

7 After checking the measurement accuracy, firmly turn the knob of the flow
regulator clockwise to stop the CO2 gas.
NOTE: Once the pressure meter of the flow regulator shows a reading of
0, the gas cylinder for sensitivity calibration should be replaced
with a new one.
3
Supplement
• The TG-901T4 / 921T4 is calibrated at a temperature of 37 °C in exhaled
gas; therefore, the indication will show a change of approximately
–0.4 %/°C at any other temperature. Generally, the gas to be calibrated is
low temperature which might indicate a pressure of 40 mmHg.
• With the TG-901T4/921T4, the unit of 1 atm is used for calibration. The
indication will change at a rate of 1 mmHg/30 hPa in an environment of
other than 1 atm.
Example 1: Checking the accuracy at high air pressure
Condensation of CO2 calibration gas: 38 mmHg (5 %); atmospheric
pressure: an increase of 60 hPa
The measurement is higher by 1 mm Hg × (60hPa / 30hPa) = 2
mmHg.
Therefore, 40 mmHg is indicated.
Example 2: Checking the accuracy at a high altitude
Condensation of CO2 calibration gas: 38 mmHg (5 %); altitude:
1,000 m
Change in atmospheric pressure = 1013 hPa × 0.1 (altitude-based
rate of change in atmospheric pressure) = 101.3 hPa
101.3 hPa / 30 hPa = 3.4 mmHg
38 mmHg – 3.4 mmHg = 34.6 mmHg
Therefore, 34.6 mmHg is indicated.

Checking the Accuracy of the TG-971T4/TG-981T4
1 Rotate the flow regulator to attach it firmly to the top of the gas cylinder for
sensitivity calibration.
2 Connect the CO2 sensor kit to the CO2 socket.
3 Connect the airway adapter to the CO2 sensor.
CO2 sensor
Airway adapter

4 Follow steps i) to iv) to perform zero calibration of the CO2 sensor (Air
calibration).
i) Expose the airway adapter placed in the CO2 sensor kit to room air.
ii) Touch the [RESP/CO2] → [CO2 ZERO CAL] key. Touch the [AIR CAL]
key for the calibration method. 3
iii) When the “EXPOSE SENSOR TO AIR” message appears, touch YES
to perform air calibration. While the calibration is being performed, the
“CALIBRATING” message is displayed.
iv) When calibration is complete, the “CALIBRATION COMPLETE”
message appears, followed by the date of calibration and the method of
calibration.
5 Turn the knob of the flow regulator counterclockwise about a half turn to let
the CO2 gas flow. Turn the knob slowly.
Pressure meter Knob

Turn the knob
counterclockwise to open.
Slip joint
There is no need to form

the expiratory phase or
the inspiratory phase

6 Connect the split joint and the airway adapter. Check that the value of the
CO2 partial pressure displayed on the screen is between 36 and 40 mmHg.
7 After checking the measurement accuracy, firmly turn the knob of the flow
regulator clockwise to stop the gas.
NOTE: Once the pressure meter of the flow regulator shows a reading of
0, the gas cylinder for sensitivity calibration should be replaced
with a new one.
Supplement
• The TG-971T4/TG-981T4 is calibrated at a temperature of 37 °C
in exhaled gas; therefore, the indication will show a change of
approximately –0.4 %/°C at any other temperature. Generally, the gas to
be calibrated is low temperature which might indicate a pressure of 40
mmHg.
• When the TG-971T4/TG-981T4 is used, atmospheric compensation is
already performed. There is no need to read the indication again.

are stipulated in ISO 80601-2-55.
MEASUREMENT ACCURACY and GAS READING
a
201.12.1.101
ALARM CONDITION 208.6.1.2
or generation of a TECHNICAL ALARM CONDITION 201.11.8.101.1

a Methods of evaluating MEASUREMENT ACCURACY as acceptance criteria
following specific tests required by this International Standard are found in
202.6.2.1.7.
Checking Other Essential Performance of the Monitor

