BeneVision TMS60

Telemetry Monitoring System

Service Manual
Intellectual Property Statement
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray)
owns the intellectual property rights to this product and this manual. This manual may
refer to information protected by copyrights or patents and does not convey any license
under the patent rights of Mindray, nor the rights of others. Mindray does not assume any
liability arising out of any infringements of patents or other rights of third parties.
Mindray intends to maintain the contents of this manual as confidential information.
Disclosure of the information in this manual in any manner whatsoever without the
written permission of Mindray is strictly forbidden.

Release, amendment, reproduction, distribution, rent, adaptation and translation of this

manual in any manner whatsoever without the written permission of Mindray is strictly
forbidden.

, and are the registered trademarks or trademarks

owned by Mindray in China and other countries. All other trademarks that appear in this
manual are used only for editorial purposes without the intention of improperly using
them. They are the property of their respective owners.

Contents of this manual are subject to changes without prior notice.

For this manual, the issued Date is December 2015 (Version: 2.0).

© 2015 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved

NOTE

 This manual describes all features and options. The equipment may not
have all of them. Contact Mindray service department for any questions.

BeneVision TMS60 Service Manual I

Manufacturer’s Responsibility
Contents of this manual are subject to changes without prior notice.

All information contained in this manual is believed to be correct. Mindray shall not be
liable for errors contained herein nor for incidental or consequential damages in
connection with the furnishing, performance, or use of this manual.

Mindray is responsible for the effects on safety, reliability and performance of this
product, only if:
 All installation operations, expansions, changes, modifications and repairs of
this product are conducted by Mindray authorized personnel;
 The electrical installation of the relevant room complies with the applicable
national and local requirements;
 The product is used in accordance with the instructions for use.

WARNING
 This manual is for biomedical engineers or technicians responsible for
troubleshooting, repairing, and maintaining the telemetry monitoring
system.

II BeneVision TMS60 Service Manual

Warranty
Mindray warrants that components within its products will be free from defects in
workmanship and materials for a period of three years from the date of purchase except
that disposable or one-time use products are warranted to be free from defects in
workmanship and materials up to a date one year from the date of purchase or the date
of first use, whichever is sooner.

This warranty does not cover consumable items such as, but not limited to, batteries,
external cables, and sensors.

Mindray shall not be liable for any incidental, special, or consequential loss, damage, or
expense directly or indirectly arising from the use of its products. Liability under this
warranty and the buyer’s exclusive remedy under this warranty is limited to servicing or
replacing the affected products, at Mindray option, at the factory or at an authorized
distributor, for any product which shall under normal use and service appear to Mindray
to have been defective in material or workmanship. Recommended preventative
maintenance, as prescribed in the service manual, is the responsibility of the user and is
not covered by this warranty.

No agent, employee, or representative of Mindray has any authority to bind Mindray to

any affirmation, representation, or warranty concerning its products, and any affirmation,
representation or warranty made by any agent, employee, or representative shall not be
enforceable by buyer or user.

THIS WARRANTY IS EXPRESSLY IN LIEU OF, AND MINDRAY EXPRESSLY DISCLAIMS, ANY
OTHER EXPRESS OR IMPLIED WARRANTIES, INCLUDING ANY IMPLIED WARRANTY OF
MERCHANTABILITY, NON-INFRINGEMENT, OR FITNESS FOR A PARTICULAR PURPOSE, AND
OF ANY OTHER OBLIGATION ON THE PART OF MINDRAY.

Damage to any product or parts through misuse, neglect, accident, or by affixing any
non-standard accessory attachments, or by any customer modification voids this
warranty. Mindray makes no warranty whatsoever in regard to trade accessories, such
being subject to the warranty of their respective manufacturers.

A condition of this warranty is that the equipment or accessories which are claimed to be
defective be returned when authorized, freight prepaid to Mindray DS USA, Inc., Mahwah,
New Jersey 07430 or its authorized representative. Mindray shall not have any
responsibility in the event of loss or damage in transit.

BeneVision TMS60 Service Manual III

Exemptions
Mindray's obligation or liability under this warranty does not include any transportation
or other charges or liability for direct, indirect or consequential damages or delay
resulting from the improper use or application of the product or the use of parts or
accessories not approved by Mindray or repairs by people other than Mindray authorized
personnel.

This warranty does not extend to:

 Malfunction or damage caused by improper use or man-made failure.
 Malfunction or damage caused by unstable or out-of-range power input.
 Malfunction or damage caused by force majeure events, such as (i) flood, fire
and earthquake or other similar elements of nature or acts of God; (ii) riots, war,
civil disorders, rebellions, or revolutions in any country; or (iii) any other cause
beyond the reasonable control of Mindray.
 Malfunction or damage caused by improper operation or repair by unqualified
or unauthorized service people.
 Malfunction of the instrument or part whose serial number is not legible.
 Others not caused by instrument or part itself.

Return Policy
In the event that it becomes necessary to return a unit to Mindray, follow the instructions
below.
1. Obtain a return authorization.
Contact the Mindray Service Department and obtain a Mindray Customer Service
Authorization Number. The Mindray Customer Service Authorization Number must
appear on the outside of the shipping container. Return shipments will not be accepted if
the Mindray Customer Service Authorization Number is not clearly visible. Please provide
the model number, serial number, and a brief description of the reason for return.

2. Freight policy
The customer is responsible for freight charges when this product is shipped to Mindray
for service (including any relevant customs fees or other freight related charges).

3. Return address
Please send the part(s) or equipment to the address offered by Customer Service
Department.

IV BeneVision TMS60 Service Manual

Contact Information
Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Address: Mindray Building,Keji 12th Road South,High-tech industrial
park,Nanshan,Shenzhen 518057,P.R.China
Website: www.mindray.com
E-mail Address: service@mindray.com
Tel: +86 755 81888998
Fax: +86 755 26582680

Distributor: Mindray DS USA, Inc.

Address: 800 MacArthur Boulevard, Mahwah, New Jersey 07430, USA
Tel: 1.800.288.2121, 1.201.995.8000
Website: http://www.mindraynorthamerica.com/

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VI BeneVision TMS60 Service Manual

