BeneVision N17/BeneVision N15/

BeneVision N12/BeneVision
N12C

Patient Monitor

Service Manual
In
ntellec
ctual Prope
P erty Statem
ment
SHENZHEN MINDRAY
M BIO
O-MEDICAL E LECTRONICS
S CO., LTD. (h
hereinafter callled Mindray) owns
o
the intellectua
al property righ
hts to this prod
duct and this manual.
m This manual
m may reefer to informa
ation
protected by copyrights
c or patents
p and do
oes not conve
ey any license under the pattent rights of
Mindray, nor the sume any liabiility arising outt of any
t rights of otthers. Mindrayy does not ass
infringementss of patents or other rights o
of third parties..

,, and are the registtered tradema

arks or tradem
marks owned by
b
hina and otherr countries.
Mindray in Ch

Re
evisio
on His
story
This manual has
h a revision number. This revision number changes whenever
w the manual is upd
dated
due to software or technica
al specification
n change. Con
ntents of this manual
m are subbject to chang
ge
without prior notice.
n

 Version n
number 3.0

 Rele ase time:

t Augest 2017

7 Shenzhen Mindray Bio-Me

© 2016 -2017 edical Electron
nics Co., Ltd. All
A rights reserrved.

I
Preface
Manual Purpose
This manual provides detailed information about the assembling, dissembling, testing and
troubleshooting of the equipment to support effective troubleshooting and repair. It is not intended to
be a comprehensive, in-depth explanation of the product architecture or technical implementation.
Observance of the manual is a prerequisite for proper equipment maintenance and prevents
equipment damage and personnel injury.

Intended Audience
This manual is for biomedical engineers, authorized technicians or service representatives
responsible for troubleshooting, repairing and maintaining the monitors

Passwords
A password may be required to access different modes. The passwords are listed below:

 User maintenance: 888888

 Manage Configuration: 315666

 Factory maintenance: 332888

 Demo mode: 2088

II
Contents
1 Safety ..........................................................................................................................................1-1 
1.1 Safety Information....................................................................................................................1-1 
1.1.1 Dangers ........................................................................................................................1-1 
1.1.2 Warnings .......................................................................................................................1-2 
1.1.3 Cautions ........................................................................................................................1-2 
1.1.4 Notes.............................................................................................................................1-3 
1.2 Equipment Symbols .................................................................................................................1-3 

2 Operation Theory .......................................................................................................................2-1 

2.1 Overview ..................................................................................................................................2-1 
2.2 Product System Architecture ...................................................................................................2-1 
2.2.1 Main Control Board .......................................................................................................2-3 
2.2.2 Internal Module Rack COM Board ................................................................................2-3 
2.2.3 Power Architecture ........................................................................................................2-4 
2.2.4 Independent Display Board (for the N17 Only) .............................................................2-5 
2.2.5 iView Module (for the N17 Only) ...................................................................................2-5 
2.2.6 Alarm LAMP Board........................................................................................................2-5 
2.2.7 Power Switch Board ......................................................................................................2-5 
2.3 Data Logic Flow .......................................................................................................................2-5 

3 WLAN Installation ......................................................................................................................3-1 

3.1 Introduction ..............................................................................................................................3-1 
3.2 Network Deployment Process..................................................................................................3-1 
3.2.1 List of outputs................................................................................................................3-2 
3.3 Network Requirements ............................................................................................................3-4 
3.4 Network Verification .................................................................................................................3-5 
3.4.1 Tools and Resources.....................................................................................................3-5 
3.4.2 Wi-Fi Signal Calibration.................................................................................................3-6 
3.4.3 Network Verification Process ........................................................................................3-6 
3.5 Network Coverage Assessment with Patient Monitors .............................................................3-9 
3.6 Recommended Devices for WLAN ........................................................................................ 3-10 
3.7 Setting Wireless Parameters for Patient Monitors ................................................................. 3-10 
3.8 Troubleshooting ..................................................................................................................... 3-14 

4 Testing and Maintenance ..........................................................................................................4-1 

4.1 Introduction ..............................................................................................................................4-1 
4.1.1 Test Equipment .............................................................................................................4-1 
4.1.2 Test Report ....................................................................................................................4-1 
4.1.3 Preventative Maintenance.............................................................................................4-1 
4.1.4 Recommended Frequency ............................................................................................4-2 
4.2 Preventative Maintenance Procedures ....................................................................................4-3 

1
 4.2.1 Visual Inspection ...........................................................................................................4-3 
4.2.2 NIBP Tests ....................................................................................................................4-4 
4.2.3 Sidestream and Microstream CO2 Tests .......................................................................4-6 
4.2.4 AG Tests ........................................................................................................................4-9 
4.3 Power On Test ....................................................................................................................... 4-11 
4.4 Module Performance Tests .................................................................................................... 4-12 
4.4.1 ECG Tests ................................................................................................................... 4-12 
4.4.2 Resp Performance Test............................................................................................... 4-13 
4.4.3 SpO2 Test .................................................................................................................... 4-13 
4.4.4 NIBP Tests .................................................................................................................. 4-13 
4.4.5 Temp Test .................................................................................................................... 4-14 
4.4.6 IBP Tests ..................................................................................................................... 4-14 
4.4.7 C.O. Test ..................................................................................................................... 4-16 
4.4.8 Mainstream CO2 Tests ................................................................................................ 4-16 
4.4.9 Sidestream and Microstream CO2 Tests ..................................................................... 4-17 
4.4.10 AG Tests .................................................................................................................... 4-17 
4.4.11 EEG Test ................................................................................................................... 4-18 
4.4.12 BIS Test..................................................................................................................... 4-19 
4.4.13 RM Test ..................................................................................................................... 4-20 
4.4.14 CCO/SvO2 Tests ........................................................................................................ 4-21 
4.4.15 PiCCO Test ............................................................................................................... 4-22 
4.4.16 NMT Tests ................................................................................................................. 4-25 
4.5 Nurse Call Relay Performance Test .......................................................................................4-26 
4.6 Analog Output Performance Test ...........................................................................................4-26 
4.7 Electrical Safety Tests ............................................................................................................ 4-27 
4.8 Recorder Check ..................................................................................................................... 4-28 
4.9 Network Print Test .................................................................................................................. 4-28 
4.9.1 Device Connection and Setup..................................................................................... 4-28 
4.10 Device Integration Check ..................................................................................................... 4-29 
4.10.1 Device Connection and Setup ................................................................................... 4-29 
4.10.2 Device Integration Function Test ...............................................................................4-32 
4.10.3 Installation and Test Report .......................................................................................4-39 
4.11 Battery Check ...................................................................................................................... 4-40 
4.12 Mounting Check ................................................................................................................... 4-40 
4.12.1 Safety check ............................................................................................................. 4-40 
4.12.2 Overall Test and Check of Installed System .............................................................. 4-40 
4.13 Factory Maintenance ........................................................................................................... 4-41 
4.13.1 Accessing Factory Maintenance Menu...................................................................... 4-41 
4.13.2 Monitor Information ...................................................................................................4-41 
4.13.3 Production Test ......................................................................................................... 4-42 
4.13.4 Setup......................................................................................................................... 4-42 
4.13.5 Debug ....................................................................................................................... 4-43 
4.13.6 Power Info ................................................................................................................. 4-43 
4.13.7 ClinicalData ............................................................................................................... 4-43 

2
 4.13.8 Transferring Clinical Data ......................................................................................... .4-44 
4.13.9 Software Version ....................................................................................................... 4-44 
4.13.10 Monitor Information .................................................................................................4-44 

5 Troubleshooting .........................................................................................................................5-1 
5.1 Introduction ..............................................................................................................................5-1 
5.2 Part Replacement ....................................................................................................................5-1 
5.3 Check before Powering on the Monitor ....................................................................................5-1 
5.4 Software Version Check ..........................................................................................................5-2 
5.5 Technical Alarm Check.............................................................................................................5-2 
5.6 Troubleshooting Guide .............................................................................................................5-2 
5.6.1 Power On/Off Failures...................................................................................................5-2 
5.6.2 Display Failures ............................................................................................................5-3 
5.6.3 Module Rack Failures ...................................................................................................5-4 
5.6.4 Alarm Failures ...............................................................................................................5-5 
5.6.5 Recorder Failures .........................................................................................................5-6 
5.6.6 Output Interface Failures...............................................................................................5-6 
5.6.7 Power Supply Failures ..................................................................................................5-7 
5.6.8 Network Related Problems ...........................................................................................5-9 
5.6.9 Software Upgrade Problems .......................................................................................5-10 
5.6.10 Device Integration Failures ....................................................................................... 5-11 

6 Upgrade ......................................................................................................................................6-1 
6.1 Overview ..................................................................................................................................6-1 
6.2 Upgrade of Parameter Function Modules ................................................................................6-2 
6.3 Upgrade of Functional Assemblies ..........................................................................................6-5 
6.3.1 Upgrading SMR ............................................................................................................6-6 
6.3.2 Upgrading Wireless Network Functions ........................................................................6-6 
6.3.3 Upgrading Recorder ......................................................................................................6-6 
6.3.4 Upgrading iView System ...............................................................................................6-7 
6.3.5 Upgrading Independent Display Function .....................................................................6-7 
6.4 Upgrading Software .................................................................................................................6-8 
6.4.1 Description of Network Upgrade Tool ............................................................................6-9 
6.4.2 Guide to Software Upgrade Operations ...................................................................... 6-12 
6.4.3 Guide to Upgrade through a USB Disk .......................................................................6-14 
6.5 Upgrading CAA license function ............................................................................................ 6-17 

7 Repair and Disassembly............................................................................................................7-1 

7.1 Tools ........................................................................................................................................7-1 
7.2 Preparations for Disassembly ..................................................................................................7-1 
7.3 Whole Unit Disassembly ..........................................................................................................7-2 
7.3.1 Basic Disassembly ........................................................................................................7-2 
7.3.2 Disconnecting the Base ................................................................................................7-3 
7.3.3 Separating the Front and Rear Half of the Monitor .......................................................7-4 

3
 7.4 Further Disassembly of the Front Case Assembly ...................................................................7-8 
7.4.1 Removing the PowerSwitch Board ................................................................................7-8 
7.4.2 Removing the Alarm Lamp and Light Sensor Board .....................................................7-8 
7.4.3 Removing the Screen Assembly Connection Line ........................................................7-9 
7.5 Further Disassembly of the Rear Case Assembly.................................................................. 7-10 
7.5.1 Removing the Recorder ..............................................................................................7-10 
7.5.2 Further Disassembly of the Recorder ......................................................................... 7-11 
7.5.3 Removing the MPAN Board ........................................................................................7-12 
7.5.4 Removing the WiFi Module .........................................................................................7-13 
7.5.5 Removing the Internal Module Rack Assembly ........................................................... 7-14 
7.5.6 Removing the Main Support Assembly ....................................................................... 7-18 
7.5.7 Removing the iView Board Assembly (N17 Series)..................................................... 7-22 
7.5.8 Removing the Independent Display Board Assembly (N17 Series) ............................7-24 
7.5.9 Removing the Handle .................................................................................................7-25 
7.6 Further Disassembly of the Base Assembly ..........................................................................7-25 
7.7 Disassembling the Module Rack............................................................................................ 7-26 
7.8 Disassembling the M51C Module ..........................................................................................7-29 

8 Parts ............................................................................................................................................8-1 
8.1 N12 Parts .................................................................................................................................8-1 
8.1.1 N12 Whole Unit .............................................................................................................8-1 
8.1.2 N12-NLT Front Housing Assembly ................................................................................8-3 
8.1.3 N12-SHARP Front Housing Assembly ..........................................................................8-5 
8.1.4 N12 Rear Housing ........................................................................................................8-6 
8.1.5 N12 Rear Housing Assembly (FRU)(115-044499-00) ...................................................8-8 
8.1.6 N12 Battery Cavity Assembly (FRU)(115-044504-00) ...................................................8-9 
8.1.7 N12 Module Rack Body Assembly (FRU) (115-044507-00) ........................................8-10 
8.2 N 15 Parts .............................................................................................................................. 8-11 
8.2.1 N15 Whole Unit ........................................................................................................... 8-11 
8.2.2 N15-NLT Front Housing Assembly ..............................................................................8-12 
8.2.3 N15-SHARP Front Housing ........................................................................................8-14 
8.2.4 N15 Rear Housing ...................................................................................................... 8-16 
8.2.5 N15 Rear Housing Assembly (FRU) (115-044541-00) ................................................8-18 
8.2.6 N15 Base Assembly (FRU)(115-044543-00) ...............................................................8-19 
8.2.7 N15N17 Module Rack Body Assembly (FRU) (115-044546-00) .................................8-20 
8.3 N17 Parts ............................................................................................................................... 8-21 
8.3.1 N17 Whole Unit ........................................................................................................... 8-21 
8.3.2 N17-NLT Front Housing Assembly ..............................................................................8-22 
8.3.3 N17-SHARP Front Housing ........................................................................................8-23 
8.3.4 N17 Rear Housing ...................................................................................................... 8-25 
8.3.5 N17 Rear Housing Assembly (FRU)( 115-044548-00) ................................................8-27 
8.3.6 N17 Base Assembly (FRU)( 115-044550-00) ..............................................................8-28 
8.3.7 Independent Display Upgrade Package (Without Mainboard) (115-044554-00) .........8-29 
8.3.8 Independent Display Upgrade Package (With Mainboard) (115-044579-00) ..............8-30 

4
 8.3.9 Independent Display Assembly ...................................................................................8-31 
8.3.10 iView Module Assembly ............................................................................................8-32 
8.4 External Satellite Module Rack (SMR) ................................................................................... 8-34 
8.5 M51C Module ........................................................................................................................ 8-35 

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 Protective Earth Resistance ................................................................................................... A-2 
A.5 Earth Leakage Test ................................................................................................................ A-4 
A.6 Patient Leakage Current ........................................................................................................ A-6 
A.7 Mains on Applied Part Leakage .............................................................................................. A-7 
A.8 Patient Auxiliary Current ......................................................................................................... A-9 

5
FOR YOUR NOTES

6
1 Safetyy
1.1 Safety Informat
I ion

DAN GER

 Indicates
s an imminen
nt hazard thatt, if not avoid
ded, will resullt in death or serious injurry.