Delays to or from a DISTRIBUTED ALARM SYSTEM 208.6.4.2

Safety Check
Safety check is performed while the components are connected. You need
to measure four different currents (earth leakage current, enclosure leakage
current, patient leakage current and patient auxiliary current) in both the normal
3
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 for
measuring leak current.
Measuring earth leakage current

Make sure that the measured value is within the range below.
Normal condition 500 μA or less
Single-fault condition 1 mA or less
When you set the network system or change the network system composition,
check the enclosure leakage current of the metal connector of the LAN cable.
Measuring patient leakage current

Measure the patient leak current flowing in the measurement system for each
parameter. For the ECG, short-circuit all the electrode leads before measurement.
For the other parameters, wrap the transducer with aluminum foil before
measurement.
Single-fault condition 50 μA or less
Measuring patient auxiliary current

For the ECG, measure the patient auxiliary current (AC). Short-circuit the non-
red electrode leads for the ECG and measure the value with respect to the red
one.
Single-fault condition 50 μA or less

4 Disassembly and
Assembly
Disassembling the Power Supply Unit (PSU)..................4-2

4
Disassembling the Speaker.............................................4-8
Disassembling the USB&LAN Board...............................4-8
Disassembling the Input Panel Unit................................4-9
Disassembling the Valve...............................................4-13
Disassembling the Rolling Pump...................................4-14
Disassembling the Main Board......................................4-16
Disassembling the SW Panel........................................4-18
Disassembling the ALARM LED Board.........................4-18
Disassembling the Touch Panel....................................4-19
Disassembling the LCD.................................................4-20
Disassembling the Recorder.........................................4-21
Assembling....................................................................4-24
4. DISASSEMBLY AND ASSEMBLY
Disassembling the Power Supply Unit (PSU)
1 Remove the screw on the battery cover with a screwdriver.
2 When the monitor is not installed with a battery pack, remove the battery
cover by pulling the tape on it.
3 When the monitor is installed with a battery pack, the battery cover
spontaneously cocks up slightly. Raise the cover and remove it. Then remove
the battery pack.

4 Remove the six screws on the rear enclosure.
5 Push the two claws with your fingers to release them and remove the rear
enclosure.
6 Remove two screws on the insulator and remove the insulator.

7 Remove the four screws on the front of the PSU unit.
8 Remove the screw on the side of the PSU unit.
9 Remove the power internal cable from the hook.
10 Remove the power internal cable from the clamp.

11 Pull out the PUS-side plug of the power internal cable.
12 Pull out the two tubes on the side of NIBP connector.
13 Remove the screw on the tube bracket. Then remove the tube bracket.
14 Cut and remove the cable tie on the cables of the speaker. Remove the PSU
unit in the direction of arrow.

15 Pull out the speaker plug from the main board.
16 Pull out the plug of the USB&LAN board lead from the main board. And
remove the USB&LAN board lead from the main board.
17 Remove the five screws on the front of the power board shielding.
18 Remove the screw on the side of the power board shielding.

19 Remove the screw on the ground cable and the two screws on the FET
radiators. Remove the two FET radiators.
20 Remove the five screws on the PSU board and remove the PSU.

Disassembling the Speaker

To remove the rear enclosure, please refer to “Disassembling the Power Supply
Unit (PSU)” section.
To remove PSU unit, please refer to “Disassembling the Power Supply Unit
(PSU)” section.
1 Remove the four screws on the speaker and remove the speaker.
Disassembling the USB&LAN Board

(PSU)” section.
1 Remove the two screws on the USB&LAN board and remove the
USB&LAN board.

Disassembling the Input Panel Unit

(PSU)” section.
4
1 Pull out the plug of the TEMP board lead from the main board.
2 Remove the two screws on the TEMP board and remove the TEMP board.
3 Remove the two screws on the input panel.