Contents

1 Safety..................................................................................................................1-1
1.1 Safety Information ......................................................................................................................1-1
1.1.1 Warnings...........................................................................................................................1-2
1.1.2 Cautions............................................................................................................................1-2
1.1.3 Notes .................................................................................................................................1-2
1.2 Equipment Symbols ...................................................................................................................1-3
2 Principles ....................................................................................................................2-1
2.1 System Operating Principle ......................................................................................................2-1
2.2 Hardware Operating Principles ...............................................................................................2-2
2.2.1 Transmitter Principle .....................................................................................................2-2
2.2.2 Overview ..........................................................................................................................2-2
2.2.3 Receiver ............................................................................................................................2-3
2.2.4 Central Station (CS) ........................................................................................................2-5
2.2.5 Central Charger...............................................................................................................2-5
2.3 Software Principles .....................................................................................................................2-8
2.3.1 Transmitter Software System ......................................................................................2-8
2.3.2 Receiver System Software............................................................................................2-9
3 Receiver Physical Views ..............................................................................................3-1
3.1 Front View .....................................................................................................................................3-1
3.2 Rear View .......................................................................................................................................3-2
3.3 Restoring Latest Configuration Automatically ....................................................................3-3
4 Central Charger Physical Views ..................................................................................4-1
4.1 Front View .....................................................................................................................................4-1
4.2 Rear View .......................................................................................................................................4-1
5 Maintenance...............................................................................................................5-1
5.1 Recommended Maintenance and Test Frequency .............................................................5-1
5.2 Parameter Performance Test ....................................................................................................5-2
5.2.1 ECG Performance Test ...................................................................................................5-2
5.2.2 SpO2 ...................................................................................................................................5-3
5.3 Miscellaneous Tests ....................................................................................................................5-4
5.3.1 Visual Inspection ............................................................................................................5-4
5.3.2 Power-On Test .................................................................................................................5-4
5.3.3 Nurse Call Test .................................................................................................................5-4
5.3.4 Electric Safety Test..........................................................................................................5-5
5.3.5 Network Print Test ..........................................................................................................5-5
5.3.6 Battery Check ..................................................................................................................5-5
5.3.7 Tests in Service Menu ....................................................................................................5-5
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6 Service Menu ..............................................................................................................6-1
6.1 Entering the Service Menu .......................................................................................................6-1
6.2 Performing Software Update ...................................................................................................6-1
6.3 Service Log ...................................................................................................................................6-1
6.4 Factory Test ...................................................................................................................................6-1
6.4.1 Device Test .......................................................................................................................6-1
6.4.2 Screen Test .......................................................................................................................6-2
6.4.3 Touch Screen Test ...........................................................................................................6-2
6.4.4 Keys Test ...........................................................................................................................6-2
6.4.5 Sound & Light Test .........................................................................................................6-3
6.4.6 USB Interface Test ..........................................................................................................6-3
6.4.7 System Watchdog Test ..................................................................................................6-3
6.4.8 MO Module Watchdog Test .........................................................................................6-3
6.4.9 Bluetooth Module Test..................................................................................................6-4
6.4.10 Processing Method......................................................................................................6-4
6.5 Checking System Software Version ........................................................................................6-5
7 Troubleshooting .........................................................................................................7-1
7.1 Telemetry Monitoring System Problems...............................................................................7-1
7.1.1 Troubleshooting Tools ..................................................................................................7-1
7.1.2 Technical Alarm Messages ...........................................................................................7-1
7.1.3 Error Codes ......................................................................................................................7-3
7.1.4 Other Failures ..................................................................................................................7-7
7.1.5 Failure Examinations .....................................................................................................7-9
7.2 Central Charger Problems...................................................................................................... 7-16
8 Parts ...........................................................................................................................8-1
8.1 Transmitter (P/N 115-029485-00) ............................................................................................8-1
8.1.1 Exploded View of Main Unit ........................................................................................8-1
8.2 Receiver (P/N 115-029486-00) .................................................................................................8-5
8.2.1 Exploded View of Receiver...........................................................................................8-5
8.2.2 Front Cover Assembly of Receiver .............................................................................8-8
8.2.3 Power Assembly of Receiver .......................................................................................8-9
8.2.4 Amplifying and Branching Assembly of Receiver (P/N 0152-30-39691) ...... 8-10
8.2.5 4-Channel Receiver Module Assembly (P/N 115-029487-00).......................... 8-11
8.3 Power Injector (P/N 115-035637-00) ................................................................................... 8-12
8.4 Signal Switching Box (P/N 115-020216-00)....................................................................... 8-13
8.5 Exploded View of Central Charger ....................................................................................... 8-14
8.6 Micellaneous: ............................................................................................................................ 8-15
A Electrical Safety Inspection....................................................................................... A-1
A.1 Power Cord Plug........................................................................................................................ A-1
A.2 Device Enclosure and Accessories........................................................................................ A-2
A.3 Device Labeling ......................................................................................................................... A-2
A.4 Scheduled Electrical Safety Inspection ............................................................................... A-2

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 A.5 Electrical Safety Inspection after Repair ............................................................................. A-2
A.6 Electrical Safety Inspection Form ......................................................................................... A-3

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4 BeneVision TMS60 Service Manual

1 Safety

1.1 Safety Information

WARNING
 Indicates a potential hazard or unsafe practice that, if not avoided, could
result in death or serious injury.

CAUTION
 Indicates a potential hazard or unsafe practice that, if not avoided, could
result in minor personal injury or product/property damage.

NOTE
 Provides application tips or other useful information to ensure that you
get the most from your product.

BeneVision TMS60 Service Manual 1-1

1.1.1 Warnings
WARNING
 There is high voltage inside the system. Never disassemble the system
before it is disconnected from the AC power source.
 The system must be connected to a properly installed power outlet with
protective earth contacts only. If the installation does not provide for a
protective earth conductor, disconnect it from the power line.
 To completely disconnect the power supply, unplug the power cord.
 To avoid the electric shock, disassemble the central charger after the
central charger is disconnected from the AC power source for five minutes
later.
 Dispose of the package material, observing the applicable waste control
regulations and keeping it out of children’s reach.

1.1.2 Cautions
CAUTION
 Make sure that no electromagnetic radiation interferes with the
performance of the system when preparing to carry out performance tests.
Mobile phone, X-ray equipment or MRI devices are a possible source of
interference as they may emit higher levels of electromagnetic radiation.
 Before connecting the system to the power line, check that the voltage and
frequency ratings of the power line are the same as those indicated on the
system’s label or in this manual.
 Protect the system from damage caused by drop, impact, strong vibration
or other mechanical force during servicing.

1.1.3 Notes
NOTE
 Refer to Operator’s Manual for detailed operation and other information.

1-2 BeneVision TMS60 Service Manual

1.2 Equipment Symbols

General warning sign

Refer to instruction manual/booklet

Power On/Off key

Main menu key

Nurse call key

Equipotentiality

Alternating current (AC)

Defibrillation-proof Type CF applied part

Serial number

Date of Manufacture

Symbol for “MANUFACTURER”

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 MR Unsafe – do not subject to magnetic resonance imaging (MRI)

Protection against fluid ingress

Interference may occur in the vicinity of equipment marked with

this symbol

The presence of this label indicates the machine was certified by

ETL with the statement:
Conforms to AAMI Std ES 60601-1, IEC 60601-1-6, IEC Std 60601-1-8,
IEC Std 60601-2-27, IEC Std 60601-2-49, ISO Std 80601-2-61
Certified to CSA Std C22.2 NO. 60601-1, NO. 60601-1-6, NO.
60601-1-8, NO.60601-2-27, NO. 60601-2-49, NO.80601-2-61

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2 Principles

2.1 System Operating Principle

TMS60 is a digital telemetry system consisting of the transmitter (TD60), the receiver
(RC60), the central station and the antenna array. The transmitter sends the patient’s
physiological information to the receiver, which then transmits the information to the
central station for analysis, displaying, storage and printing. The transmitter is attached to
the patient, whereas the receiver is used together with the central station. TMS60
telemetry system is intended to monitor and display a fixed set of parameters including
ECG, SpO2, HR and PR under hospital environments. The SpO2 module is optional.

The following is a simple illustration:

Figure 2-1 TMS60 Telemetry Monitoring System Diagram

NOTE
 The distance between the TD60 and the antenna should be at least one
meter.

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2.2 Hardware Operating Principles
2.2.1 Transmitter Principle

Power Display and

Circuit Control Module

Antenna

Bluetooth
TCXO module
LDO
12.8M

MCU

ECG LPF Match WMTS IC

leadwire
PLL
Externally
SpO2
ECG circuit connecting with
connector
SpO2 module

Figure 2-2 Transmitter Principle Diagram

2.2.2 Overview
The transmitter mainly consists of the MCU, ECG circuit, SpO2 connector, WMTS circuit,
Bluetooth module, Power Circuit, and Display and Control Module.

The ECG circuit provides the amplified ECG signals, which supports 3-lead and 5-lead
modes.

SpO2 module is externally connected to the transmitter.

WMTS circuit is to send ECG data, SpO2 data and status information out .The shielding
layer of the ECG lead is the transmitter antenna.

Bluetooth module is used to transfer configuration between the transmitters.

The Display and Control Module consists of a LCD, a touch screen, a LED indicator, a
speaker, and three keys. It is used to display ECG, SpO2 waveforms and transmitter status,
etc, and allow users to control transmitter.

The MCU circuit is the core of the transmitter, enabling the following functions:
 Button signal detection
 SpO2 connector

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  Status detection, such as ECG overload detection, lead off detection, PACE
detection, etc.
 ECG data processing
 MWTS circuit control and Baseband signal generation
 Bluetooth module control

2.2.3 Receiver
2.2.3.1 Principle Diagram

Figure 2-3 Receiver Principle Diagram

The receiver comprises the AC/DC power source, power adapter board, amplifying and
branching module, 4-channel receiver, LED board, main control board and network
interface board.

2.2.3.2 AC/DC Source

The AC/DC source is to convert the externally inputted AC source into a 9V DC by means
of isolation. The inputted AC voltage range is from 90V to 264V, and the outputted
voltage/current is 9V/6.5A.

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2.2.3.3 Power Adapter Board
The power adapter board is to drop the 9V DC coming from the AC/DC source to a 5V DC
and then output it with the 9V DC.