WA RNING
R

 Indicates
s a potential hazard or uns
safe practice
e that, if not avoided,
a could
d result in de
eath
or seriou
us injury.

CAUT
TION

 Indicates
s a potential hazard or uns
safe practice
e that, if not avoided,
a could
d result in minor
personal injury or pro
oduct/properrty damage.

NOTE
 Provides
s application tips or other useful inform
mation to ensure that you get the most from
your pro
oduct.

1.1.1 Dange
ers
There are no dangers that refer
r to the pro
oduct in general. Specific “D
Danger” statem
ments may be
e
given in the re
espective secttions of this m
manual.

1-1
1.1.2 Warnings

WARN
NING

 All installlation operattions, expans

sions, change
es, modifications and repaairs of this
product are conducte
ed by Mindray
y authorized personnel.

 There is high voltage inside the eq

quipment. Ne
ever disassem
mble the equiipment before
e it is
disconne
ected from th
he AC power source.

 When yo
ou disassemb
ble/reassemb
ble a parameter module, a patient leakaage current te
est
ed again for monitoring.
must be performed before it is use

 d to a properrly installed power

The equiipment must be connected p outlet w
with protectiv
ve
earth contacts only. If
I the installattion does nott provide for a protective eearth conduc
ctor,
disconne
ect it from the power line and operate it on battery power, if posssible.

 Dispose of the package material, o

observing the
e applicable waste
w contro
ol regulations
s and
keeping it out of child
dren’s reach..

1.1.3 Cautio
ons

CAUT
TION

 Make sure that no ele

ectromagnetic
c radiation in
nterferes with
h the perform
mance of the
equipme
ent when prep mance tests. Mobile phon
paring to carrry out perform ne, X-ray
equipme
ent or MRI devices are a p
possible source of interference as theyy may emit hig
gher
netic radiatio n.
levels off electromagn

 Before connecting the equipment to the powerr line, check that

t the voltaage and frequ
uency
ratings of
o the power line are the s
same as those
e indicated on the equipm
ment’s label or
o in
this man
nual.

 Protect the
t equipmen
nt from dama
age caused by
y drop, impac
ct, strong vib
bration or other
mechaniical force durring servicing
g.

1-2
 1.1.4 Notes

NOTE

 Refer to Operation Ma
anual for deta
ailed operatio
on and other information..

1.2
2 Equipm
ment Sym
mbols
Sym
mbol D
Description Symbol Description

Refer to instruuction
G
General warning sign
manual/bookleet

S
Serial number Catalogue Nuumber

D
Date of manuffacture Manufacturer

Protected agaainst vertically

U
USB connecto
or falling
f water ddrops per IEC
60529

B
Battery indicattor Direct currentt

E
Equipotentialit
ty Alternating
A cuurrent

D
DEFIBRILLAT
TION-PROOF TYPE DEFIBRILLAT
TION-PROOF
C APPLIED PART
CF P TYPE
T BF APP
PLIED PART

S
Stop USB Zero
Z key

Calibrate key
N
NIBP start/stop key

S
Setup menu ke
ey Main menu keey

1-3
Symbol Description Symbol Description

Check sensor Graphical record

Gas outlet Input/output

Output Input

Dispose of in accordance to your Authorised representative in the

country’s requirements European Community

The product bears CE mark indicating its conformity with the provisions of the Council
Directive 93/42/EEC concerning medical devices and fulfils the essential requirements
of Annex I of this directive.
Note: The product complies with the Council Directive 2011/65/EU.

1-4
2 Operation Theory
2.1 Overview
As a bedside workstation for multi-parameter monitoring, the N series can provide the complete
patient management, abundant physiological parameter monitoring and physiological alarm
functions, as well the powerful data review function and the flexible wired and wireless network
configuration and application capabilities. The third-party application can be accessed easily
through the iView application, meeting the increasingly common information requirements of
hospitals. The provided series of CAA applications can help doctors to make auxiliary diagnosis for
patients. Meanwhile, the N series provide the hospital management personnel with more excellent
monitor management applications, rendering assistance in fixing the efficiency and quality problems
during monitor equipment management of hospitals.

The N series provide the product models with display screens of different sizes according to the
demand of clinical application. In addition to touch screen operations, the user can use the mouse
and keyboard to operate the monitor. The N series can connect to multiple display screens to
function as mirror screens or extension screens.

The series of products are compatible with the BeneView T series plug-in modules and related
accessory products. They can work together with the TDS to implement the intra-hospital transfer
application of patients.

In comparison with the BeneView T series products, the N series boast better human-computer
interaction design and clinical applicability, more complete IT solution capability of hospitals, and
more abundant CDS applications.

2.2 Product System Architecture

All the N17/N15/N12 monitors have only one main unit:

 The N12 main unit uses the 12.1” TFT WXGA display screen.
 The N15 main unit uses the 15.6” TFT FHD display screen.
 The N17 main unit uses the 18.5”TFT FHD display screen.
 All of them use the touch screen as an input device and can extend the mouse, keyboard
and remote control.
 An internal module rack is integrated, with 4 slots (N12) or 6 slots (N15/N17).
 The MPAN and WiFi modules are optional.
 The built-in recorder is optional.

2-1
 The N15/N17 can connect to the external module rack and TDS; the N12 can connect to
the TDS.

Figure 2-1 System block diagram of the N17/N15/N12/N12C

2-2
2.2.1 Main Control Board
There are the main control CPU, program memory, data memory, system configuration memory,
system FPGA, WiFi module (optional), power management MCU, battery charging circuit, and
DC-DC circuit on the main control board. The internal interface and external interfaces are also
provided on the board. The internal interface is an interface between the recorder, internal module
rack COM board, AC-DC, and the battery. The external interfaces refer to the DVI display interface,
USB interface, and Ethernet interface.

Figure 2-2 Diagram of the main control board

2.2.2 Internal Module Rack COM Board

Two models of internal module rack COM boards are available. The N12 uses the 4-slot COM board,
and the N15/N17 uses the 6-slot COM board. The internal module rack COM board is used to
provide the interface for communication with the parameter module, the SMR interface and nurse
call interface, and the MPAN module interface. Besides, the data forwarding FPGA and
corresponding power circuit are also provided on the internal module rack COM board.

2-3
2.2.3 Power Architecture

Figure 2-3 Diagram of power architecture

The AC/DC power module outputs 15V to the main control board, and 3.3V, 5V and 12V can be
generated through the internal DC-DC conversion circuit in the main control board to provide a
power supply to other modules or boards in the main unit. The battery charging circuit is powered by
15V, and the AC power supply and battery power supply can be switched according to AC on-line
detection.

The +12V power supply is provided to the power supply, including the external module rack, and the
DC-DC isolation design is implemented at the module end.

The iVIew assembly uses the power rail Vbus, which is the switching output between the AC-DC
output and battery and aims to avoid abnormal power failure of the iView module and running
exception of the Windows OS running on other modules due to an unexpected power failure of the
AC power supply. The battery supports the main unit to stop the iView module in the normal
power-off mode. In the case of battery power supply, the iView module cannot start.

2-4
 2.2.4 Independent Display Board (for the N17 Only)
It is used to connect the main unit to a display and extend the main screen display. It adopts the DVI
interface. Moreover, the external display with a touch screen can be supported through the USB
interface of the main unit. At present, the supported display with a touch screen is Elo 1919LM.

2.2.5 iView Module (for the N17 Only)

As an embedded computer module, it provides the following external interfaces: the network
interface, DVI interface, and the USB interface. It can connect to the keyboard, mouse, network
cable, and display independently. The configuration of the iView module is mutually exclusive with
that of the independent display module.

2.2.6 Alarm LAMP Board

The LED alarm lamp and light sensor are provided on the board. The light sensor implements the
ambient light detection and is used to adjust brightness of the LCD background light.

2.2.7 Power Switch Board

There are the power switch and three indicators on the power switch board, which are the AC on-line
indicator, battery indicator, and the power-on indicator.

2.3 Data Logic Flow

Figure 2-4 Data flow diagram

The monitoring parameters are collected and analyzed through the module, and then forwarded to
the system software through the internal or external module rack. The system software displays the
waveform, numerical value and alarm information, and the data, alarm information and numerical
value are also stored in the internal data memory at the same time. Meanwhile, they can also be
sent to the central station or other monitors through the wired or wireless network.

2-5
FOR YOUR NOTES

2-6
 3 WLAN Installation
3.1 Introduction
This chapter describes how to install Mindray patient monitors using WLAN.

3.2 Network Deployment Process

If the hospital has built its WLAN, the installation process is illustrated as follows:

Mindray/agent A0 Provide network

marketing or sales requirements
personnel

Mindray A1 Communicate with

headquarters the hospital about
intention to order

Mindray/agent
service personnel A2 Communicate with the
hospital about network
requirements and ask the
hospital to perform
corresponding setting and
adjustment

A3 Do site survey

Pass or fail

Pass

A4 Sign the contract

A5 Install the device

and confirm system
operation

Figure 3-1 Network Deployment Process

3-1
 3.2.1 List of outputs
Action Output Requirements Template
A0 Wireless Network Determine requirements for Wireless
requirements for deployment of the wireless Network
Mindray patient monitors network for Mindray patient Requirement
monitors. Table in 3.3
Network
Requirements
A3 Netw ork acceptance Confirm that the customer Wireless
report network meets requirements Network
of Mindray patient monitors by Acceptance
means of questionnaire and Table in 3.4.3
measurement. Network
Verification
Process
A5 Installation confirmation Confirm the actual operation Patient Monitor
report of the Mindray patient Installation
monitors after installation. Confirmation
Table in 3.5
Network
Coverage
Assessment
with Patient
Monitors

If the hospital plans to build a new WLAN for the Mindray patient monitors, make sure
that there is at least one idle wifi channel that is not in use. Otherwise, you can’t make
co-channel interference meet Mindray patient monitors’ requirement after the new WLAN
is built. The installation process is illustrated as follows:

3-2
 Mindray/agent A0 Provide network
marketing or sales requirements
personnel

Mindray A1 Communicate with

headquarters the hospital about
intention to order

Mindray/agent
service personnel A2 Do site survey and
design network

A3 Sign the contract

A4 Install network

A5 Install the device

and confirm system
operation

Figure 3-2 Installation Process for a New WLAN

3-3
 Action Output Requirements Template
A0 Wireless Determine requirements for Wireless Network
Network deployment of the wireless network Requirement Table
requirements for Mindray patient monitors. in 3.3 Network
for Mindray Requirements 
patient
monitors
A2 Network design / /
document,
Bill of material
A5 Installation Confirm the actual operation of the Patient Monitor
confirmation Mindray patient monitors after Installation
report installation. Confirmation Table
in 3.5 Network
Coverage
Assessment with
Patient Monitors 

NOTE
 Network design and deployment project needs much more complex process,
you need professional IT engneer ’s help to finish the job. This document does
not include these contents.