4 Remove the input panel unit.

● For SVM-7501/7521:
Pull out the plugs of ECG internal cable and SpO2 internal cable and remove
the input panel unit.
● For SVM-7503/7523:
Pull out the plugs of ECG internal cable, SpO2 internal cable, IBP internal
cable and CO2 internal cable and remove the input panel unit.
5 Cut and remove the cable tie of SpO2 internal cable.

6 Remove the two screws on the connector bracket unit and separate the
connector bracket from the input panel.
7 Remove internal cable

● For SVM-7501/7521:
Remove SpO2 internal cable.
● For SVM-7503/7523:
Remove CO2 internal cable, IBP internal cable and SpO2 internal cable
individually.

8 Remove the four screws on the ECG internal cable and remove the ECG
internal cable.
9 Remove the two screws on the NIBP connector and remove NIBP connector.

Disassembling the Valve

(PSU)” section.
4
1 Pull out the plug of the rolling pump and the valve from the main board.
The Socket of the Valve Lead
The Socket of the Rolling Pump Lead
2 Remove the two screws on the valve unit and remove the valve unit.
3 Remove the four screws on the valve and remove the valve.

Disassembling the Rolling Pump

(PSU)” section.
1 Cut the cable tie on the ALARM LED board lead and remove it.
2 Pull out the plug of ALARM LED board lead.

3 Loosen the lock of the socket and pull out the lead of the touch panel.
4 Remove the five screws on the main shielding unit and remove the main
shielding unit.
5 Cut and remove the two cable ties on the rolling pump and remove the
rolling pump.

Disassembling the Main Board

(PSU)” section.
To remove the input panel unit, please refer to “Disassembling the Input Panel
Unit” section.
To remove the valve unit, please refer to “Disassembling the Valve” section.
To remove the main shielding unit, please refer to “Disassembling the Rolling
Pump” section.
1 Remove the tube unit from the main board.
2 Pull out the plug of the power internal cable from the main board.
3 Pull out the plug of SW board lead from the main board.

4 Pull out the plug of LVDS cable from the main board.
5 Pull out the plug of LCD Backlight cable from the main board.
The plug of LCD BL LED cable of SVM-7521/7523 is on the front of the
main board.
The plug of LCD BL LED cable of SVM-7501/7503 is on the back of the
main board.
6 Remove the two stanchions on the main board.
7 Remove the six screws on the main board and remove the main board.

Disassembling the SW Panel

To remove the PSU unit, please refer to “Disassembling the Power Supply Unit
(PSU)” section.
1 Pull out the plug of the SW board lead from the main board.
2 Remove the two screws on the SW board and remove the SW board.
Disassembling the ALARM LED Board

To remove the front enclosure, please refer to “Disassembling the Touch Panel”
section.
To cut and remove the cable tie on the ALARM LED board lead, please refer to
“Disassembling the Rolling Pump” section.
To pull out the plug of ALARM LED board lead, please refer to “Disassembling
the Rolling Pump” section.
1 Remove the two screws on the ALARM LED board and remove the
ALARM LED board.

Disassembling the Touch Panel

1 Remove the three screws on the front enclosure and remove the front
enclosure. 4
2 Remove the touch panel.
3 Remove the sponge from the touch panel.

Disassembling the LCD

(PSU)” section.
To remove the input panel unit, please refer to “Disassembling the Input Panel
Unit” section.
To remove the valve unit, please refer to “Disassembling the Valve” section.
To remove the main shielding unit, please refer to “Disassembling the Rolling
Pump” section.
To remove the main board, please refer to “Disassembling the Main Board”
section.
To remove the front enclosure, please refer to “Disassembling the Touch Panel”
section.
1 Remove the four screws on the LCD and remove the LCD.
SVM-7501/7503 SVM-7521/7523
NOTE: The cable should pass through the hole on the LCD chassis.