2.2.3.4 Amplifying and Branching Module

The amplifying and branching module is to amplify, filter and branch RF signals. The
module allows two amplifying, filtering & branching circuits with circuit parameters in full
symmetry. Each circuit amplifies, filters and branches the RF signals received by its
corresponding antenna and then outputs 4 channels of RF signals. Therefore, there are a
total of 8 channels of RF signals, which are then sent to the 4-channel receiver for
processing. The 9V DC linearly drops down to an 8V DC, which then goes to the
amplifying and branching module. The antenna array is shared by all receiving modules.
Therefore, in order to compensate for the branching attenuation of the signal, a LNA (low
noise amplification) is added before the branch divider. Besides, to avoid that the LNA is
blocked by strong out-band signal interference, filtering circuits shall be added in front of
and behind the LNA.

2.2.3.5 4-Channel Receiver

The 4-channel receiver divides the two channels of antenna signals coming from the
amplifying and branching module into four channels of RF signals through the 4-channel
branch divider. The MCU of the 4-channel receiving board will estimate the received
signal strength (RSSI) and then select the corresponding antenna signals through the
antenna switch. The selected signals will be respectively sent to the receiving modules for
filtering, amplifying, mixing, filtering and demodulating. The demodulated 4-channel
analog signals will then be sent to the MCU system for clock and data regenerating. The
regenerated data is packed by CPU and then delivered via the asynchronous serial port to
the main control board for processing. The 9V DC linearly drops down to an 8V DC, which
is then stabilized into a 5V and a 3.5 V supplying power for the 4-channel receiver.

2.2.3.6 Main Control Board

After receiving the data coming from the 4-channel receiving board, the main control
board will pack them and then delivers them to the central station through the Ethernet.
The speaker of the main control board will give a short beep when the initialization is
over, and will beep continuously when an initialization failure or a hardware fault occurs.

2.2.3.7 LED Board

The LED board has two green LEDs, respectively indicating the power status and the
communication status of the receiving module.

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2.2.3.8 Network Interface Board
The interface between the main control board and Ethernet consists of the network
isolating transformer and interface connector.

2.2.4 Central Station (CS)

BeneVision Central Station comprises powerful system software and high-performance
computer components. It constructs a monitoring network by connecting monitors and
telemetry transmitters. By collecting, processing, analysing and outputting the
information coming from monitors and telemetry transmitters, the central station can
achieve centralized monitoring over multiple patients so as to greatly promote the
efficiency and quality of the monitoring work.

The CS is capable of connecting up to 32 telemetry transmitters.

2.2.5 Central Charger

The central charger inner structure consists of three boards, as shown in Figure 2-4:

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 3 2

Figure 2-4 Central Charger Inner Structure

1. AC-DC board (one)

Switching the AC circuit to the DC circuit.
2. Main board (one)
Including the charge circuit, MCU, and LED indicator.
3. Battery interface board (10)
Switching the circuit from the battery contact terminal to the main board.

Three kinds of wires connect with those boards:

 AC-DC socket + wire (P/N 0651-20-76879)
The wire connects the AC socket and the AC-DC board.
 Main board wire (P/N 009-003327-00)
The wire connects the AC-DC board and the main board.
 Battery interface board wires (10) (P/N 009-003325-00)
The wires connect the main board and the battery interface boards.

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 AC-DC socket MCU power supply
circuit

socket
Battery switch board
EN Circuit Charge current
selecting circuit

Charge NTC detection

voltage circuit

socket
Battery interface
terminal
Battery contact
selecting
circuit
Battery
AC-DC AC-DC Main Charge Circuit (10) interface
socket+ board board board wire
wire wire (10)
LED control Burning upgrade Battery
interface board
I2C access EN control (10)

Charge voltage Charge current

control control
MCU (10)

Battery-LED AC-LED
circuit (10) circuit

Main board

Figure 2-5 Central Charger Hardware Boards and Wires

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2.3 Software Principles
2.3.1 Transmitter Software System
2.3.1.1 Overview

Figure 2-6 Interfacing Diagram between the Transmitter Single-Chip Software and
Peripherals

Inside the solid frame is the transmitter software system (hereinafter called the software
system), and outside the solid frame are the inputs and outputs of the software system.
The patient’s ECG data are inputted into the software system by means of sampling.

The external SpO2 module communicates with the transmitter through the serial port,
and the collected SpO2 data are inputted into the software system via the serial port. The
central station and external SpO2 module communicate with the transmitter through the
same serial port. The user commands and online upgrade files of the transmitter software
are inputted into the software system through this serial port.

Patient calls can be inputted into the software system through the nurse call button. The
patient’s ECG and SpO2 parameter signals and the transmitter’s status data are processed
by the software system and then transmitted to the RF module. In addition, the indicator
and speaker are also controlled by the software system.

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2.3.1.2 Transmitter System Task
The transmitter collects the patient’s ECG and SpO2 signals, and then detects the pace
pulse, SpO2 and other status information in them by amplifying and digitalizing them,
and finally sends the detected information to the receiver through wireless channels.

The transmitter supports the auto detection of 3-lead or 5-lead leadwire, lead off
detection and PACE detection. It also supports the external SpO2 module through the
SpO2 connector, through which the central station can perform the parameter
configuration and online software upgrade to the transmitter.

The transmitter also enables these functions including battery voltage detection,

hardware button detection including the Power On/Off and Display On/Off button ,

Nurse Call button , Main menu/Main screen button . Besides, it supports

audible and visual alarms and enables the standby mode, sleep mode, and lock screen
mode.

2.3.2 Receiver System Software

2.3.2.1 Overview

Figure 2-7 Receiver system software diagram

Inside the dashed frame is the system software of the main control board (hereinafter
called the software system), and outside the dashed frame is the inputs and outputs of
the software system. The data coming from the 4-channel receiver are sent to the
software system through the serial port.

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The main control board and receiver controller communicate through the serial port. The
main control board directly controls the LED indicator through the I/O port and
communicates with the central station through the Ethernet.

2.3.2.2 Receiver System Task

The receiver receives data from boards, descrambles data, analyses the integrity of data,
generates relevant alarm messages and sends them together with data to the central
station.

Through the receiving controller, the receiver obtains and controls the operating status of
the receiving demodulator, including the operating frequency and signal strength of the
demodulator. After detecting the operating status, the receiver will give prompt
information through the communication status indicator.

2.3.2.3 Overview of the 4-Channel Receiver Software

Figure 2-8 Diagram for the 4-Channel Receiver Software

Inside the dashed frame is the receiving module control software (hereinafter call
software system), and outside the dashed frame are the inputs and outputs of the
software system. Through the serial port and signal line, the software system
communicates with the receiving demodulator, resolves the data coming from the
data-generating module and controls the antenna system via switch. Besides, it also
communicates with the main control board via the serial port.

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2.3.2.4 4-Channel Receiver Software Task
The 4-channel receiver mainly undertakes the following tasks:
 Recover and resolve the wireless transmission space protocol;
 Configure frequency for the 4-channel receiver on the receiving board;
 Collect the RSSI from the 4-channel receiver on the receiving board;
 Select antenna according to the received signal strength;
 Collect the status information of the 4-channel receiver on the receiving board;
 Carry out the communication with the main control board.

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3 Receiver Physical Views

3.1 Front View

Figure 3-1 Receiver Front View

1. Communications indicator
 Flashes periodically: communications is occurring.
 On: communications is not occurring.
 Off: there is a startup failure or hardware failure.
2. Power indicator
 On: the receiver is powered on.
 Off: the receiver is powered off.

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3.2 Rear View

Figure 3-2 Receiver Rear View

1. Antenna connectors
The receiver has two antenna connectors. Each connector connects an antenna
cable.
2. Power switch
Place the switch to “┃” to turn the receiver on. Place the switch to “〇” to turn the
receiver off.
3. Fuse holder
You can open the cover to replace the fuse.
4. AC power input connector
5. Equipotential grounding terminal
When the receiver and other device are to be used together, their equipotential
grounding terminals should be connected together to eliminate the potential
difference.
6. Network connector
A standard RJ45 connector that connects the receiver to the central monitoring
system.