3.3 Network Requirements

The Wireless infrastructure needs to meet the following requirements.

Table 3-1 Wireless Network Requirement Table

No.  Item  Content of Requirements 
Wireless coverage requirements

1 Received signal strength -65 dBm

(RSSI) RSSI is the value displayed on the patient monitor
2 Co-channel interference -20dB(co-channel interference AP’s RSSI shall
be at least 20 dB lower than the AP that patient
monitor uses.)
3 Ping delay The mean delay of PC or cell phone is smaller than 100ms and
The packet lost rate shall be less than 1%.
Requirements of AP capability 
1 AP capability 1． The anticipated number of devices connecting to one AP
must be lower than 50% of the AP capability. For example,

3-4
No.  Item  Content of Requirements 
In the coverage of one AP, the typical number of devices
connected to this AP is 16, then the announced number of
devices that can connect to AP simultaneously must be
more than 32.
2． The AP Can create several SSIDs.
2 Device density The maximum number of devices connected to one AP
simultaneously is 16 (including patient monitors and other
devices).
WLAN features
1 AP channel width Set the channel width to 20MHz, don’t use HT40 or even HT80.

2 802.11 protocol WLAN can't use protocols that Mindray patient monitor can’t
support, e.g 802.11ac

3 Security mode WLAN can't use Security mode that Mindray

patient monitor can’t support.
WPA2-PSK is highly recommended.
WPA2-Enterprise may increase probability of
offline when roaming, so not be recommended.
4 Dedicated The patient monitors need to work on a dedicated
VLAN VLAN.
Using VLAN can minimize Broadcast or multicast data which can
affect patient monitors’ stability.
Important settings
1 DHCP The DHCP server reserves a sufficient number of
IP addresses to ensure that the patient monitors
can obtain an IP address.
2 IGMP snooping If patient monitors use multicast, enable IGMP
snooping
3 Multicast If patient monitors use multicast, the multicast
function of network should be enabled.
4 Beacon & DTIM AP DTIM = 1, Beacon = 100ms
5 Service port Refer to Mindray Patient Monitoring Network
Whitepaper; patient monitors need some certain
TCP/UDP ports to be opened

3.4 Network Verification

3.4.1 Tools and Resources
 Laptop computer, where Windows 7 or later version is installed and wireless network
card is equipped. We recommended laptop configured with Intel Centrino Wireless-N

3-5
 adapter. If your laptop is configured with some other wireless adapter, please make
sure the adapter has a high degree of accuracy.
 Wireless network survey tool, we suggest to use professional survey tool such as
tamograph, Wirelessmon or other professional network survey tool.
 Professio nal network engineer.

NOTE
 The personnel who implement the Wi-Fi network survey should be well trained
about Wi-Fi. If professional network engineers are not available, please ask
some third party for help.

3.4.2 Wi-Fi Signal Calibration

Before a wireless network survey tool (running on laptop computer) is used to test
network coverage, follow this procedure to calibrate the RSSI of wireless network survey
tool with a patient monitor

1. Keep the patient monitor and wireless network survey tool close. The distance
between them is not greater than 30cm and the distance from human body is above
50 cm.
2. Move the patient monitor and Wireless network survey tool at the same time (keep
the previous distance).
3. When the patient monitor reads the following RSSI values: -50 dBm, -60 dBm, -70
dBm and -80 dBm, record the RSSI values read by Wireless network survey tool.
4. Calibrate the RSSI of Wireless network survey tool to patient monitor when do site
survey (the RSSI of Patient monitor is the benchmark to wireless coverage).

3.4.3 Network Verification Process

This part is completed through two ways: First the hospital completes items requiring
self-check of the hospital’s IT Dept., as indicated in the Network Verification Table. Then
customer service personnel or authorized party confirms items on site and finally
completes the Network Acceptance Table. If any item is found incompliant during
network Verification test, adjustment should be made before the patient monitors
installation.

When in test, the wifi network SSID broadcast needs to be enabled to ensure that the wifi
SSID can be scanned.

Table 3-2 Wireless Network Acceptance Table

3-6
N Item Content of Verification Method Check Results
o. Requirements
Wireless coverage requirements

1 Received -65 dBm Service person

signal RSSI is the value performs the test by
strength displayed on the using network
(RSSI) patient monitor survey tool.
Make sure that all
expected coverage
areas such as
ward, corridor,
toilet, stairs, and
elevator are tested.
2 Co-chann -20dB Service person
el performs the test by
interferen using network
ce survey tool.
Make sure that all
expected coverage
areas such as
ward, corridor,
toilet, stairs, and
elevator are tested.
3 Ping The mean delay of PC or cell Service person performs the
delay phone with normal wifi test:
module is smaller than 1. Connect PC or cell phone
100ms and The packet lost with normal wifi module to
rate shall be less than 1%. AP.
2. Connect another PC to
the LAN port where the
central monitoring system is
connected to.
3. Run the command” “ping
–t –l 32 –w 1000
IPaddress-of -cellphone” for
10 minutes.
4. Run“ ctrl+c”.
Requirements of AP capability
1 AP 1. The anticipated number Service personnel
capability of devices connecting to get the AP model
one AP must be lower from related
than 50% of the AP hospital people or
capability. For example, observe directly.
In the coverage of one According to the

3-7
N Item Content of Verification Method Check Results
o. Requirements
AP, the typical number model, get the data
of devices connected to sheet of AP to
this AP is 16, then the make sure the
announced number of capability.
devices that can
connect to AP
simultaneously must be
more than 32.
2. The AP can create
several SSIDs.
2 Device The maximum number of Check with hospital IT if this
density devices connected to one requirement is met or not.
AP simultaneously is 12
(including patient monitors
and other devices).
WLAN features
1 AP Set the channel width to Check with hospital IT if this
channel 20MHz, don’t use HT40 or requirement is met or not.
width even HT80.
2 802.11 WLAN can't use protocols Check with hospital IT if this
protocol that Mindray patient monitor requirement is met or not.
can’t support, e.g 802.11ac
3 Security WLAN can't use Check with hospital
mode Security mode that IT if this
Mindray patient requirement is met
monitor can’t or not.
support.
WPA2-PSK is
highly
recommended.
WPA2-Enterprise
may increase
probability of offline
when roaming, so
not be
recommended.
4 Dedicate The patient monitors need to Check with hospital IT if this
d VLAN work on a dedicated VLAN. requirement is met or not.
Using VLAN can minimize
Broadcast or multicast data
which can affect patient
monitors’ stability.

3-8
N Item Content of Verification Method Check Results
o. Requirements
Important settings
1 DHCP The DHCP server reserves a Check with hospital IT if this
sufficient number of IP requirement is met or not.
addresses to ensure that the
patient monitors can obtain
an IP address.
2 IGMP If patient monitors use Check with hospital IT if this
snooping multicast, enable IGMP requirement is met or not.
snooping
3 Multicast If patient monitors use Check with hospital IT if this
multicast. The multicast requirement is met or not.
function of network should
be enabled.
4 Beacon & AP DTIM = 1, Beacon = Check with hospital IT if this
DTIM 100ms requirement is met or not.
Service Refer to Mindray Patient Check with hospital IT if this
port Monitoring Network requirement is met or not.
Whitepaper; patient
monitors need some certain
TCP/UDP ports to be
opened

3.5 Network Coverage Assessment with Patient Monitors

To confirm coverage, perform coverage test in the areas where patients often go.

Check whether coverage meets requirements by observing the signal strength (RSSI)
showing on Patient monitor, and by observing whether an offline event occurs.

When necessary, adjust locations of APs or add APs to ensure the overage effect.
Do as follows:
1. Set the patient monitor to access to CMS.
2. Ping the patient monitor on the CMS (input “ping –t –l 32 –w 1500 IP address” in
window CLI (Ping the patient monitor persistently. The packet is 32 bytes and the
timeout of reply is 1500ms). After ten minutes, input “ ctrl + c”(finish the ping), make
sure that the mean delay is less than 250ms and the packet lost rate shall be less
than 1%.
3. Hold the patient monitor with a hand and avoid blocking by people. Walk in the
expected coverage areas, for example, all corners of the ward, toilet, smoking area,
corridor, and elevator.

3-9
 4. Offline event time should be less than 10% of patient monitor roaming times; the
RSSI value displayed on the patient monitor is not lower than -65dBm.
5. If the signal strength is lower than -65dBm during walking, stop at the location and
observe for 30s. If the RSSI value is not lower than -65 dB in more than 66 percent
of the time, the coverage requirement is met.

Table 3-3 Patient Monitor Installation Confirmation Table

Test or Observation Item Result (Pass, Fail or NA)
Ping the patient monitor from the CMS and make
sure that the mean delay is less than 250 ms and the
packet lost rate shall be less than 1%.
Hold the patient monitor and walk in the scope of
different APs. After walking through the whole
expected coverage area, observe continuous
waveform on the CMS. Offline event times should be
less than 10% of patient monitor roaming times.
In the location where coverage is the poorest,
signal strength displayed on the screen is higher than
-65dBm.

NOTE
 If patient monitors do not need to roam between Aps, you can just place
patient monitor where RSSI is lowest, and check the RSSI and ping results.

3.6 Recommended Devices for WLAN

The following Cisco devices listed in table below are recommended.
Device Part Number
2500 Wireless Controller AIR-CT2504-x-K9
2600 Access Point AIR-CAP2802I-K9

3.7 Setting Wireless Parameters for Patient Monitors

Follow the table below to configure the WLAN parameters of a patient monitor:
Parameter Recommended Comments
Setting
Main Menu→Maintenance→User Maintenance→Network Setup →WLAN
SSID Set according to the /
WLAN deployment
Security Mode WPA2-PSK Should be the same as that of the WLAN deployed

3-10
 for patient monitor.
If EAP used, choose the security mode according to
the WLAN deployment.
Password Set the password /
according to the WLAN
deployment
Main Menu→Maintenance→User Maintenance→Network Setup→WLAN→WLAN Setup
WLAN Band 5G Options are: 2.4G, 5G and Auto.
2.4G = only use 2.4GHz band
5G = only use 5GHz band
Auto = use both 2.4GHz and 5GHz bands(5GHz
takes priority)
AUT. Server Type ACS Options are: ACS and SBR.
ACS means Cisco Access Control Server.
SBR means another server different from ACS.
This only applies if the security type is Enterprise.
BG Channel Specified Options are: All, Specified, None.
Specifying the channels improves stability and
roaming performance by restricting the channels
scanned to only those specified. For example, on a
2.4GHz network set channels 1, 6, and 11.
BG channel settings on the monitor must match the
WLAN AP channel settings.
A Channel Specified Options are: All, Specified, None.
Specifying the channels improves stability
and roaming performance by restricting
the channels scanned to only those
specified.
The 5GHz channel settings on the
monitor must match the WLAN AP
channel settings.
Main Menu→Maintenance→User Maintenance→Network Setup→WLAN →Certificate
Management
Local / Display the existing EAP certificates in a
patient monitor
USB Drive / Display the existing EAP certificate in the
USB drive
Main Menu→Maintenance→Factory Maintenance→Setup→WLAN Setup
Regulatory Worldwide Korea, Turkey, Russia, and Brazil need to
Domain be configured separately. For other
countries, just choose worldwide.
You need to restart the monitor for the
monitor settings to take effect.
CCX Features Support This means that it supports CCX 4.0 and

3-11
 fast roaming
PMK Caching Standard Options are: Standard, OPMK.
Standard indicates PMK caching.
OPMK indicates opportunistic key
caching.
Trigger -70 When the RSSI is lower than the roam
trigger, the radio will try to roam.
Scan Period 5 When the RSSI is lower than the roam
trigger, the period of the probe request is
5s.

Patient monitor support the following security modes:

Menu Basic Authentication Mode Encryption CCKM
Selection Algorithm Support
WPA WPA PSK TKIP/RC4 No
PSK
WPA2 WPA2 PSK CCMP/AES No
PSK
WPA WPA PSK CCMP/AES No
PSK AES
WPA WPA EAP TKIP/RC4 No
TKIP
WPA2 WPA2 EAP CCMP/AES No
AES
WPA WPA EAP CCMP/AES No
AES
CCKM CCKM EAP TKIP/RC4 Yes
TKIP
CCKM CCKM EAP CCMP/AES Yes
AES

3-12
After Security Mode of EAP is selected, corresponding configuration item will be
displayed. The following table lists the configuration items for different EAP methods.
Identit Anony Passwor CA User PAC PAC
y mity d Certificate Certificat Certificate passwor
e d
PEAP-M Y O Y Y N N N
SCHAP
V2
PEAP-G Y O Y Y N N N
TC
PEAP-T Y O Y Y Y N N
LS
TTLS Y O Y Y N N N
TLS Y N Y Y Y N N
FAST Y O Y N N Y Y
LEAP Y N Y N N N N

Note: Y means yes, N means No, O means optional.