Disassembling the Recorder
1 Remove the four screws on the recorder PCBA and remove the recorder
PCBA.

2 Remove the screw on the recorder bracket and remove the recorder bracket.
3 Remove the screw on the recorder case and remove the recorder case.

Assembling
Follow the opposite steps to assemble the units and parts.

5 Maintenance Check
Sheet
Maintenance Check Sheet..............................................5-2

5
5. MAINTENANCE CHECK SHEET
Maintenance Check Sheet

Issuance No.
Facility name Address of facility Installation site Installation date
Date of maintenance check Sign by engineer who did the Representative (or service Customer’s signature
maintenance check company)
Instrument model Instrument serial number Software version Models of main unit and optional units
number installed
Measuring instrument employed Attachments/Consumables

Product name Maintenance No. Product name No. Product name No.
Overall judgment Use situation

[ ] The instrument is working normally. Status of usage: Continually, Intermittently
[ ] The instrument is working normally with the following minor Duration of usage: year(s)
points.
Used by: Nurse, Doctor, Technician
( )
[ ] The instrument must be repaired as soon as possible.
Check
No. Item Action
result
1 Appearance Check that there is no dirt, rust, scratch or crack on the instrument.
Check that there is no stain which shows that liquid such as blood or
medical liquid got inside the instrument.
Check that the instrument has no loose screws.
Check that the instrument has no loose connectors or switches.
Check that the labels on the instrument are not peeled or damaged.
2 Power cord Check that the power cord is not folded and none of the 3 internal wires in
the power cord are exposed.
Standard Configuration
3 Power on Check that “OK” is displayed at the POWER ON CHECK RESULT on

the DIAGNOSTIC CHECK screen.
4 NAND Check NAND on the MAIN board in the MANUAL CHECK mode.
Select NAND from the CPU CHECK items on the MANUAL CHECK
screen.
5 FRAM Check the Synchronous FRAM on the MAIN board in the MANUAL
CHECK mode. Select FRAM from the CPU CHECK items on the
MANUAL CHECK screen.
6 Touch key Check the touch screen. Select TOUCH KEYS from the CPU CHECK
items on the MANUAL CHECK screen.
7 RAM Check the Ferroelectric RAM on the MAIN DIGITAL board in the
MANUAL CHECK mode. Select RAM from the CPU CHECK items on
the MANUAL CHECK screen.
8 Sound Check the alarm sound, QRS synchronization sound and click sound.
Select SOUND from the CPU CHECK items on the MANUAL CHECK
screen.
9 Alarm indicator Check the alarm indicator. Select ALARM INDICATOR from the CPU
CHECK items on the MANUAL CHECK screen.