3-2 BeneVision TMS60 Service Manual

 WARNING
 Only use the approved power cord with the grounded mains plug to firmly
connect the receiver to a grounded AC mains socket. Never refit the mains
plug to fit an ungrounded AC mains socket.
 Do not use the Multiple Portable Socket Outlets (MPSO) or AC mains
extension cords. Use an IEC 60601-1 approved isolation / separation
transformer, otherwise, it may result in leakage current. Insure that the
sum of the individual ground leakage currents does not exceed the
allowable limits.

3.3 Restoring Latest Configuration Automatically

To prevent the changes from losing in case of a sudden power failure, the device, such as
the receiver or the BeneVision Central Station, stores the configuration in real time. The
saved configuration is the latest configuration.

The device restores the latest configuration if it restarts within 60 seconds after the power
failure. And the device will restore the default configuration rather than the latest
configuration if it restarts 120 seconds after the power failure. The device may load either
the latest configuration or the default configuration if it restarts from 60-120 seconds
after the power failure.

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4 Central Charger Physical Views

4.1 Front View

Figure 4-1 Central Charger Front View

1. Charging slot
2. AC power indicator
Off: No AC power supply connected, or the AC-DC board is abnormal.
Green: AC power supply is connected.
3. LED indicators: indicates the charging status for the corresponding charging slot.

4.2 Rear View

Figure 4-2 Central Charger Rear View

1. AC power socket

For further details about the central charger such as how to mount the central charger
and how to charge and remove batteries, refer to the BeneVision Central Charger
Operator’s Manual (P/N 046-007059-00).

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5 Maintenance

To ensure that the telemetry monitoring system always functions normally, qualified
service personnel should perform regular inspection, maintenance and test. This chapter
provides a checklist of the testing procedures for the telemetry monitoring system with
recommended test equipment and frequency. The service personnel should perform the
testing and maintenance procedures as required and use appropriate test equipment.

The testing procedures provided in this chapter are intended to verify that the telemetry
monitoring system meets the performance specifications. If the telemetry monitoring
system fails to perform as specified in any test, repairs or replacement must be done to
correct the problem. If the problem persists, contact our Customer Service Department.

CAUTION
 All tests should be performed by qualified service personnel only.
 Care should be taken to change the settings in the Maintenance menu to
avoid loss of data.
 Service personnel should acquaint themselves with the test tools and
make sure that test tools and cables are applicable.

5.1 Recommended Maintenance and Test Frequency

Check/Maintenance Item Frequency

Visual inspection When first installed or reinstalled.
1. When first installed or reinstalled
Power-on test 2. Following any repairs or replacement
of transmitter components
Performance test
ECG test
Calibration 1. If the user suspects that the measurement
is incorrect.
2. Following any repairs or replacement of
SpO2 test relevant module.
3. At least once every two years.

If the user suspects that the measurement is

Nurse call test
incorrect.

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 Check/Maintenance Item Frequency
1. After the transmitter or central charger
falls off.
Electrical safety tests
2. Performed at least once every two years or
as needed
1. When first installed.
Network print test 2. Whenever the printer is serviced or
replaced.
1. When first installed.
Functionality test
2. Whenever a battery is replaced.
Battery check
Once every two months or when the battery’s
Performance test
run time becomes noticeably shorter.

5.2 Parameter Performance Test

5.2.1 ECG Performance Test
Tool required:
 Medsim 300B patient simulator recommended
Follow this procedure to perform the test:
1. Connect the patient simulator with the ECG module using an ECG cable.
2. Set the patient simulator as follows: ECG sinus rhythm, HR=80 bpm with the
amplitude as 1mV.
3. Check the ECG waves are displayed correctly without noise and the displayed HR
value is within 80±1 bpm.
4. Disconnect each of the leads in turn and observe the corresponding lead off
message displayed on the screen.
5. Set that the simulator outputs paced signals and set Paced to Yes on the transmitter.
Check the pace pulse marks on the transmitter’s screen.

5.2.1.5 ECG Calibration

The ECG signal may be inaccurate due to hardware or software problems. As a result, the
ECG wave amplitude becomes greater or smaller.
Tool required:
 Vernier caliper
To verify the ECG waveform amplitude:
1. In the main menu, select Parameter Setup.
2. Select ECG.
3. Set Filter to Monitor.
4. Return to the main menu and select Maintenance.
5. Input the maintenance passcode.
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6. Tap Accept.
7. In the Maintenance menu, select General.
8. Enable Calibrate ECG. A square wave appears on the screen and the message ECG
Calibrating is displayed in the technical alarm area of the transmitter’s screen.
Compare the amplitude of the square wave with the wave scale. The difference
should be within 5%.
9. After completing the verification, disable Calibrate ECG. If necessary, you can print
out the square wave and wave scale through the recorder and then measure the
difference.

5.2.2 SpO2
Tool required:
 None
Follow this procedure to perform the test:
1. Connect an adult SpO2 sensor to the SpO2 connector of the transmitter.
2. In the main menu, select Patient Info and set Patient Category to Adult on the
transmitter
3. Measure SpO2 on your finger. (Assume that you stay healthy)
4. Check the Pleth wave and PR reading on the screen and make sure that the
displayed SpO2 is within 95%-100%.
5. Remove the SpO2 sensor from your finger and make sure that an alarm of SpO2
Sensor Off is triggered.

Measurement accuracy verification:

The accuracy of Masimo and Nonin SpO2 modules has been verified in human
experiments by comparing with arterial blood sample reference measured with a
CO-oximeter. Pulse oximeter measurements are statistically distributed and about
two-thirds of the measurements are expected to come within the specified accuracy
range compared to CO-oximeter measurements.

NOTE
 A functional tester cannot be used to assess the accuracy of a pulse
oximeter monitor. However, it can be used to demonstrate that a particular
pulse oximeter monitor reproduces a calibration curve that has been
independently demonstrated to fulfill a particular accuracy specification.

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5.3 Miscellaneous Tests
5.3.1 Visual Inspection
Perform a visual inspection before the equipment is first used every day. Verify that the
equipment meets the following requirements:
 The housing and display screen are free from cracks or other damages.
 All keys function properly.
 Connectors are not loose, cracked, or bent and cables have no cuts, nicks, or
fraying.
 ECG leadwires are securely connected with the equipment.
 Battery pack is installed and has sufficient charge.
 Chest electrodes are free from cracks and limb electrodes can properly clamp.

5.3.2 Power-On Test

This test is to verify that the transmitter can power up correctly.
Follow this procedure to perform the test:
1. Install a lithium-ion rechargeable battery pack or AA batteries into the transmitter’s
battery compartment.
2. Press the Power on/off key to turn on the transmitter. The cyan alarm light will
momentarily turn on to indicate that the device is starting.
When the boot screen appears, the device sounds a beep, and the alarm light
serially turns red, yellow, cyan, and then off. This indicates that the alarm system
functions correctly. When the boot screen disappears, the main screen displays and
the device finishes starting.

WARNING
 Check that visual and auditory alarm signals are presented correctly when
the equipment is powered on. Do not use the equipment for any
monitoring procedure on a patient if you suspect the equipment is not
working properly or if the equipment is mechanically damaged. Contact
your service personnel or Mindray.

5.3.3 Nurse Call Test

Follow this procedure to perform the test:
1. Press the nurse call button on the transmitter.
2. Observe corresponding display on the central station. If a nurse call icon appears, it
indicates that the nurse call test passes.

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5.3.4 Electric Safety Test
Refer to A Electrical Safety Inspection for details.

5.3.5 Network Print Test

Follow this procedure to perform the test:
1. Power on the transmitter.
2. Connect the transmitter to the central station wirelessly.

3. Press to enter the main menu of the transmitter or swipe your finger up from
the bottom of the main screen to display the quick keys area.
4. Select Print.
5. Verify that the network printer shall print out a report correctly.

5.3.6 Battery Check

Refer to 11 Battery in the BeneVision TMS60 Telemetry Monitoring System Operator’s
Manual (P/N 046-007056-00) for methods to check battery status and verify battery
supply specifications.

5.3.7 Tests in Service Menu

Refer to 6 Service Menu for test items in the service menu.

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6 Service Menu

In the Service menu, you can update TD60 software, check the service log, perform the
factory test, and check the system software version.

6.1 Entering the Service Menu

1. Press to enter the main menu
2. Select Maintenance.
3. Input the password, and then tap Accept.
4. Select Service.
5. Input the password, and then tap Accept.