The meaning of each configuration item is shown below:

 AUT. Protocol (Phase2 Auth): When PEAP in the EAP Method is selected, the user
can configure the following PEAP inner methods: EAP-MSCHAPV2, EAP-GTC,
EAP-TLS.
 Identity: user identity, it is the user name in the AD, LDAP or local user management
on the RADIUS server.
 Anonymity: This item does not impact the authentication process. The function of this
item is to hide the real name (Identity).
 Password: the password for the Identity.
 CA Certificate: choose the CA Certificate from the imported certificates.
 User Certificate: choose the User Certificate from the imported certificates.
 PAC Certificate: When the EAP-FAST is selected, choose the PAC certificate from
the imported certificates. If the RADIUS server has support In-band PAC provisioning
to provision the client with a PAC, then there is no need to setup the PAC Certificate
and password.
 PAC password: When the EAP-FAST is selected, input the PAC password for the
PAC Certificate. If the RADIUS server has support In-band PAC provisioning to
provision the client with a PAC, then there is no need to setup the PAC Certificate
and password.

3-13
3.8 Troubleshooting
Symptom Possible Cause Recommended Measure
The monitor The nearby AP is not turned Ensure that the AP is turned on and belong to
cannot connect to on. the VLAN where the monitor resides.
the AP and an X is The monitor is not turned on in Walk to the coverage area of the AP and turn on
displayed on the the coverage area of the AP. the monitor. Ensure that the signal strength
Wi-Fi signal icon indicated on the monitor is larger than –65 dBm.
on the monitor. Ensure that the intra-frequency interference
meets the requirement.
The SSID, IP address Configure the information again by referring to
acquisition mode, and security this manual.
mode are not correctly
configured on the monitor.
The monitor fails. Check whether another monitor can get online. If
yes, restart the monitor and ensure that the
configurations of the two monitors are
consistent. If the monitor still cannot get online,
return the monitor to Mindray for repair.
The monitor can The monitor is not admitted on Admit the monitor on the CMS.
connect to the AP the CMS.
but cannot connect The monitor cannot obtain any Enable other network equipment to connect to
to the CMS. IP address and the IP the CMS and check whether an IP address can
addresses in the IP address be obtained.
pool on the DHCP server are If the problem cannot be solved, contact the IT
used up. department.
A static IP address conflict Observe whether a prompt indicating IP address
occurs. conflict is displayed on the monitor.
If so, make sure all network devices have unique
IP addresses.

The network link fails. Check whether the CMS can be pinged by
using PC or cell-phone.
If the problem cannot be solved, contact the IT
department.
The services required by the Check whether the services required by the
monitor are not enabled on the monitor are enabled on the hospital network and
hospital network. enable related services, such as certain UDP
ports and multicast.
If the problem cannot be solved, contact the IT
department.
A single monitor The monitor moves to a Ensure that the signal strength is larger than –65
becomes coverage hole. dBm at the position where the monitor is

3-14
Symptom Possible Cause Recommended Measure
disconnected disconnected.
intermittently The monitor is faulty. Check whether the monitor is disconnected
easily at the same position. If the problem
cannot be solved after the monitor is restarted,
return the monitor to Mindray for repair.
A static IP address conflict Observe whether a prompt indicating IP address
occurs. conflict is displayed on the monitor.
Check whether an IP address is assigned to
more than one device.
Multiple monitors The APs in some areas are Ensure that the APs are turned on and run
become damaged. properly.
disconnected The interference is intense in Check whether the interference is intense by
intermittently certain areas. using a network survey tool and remove obvious
interference sources or adjust WLAN
deployment to meet the requirements of
Mindray.
The signal coverage is Check the signal coverage by using network
insufficient in some areas. survey tool. If signal coverage is insufficient in
any area, adjust the position of the AP or add an
AP.
All monitors The wired network is Check the wired network configuration by using
become configured improperly. a wired monitor. Ensure that the WLAN
disconnected bandwidth configured on the switch is sufficient
intermittently with a margin of 50%.
There is radio interference. Check whether there is radio interference by
usingnetwork survey tool and remove obvious
interference sources or adjust WLAN
deployment to meet the requirements of
Mindray.

3-15
FOR YOUR NOTES

3-16
 4 Testting andd Mainteenance
4
4.1 Introd
duction
To en
nsure the patie
ent monitor alw
ways function
ns properly, qu
ualified service
e personnel shhould perform regular
inspe
ection, maintenance and tes
st. This chapte
er provides a checklist
c e testing proceedures for the
of the e patient
moniitor with recom nd frequency. The service personnel shouuld perform the testing
mmended test equipment an
and m
maintenance procedures
p as
s required and
d use appropriate test equipment.

The ttesting proced

dures provided
d in this chapte ed to verify tha
er are intende at the patient m
monitor meets
s the
perfo
ormance speciifications. If the patient mon
nitor or a modu
ule fails to perfform as speciffied in any tes
st, repairs or
repla
acement must be done to co
orrect the prob
blem. If the pro s, contact our Customer Service
oblem persists
Depa
artment.

CAUTION
N
 A
All tests shou
uld be perforrmed by qualiified service personnel on
nly.

 C
Care should be taken whe i Maintenan
en changing tthe settings in nce and Connfiguration menus
m to
a
avoid loss off data.

 S
Service perso
onnel should
d possess a w
working know
wledge of the test tools an
nd make sure that test
e
equipment an
nd cables are
e applicable.

4.1.1 Test Equipment

See tthe following sections.
s

4.1.2 Test Repo

ort
Upon
n completion of
o the tests, the table of prevventative main
ntenance test reports and thhe table of ma
aintenance
test rreports in this chapter shoulld be kept pro perly.

4.1.3 Preventattive Mainte

enance
The ffollowing sectiions provide a list of recomm
mended preve
entative mainte
enance proceddures. It is rec
commended
to ma
aintain the pattient monitor at every two yearrs (and once a year for CO22 and AG modules). (See
a least once e
the fo
ollowing sectio
ons for detaile
ed test procedu
ures and conttents)

4-1
4.1.4 Recommended Frequency
Check/Maintenance Item Frequency
Preventative Maintenance Tests
Visual inspection When first installed or reinstalled.
Pressure check
NIBP tests 1. If the user suspects that the measurement is incorrect.
Leakage test
2. Following any repair or replacement of relevant module.
Sidestream and Leakage test
3. For NIBP module, at least once every two years; for CO2
Microstream CO2 Performance test
and AG modules, once a year.
tests Calibration
4. AG leakage test should be performed before AG
Performance test
AG tests measurement.
Calibration
Performance Tests
Performance test
ECG tests
Calibration
Resp performance test

SpO2 test
Pressure check
NIBP test
Leakage test

Temp test

Performance test
IBP tests
Pressure calibration
C.O. test 1. If the user suspects that the measurement is incorrect.
2. Following any repair or replacement of relevant module.
Mainstream CO2 test
3. At least once every two years. For CO2, AG and NMT
Sidestream and Leakage test
modules, at least once a year.
Microstream CO2 Performance test
4. AG leakage test should be performed before AG
tests Calibration
measurement.
Leakage test
AG tests Performance test
Calibration
EEG test
BIS test
RM test
Interconnecting function
CCO/SvO2 tests
Output calibration
Performance test
NMT tests
Sensor check
PiCCO test
Nurse call relay performance test If the user suspects that the nurse call or analog output does
Analog output performance test not work well.

4-2
Electrical Safety Tests
Earth impedance
1. Following any repair or replacement of the power module.
Earth leakage test
Electrical safety tests 2. When the patient monitor is dropped.
Patient leakage current
3. At least every two years or as required.
Patient auxiliary current
Other Tests
1. When first installed or reinstalled.
Power on test 2. Following any maintenance or the replacement of any main
unit parts.
Recorder check Following any repair or replacement of the recorder.
1. When first installed.
Network print test
2. Whenever the printer is serviced or replaced.
1. When first installed.
Device integration check
2. Following any repair or replacement of the external device.
1. When first installed.
Function test
2. Whenever a battery is replaced.
Battery check
Once every three months or when the battery run time is reduced
Performance test
significantly.
1. When first installed.
Mounting check
2. At least every two years or as required.

Note: Performance test is not required for the ICG, rSO2, Tympanic Temp and ScvO2 modules, because the first
three modules perform self tests, and the last one needs to be calibrated prior to use.

4.2 Preventative Maintenance Procedures

4.2.1 Visual Inspection
Inspect the equipment for obvious signs of damage. The test is passed if the equipment has no obvious signs of
damage. Follow these guidelines when inspecting the equipment:

 Carefully inspect the case, display screen, buttons and handle for obvious signs of damage.

 Inspect the SMR and parameter modules for obvious signs of damage.

 Inspect the power cord, bracket and module accessories for obvious signs of damage.

 Inspect all external connections for loose connectors, bent pins or frayed cables.

 Inspect all connectors on the equipment for loose connectors or bent pins.

 Make sure that safety labels and data plates on the equipment are clearly legible.

4-3
 4.2.2 NIBP Tests
NIBP Accuracy Test

Tools required:

 T-shape connector

 Tubing

 Squeeze bulb

 Rigid vessel with volume 500±25 ml

 Reference manometer (calibrated with accuracy equal to or greater than 1 mmHg)

Follow this procedure to perform the test:

1. Connect the equipment as shown below.

Monitor Manometer

Tubing
NIBP connector

Squeeze bulb Rigid vessel

2. Before inflation, the reading on the manometer should be zero. If not, open the valve of the squeeze bulb to
let the whole airway open to the atmosphere. Close the valve after the reading turns to zero.

3. Select Main Menu → Maintenance → enter the required password → Module → NIBP → NIBP
Accuracy Test.

4. Check the reading of the manometer and the reading of the patient monitor. Both should be 0 mmHg.

5. Raise the pressure in the rigid vessel to 50 mmHg with the squeeze bulb. Then, wait for 10 seconds until
the measured values become stable.

6. Compare the reading of the manometer with the reading of the patient monitor. The difference should be 3
mmHg. If it is greater than 3 mmHg, contact your service personnel.

7. Raise the pressure in the rigid vessel to 200 mmHg with the squeeze bulb. Then, wait for 10 seconds until
the measured values become stable. Repeat step 6.

NOTE
 You can use an NIBP simulator to replace the squeeze bulb and the reference manometer
to perform the test.

 You can use an appropriate cylinder and a cuff instead of the rigid vessel.

4-4
Leakage Test

Tools required:

 NIBP cuff for adult patient

 Tubing

 Cylinder

Follow this procedure to perform the test:

1. Set Patient Category to Adult.

2. Connect the NIBP cuff to the NIBP connector on the patient monitor.

3. Wrap the cuff around the rigid cylinder as shown below.

Cylinder
Monitor

Hose
NIBP Cuff

4. Select Main Menu → Maintenance → enter the required password → Module → NIBP → NIBP
Leakage Test. The message NIBP Leakage Test is displayed in the NIBP parameter area.

5. The cuff automatically deflates after 20s, which means NIBP leakage test is completed.

6. If no message is displayed in the NIBP parameter area, it indicates that the system has no leak. If the
message NIBP Pneumatic Leak is displayed, it indicates that the system may have a leak. In this case,
verify the connections and make sure that the NIBP cuff, hose, and connectors are not leaking. Then,
perform the test again.

You can also perform a manual leakage test:

1. Perform steps 1-4 in the NIBP Accuracy Test section.

2. Raise the pressure in the rigid vessel to 250 mmHg with the squeeze bulb. Then, wait for 5 seconds until
the measured values become stable.

3. Record the current pressure value and meanwhile count time with a timer. Then, record the pressure value
after counting to 60 seconds.

4. Compare the two values and make sure the difference is not greater than 6 mmHg.

4-5
NIBP Overpressure Protection Circuit Test

Tools required:

 T-shape connector

 Approprating tubing

 Balloon pump

 Metal Vessel with volume 500 ± 25 ml

 Reference manometer (calibrated with accuracy equal to or greater than 1 mmHg)

Follow this procedure to perform a NIBP calibration:

1. Perform procedures 1-4 in the NIBP Accuracy Test section.

2. Select [Main Menu]→ [Maintenance ]→enter the required password →[Factory Maintenance]→ [NIBP].

3. Set [Patient Category] to [Adult/Ped] in the [Overpressure Protection Circuit Test]. Raise the pump
pressure to 320-330 mmHg. After the pressure value is stabilized, select the [Test] button to start a
calibration, and the [NIBP] menu will display [Test successful] ,When raise the pump pressure out of the
range of 320-330 mmHg, and select the [Test] button to, the [NIBP] menu will display [Test Failed].