Check
No. Item Action
result
10 Screen brightness Check the backlight lamp. Select BACKLIGHT from the CPU CHECK
items on the MANUAL CHECK screen.
11 Recorder (if Check the optional WS-752P recorder module. Select WS RECORDER
installed) from the COM CHECK items on the MANUAL CHECK screen.
12 NIBP Check the accuracy of two pressure sensors for NIBP measurement.
Select NIBP from the DPU CHECK items on the MANUAL CHECK
screen and select “1. CALIBRATION” on the NIBP CHECK screen.
Check the zeroing for NIBP measurement. Select NIBP on the MANUAL
CHECK screen and select “2. ZERO CALIBRATION” on the NIBP
CHECK screen. 5
Check the NIBP safety circuit. Select NIBP on the MANUAL CHECK
screen and select “3. SAFETY CHECK” on the NIBP CHECK screen.
Check the inflation speed. Select NIBP on the MANUAL CHECK screen
and select “4. INFLATION SPEED” on the NIBP CHECK screen.
Check the pressure holding time. Select NIBP on the MANUAL CHECK
screen and select “5. PRESSURE HOLD” on the NIBP CHECK screen.
Check the two valves. Select NIBP on the MANUAL CHECK screen and
select “6. STEP DEFLATION” on the NIBP CHECK screen.
Check the NIBP circuit. Select NIBP on the MANUAL CHECK screen
and select “8. AIR CIRCUIT” on the NIBP CHECK screen.
13 Date/time Check that the date and time are properly set on the monitoring screen.
14 ECG Check the heart rate accuracy with an AX-410G vital sign simulator or
equivalent.
Check the heart rate alarm, alarm message, alarm sound and alarm
indication with a JC-906P ECG connection cord and BR-903P electrode
lead with an AX-410G vital sign simulator or equivalent.
15 RESP Check the respiration rate accuracy with an AX-410G vital sign simulator
or equivalent.
Check the respiration rate alarm, alarm message, alarm sound and alarm
indication with an AX-410G vital sign simulator or equivalent.
16 SpO2 Check the accuracy of SpO2 and pulse rate with an AX-410G vital sign
simulator or equivalent.
Check the SpO2 alarm, alarm message, alarm sound and alarm indication
with an AX-410G vital sign simulator or equivalent.
17 IBP (SVM- Check that the zeroing for IBP measurement is within the specified range
7503/7523 only) with an AX-410G vital sign simulator or equivalent.
Check the blood pressure accuracy with an AX-410G vital sign simulator
or equivalent.
Check the blood pressure alarm, alarm message, alarm sound and alarm
indication with an AX-410G vital sign simulator or equivalent.
Check the alarm message, alarm sound and alarm indication with an
AX-410G vital sign simulator or equivalent when disconnecting the IBP
connection cord from the instrument.
18 TEMP Check the temperature accuracy with an AX-410G vital sign simulator or
equivalent.
Check the alarm message, alarm sound and alarm indication with an AX-
410G vital sign simulator or equivalent when disconnecting the TEMP

Check
No. Item Action
result
19 CO2 (SVM- Check that the CO2 wave, data and respiration rate are properly displayed
7503/7523 only) with an AX-410G vital sign simulator or equivalent.
Check the alarm message, alarm sound and alarm indication with an
AX-410G vital sign simulator or equivalent when disconnecting the CO2
Check the accuracy of the CO2 sensor with CO2 calibration gas.
20 Battery (if When an optional SB-752P battery pack is used, check the battery pack.
installed)
21 Check that the earth leakage current is less [ ] μA under normal condition
than the prescribed limits. [ ] μA under single-fault condition
22 Check that the enclosure leakage current is [ ] μA under normal condition
less than the prescribed limits. [ ] μA under single-fault condition
Safety
23 Check that the patient leakage current is less [ ] μA under normal condition
24 Check that the patient auxiliary current is less [ ] μA under normal condition