6.2 Performing Software Update

Software upgrade must be performed by Mindray. Please contact Mindray for
software upgrade.

6.3 Service Log

The service log stores and displays the error codes.
To check the service log, select Service Log in the Service menu.
For details on the error codes, refer to 7.1.3 Error Codes.

6.4 Factory Test

To enter the Factory Test menu, select Factory Test from the Service menu.

6.4.1 Device Test

The option is to do the device self-test.
1. In the Factory Test menu, select Device Test.
2. Tap Start.
The device self-tests including device test, MO module test, and Bluetooth module
test start.

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 The test results will correspondingly display to the right of the test. If the test fails,
refer to 6.4.10 Processing Method.

6.4.2 Screen Test

This option is to test the screen.
1. In the Factory Test menu, select Screen Test.
2. Tap the screen in turn.
If the screen color turns red, green, cyan, white, and then off, tap Pass. If the screen color
is not displayed in this way, tap Fail.
If the test fails, refer to 6.4.10 Processing Method.

6.4.3 Touch Screen Test

This option is to test the touch screen.
1. In the Factory Test menu, select Touch Screen Test.
2. Touch the white blank screen, and move around.
If a touch line appears on the screen, tap Pass.
If a touch line does not appear on the screen, tap Fail. If the test fails, refer to 6.4.10
Processing Method.

6.4.4 Keys Test

This option is to test the hard keys.
1. In the Factory Test menu, select Keys Test.
2. Press each key to test.

 Press and the screen displays “Power Key is Pressed Shortly”; or keep

pressing and the screen displays “Power Key is Pressed Long”.

 Press and the screen displays “Nurse Call Key is Pressed”.

 Press and the screen displays “Menu Key is Pressed”.

3. Tap Pass to finish the keys test.
If any key test fails, refer to 6.4.10 Processing Method.

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6.4.5 Sound & Light Test
This option is to test speaker, and red, yellow, cyan LEDs.
1. In the Factory Test menu, select Sound & Light Test.
2. Select Sound Test. If the speaker sounds, tap Pass.
3. Select Red Light Test. If the red light flickers, tap Pass.
4. Select Yellow Light Test. If the yellow light flickers, tap Pass.
5. Select Cyan Light Test. If the cyan light flickers, tap Pass.

6.4.6 USB Interface Test

This option is to test USB interface.
1. Insert a USB drive.
2. In the Factory Test menu, select USB Interface Test.
If the test is completed successfully, tap Pass. If it fails, refer to 6.4.10 Processing
Method.

NOTE
 The upgrade tools kit (Dubhe) P/N 115-033434-00 is required to perform
the USB interface test.

6.4.7 System Watchdog Test

This option is to test the system watchdog.
1. In the Factory Test menu, select System Watchdog Test.
2. Tap Yes. Then, the device will be restarted. If the test fails, refer to 6.4.10 Processing
Method.

6.4.8 MO Module Watchdog Test

This option is to test the MO module watchdog.
1. In the Factory Test menu, select MO Module Watchdog Test.
2. Tap Yes. The device will be restarted. If the test fails, refer to 6.4.10
Processing Method.

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6.4.9 Bluetooth Module Test
This option is to test the Bluetooth module. Two or more TD 60 devices are required for
this test. To show the test procedures clearer, we use two TD 60 devices which are called
as TD 60-2 and TD 60-1 hereinafter.
1. For TD 60-2, in the Factory Test menu, select Bluetooth Module Test.
2. For TD 60-1, in the Maintenance menu, select Defaults and then select Import
Device Settings.
3. Slide the MPAN on/off switch of TD 60-2 to right. Then, TD 60-2 starts searching
devices.
4. Tap Connect when TD 60-1 was found. When they are connected successfully, the
connection status on the right of TD 60-1 will be changed to Connected, as shown in
Figure 6-1.

Figure 6-1 Example of Bluetooth Module Test Screen

If the test fails, refer to 6.4.10 Processing Method.

6.4.10 Processing Method

If the factory test fails, please contact your service personnel or Mindray.

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6.5 Checking System Software Version
In the Service menu, select System Software Version.
The screen displays the software version of development as follows:
Format: xx.xx.xx.xx.
Compile Time: Month day, year

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7 Troubleshooting

7.1 Telemetry Monitoring System Problems

The section describes the troubleshooting about the transmitter, and the receiver.

7.1.1 Troubleshooting Tools

 Receiver
 Transmitter

7.1.2 Technical Alarm Messages

Alarm Possible Cause Processing Method

Message
Low Battery The battery charge of the Replace the battery of the
transmitter is to be depleted. transmitter.
No RF signal (The 1. The battery charge of the 1. Check if the battery charge of
receiver does not transmitter is to be the transmitter is depleted.
receive valid depleted. 2. Check if the corresponding
data for 2. The transmitter in the transmitter is in dormant
consecutive 5 dormant status. status.
seconds) 3. The patient is out of the 3. Check if the patient is out of
antenna array coverage the coverage area.
area. 4. Check if there is an error in the
4. There is an error in the antenna array. Refer to 7.1.5.1
antenna array. Determining RF Signal
5. The transmitter is not Interference and 7.1.5.2 Low
connected with the ECG RSSI Signal Check for details.
cable. 5. Check if the transmitter is
6. The receiver frequency is connected with the ECG cable
not paired with the properly.
transmitter frequency. 6. Check if the receiver frequency
7. There is an IP addresses configuration that is
conflict. consistent with the
transmitter.
7. Reset the IP addresses at the
central station.
RF interference 1. The transmitter signal is 1. Check if the Patient is at the
(The transmitter weak. edge of the coverage area or
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 Alarm Possible Cause Processing Method
Message
receives three 2. There is RF interference in an elevator. Remove behind
consecutive around. a reinforced concrete wall.
wrong frames.) 2. Check for RF Interference.
Refer to 7.1.5.1 Determining
RF Signal Interference and
7.1.5.2 Low RSSI Signal Check
for details.
Wrong Channel 1. The channel name for 1. Reset the channel name at the
the transmitter is central station.
incorrect. 2. Check if there is another
2. The receiver receives the telemetry system in the
data sent from the vicinity. Re-configure the
transmitter, but the ID frequency. Refer to 7.1.5.3
code does not belong to Programming Telemetry
the system. Packs for details.
Receiver Offline 1. The receiver is not 1. Check if the receiver is
powered on. powered on;
2. The receiver cannot be 2. Check if the network cable is
connected to the central properly connected.
station.
SpO2 No Pulse The SpO2 sensor failed to Check the patient’s condition and
obtain pulse signal. change the sensor application site.
If the error persists, replace the
sensor.
Transmitter key The transmitter detects that a Check if the key is pressed by a
error key has been pressed for over foreign object or jammed.
10 seconds.
Receiver Fault An error occurred to the Restart the receiver.
receiver.

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7.1.3 Error Codes

Error Message Displayed Possible Cause Processing Method

Code on the Screen
Power off and then on
the transmitter to see if
Module Selftest The parameter board the fault disappears. If
001
Err(0xff ) MCU is faulty. the fault persists,
change the parameter
board.
Power off and then on
the transmitter to see if
The ECG ASIC chip is the fault disappears. If
002 ECG ASIC Init Err
faulty. the fault persists,
change the parameter
board.
Power off and then on
the transmitter to see if
The power supply for
the fault disappears. If
003 ECG ASIC 3.3V Err the parameter board
the fault persists,
is abnormal.
change the parameter
board.
1. The SpO2 1. Replug the SpO2
module is faulty. module.
2. The SpO2 2. Replace with a
module is not SpO2 module
supported by supported by the
004 SPO2 Init Err the transmitter. transmitter.
3. The SpO2 3. Replace the SpO2
connection connection circuit
circuit of the or the parameter
transmitter is board.
abnormal.
1. The Bluetooth 1. Power off and
firmware is then on the
abnormal. transmitter to see
2. The Bluetooth if the fault
firmware is disappears.
006 Bluetooth Init Err faulty. 2. Upgrade the
3. The power Bluetooth
supply for the firmware.
Bluetooth 3. Replace the
module is parameter board.
abnormal.