4. Set [Patient Category] to [Neo] in the [Overpressure Protection Circuit Test], and raise the pressure to
160-165 mmHg. After the pressure value is stabilized, select [Test] to start a calibration. and the [NIBP]
menu will display [Test successful] ,When raise the pump pressure out of the range of 160-165 mmHg, and
select the [Test] button, the [NIBP] menu will display [Test Failed].

4.2.3 Sidestream and Microstream CO2 Tests

Leakage Test

1. Plug the module into the module rack.

2. Wait until CO2 warmup is finished and then completely block the gas inlet of the module or water trap (by
using your finger or other objects). The sidestream and microstream CO2 modules will behave as follows:

 Sidestream: Plug the sidestream CO2 module into the module rack of the main unit. Wait one minute
until the module warmup is finished and then completely block the gas inlet of the module (you may
use a pneumatic plug or your finger to manually occlude the port). An alarm message CO2 Airway
Occluded will appear on the screen. Block the gas inlet for another 60 seconds. Select Main Menu →
Maintenance → enter the required password → Module → CO2 → Calibration. If the flow rate is
less than 10 ml/min and the alarm message continues, it indicates that the module does not leak. If the
alarm message CO2 Airway Occluded disappears, or the flow rate is greater than or equal to 10
ml/min, it indicates that the module leaks.

 Microstream: The alarm message CO2 Purging is displayed on the screen after 3 seconds. Block the
gas inlet for another 30 seconds. If alarm message CO2 Airway Occluded is displayed, it indicates that
the module does not leak.

4-6
Accurac
cy Test

Toolss required:

 A steel gas cyylinder with 6±

±0.05% CO2 an
nd balance ga
as N2

 A steel gas cyylinder with >4

40% O2 and ba
alance gas N2 (applicable to
o sidestream C
CO2 module with
w O2
m
module equipped)

 T
T-shape conn
nector

 T
Tubing

 Flowmeter

1. P
Plug the modu
ule into the mo
odule rack.

2. W
Wait until the CO
C 2 module warmup
w is finisshed. Check th
he airway for leak and perfoorm a leakage test as well
tto make sure that the airway has no leak .

3. S
Select Main Menu
M → Mainttenance → en
nter the require
ed password → Module → CO2 → Caliibration.

4. C
Connect the te
est system as follows:

Flowmeter

Tubing

Relief valve
Monitor
T-shape con
nnector

Gas cyylinder

5. O
Open the relie
ef valve, and adjust
a it until th
he flowmeter has
h a stable re
eading betweeen
10 ml/min and
d 50 ml/min.

6. V
Verify that the
e real-time CO2 value is with
hin 6±0.2% in the Calibrate CO2 menu (foor microstream
m CO2, the
vvalue is 45±2 mmHg).

4-7
 7. Rep
place the cylind
der to the stee
el gas cylinderr with >40% O2 and balance
e gas N2(appllicable to sides
stream
CO2 module with O2 module eq
quipped) and vverify that the real-time O2 value
v error is w
within ±2% (w
when
O2≤
≤80%) or ±3% (80%≤O2≤100
0%).

Calibration

Tools req
quired:

 A stteel gas cylind

der with 6±0.05
5% CO2 and b
balance gas N2

 A stteel gas cylind

der with >40% O2 and balan
nce gas N2 (ap
pplicable to sid
destream CO22 module with O2
dule equipped)
mod

 T-sh
hape connecto
or

 Tub
bing

 Flow
wmeter

1. Makke sure that th

he sidestream or microstream
m CO2 module has been wa
armed up or sstarted up.

2. Che
eck the airway for leaks and perform a lea
akage test as well
w to make sure that the aiirway has no leakage.

3. Sele
ect Main Menu
u → Maintenance → ente d password → Module → CO2.
er the required

4. he CO2 menu, select Zero.

In th

5. Afte shed successffully, connect the equipment as follows:

er the zero caliibration is finis

er
Flowmete

Tu
ubing

Relief valvve
Mon
nitor
T-shape con
nnector

Gas cylind
der

6. Ope
en the relief va
alve, and adjus
st it until the fllowmeter has a stable readiing between
10 m
ml/min and 50
0 ml/min.

7. In th
he Calibrate CO2
C menu, entter 6% (the CO
O2 concentration) in the CO
O2 field.

8. In th
he Calibrate CO2
C menu, the O2 concentrattion is displaye
e measured CO ed. After the m
measured CO2
conccentration beccomes stable, select Calibra
ate CO2 to calibrate the CO
O2 module.

4-8
 9. Replace the cylinder to the steel gas cylinder with >40% O2 and balance gas N2(applicable to sidestream
CO2 module with O2 module equipped) and calibrate O2.

If the calibration is finished successfully, the message Calibration Completed! is displayed in the Calibrate CO2
menu. If the calibration failed, the message Calibration Failed! is displayed. In this case, check whether the
operations are correct and perform another calibration. If the calibration fails several times, return the module to
Mindray for repair.

4.2.4 AG Tests
Leakage Test

1. Plug the AG module into the module rack.

2. Wait until the AG module warmup is finished and then completely block the gas inlet of the AG module (you
may use a pneumatic plug or your finger to manually occlude the port). An alarm message AG Airway
Occluded will appear on the screen.

3. Block the gas inlet for another 60 seconds. Select Main Menu → Maintenance → enter the required
password → Module → AG → Calibration. Check that the flow rate is less than 10 ml/min. If the alarm
message continues, it indicates that the module does not leak.

If the alarm message disappears, or the flow rate is greater than or equal to 10 ml/min, it indicates that the
module leaks.

Accuracy Test

Tools required:

 Gas cylinder with a certain standard gas (such as 6±0.05% CO2, Bal N2) or standard gas mixture. Gas
concentration should meet the following requirements: AA > 1.5%, CO2 > 1.5%, N2O > 40%, O2 > 40%, of
which AA represents an anesthetic agent. Precision requirement: a/c  0.01 (a is the gas absolute
concentration accuracy; c is the gas concentration)

 T-shape connector

 Tubing

 Flowmeter

1. Plug the AG module into the module rack.

2. Wait at least 10 min and then perform a leakage test to make sure that the airway has no leakage.

3. Connect the test system as follows:

4-9
 Flowmetter

Tubing

Relief vallve
Monitor
T-shape cconnector

der
Gas cylind

4. Ope
en the relief va
alve, and adjus
st it until the fllowmeter has a stable readiing between 110 ml/min and 50
ml/m
min.

5. Veriify that the con

ncentration of each compossition meets th
he specification stated in thee Operator's Manual.
M

Calibration

Tools req
quired:

 Gass cylinder with a certain stan

ndard gas (succh as 6±0.05%
% CO2, Bal N2
2) or standardd gas mixture. Gas
conccentration sho
ould meet the following requ
uirements: AA
A [1.5%,7.0%], set step lengtth: 0.1, CO2
[1.5%,7.0%], set step
s length: 0.1, N2O [40% ,100%], set sttep length: 5, O2
O [40%,100%
%], set step le
ength: 5,
of w quirement: a/c  0.01 (a is thhe gas absolute
esents an anesthetic agent. Precision req
which AA repre
conccentration acccuracy; c is the
e gas concenttration)

 T-sh
hape connecto
or

 Tub
bing

 Flow
wmeter

Follow th
his procedure to perform a calibration:
c

1. Sele
ect Main Menu
u → Maintenance → ente
er the required AG.
d password → Module → A

2. Che
eck the airwayy and make sure that there a
are no occlusio
ons or leaks.

 ate and Set F low Rate are

mpling tubing to the air and ccheck if the Current Flow Ra
Vent the sam
approximatelly the same. Iff the deviation dicates that there is an occluusion in the tu
n is great, it ind ubing.
Check the tubing for an oc
cclusion.

 Perform a lea
akage test to make
m sure tha
at the airway has
h no leakage
e.

3. Con
nnect the test system
s as follows:

4. Ope
en the relief va
alve and vent a certain stand
dard gas or ga
as mixture. Ad
djust the relieff valve until the
e
flow
wmeter has a stable
s reading between 10 m
ml/min and 50
0 ml/min.

4-10
 Fllowmeter

Tubing

Relieff valve
Monitor
M
T sh ape connector

Gas ccylinder

5. IIn the Calibratte AG menu, the

t concentrattion and flowra
ate of each me
easured gas aare displayed.

 If the diffe
erence betwee
en the measurred gas conce
entration and the
t actual onee is within tolerrance, a
calibration is not neede
ed.

 If the diffe
erence is not within
w tolerancce, a calibratio
on should be performed.
p Seelect Calibrate.

6. E
Enter the ventted gas conce
entration. If you
u use only one
e gas for calib
bration, set othher gases' con
ncentration
tto 0. If the ca
alibration is performed
p forr all gases, th
he gas with an
a entered ca
calibration value of 0 is
not calibrated.
7. S
Select Calibra
ate to start a ca
alibration.

8. IIf the calibratio

on is finished successfully,
s tthe message Calibration
C Co
ompleted! is diisplayed. If the
e calibration
ation Failed! iss displayed. In this case, perrform another calibration. If the
ffailed, the messsage Calibra
ccalibration faills several time
es, return the m
module to Min
ndray for repaiir.

CAUTION
N
 C
Calibrate the O2 module, if it has been transported for long dista
ance.

4
4.3 Powerr On Tes
st
This test is to veriffy that the patient monitor ca
an power up correctly.
c The test
t is passedd if the patient monitor
startss up by following this proced
dure:

1. C
Connect the patient
p monitorr to the AC ma
ains. The AC mains
m LED an
nd battery LED
D light up.

2. P
Press the pow
wer on/off switc
ch to switch o
on the patient monitor.
m The system
s soundss a beep indic
cating the
sself test on ala
arm sounds is
s passed. The alarm lamps light red, yello
ow and cyan reespectively, and then go
o
off, indicating the self test on
o alarm is passsed.

3. T
The patient monitor enters the
t main scree
en and start-u
up is finished.

4-11
 4.4 Module Performance Tests
4.4.1 ECG Tests
ECG Performance Test

Tools required:

 Medsim300B patient simulator

1. Connect the patient simulator with the ECG module using an ECG cable.

2. Set the patient simulator as follows: ECG sinus rhythm, HR = 60 bpm with the amplitude as 1 mV.

3. Verify that the ECG waves are displayed correctly without noise and the displayed HR value is within 60±1
bpm.

4. Disconnect each of the leads in turn and observe the corresponding lead off message displayed on the
screen.

5. Set the output of the simulator to deliver a paced signal and set Paced to Yes on the monitor. Check the
pace pulse marks on the monitor screen.

ECG Verification

Tools required:

 Vernier caliper

1. Select the ECG parameter window or waveform area → Filter → Diagnostic.

2. Select Main Menu → Maintenance → enter the required password → Module.

3. Select Calibrate ECG. A square wave appears on the screen and the message ECG Calibrating is
displayed.

4. Compare the amplitude of the square wave with the wave scale. The difference should be within 5%.

5. After completing the calibration, select Stop Calibration.

If necessary, you can print out the square wave and wave scale through the recorder and then measure the
difference.

4-12
4.4.2 Resp Performance Test
Tools required:

 Medsim300B patient simulator

1. Connect the patient simulator to the module using a non ESU-proof cable and set lead II as the respiration
lead.

2. Configure the simulator as follows: lead II as the respiration lead, base impedance line as 500 Ω; delta
impedance as 1 Ω, respiration rate as 20 rpm.

3. Verify that the Resp wave is displayed without any distortion and the displayed Resp value is within 20±1
rpm.

4.4.3 SpO2 Test

Tools required:

 None.

1. Connect SpO2 sensor to the SpO2 connector of the monitor. Set Patient Category to Adult and PR Source
to SpO2 on the monitor.

2. Apply the SpO2 sensor to the ring finger of a healthy person.

3. Check the Pleth wave and PR reading on the screen and make sure that the displayed SpO2 is within 95%
and100%.

4. Remove the SpO2 sensor from your finger and make sure that an alarm of SpO2 Sensor Off is triggered.

Measurement accuracy verification:

The SpO2 accuracy of the MPM module 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 simulator cannot be used to assess the accuracy of a pulse oximeter monitor or a SpO2
sensor. Instead, it can only verify that whether the monitor is functional. The accuracy of
a pulse oximeter monitor or a SpO2 sensor needs to be verified by clinical data.