6 Replaceable Parts
List
Replaceable Parts List....................................................6-2

6
6. REPLACEABLE PARTS LIST
Replaceable Parts List

No. Code No. Q’ty Description
1 6124-912740 1 Power panel (for SVM-7501/7503/7521/7523)
2 6112-912271 1 Front enclosure (for SVM-7501/7503)
6112-912273 1 Front enclosure (for SVM-7521/7523)
3 6113-924483 1 Alarm indicator (for SVM-7501/7503/7521/7523)
4 6114-936104 1 Alarm indicator packing
5 6113-925791 1 Touchscreen edge protector (for SVM-7501/7503)
6113-925792 1 Touchscreen edge protector (for SVM-7521/7523)
6 6113-925921 1 LCD Chassis (for SVM-7501/7503)
6113-925920 1 LCD Chassis (for SVM-7521/7523)
7 6114-936133 1 SPONGE ZG
8 6114-936076 2 HEX spacer
9 6114-936359 1 Tube A2
10 9000-059725 1 T type joint
11 6114-936360 1 Tube B1
12 6114-936361 1 Tube B2
13 9000-067612 1 Y type joint
14 6114-936110 1 Joint
15 9000-052079 1 Check valve
16 6114-936111 1 Joint B
17 6114-936358 2 Tube A1
18 6113-924476 1 Mainboard shielding
19 6114-936127 1 Valve holder
20 6114-936121 1 Pump vibration absorber
21 6113-924640 1 Connector bracket
22 6114-936333 1 NIBP socket
23 6113-924501 1 Input socket panel (for SVM-7501/7521)
6113-924637 1 Input socket panel (for SVM-7503/7523)
A 9000-062198 1 Touchscreen (for SVM-7501/7503)
6104-900129 1 Touchscreen (for SVM-7521/7523)
B 9000-062106 1 LVDS CABLE (for SVM-7501/7503)
9000-062108 1 LVDS CABLE (for SVM-7521/7523)
C 9000-000313 1 LCD (for SVM-7501/7503)
6104-900130 1 LCD (for SVM-7521/7523)
D UR-43052-SK 1 UR-43052 Mainboard (for SVM-7501/7521)
UR-43051-SK 1 UR-43051 Mainboard (for SVM-7503/7523)
E 9000-062107 1 LCD BL LED Cable (for SVM-7521/7523)
F 6104-900035 1 Power cable
G 6104-900040 1 NIBP Pump
H 6104-900131 1 Valve set
I 6104-900046 1 Pump cable
J 6104-900132 1 Ferrite core
K 6104-900028 1 CO 2 Cable (for SVM-7503/7523)
L 6104-900029 1 ECG CABLE

M 6104-900038 1 SpO2 CABLE

N 6104-900031 1 IBP Cable (for SVM-7503/7523)
R 6104-900136 1 UR-4306 LC TEMP BOARD
S 6104-900135 1 UR-4307 LC PWR SW BOARD
T 6104-900134 1 UR-4308 LC ALARM BOARD
3
23
2 4
6
N
M
L
22
K
5
21
A
R
J
7
T
B D
C
9
10 14 15
6
8 16
12
11 13 17
20
G
I
S
F
18
19
H


24 6114-936077 1 Insulator
25 6113-924491 1 Power board chassis
26 9000-062373 2 CLAMP
27 6124-912658 1 GROUND LABEL
28 6114-935994 1 Ground pin
29 6144-902342 2 FET radiator
30 9000-059360 2 ASB, NK, SILICONE_CAP, L21.5mm
31 458612 2 Edge holder
32 6114-936109 1 Tube holder
33 6113-924492 1 Power board shielding
34 6114-937653 4 Rubber foot
35 6111-905730 1 Rear enclosure
36 6113-924636 1 Recorder cover
37 6113-924639 1 Handle
38 6124-912662 1 Battery Direction Label
39 6114-936290 1 ESD LABEL
40 6113-924635 1 Battery cover
41 6124-041901A 1 WEEE mark label
42 6184-941997 1 SVM-7500 Mass label (for SVM-7503/7523)
43 6184-941999 1 SVM-7501 version label
6184-942002 1 SVM-7503 version label
44 6183-905618 1 SVM-7501 nameplate
6183-905620 1 SVM-7503 nameplate
6183-905622 1 SVM-7521 nameplate
6183-905624 1 SVM-7523 nameplate
45 6124-912773 1 CE label
O 6104-900110 1 UR-4303 PSU board
P 930708 1 Speaker
Q 6104-900030 1 Ground cable
U 6104-900133 1 UR-4309 LC LAN&USB BOARD
WS-752P
100 RG-750X 1 Paper drive unit
101 6113-924480 1 Recorder case (LC)
102 6114-936106 1 Shielding gasket
103 6113-924479 1 Recorder bracket (LC)
104 6104-900050 1 Recorder cable
105 6104-900067 1 UR-4304 Recorder PCBA

O P
24
30
29 31
25
27
32 6
U
28
Q
35
33
26
38
34
39
41
42
36
45
40
43 37
44
102
103
104 105
101
100
WS-752P

SVM-7500 - EngSM - NIHON KOHDEN

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Service Manual

Service Manual (this manual)