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 Error Message Displayed Possible Cause Processing Method
Code on the Screen
1. Reinstall batteries
1. Batteries are not per instructions in
installed Operator’s
properly. Manual.
2. The battery 2. Check that the
contacts inside battery contacts
the battery are not depressed.
008 Battery Comm Err
compartment of If they are
the transmitter depressed, pull
are damaged or the battery
distorted. contacts to the
3. Batteries are original positions.
faulty. 3. Replace with new
batteries.
1. Battery voltage 1. Replace with new
is low. batteries.
2. The power 2. Replace the
011 Power 2.5V Err(0xff ) supply circuit of parameter board
the parameter with a known
board is good one.
abnormal.
1. Move the
transmitter away
from interference
The ECG detection
020 ECG Selftest(0xff ) sources and then
circuit is abnormal.
restart it.
2. Replace the
parameter board.
1. Power off and
The watchdog circuit then on the
021 Module Watchdog Err on the parameter transmitter.
board is abnormal. 2. Replace the
parameter board.
1. RTC battery is 1. Replace the RTC
low. battery.
103 RTC Comm Err
2. RTC chip is 2. Replace the
faulty. parameter board.
The main control Replace the parameter
104 E2PROM Err
EEPROM is faulty. board.
An error occurred 1. Move the
while initializing the transmitter away
105 ECG Init Err
parameter board from interference
ECG. sources and then

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Error Message Displayed Possible Cause Processing Method
Code on the Screen
restart it.
2. Replace the
parameter board.
1. Move the
transmitter away
from interference
sources and then
Communication restart it.
between the 2. Check the FPC
106 ECG Comm Stop parameter board and connection
the main control between the
board is abnormal. parameter board
and the main
control board.
3. Replace the
parameter board.
1. Move the
transmitter away
from interference
sources and then
Communication restart it.
between the 2. Check the FPC
107 ECG Comm Abnormal parameter board and connection
the main control between the
board is abnormal. parameter board
and the main
control board.
3. Replace the
parameter board.
1. Move the
transmitter away
from interference
sources and then
Communication restart it.
between the 2. Check the FPC
108 ECG COMM Err parameter board and connection
the main control between the
board is abnormal. parameter board
and the main
control board.
3. Replace the
parameter board.

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 Error Message Displayed Possible Cause Processing Method
Code on the Screen
1. Move the
transmitter away
from interference
An error occurred sources.
109 SPO2 Init Err while initializing the 2. Replug the SpO2
SpO2 module. module.
3. Replace with a
known good SpO2
module.
1. Move the
transmitter away
Communication from interference
between the SpO2 sources.
110 SPO2 Comm Stop module and the 2. Replug the SpO2
transmitter is module.
abnormal. 3. Replace with a
known good SpO2
module.
1. Move the
transmitter away
Communication from interference
between the SpO2 sources.
SPO2 Comm
111 module and the 2. Replug the SpO2
Abnormal
transmitter is module.
abnormal. 3. Replace with a
known good SpO2
module.
1. Move the
transmitter away
Communication from interference
between the SpO2 sources.
112 SPO2 Comm Err module and the 2. Replug the SpO2
transmitter is module.
abnormal. 3. Replace with a
known good SpO2
module.
The parameter board Replace the parameter
114 Module Init Err
MCU is abnormal. board.
Communication 1. Move the
between the transmitter away
115 Module Comm Err parameter board from interference
MCU and the main sources and then
control board is restart it.

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 Error Message Displayed Possible Cause Processing Method
Code on the Screen
abnormal. 2. Check the FPC
connection
between the
parameter board
and the main
control board.
3. Replace the
parameter board.
1. Power off and
then on the
The main board
116 Main Board Selftest Err transmitter.
selftest error
2. Replace the main
control board.

7.1.4 Other Failures

Symptom Possible Cause Processing Method

The receiver 1. Bad network cable 1. Replug the network cable of
cannot connect connection the receiver and make sure
to network. 2. The IP address of the that it is connected securely.
receiver is set incorrectly. 2. Connect the receiver to the
PC via a network cable. The
PC is installed with a
telemetry configuration tool.
Change the receiver IP
address and confirm the
change at the PC side. If the IP
address of the central station
is set to DHCP, the IP address
of the receiver should be set
to DHCP. If the IP address of
the central station is set to a
static IP, the IP address of the
receiver should be set to a
static IP in the same network
segment.
The telemetry 1. Incorrect network cable 1. Check the network cable
system cannot connection. connection.
connect to the 2. Incorrect IP address 2. Configure correct IP address.
network of the setting
central station.

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 Symptom Possible Cause Processing Method
The CS does not 1. The SpO2 module is not 1. Connect the SpO2 module to
display the SpO2 connected to the the transmitter.
data. transmitter. 2. If there is an error in the SpO2
2. There may be error in the module, replace the SpO2
SpO2 module. module with a new one.
ECG noise ECG waveforms are Check that the electrodes are
overlapped with the noise properly attached, the leadwires
interference. are secured properly, and the
patient does not come into
contact with any ungrounded
electric device.
ECG signal The transmitter detects that 1. Check if patient has excessive
saturation ECG signal saturation or movement.
overload. 2. Check if the electrodes are in
good contact with the skin.
3. Check if the electrodes
operating time is over the
electrode service life.

Low signal The signal of the central 1. Check if the ECG cable is
intensity station (average value) is less firmly connected to the
than 180 transmitter.
2. Check if there is signal
intensity between the
receiver and transmitter.
Refer to 7.1.5 Failure
Examinations for details.

The AC power 1. The receiver is not 1. Check if the receiver is

indicator on the connected to the power. connected to the power.
receiver is off. 2. The receiver is power off. 2. Check if the receiver sounds a
beep when turn the receiver
on.
Transmitter or The battery charge of the Replace the battery of the
SpO2 module transmitter is to be depleted. transmitter.
restarting
repeatedly.

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7.1.5 Failure Examinations
7.1.5.1 Determining RF Signal Interference
1. Connect a receiver to the antenna array.
2. Turn on the telemetry system and the central station. Ensure that the telemetry
system works normally.
3. Remove the battery of interference transmitter; make sure its RSSI in the Telemetry
window of CS is not higher than 130 (-105dBm). If the RSSI is higher than 130
(-105dBm), use the CS configuration tool to scan all of the frequencies, and choose a
frequency, of which the signal is lower than -105dBm, and program it to the
interference transmitter.
4. If there is more than one transmitter with interference, resolve each transmitter one
by one according to step 2.

Figure 7-1 Example of Telemetry Tab

7.1.5.2 Low RSSI Signal Check

1. When a transmitter has a low signal strength indication, access the “Telemetry” tab
and check the RSSI to see if it is low.
2. Choose a known good transmitter whose RSSI is above 180.
3. Program the known good transmitter to the frequency of the suspected bad
transmitter and vice versa.
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4. If the low RSSI follows the transmitter, the transmitter is defective. If the low RSSI
stays with the channel, the receiver board is defective.

7.1.5.3 Programming Telemetry Packs

NOTE
 When the number of the beds is greater than 80 beds, follow the below
rule to configure the frequencies:
The start frequency is 608 MHz, the end frequency is 613.975 MHz, and the
channel interval is 25 KHz.

1. Connect one end of the dedicated programming cable to the serial port 1 (COM1) on
the CS, and the other end to the SpO2 connector on the transmitter.
2. At the CS, select System Setup and then select Admin Setup. After entering a
password, tap OK to enter the “Admin Setup” window.
3. Select the Telemetry tab, and then select Frequency Setup. The “Telemetry” tab
displays as shown in Figure 7-2.

Figure 7-2 Example of the Telemetry Tab

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4. View the transmitter SN number, and remember the last eight digitals, such as
12345678.
5. In the “Frequency Setup” field, select the desired transmitter name, such as
“TEL-0001”, from the “Monitor Name” column.
6. Tap Program to display the “Program” window as shown in Figure 7-3.

Figure 7-3 Example of Program Window

7. In the “Frequency” input field, enter the frequency as desired.

8. Tap OK to start programming.

NOTE

 The power is 23. Do not change the power level.

9. After the programming succeeds, the prompt message “Frequency setup completed
successfully” displays.
10. Tap OK to close the dialog. So far the programming of a pair of transmitter and
receiver is finished.

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 If you want to program another pair of transmitter and receiver, repeat the above
step 6-10.