4.4.4 NIBP Tests

See section 4.2.24.2.2NIBP Tests.

4-13
 4.4.5 Temp Test
Tools required:

 Resistance box (with accuracy above 0.1 Ω)

1. Connect the two pins of any Temp connector of a module to the two ends of the resistance box using two
wires.

2. Set the resistance box to 1354.9 Ω (corresponding temperature is 37ºC).

3. Verify each Temp channel of the monitor and make sure that the displayed value is within 37±0.1ºC.

4.4.6 IBP Tests

Performance Test

Tools required:

 Medsim300B patient simulator, MPS450, or other equivalent equipment

 Dedicated IBP adapter cable (300B, P/N 00-002199-00) (use P/N 00-002198-00, if the simulator is
MPS450)

1. Connect the patient simulator to the monitor's IBP connector.

2. Set the patient simulator output to the IBP channel to 0 mmHg.

3. Press the Zero key on the module to make a zero calibration.

4. Set static pressure to 200 mmHg on the patient simulator.

5. The displayed value should be within 200±2 mmHg.

6. If the value is outside of these tolerances, calibrate the IBP module. If the IBP module was calibrated with a
dedicated reusable IBP sensor, check the calibration together with this IBP sensor.

7. Make the patient simulator outputs 120/80 mmHg ART signals and 120/0 mmHg LV signals respectively to
each IBP channel and check that the IBP wave is displayed correctly.

Pressure Calibration

Method 1:
Tools required:

 Medsim300B patient simulator, MPS450, or other equivalent equipment

 Dedicated IBP adapter cable (300B, P/N 00-002199-00) (use P/N 00-002198-00, if the simulator is
MPS450)

4-14
1. C
Connect the patient
p simulattor to the mon itor's IBP conn
nector.

2. S nt simulator to 0 pressure fo r the desired IBP

Set the patien I channel.

3. P
Press the Zero
o key on the module
m to makke a zero calib
bration.

4. S
Set static presssure to 200 mmHg
m on the p
patient simula
ator.

5. S
Select Main Menu
M → Main
ntenance → e
enter the required password
d → Module → IBP. In the
e Cal. IBP
Press. menu, set the calibra
ation value to 200 mmHg.

6. Select the Callibrate button next to the de

S esired IBP cha
annel to start a calibration.

7. IIf the calibratio

on is complete ge Calibration Completed! w
ed successfullly, the messag will be displaye
ed.
O
Otherwise, a corresponding
c g message wil l be displayed
d.

Meth
hod 2:
Toolss required:

 S
Standard sphyygmomanome
eter

 S
Squeeze bulb
b

 T
Tubing

 T
T-shape conn
nector

1. C
Connect the 3-way
3 momanometer and the squee
stopcock, the sphygm eze bulb throuugh a T-shape
e connector,
a
as shown belo
ow.

2. Z
Zero the transsducer, and then open the sstopcock to the
e sphygmoma
anometer.

Pressure
e transducer

3-w
way stopcock

Pre
essure adapter cable

IBP
T-shape co
onnector
module

Sphygmoman
nometer

3. S
Select Main Menu→
M Mainte nter the requirred password → Module → IBP. In the displayed
enance → en
iinterface, set the
t target calibration value of the target channel.
c Value
e range: 80 to 300 mmHg.

4. IInflate using th
he squeeze bu
ulb until the re
eading of sphy
ygmomanometer approximaates the preset calibration
vvalue.

5. A
Adjust the caliibration value in the Maintaiin IBP menu until
u it is equal to the readingg of sphygmomanometer

6. S
Select the Callibrate button next to the de
esired IBP cha
annel to start a calibration.

If the
e calibration is completed su
uccessfully, the
e message Ca
alibration Com
mpleted! will bee displayed. Otherwise,
O a

4-15
 corresponding message will be displayed.

4.4.7 C.O. Test

Tools required:

 Medsim300B patient simulator

 C.O. adapter box (for 300B)

1. Connect the patient simulator to the C.O. module using a C.O. main cable.

2. Set the blood temperature (BT) to 37ºC on the patient simulator and check the temperature value is
37±0.1ºC.

3. Switch off Auto TI and adjust TI (IT) to 24ºC. Select C.O. Measure to enter the C.O. measurement window
and set Comp. Const. to 0.595.

4. Set the injectate temperature to 24ºC and the C.O. to 5 L/min on the C.O. simulator. Select Start in the C.O.
measurement window to start C.O. measurements, and press the run key on the simulator after 3-10
seconds.

6. Verify that the C.O. value is 5±0.25 L/min.

4.4.8 Mainstream CO2 Tests

NOTE
 Make sure that the barometric pressure set in Main Menu → Maintenance → en ter
the required password → Other accords with the local barometric pressure before
performing mainstream CO2 tests.

Tools required:

 A steel gas cylinder with 6±0.05% CO2 and balance gas N2

 A steel gas cylinder with100% N2

 T-shape connector

 Tubing

 Flowmeter

4-16
 1. P
Plug the modu
ule into the mo
odule rack and
d connect the sensor.

2. W
Wait until CO2 warmup is fin
nished. Selectt the CO2 wav
veform or parameter to enterr the CO2 Settup menu.
T
Then, select Start
S Zero Cal.. to start a zero
o calibration. If
I the zero calibration fails, tthe prompt me
essage CO2
Z
Zero Failed is displayed. Ottherwise, the b
baseline of wa
aveform recov
vers to zero.

3. S
Set Apnea Tim
me to 10s in th
he CO2 Setup
p menu.

4. B
Blow to the CO
O2 sensor to generate
g a CO
O2 waveform and
a then place
e the sensor inn the air. Chec
ck if the
a ge *** Apnea is displayed o
alarm messag on the screen.
5. C
Connect the te
est system as follows:

Relief valve
v Flowmeter

N2 gas cyylinder Mainstrea

am sensor proobe

T-shape
e
connecto
or

Monittor
T-sha
ape connector
R
Relief valve

C 2 gas cylinder
CO

6. T
Turn on the re
elief valves of N2 gas cylinde
er and CO2 cy
ylinder respecttively to ensurre that only on
ne gas
ccylinder is con
nnected to the
e T-shape con nector at a tim
me.

7. A
Adjust the relie
ef valves resp
pectively to enssure a stable flow
f by mainta
aining the readding on the flow
wmeter at a
vvalue between
n 2 and 5 L/min.

8. S
Switch betwee
en the two cylinders to conn
nect Mainstrea
am CO2 senso
or at intervals oof
6 -10s and check if the disp
played CO2 va
alue is 45±2 mmHg.

4.4.9 Sidestrea
am and Mic
crostream
m CO2 Testts
See ssection 4.2.3S
Sidestream an
nd Microstrea
am CO2 Testts.

4.4.10
0 AG Tests
s
See ssection 4.2.4A
AG Tests.

4-17
4.4.11 EEG Test
You can choose either of the following methods to perform the test:

Method 1:
Tools required:

 ECG simulator with Sine wave output function.

1. Connect pins of EEG lead wires to an ECG simulator.

Set the ECG simulator to output Sine wave and frequency to between 0.5 and 30Hz. The range is 2mV. The
GND pin of EEG module connects to RL of ECG simulator. The A+ pin of EEG module connects to LA of ECG
simulator. The other pins of EEG lead wires connect to any ECG lead as you wish.

2. Open the EEG setting menu on monitor, Set the Scale of EEG to be 2000uV. Then you can find a Sine
wave on screen of Patient Monitor.

Method 2:
Tools required:

 None.

Connect all the pins of EEG lead wire together, for example, you can connect them to some metal materials.
Then check the EEG module resistance test, if all the leads are green then pass.

Method 3:
Tools required:

 Resistance box

 Multimeter

1. Connect the EEG module/cable to the EEG simulator and the monitor.

2. Set Montage Type: Bipolar Mode.

3. Adjust the resistance box to 1 kΩ, verify the resistance value displayed on the monitor is 1kΩ.

4. Test the lead type of the monitor to B+, C+ and D+ respectively instead of lead A+.

5. Set Montage Type: Monopolar Mode , then repeat the step 3~4.

4-18
 BIPOLAR

RA = 10 K A+

RA = 10 K A-

RA = 10 K PGND

MONOPOLAR
RA = 10 K A

RA = 10 K NE

RA = 10 K PGND

4.4.12 BIS Test

You can choose either of the following methods to perform the test:

Method 1:
Tools required:

 None.

1. Connect the BIS sensor to a healthy, wide-awake adult as directed in the Operator's Manual.

2. Check the EEG wave and BIS numerics displayed on the screen and make sure the BIS value is within 80
and 100.

Method 2:
Tools required:

 BIS simulator (Covidien PN: 186-0137)

1. Connect the BIS sensor with the BIS simulator. Select BIS area parameter or waveform to access BIS
Setup. Then, select Sensor Check to perform a cyclic impedance check.

2. After the cyclic impedance check is finished, check that the result for each electrode is passed.

Method 3:
Tools:

 Signal generator, （Maker: NF, Model:WF1946B）

 Covidien Signal simulator (Covidien PN:189-0137)

4-19
 1. Insert the BIS module to the monitor, connect the BIS module/cable to the Covidien Signal simulator, signal
generator.

2. Adjust the signal generator to produce a 90Hz, 35.4mV(RMS) sine signal to the Convidien Signal simulator.

3. Set the time length of the review window to the shortest.

4. Verify the EMG value range from 65 to 75, and SQI value should be 100 displayed on Graphic Trends.

4.4.13 RM Test
Method 1:
Tools required:

 T-shape connector

 Tubing

 Squeeze bulb

 Rigid vessel with volume 500±25 ml

 Reference manometer (calibrated with accuracy equal to or greater than 1 mmHg)

 Flow sensor for adult patient

1. Connect the equipment as shown below.

2. Set the monitor to be tested to mechanical ventilation mode.

3. Use the squeeze bulb to exert a test pressure of 60cmH2O, and check whether the RM airway pressure
precision meets the requirement of 58.2~61.8cmH2O.

Monitor Reference
manometer
RM sensor
RM connector

Squeeze bulb Rigid vessel

Method 2:
Tools required:

 Tubing

 Pressure gauge （Accuracy not less than 0.1cmH2O）

 Air Pump （-95~400 kPa）

1. Connect the module, RM sensor, air pump and pressure gauge according to picture below.

2. Select monitor as mechanical ventilation mode.

4-20
 3. Use air pump to inflate to -20, 0, 10, 60, 120cmH2O pressure, verify RM module measured airway pressure
accuracy is ±3％ of reading.

4.4.14 CCO/SvO2 Tests

Interconnecting Function

Tools required:

 None.

1. Connect and set the patient monitor and Vigilance II monitor per the procedures in the Operator's Manual.

2. Set the Vigilance II monitor to Demo mode. Start the CCO and SvO2 tests in Demo mode.

3. Verify that the CCO/SvO2 numerics displayed on the patient monitor and Vigilance II monitor are consistent.

Output Performance

Tools required:
Multimeter

1. Connect the signal output end of the connecting cables of the CCO/SvO2 module to the oscilloscope.

2. Select CCO Setup → Signal Output Setup and then select Simulated High Value from the pop-up menu.
Check that the amplitude of electrical level at the signal output port of ECG, MAP, CVP and SpO2 are
5±0.015 V, 5±0.25 V, 5±0.25 V and 10±0.5 V respectively.

4-21
 4.4.15 PiCCO Test
Performance Test

Tools required:

 Medsim300B patient simulator or Prosim 8

 PiCCO IBP test cable (PN: 040-001300-00)

1. Connect the patient simulator, the PiCCO IBP test cable and the PiCCO module.

2. Let the patient simulator outputs 0 mmHg respectively to the pArt channel and the pCVP channel.

3. Select the pArt parameter interface to access the pArt Setup menu, and then select Zero.

4. Select the pCVP parameter interface to access the pCVP Setup menu, and then select Zero.

5. Let the patient simulator output static pressure 200 mmHg to pArt channel and 20 mmHg to pCVP channel.

6. The pArt value displayed on the monitor should be within 200±4 mmHg, and pCVP value within 20±1
mmHg.

7. If the pArt error is beyond ±4 mmHg or pCVP error beyond ±1 mmHg, calibrate the PiCCO module. If the
module was calibrated with a dedicated reusable IBP sensor, check the calibration together with this IBP
sensor.

8. Let the patient simulator output ART signal to the pArt channel and CVP signal to the pCVP channel, check
whether the IBP waveform is correctly displayed.