Introduction............................................................... 1-2 Replaceable Parts List............................................. 6-2 6

3 Diagnostic Check and Safety

4 Disassembly and Assembly

SVM-7500 Series Service Manual Contents 1

2. When installing or storing the instrument, take the following precautions:

5. To Shutdown After Use

7. The instrument must not be altered or modified in any way.

SVM-7500 Series Service Manual i

11. Contraindications: None.

12. The electrodes cannot be applied directly on the heart.

ii SVM-7500 Series Service Manual

3. Effect of direct or indirect electrostatic discharge:

6. Use with other equipment:

7. Use of unspecified accessory, transducer and/or cable:

SVM-7500 Series Service Manual iii

8. Use of unspecified configuration:

9. Measurement with excessive sensitivity:

iv SVM-7500 Series Service Manual

SVM-7500 Series Service Manual v

Note: A note provides specific information, in the form of recommendations,

vi SVM-7500 Series Service Manual

Introduction.................................................1-2 Environment....................................................... 1-21

Influence on Measuring Accuracy System Composition for EMC Test..................... 1-26

Alarm.................................................................... 1-9 Left Side Panel................................................... 1-28

Alarm Delay Time............................................... 1-10 Right Side Panel................................................. 1-29

ECG (IEC 60601-2-27: 2011)............................. 1-11 Rear Panel......................................................... 1-29

Respiration (Impedance Method)....................... 1-13

The SVM-7501/7521 bedside monitor is installed near a patient and displays

1-2 SVM-7500 Series Service Manual

Cleaning after use

Disinfection and cleaning

SVM-7500 Series Service Manual 1-3

- Glutaraldehyde solution: 2.0 %

Handling the instrument

Measuring and test equipment

1-4 SVM-7500 Series Service Manual

Only disassemble the instrument or replace a board or unit in an environment

As background knowledge for repair, pay special attention to the following:

Patient Safety Checks

SVM-7500 Series Service Manual 1-5

Monitor Status on Power Interruption

When there is a power failure or sudden power interruption during AC operation,

1-6 SVM-7500 Series Service Manual

UR-4303 PSU BOARD

UR-43052 MAIN BOARD (BASIC)

UR-4306 TEMP BOARD

UR-4307 PWR SW BOARD

UR-4308 ALARM BOARD

UR-4309 LAN&USB BOARD

WS-752P RECORDER MODULE

UR-4304 RECORDER CTRL BOARD

RG-750X PAPER DRIVE UNIT

SB-752P BATTERY PACK

UR-4303 PSU BOARD

UR-43051 MAIN BOARD (PLUS)

UR-4306 TEMP BOARD

UR-4307 PWR SW BOARD

UR-4308 ALARM BOARD

UR-4309 LAN&USB BOARD

WS-752P RECORDER MODULE

UR-4304 RECORDER CTRL BOARD

SVM-7500 Series Service Manual Contents 1

SVM-7500 Series Service Manual i

ii SVM-7500 Series Service Manual

SVM-7500 Series Service Manual iii

iv SVM-7500 Series Service Manual

SVM-7500 Series Service Manual v

vi SVM-7500 Series Service Manual

1-2 SVM-7500 Series Service Manual

SVM-7500 Series Service Manual 1-3

1-4 SVM-7500 Series Service Manual

SVM-7500 Series Service Manual 1-5

1-6 SVM-7500 Series Service Manual

SVM-7500 Series Service Manual 1-7

1-8 SVM-7500 Series Service Manual

SVM-7500 Series Service Manual 1-9

1-10 SVM-7500 Series Service Manual

SVM-7500 Series Service Manual 1-11

1-12 SVM-7500 Series Service Manual

SVM-7500 Series Service Manual 1-13

1-14 SVM-7500 Series Service Manual