7.1.5.4 Admitting the Transmitter

After programming the telemetry packs, you can continue to admit the transmitter at the
CS.
1. In the “Admin Setup” window, select the “Monitor List” tab. The “Monitor List” tab
displays, as shown in Figure 7-4.

Figure 7-4 Example of the Monitor List Tab

2. Select your desired transmitter name from the “Monitor Name” column, such as TEL
7398.
3. Tap Admit.
4. Click the button to enter the multi-bed menu and then select Admit Telemetry
Patient by clicking the patient admission button. Then, the patient will be
admitted successfully.

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 Figure 7-5 Example of Admit Telemetry Patient

7.1.5.5 Discharging and Freeing the Transmitter Channel/Frequency from the CS

1. Connect one end of the dedicated programming cable to the serial port 1 (COM1) on
the CS, and the other end to the SpO2 connector on the transmitter.
2. At the CS, select Admin Setup from System Setup, input the correct password, and
then tap OK to enter the “Admin Setup” window.
3. Select the “Telemetry” tab.
4. In the “Frequency Setup” field, select the desired transmitter name, such as TEL 7398
from the “Monitor Name” column.
5. Tap Discharge to release the transmitter from the CS. Please be noted that if there is
still a valid waveform on the transmitter, the transmitter will be connected to the CS
automatically after a patient is discharged from the CS.

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7.1.5.6 Programming the Replacement Telemetry Packs
If a telemetry transmitter is damaged, you need to replace a new telemetry transmitter.
1. At the CS, select Admin Setup from System Setup, input the correct password, and
then tap OK to enter the “Admin Setup” window.
2. Select the “Telemetry” tab. The “Telemetry” tab displays.
3. In the “Frequency Setup” field, select the damaged transmitter name, such as “TEL
0007”, from the “Monitor Name” column.
4. Tap the Discharge button to free the transmitter channel/frequency from the CS.
5. Connect one end of the dedicated programming cable to the serial port 1 (COM1) on
the CS, and the other end to the SpO2 connector on the new transmitter.

Figure 7-6 Example of COM1 Serial Port

6. Tap the Program button to display the “Program” window.

7. In the “Frequency” input field, enter a frequency that is not being use or the same
frequency as the transmitter that was replaced, as shown in Figure 7-6.

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 Figure 7-7 Example of Program Window

8. Tap OK to start programming.

9. After the programming succeeds, the prompt message “Frequency setup
completed successfully” displays.
10. Tap OK to close the dialog. So far the programming the replaced telemetry
transmitter is finished.

NOTE

 For how to admit a transmitter, refer to 7.1.5.4 Admitting the Transmitter.

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7.2 Central Charger Problems
Symptom Possible Cause Processing Method
The AC power indicator 1. The AC power socket 1. Change another available
is off. is unavailable. AC power socket. Check if
2. The connection is not the AC power indicator is
good. still off.
3. The main board is 2. Correctly reconnect the
abnormal. central charger to the AC
4. The AC-DC board is power socket. Check if
abnormal. the AC power indicator is
still off.
3. Replace the main board
with a new one, check if
the AC power indicator is
off.
4. Replace the AC-DC board
with a new one.

After the lithium-ion 1. The battery is not 1. Pull the battery from the
battery is plugged in the plugged in the charger slot, and then
charger slot, the charger slot correctly. re-plug the battery to the
corresponding LED 2. The corresponding end of the charger slot.
indicator is still off. LED indicator is Check if the LED indicator
broken. is still off.
3. The corresponding 2. Remove the battery from
battery interface the current charger slot.
board is abnormal. Try to use other charger
4. The main board is slots. Check if the LED
abnormal. indicator is still off.
3. Replace the battery
interface board with a
new one. Check if the
LED indicator is still
off.
4. Replace the main
board with a new one.

7-16 BeneVision TMS60 Service Manual

WARNING
 To avoid the electric shock, disassemble the central charger after the
central charger is disconnected from the AC power source for five minutes
later.

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7-18 BeneVision TMS60 Service Manual

8 Parts

8.1 Transmitter (P/N 115-029485-00)

8.1.1 Exploded View of Main Unit

Figure 8-1 Exploded View of Main Unit

No. P/N Description

1 115-026846-00 Front cover assembly
2 / Back cover assembly FRU
3 030-000659-00 Screws M1.6x13.3mm color zinc plating
4 030-000660-00 Screws M1.6x9.8mm color zinc plating
5 047-014418-00 Blank label

BeneVision TMS60 Service Manual 8-1

6 047-014659-00 The host label (FDA)
No. P/N Description
115-030105-00 Battery frame (2AA) (with 3pcs)
7
115-030106-00 Battery frame (3AA) (with 3pcs)
8 0000-10-10902 AA battery
9 030-000658-00 Screws M1.6x3.5mm color zinc plating
10 030-000661-00 Screws M1.6x2.4mm color zinc plating

8.1.1.1 Exploded View of Front Cover Assembly（P/N 115-026846-00）

Figure 8-2 Exploded View of Front Cover Assembly

8-2 BeneVision TMS60 Service Manual

 No. P/N Description
1 LCD TFT 3.5" 480*272 3.3V PCT
2 TP Front Cover
3 115-032157-00 TP key gasket (small)
4 TP key gasket (big)
7 Seal
5 051-001986-00 0155 main board PCBA
6 030-000661-00 Screws M1.6x2.4mm color zinc plating
8 048-004511-00 TP warning light PCBA gasket
9 048-004512-00 TP outlet gasket

8.1.1.2 Exploded View of Back Cover Assembly

Figure 8-3 Exploded View of Back Cover Assembly

BeneVision TMS60 Service Manual 8-3

 No. P/N Description
1 030-000658-00 Screws M1.6x3.5mm color zinc plating
2 042-011883-00 Shield cover
3 050-001539-01 0156 FPC for main and parameter Board
4 051-001705-01 New Telemetry ECG Board PCBA
5 USB silica gel plug
6 Speaker 0.5W IPX8
7 ECG and SpO2 socket gasket
8 Speaker bracket
9 115-032160-00 TP horn dust network
12 Bluetooth antenna (P/N 024-000750-00)
14 TP back Cover
17 SpO2 silicone plugs (P/N 049-000782-00)
19 SpO2 gasket
10 TP battery sheet metal bayonet mount
11 115-032156-00 TP battery snaps shrapnel
13 TP battery snaps
15 ECG-connector
115-032159-00
18 ECG limit frame
16 051-001709-00 SpO2 connector assembly
20 047-013564-00 TP insulation sheet

8-4 BeneVision TMS60 Service Manual

8.2 Receiver (P/N 115-029486-00)
8.2.1 Exploded View of Receiver

Figure 8-4 Exploded View-1 of Receiver

BeneVision TMS60 Service Manual 8-5

 Figure 8-5 Exploded View-2 of Receiver

8-6 BeneVision TMS60 Service Manual

No. P/N Name and Specifications Quantity
1 0152-20-39747 Main bracket 3 of the receiver 1
2 0152-20-39746 Main bracket 2 of the receiver 1
3 801-0152-00080-00 Ethernet interface board 1
4 M04-002505--- Cross pan head screw M3×6 2
5 801-0152-00085-00 9210 main control board 1
6 900E-20-04894 Dust washer1 1
7 M04-021003--- Plain washer GB97.26 1
8 M04-004504--- Spring washer BF93 6 4
9 M04-004401--- Stainless steel hexagon nut M6 1
10 0152-20-39744 Bottom plate of the receiver 1
11 115-029487-00 4-channel receiver (608-614) 1
Cross recessed countersunk screw
12 M04-000405--- 21
M3×8

13 045-001817-00 Front cover of the receiver 1

14 0152-20-39948 Upper cover of the receiver 1

15 801-0152-00002-00 Power adapter board 1
16 0152-30-39738 Power assembly of the receiver 1
17 0152-20-39732 Rubber foot of the receiver 1
Amplifying and branching assembly
18 801-0152-00128-00
of the receiver (608-614)

BeneVision TMS60 Service Manual 8-7

8.2.2 Front Cover Assembly of Receiver

Figure 8-6 Front Cover Assembly of Receiver

No P/N Name and Specifications Quantity

1 045-001817-00 Front cover of the receiver 1
2 0152-20-39748 Main bracket 4 of the receiver 1
3 0152-30-39726 LED board 1
4 M04-004012--- Cross pan head screw M3×6 4