Pressure Calibration

Method 1:
Tools required:

 Medsim300B patient simulator or Prosim 8

 PiCCO IBP test cable (PN: 040-001300-00)

1. Connect the patient simulator, the PiCCO IBP test cable and the PiCCO module.

2. Let the patient simulator outputs 0 mmHg respectively to the pArt channel and the pCVP channel.

3. Select the pArt parameter interface to access the pArt Setup menu, and then select Zero.

4. Select the pCVP parameter interface to access the pCVP Setup menu, and then select Zero.

5. Set static pressure to 200 mmHg on the patient simulator.

6. Select Main Menu → Maintenance → enter the required password → Module. In the IBP menu, set the
calibration pressure to 200 mmHg.

7. Select the Calibrate button next to the desired IBP channel to start a calibration.

The message Calibration Completed! is displayed after a successful calibration. Otherwise, a corresponding
message will be displayed.

Method 2:
Tools required:

4-22
 S
Standard sphyygmomanome
eter

 S
Squeeze bulb
b

 T
Tubing

 T
T-shape conn
nector

1. C
Connect the 3-way
3 stopcock, the sphygm
momanometer and the squee
eze bulb throuugh a T-shape
e connector,
a
as shown belo
ow.

2. T
Turn on the 3--way stopcock
k to the air to zzero the transducer, and the
en open the sttopcock to the
e
ssphygmomano
ometer.

Pressure transducer

3-way sto
opcock

Connector cable of pressure trransducer

IBP
T-shape connector
c
module
Sphyg
gmomanomete
er

3. Select Main M
S Menu → Ma in enter the required password
ntenance → e enu, set the
d → Modu le. In the IBP me
ttarget calibrattion value of th nnel.
he target chan

4. IInflate using th
he squeeze bu eading of sphy
ulb until the re ygmomanometer approximaates the preset calibration
vvalue.

5. Adjust the caliibration value in the Maintaiin IBP menu until

A u it is equal to the readingg of sphygmomanometer

6. S esired IBP cha

Select the Callibrate button next to the de annel to start a calibration.

The m ayed after a successful calib

message Calibration Completed! is displa bration. Otherw
rwise, a corres
sponding
messsage will be diisplayed.

4-23
C.O. Test

Method 1:
Tools required:

 Medsim300B Patient simulator or Prosim 8, or equivalent equipment

 C.O. adapter box (for 300B)

 PiCCO C.O. test cable (PN: 040-001301-00)

1. Connect the patient simulator and the C.O. module using a C.O. trunk cable and a C.O. adapter box.

2. Set the blood temperature (BT) to 37ºC on the patient simulator and check the temperature value is
37±0.1ºC.

3. Select CCO parameter interface to access the C.O. Measure interface. Then, select Setup to check
whether the value of Catheter Type is PV2015L20.

4. Turn the injectate temperature (TI) knob on the C.O. adapter box to set the TI to 20±1ºC for the patient
simulator and C.O. to 5 L/min.

5. In the C.O. Measurement window, select Start to start C.O. measurement. As soon as the prompt Inject
XXml is displayed, adjust TI to 4±1ºC, and then quickly back to 20±1ºC. Simultaneously press the button on
the simulator that corresponds to 5 L/min. The whole procedure shall be finished in 10 seconds.

6. Verify that the C.O. value displayed on the monitor is correct.

Method 2:
Tools required:

 Medsim300B Patient simulator or Prosim 8, or equivalent equipment

 C.O. adapter box (for 300B)

 PiCCO C.O. test cable (PN: 040-001301-00)

1. Connect the patient simulator and the C.O. module using a C.O. trunk cable and a C.O. adapter box.

2. Set the blood temperature (BT) to 37ºC on the patient simulator and check the temperature value is
37±0.1ºC.

3. Select CCO parameter interface to access the C.O. Measure interface. Then, select Setup to check
whether the value of Catheter Type is PV2015L20.

4. Turn the injectate temperature (TI) knob on the C.O. adapter box to check whether the value of the TI is
from 0 to 30ºC.

4-24
 4.4.16 NMT Tests
Performance Test

Method 1:
Tools required:

 Resistance box

 Multimeter

1. Set the resistance value to 1kOhm. Connect the stimulation electrodes to the two wiring terminals.

2. Set the multimeter to operate in DC mode. Connect the multimeter sensors to the NMT stimulation
electrodes, making sure that the sensor and electrode connected have the same polarity.

3. Insert the NMT module into the module rack of the monitor. Select the NMT parameter area of the monitor
to access the NMT Setup menu. Set the Stimulation Current to Supra(60mA). Set the Pulse Width to 300μs.
Perform a PTC measurement.

4. Check the voltage change detected by the multimeter and verify normal output of NMT stimulation.

Method 2:
Tools required:

 Resistance box (0~9999.9 Ω)

 Oscilloscope (Agilent DS0-X3014A)

1. Set resistance box to 1kOhm, connect stimulation electrodes to the resistance box.

2. Insert the NMT module to monitor. Set [Stimulation current] to [Supra (35mA)], [Pulse width] to 200μs.
Select [ST Mode] in NMT setup menu to start a ST measure.

3. Measure the voltage wave of the resistance box by oscilloscope, verify the pulse width is range from 180 to
220us, and calculate the Stimulation Current according stimulation voltage should be range from 33 to
37mA.

Sensor Check

Tools required:

 None.

1. Connect the patient monitor, NMT module, and NMT accessories.

2. Select Main Menu → Maintenance → enter the required password → Module → NMT.

3. Follow the on-screen instructions to check the NMT sensor.

4-25
If sensor check completes successfully, the message Test passed. The function of NMT sensor is OK is
displayed, indicating a functional sensor. If the check fails, check whether the sensor is placed correctly as
instructed, and perform the sensor check again.

NOTE

 Stop NMT measurement or calibration before starting NMT sensor check.

 Avoid forcefully striking the sensor.

4.5 Nurse Call Relay Performance Test

Tools required:

 Multimeter

1. Connect the nurse call cable to the Nurse Call Connector of the patient monitor.

2. Enter Demo mode. Then, select Main Menu → Maintenance >> → enter the required password →
Alarm to access the Nurse Call setup menu.

3. In Nurse Call menu, select all options of Alarm Priority and Alarm Type. and set Contact Type to Normally
Open.

4. In Nurse Call menu, set Signal Type to Pulse. Cause the monitor to generate an alarm and verify the output
are pulses of 1s width and the relay contacts are closed (can be measured with a multimeter) when there is
an alarm.

5. In Nurse Call menu, set Signal Type to Continuous. Cause the monitor to generate an alarm and verify the
output is continuous high level and the relay contacts are closed (can be measured with a multimeter)
when there is an alarm.

4.6 Analog Output Performance Test

Tools required:

 Patient simulator

 Oscilloscope

1. Connect the patient simulator to the monitor using an ECG or IBP cable and connect the oscilloscope to the
Auxiliary Output Connector of the MPM module of the patient monitor.

2. Verify that the waves displayed on the oscilloscope are identical with those displayed on the monitor.

4-26
 4
4.7 Electrrical Safe
ety Tests
s

WARNING
G

 Electrical saffety tests are a proven me

eans of detec
cting abnorma
alities that, iff undetected,
c
could prove dangerous
d to
o either the pa
atient or the operator.

 A
All tests can be performed
d using comm
mercially ava
ailable safety analyzer testt equipment.
Maintenance personnel sh he adaptabilitty, functionall completenesss and safety
hall ensure th y
o
of these piec
ces of test equipment, and
d be familiar with
w their usa
age.

 Electrical saffety tests sha

all comply witth the followiing standards
s: IEC 60601--1 and
A
ANSI/AAMI ES60601-1.
E

 In case of oth
her stipulatio
ons in local la
aws and regulations, imple
ement electriical safety
ttests by follo
owing relevan
nt stipulations
s.

 A
All devices driven
d by AC power and co
onnected to medical
m instruments in paatient zones
m
must comply
y with the IEC ndard. And electrical safety tests on th
C 60601-1 stan hese devices
m
must be impllemented in accordance
a w
with the test interval of the
e patient mon
nitor.

 Use certified safety analyzer (for exam

mple, UL, CSA
A or AMAI) as
s instructed to
o perform
rrelevant tests
s.

NOT
TE

 Electrical saffety check sh

hall be perform
med after rep
pair or routine
e maintenancce. Ensure th
hat all cover
b
boards, pane
els and screw
ws are correcttly installed before
b implem
menting electtrical safety tests.
t

 ely detect pottential electrical safety rissks that might cause

Electrical saffety tests are used to time
d
damage to pa
atients, opera
ators or main sonnel. Electrical safety teests must be
ntenance pers e carried out
under norma
al environmen
ntal condition
ns (that is, no
ormal temperature, humid ity and barom
metric
pressure).

See A
Appendix A Electrical
E on for electrica
Saffety Inspectio al safety tests..

4-27
 4.8 Recorder Check
Tools required:

 None.

1. Print ECG waveforms. The recorder should print correctly and the printout should be clear.

2. Set the recorder to some problems such as out of paper, etc. the patient monitor should give corresponding
prompt messages. After the problem is removed, the recorder should be able to work correctly.

3. Switch automatic alarm recording for each parameter ON and then set each parameter's limit outside set
alarm limits. Corresponding alarm recordings should be triggered when parameter alarms occur.

4.9 Network Print Test

NOTE
 HP LaserJet Pro M202dw laser printer is recommended for BeneVision patient monitor
series

4.9.1 Device Connection and Setup

1 Connect the patient monitor and network printer to a network switch using common network cables as
follows:

BeneVis Network
ion printer

Network cable Network cable

Switch

2 Select Main Menu → Maintenance → enter the required password →Network Setup and set the IP
address of the patient monitor in the same network segment with that of the network printer. (See the
instructions for use accompanying the printer)

3 Select Main Menu → Maintenance → enter the required password → Print and set the IP address of the
printer to the actual IP address, and set the paper size to the actual size.

4 Set the print resolution to 300dpi or 600dpi as required.

5 Click Print Test Page to check whether the output of the printer's test page is normal. If not, recheck the
connection and configuration of the printer.

4-28
 4
4.10 Device Integrration Ch
heck
4.10.1
1 Device Connectio
C n and Settup
Toolss required:

 External devicce (anesthesia

a machine, ve ntilator)

 ID adapter tha
at matches the
e external devvice

 RJ45 connectting cable

 S
Serial port ada
apting cable th
hat matching tthe external device

Conn
nect an extern
nal device as shown
s below. T
The figure bellow is for referrence only.

BeneLink module RJ45

5 connecting ccable ID
D adapter

Label

External
device

Serial p
port adapting cable
c (optional)

1. IInsert the Ben

neLink module
e into the modu
ule slot on the
e BeneVision patient
p monitoor.

2. C
Connect the ID
D adapter thatt matches the external device to the Bene
eLink module with a RJ45 connecting
c
ccable.

3. P
Plug the ID ad
dapter into the
e RS232 port o
on the externa
al device. Som
me external dev
evices may hav
ve ports
iincompatible with
w the ID adapter. In this ccase, a serial port adapter cable
c is requireed. Please be
e sure that
yyou have sele
ected the proper cable beforre connection..

4. A
Attach a label indicating dev
vice name to tthe RJ45 conn
necting cable at the end clos
oser to the Ben
neLink
module. When
m n the BeneLink module is co
onnected to several externa
al devices, youu can tell the devices
d
a
apart easily with
w these labels.

5. S
Switch the extternal device on.
o

4-29
NOTE
 Devices in the same category cannot be connected to the BeneLink module
simultaneously.

 Use the serial port adapting cable only with its matching external device. Please see the
following table to select the correct adapting cable.

 Use the ID adapter only with the matching external device. Please see the following table
for correct ID setup in Factory Maintenance menu.