8-8 BeneVision TMS60 Service Manual

8.2.3 Power Assembly of Receiver

Figure 8-7 Power Assembly of Receiver

No P/N Name and Specifications Quantity

1 0152-20-40046 Power cover of the receiver 1
2 801-0000-00009-00 Power module AC/DC 90-264VAC 9VDC 1
3 M04-004012--- Cross pan head screw M3×6 4

BeneVision TMS60 Service Manual 8-9

8.2.4 Amplifying and Branching Assembly of Receiver (P/N
0152-30-39691)

Figure 8-8 Amplifying and Branching Assembly of Receiver

No P/N Name and Specifications Quantity

Upper cover of the amplifying and branching
1 / 1
assembly of the receiver
2 / Cross pan head screw M3×6 9
3 / Antenna socket 2
Bottom cover of the amplifying and branching
4 / 1
assembly of the receiver
5 / Amplifying and branching board (185-205) 1
6 / Feedthrough capacitor 1
7 / SMA radio frequency socket 8
8 / Cross pan head screw M2×6 66

8-10 BeneVision TMS60 Service Manual

8.2.5 4-Channel Receiver Module Assembly (P/N 115-029487-00)

Figure 8-9 4-Channel Receiver Module Assembly

No P/N Name and Specifications Quantity

1 / Cross pan head screw M2.5×8 12
2 / Back panel of the receiver module 1
3 / Receiver module cavity 1
4 / 4-channel receiving board 1
5 / Front panel of the receiver module 1

BeneVision TMS60 Service Manual 8-11

8.3 Power Injector (P/N 115-035637-00)

No P/N Name and Specifications Quantity

1 M04-051099--- Countersunk flat head screws M2.5X8 8
2 041-008877-00 Back plate signal converter(printing) 1
3 041-008875-00 Signal converter box 1
4 051-002362-00 0155 Signal Converter PCBA 1

8-12 BeneVision TMS60 Service Manual

8.4 Signal Switching Box (P/N 115-020216-00)

Figure 8-10 Signal Switching Box

No P/N Name and Specifications Quantity

1 / Countersunk flat head screws 8
2 / Back plate signal converter(printing) 1
3 / Signal converter box 1
4 / 0164 Signal Connection Board PCBA 1
5 / WIRE power cable American Domestic 1
6 022-000138-00 Adapter 100-240VAC 9V 70W 1

BeneVision TMS60 Service Manual 8-13

8.5 Exploded View of Central Charger

Figure 8-11 Exploded View of Central Charger

8-14 BeneVision TMS60 Service Manual

 No. P/N Description
1 047-014714-00 Gasket of top housing
2 049-000792-00 AC light pipe
3 M04-051134--- Pan head screw M4X8
4 042-012302-00 Charger-main-support
5 0000-10-10996 Spring, EMI
6 030-000338-00 ST3.3X8 screw
7 051-001719-00 Charger Connector Board PCBA
8 051-001720-00 Charger Charge main Board PCBA
9 0651-20-76879 AC power socket & connecting cable
10 043-005882-00 Charger bottom housing(SY)
11 047-010577-00 FOOT-VS
12 049-000814-00 Screw hole cover 1
13 049-000815-00 Screw hole cover 2
14 M04-004012--- Screw, Pan Head W/Washer Phillips M3X6
15 022-000159-00 POWER SUPPLY BOARD 15V 63W
16 047-010792-00 Thermal Pad
17 047-013600-00 AC-DC insulating trip
18 047-013598-00 Indicator label
19 049-000960-00 Light pipe of central charger
20 043-005298-00 Charger top housing
21 047-014926-00 The host label (FDA)
22 009-003327-00 Main board wire
23 009-003325-00 Battery interface board wires

8.6 Micellaneous:
No. P/N Description
1 009-005427-00 Programming cable
2 DA8K-10-14452 Power cords
3 0000-10-10902 AA batteries
4 115-030109-00 Central charger wall mount
5 115-033434-00 Upgrade tools kit (including update cable and adapter)

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8-16 BeneVision TMS60 Service Manual

A Electrical Safety Inspection

The following electrical safety tests are recommended as part of a comprehensive

preventive maintenance program. They are a proven means of detecting abnormalities
that, if undetected, could prove dangerous to either the patient or the operator.
Additional tests may be required according to local regulations.

All tests can be performed using commercially available safety analyzer test equipment.
These procedures assume the use of a 601PROXL International Safety Analyzer or
equivalent safety analyzer. Other popular testers complying with IEC 60601-1 used in
Europe, such as Fluke, Metron, or Gerb, may require modifications to the procedure.
Please follow the instructions of the analyzer manufacturer.

The consistent use of a safety analyzer as a routine step in closing a repair or upgrade is
emphasized as a mandatory step if an approved agency status is to be maintained. The
safety analyzer also proves to be an excellent troubleshooting tool to detect
abnormalities of line voltage and grounding, as well as total current loads.

A.1 Power Cord Plug

Test Item Acceptance Criteria
The power plug pins No broken or bent pin. No discolored pins.
The The plug body No physical damage to the plug body.
power No physical damage to the strain relief. No plug
The strain relief
plug warmth for device in use.
The power plug No loose connections.
No physical damage to the cord. No deterioration
to the cord.
For devices with detachable power cords, inspect
The power cord
the connection at the device.
For devices with non-detachable power cords,
inspect the strain relief at the device.

BeneVision TMS60 Service Manual A-1

A.2 Device Enclosure and Accessories
A.2.1 Visual Inspection
Test Item Acceptance Criteria
No physical damage to the enclosure and accessories.
The enclosure and No physical damage to meters, switches, connectors, etc.
accessories No residue of fluid spillage (e.g., water, coffee, chemicals, etc.).
No loose or missing parts (e.g., knobs, dials, terminals, etc.).

A.2.2 Contextual Inspection

Test Item Acceptance Criteria
No unusual noises (e.g., a rattle inside the case).
No unusual odors (e.g., burning or smoky odor, particularly
The enclosure and
from ventilation holes).
accessories
No taped notes that may suggest device deficiencies or
operator concerns.

A.3 Device Labeling

Check the labels provided by the manufacturer or the healthcare facility are present and
legible.
 Main unit label
 Integrated warning labels

A.4 Scheduled Electrical Safety Inspection

For scheduled electrical safety inspection, perform all the test items listed in A.6 Electrical
Safety Inspection Form.

A.5 Electrical Safety Inspection after Repair

The following table specifies test items to be performed after the equipment is repaired.
Refer to A.6 Electrical Safety Inspection Form for the description of the test items.

Repair with main unit not disassembled Test items: 1, 2, 3

Repair with main When neither power Test items: 1, 2, 3, 4
unit supply PCBA nor patient
disassembled electrically-connected
PCBA is repaired or
replaced

A-2 BeneVision TMS60 Service Manual

 When power supply PCBA Test items: 1, 2, 3, 4, 5
is repaired or replaced
When patient Test items: 2, 3, 6, 7, 8
electrically-connected
PCBA is repaired or
replaced
When both power supply Test items: 1, 2, 3, 4, 5, 6, 7, 8
PCBA and patient
electrically- connected
PCBA are repaired or
replaced

A.6 Electrical Safety Inspection Form

Inspection and Testing Limit
1 Power Cord Plug
2 Device Enclosure and Accessories /
3 Device Labeling /
4 Protective Earth Resistance Max 0.2 Ω
5 Earth Leakage Normal condition(NC) Max:
NC: 300μA (refer to UL60601-1)
SFC: 1000μA
Single Fault condition(SFC)

6 Patient Leakage Normal condition(NC) Max:

Current CF applied part:
Single Fault condition(SFC) NC:10μA, SFC: 50μA
BF applied part:
NC:100μA, SFC: 500μA
7 Mains on Applied Part Leakage Max:
CF applied part: 50μA
BF applied part: 5000μA
8 Patient Auxiliary Normal condition(NC) Max:
Current CF applied part:
Single Fault condition(SFC) NC:10μA, SFC: 50μA
BF applied part:
NC:100μA, SFC: 500μA

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A-4 BeneVision TMS60 Service Manual

PN: 046-007057-00 (2.0)