Type of serial port adapting

External Device ID for ID adapter
cable
No need to use the adapting cable;
the ID adapter can be plugged into
Mindray Wato 20/30/55/65 4D52B2AE
the serial port of the external device
directly.
Newport E360 4E50B1B0 Type B
SNDF: 5042AFBE
No need to use the adapting cable;
(recommended)
the ID adapter can be plugged into
Puritan Bennett 840 SNDA: 5031AFCF (support
the serial port of the external device
less parameters than
directly.
protocol SNDF)
Maquet Flow-i 4D46B2BA Type B
Maquet Servo-i/Servo-s 4D53B2AD Type B
Draeger Evita 2/Evita 2
4434BBCC Type B
dura/Evita 4/Evita XL
Hamilton G5 (protocol Polling) 3550CAB0 Type B
Hamilton C2 (protocol Polling) 3270CD90 Type B
Hamilton Galileo (protocol
4750B8B0 Type B
Polling)
Hamilton G5 (protocol Block) 3542CABE Type B
Ohmeda Avance/Aisys 4F41B0BF Type D
Ohmeda Aestiva 7100/7900 4F37B0C9 Type D
GS: No need to use the adapting
cable; the ID adapter can be
plugged into the serial port of the
Drager Fabius GS/Plus/Trio 4446BBBA
external device directly.
Plus: type C
Trio: type C
Drager Primus 4450BBB0 Type C
TCM CombiM/TCM TOSCA 5443ABBD Type C
TOF-Watch SX 5457ABA9 Type C
Expanded Model / Type A
Drager Savina 300 4441bbbf Type B
Babylog8000 plus 4442bbbe Type B

4-30
 VPRT: 5637A9C9
Philips V60 Type B
SDNA:5636A9CA
Resmed VSIII 5653a9ad Type C
SenTec TpCO2 5354ACAC Type C
No need to use the adapting cable;
the ID adapter can be plugged into
ALM monnal T75 4154BEAC
the serial port of the external device
directly.
GE CareScape R860 4F52B0AE Type B
GE Engstrom Carestation 4F45B0BB Type B
Maquet Servo-U 4d55B2AB Type B
HUL Leoni Plus 4849B7B7 Type C
HUL Leon Plus 4850B7B0 Type C
HUL Leon 484CB7B4 Type C
No need to use the adapting cable;
the ID adapter can be plugged into
Draeger ZeusIE 445abba6
the serial port of the external device
directly.
No need to use the adapting cable;
the ID adapter can be plugged into
Draeger V300 4433bbcd
the serial port of the external device
directly.
No need to use the adapting cable;
the ID adapter can be plugged into
Draeger Perseus A500 4435bbcb
the serial port of the external device
directly.
No need to use the adapting cable;
the ID adapter can be plugged into
Drager Evita infinity V500(C500) 4456bbaa
the serial port of the external device
directly.
Apollo 444fbbb1 Type C

4-31
4.10.2 Device Integration Function Test
4.10.2.1 Preparation

Prepare the tools needed for function test according to the type of the external device you install. Please see
the Instructions for Use of the corresponding external device for guidance. For the function test of ventilator and
anesthesia machine, at least the following tools are needed:

 BeneVision patient monitor with BeneLink module properly installed

 Anesthesia machine or ventilator

 Gas source(tube or gas cylinder), including air or O2 at least, and N2O or other anesthesia gases are
optional

 Tube that connects the patient(or test lung)

 Test lung and a matching Y-pipe, or other accessories

4.10.2.2 Procedure and Items to Be Checked

Follow the steps below:

1. Connect the BeneLink module to the ventilator or the anesthesia machine. Please see Device Connection
and Setup for more details.

2. Connect the gas supply and test lungs to the ventilator or anesthesia machine, turn on the device, and
configure as follows:

 Set up the serial port of the external device by referring to Serial Port Configuration List.

 Set up the pressure control mode and check if the ventilator or anesthesia machine works normally.

3. Make sure the ID adapter is correctly configured, and the green indicator of corresponding port on the
BeneLink module illuminates constantly.

4. Access Integrated Devices screen on the patient monitor. Check that the device type (ventilator or
anesthesia machine) and ventilation mode are correctly displayed.

5. Select parameters PEEP, Pmean, VTe, MV, I:E, and f(RR) respectively on the patient monitor and check if
the parameter values displayed on the patient monitor are consistent with those displayed on the ventilator
or anesthesia machine.

6. Re-configure the above parameters on the ventilator or the anesthesia machine and check if the parameter
values displayed on the patient monitor change accordingly.

7. Trigger alarms MV Too Low, Airway Pressure Too High, PAW Too High, Peak Too High, and No Gas
Supply (no Air or O2) on the ventilator or the anesthesia machine. Check whether these alarm messages
are correctly recorded in the alarm list of the patient monitor.

8. Switch the ventilator or anesthesia machine to volume control ventilation mode. Check if the ventilation
mode displayed on the patient monitor changes accordingly, and if the parameter values of PEEP, Pmean,
VTe, MV, I:E, and f(RR) are correctly displayed.

4-32
Serial Port Configuration List

External Device Setup Remark

If you need to view the

parameters of CO2, AG, and
BIS module in the anesthesia
Mindray Wato machine, select Factory
Not required.
20/30/55/65 Maintenance → Function
Configuration → Select
Module in standby mode and
tick the corresponding module.
The following information is for
further reference: Baud Rate:
Maquet Servo-i 9600 bps
Not required.
Maquet Servo-s Word Length: 8 bits
Parity: even
Stop Bits: 1
Channel A: Not required;
Channel B:
 Protocol: Medibus
Draeger Evita 2 /
 Baud rate: 19200
 Parity: even
 Stop Bits: 1

Protocol: Medibus
Draeger Evita 2 Baud Rate: 19200
dura/ Evita 4/ Evita Parity: even /
XL Stop Bits: 1
Interval: --- (Evita 2 dura)

The following information is for

further reference: Baud Rate:
38400 bps
Newport E360 Protocol: Newport
Word Length: 8 bits
Parity: NONE
Stop Bits: 1
Baud Rate: 38400
Puritan Bennett 840 Word Length: 8 bits /
Parity: NONE
Baud Rate: 9600 bps
Hamilton G5 1. Access the Configuration menu; Word Length: 7 bits
(protocol Polling) 2. Set protocol to Polling Parity: even
Stop Bits: 2
Baud Rate: 9600 bps
Hamilton C2 1. Access the Configuration menu; Word Length: 7 bits
(protocol Polling) 2. Set protocol to Polling Parity: even
Stop Bits: 2
4-33
External Device Setup Remark

Baud Rate: 9600 bps

Hamilton Galileo Word Length: 7 bits
Not required.
(protocol Polling) Parity: even
Stop Bits: 2
Baud Rate: 38400 bps
Hamilton G5 1. Access the Configuration menu; Word Length: 8 bits
(protocol Block) 2. Set protocol to Block Parity: None
Stop Bits: 1
Baud Rate: 19200 bps
Ohmeda Word Length: 7 bits
Not required.
Avance/Aisys Parity: odd
Stop Bits: 1
Baud Rate: 19200 bps
Ohmeda Aestiva Word Length: 7 bits
Not required.
7100 /7900 Parity: odd
Stop Bits: 1
1. Access the repair mode;
2. Protocol: Medibus;
Drager Fabius 3. Baud Rate: 9600 bps
/
GS/Plus/Tiro Word Length: 7 bits
Parity: even
Stop Bits: 1
1. Access the repair mode;
2. Protocol: Medibus;
3. Baud Rate: 9600 bps
Drager Primus /
Word Length: 8 bits
Parity: even
Stop Bits: 1
Baud Rate: 9600 bps
1. Access the technical maintenance menu
TCM CombiM/TCM Word Length: 8 bits
(password required);
TOSCA Parity: even
2. Set protocol to Monlink.
Stop Bits: 1
Baud Rate: 19200 bps
Word Length: 8 bits
TOF-Watch SX Not required.
Parity: NONE
Stop Bits: 1
1. Access the Savina maintenance menu and
Baud Rate: 19200 bps
set the protocol to: MEDBUS.X or
Word Length: 7 bits
Drager Savina 300 MEDIBUS1.
Parity: even
2. Serial port adapting cable between ID
Stop Bits: 1
adapter and monitor: Type B

4-34
External Device Setup Remark

Baud Rate: 9600 bps

Press the Cal. config hardkey, and select
Word Length: 8 bits
Babylog8000 plus config → com on the touchscreen; protocol:
Parity: NONE
medibus.
Stop Bits: 1
Baud Rate: 19200 bps
1. In standby mode, select System setup →
Word Length: 8 bits
Evita V500 System → Interface → COM
Parity: even
2. Set protocol to MEDBUS.X or MEDIBUS
Stop Bits: 1
1. Access Diagnosis mode and select baud
rate.
To access Diagnosis mode, do as follows:
1) Turn off V60.
2) Press and hold the confirm button (a "√"
symbol on the hardkey) in the right upper
part of the touchscreen, and then press the
power-on button.
3) A message indicating whether V60 enters
the Diagnosis mode is displayed on upper
side of the touchscreen. Release the Confirm
Philips V60 button and click it again to access the Baud Rate: 19200 bps
diagnosis mode.
4) Set the baud rate to 19200 bps
5) Restart V60 for the new settings to take
effect.
2. Serial port adapting cable between ID
adapter and monitor: 25 pin (male) to 9 pin
(female) + Type B
3. Protocol: SNDA or VPRT as required with
corresponding ID set. Since protocol VPRT
has more parameters than protocol SNDA, it
is recommended to use VPRT.
1. Serial port configurations are not required.
Resmed VSIII 2. Serial port adapting cable between ID /
adapter and monitor: Type C
1. Adopt default settings. Access
Interfaces/Serial Interface/ to verify the
following settings:
Sentec TcpCO2 Baud Rate: 115200 bps
Protocol: SenTecLink
2. Serial port adapting cable between ID
adapter and monitor: Type C
Baud Rate: 38400 bps
Word Length: 8 bits
ALM monnal T75 /
Parity: NONE
Stop Bits: 1

4-35
External Device Setup Remark

Baud Rate: 19200 bps

GE CareScape 1. Serial port adapting cable between ID Word Length: 7 bits
R860 adapter and monitor: Type B Parity: odd
Stop Bits: 1
Baud Rate: 19200 bps
GE Engstrom 1. Serial port adapting cable between ID Word Length: 7 bits
Carestation adapter and monitor: Type B Parity: odd
Stop Bits: 1
Baud Rate: 38400 bps
1. Serial port adapting cable between ID Word Length: 8 bits
Maquet Servo-U
adapter and monitor: Type B Parity: even
Stop Bits: 1
1. Access the Standby mode. Use the
interface switch button to access the Service
interface. Select Login and set User to
Baud Rate: 19200 bps
Service Engineer (password: 0002). Then,
Word Length: 8 bits
HUL Leoni Plus select Connections from the left. In Serial
Parity: NONE
Protocol, set Serial Protocol to On and set
Stop Bits: 1
Mode to request driven. Exit and restart.
2. Serial port adapting cable between ID
adapter and monitor: Type C
1. Access the Standby mode. Use interface
switch button to access the Service interface.
Select Login and set User to Service
Engineer (password: 0002). Then, select the Baud Rate: 19200 bps
Configuration menu at the bottom and Word Length: 8 bits
HUL Leon Plus
select Page2. In Serial Protocol, set Serial Parity: NONE
Protocol to On and set Mode to request Stop Bits: 1
driven. Exit and restart.
2. Serial port adapting cable between ID
adapter and monitor: Type C

1. Access the Standby mode. Use interface

switch button to access the Service interface.
Select Login and set User to Service
Engineer (password: 0002). Then, select the Baud Rate: 19200 bps
Configuration menu at the bottom and Word Length: 8 bits
HUL Leon
select Page2. In Serial Protocol, set Serial Parity: NONE
Protocol to On and set Mode to request Stop Bits: 1
driven. Exit and restart.
2. Serial port adapting cable between ID
adapter and monitor: Type C

4-36
External Device Setup Remark

Baud Rate: 38400 bps

Word Length: 8 bits
Maquet Flow-i Not required
Parity: even
Stop Bits: 1

1.Access the Standby mode through

“Biomed service”, input maintenance
password.
2.Select “Medibus setup” menu and select
Baud rate = 9600
COM1 as example for configuation.: set
Draeger ZeusIE Parity = Even
“ Commands to Medibus device” to “On” ; set
Stop bits = 1
“Medibus version” to “SW4.n; set “ Port” to
“On” , Then press “Activate” button.
3. Serial port adapting cable between ID
adapter and monitor: not required.

1. In standby mode, select System setup →

System → Interface → COM. Baud rate = 9600
Draeger V300 2. Set protocol to MEDBUS.X or MEDIBUS. Parity = Even
3. Serial port adapting cable between ID Stop bits = 1
adapter and monitor: not required.

4-37
External Device Setup Remark

1. In standby mode, select System setup →

Baud Rate: 19200 bps
System → Interface, input password.
Draeger Perseus Word Length: 8 bits
2. Set protocol to MEDBUS.X.
A500 Parity: even
3. Serial port adapting cable between ID
Stop Bits: 1
adapter and monitor: not required.

1. Press knob, change display and power

button simultaneously to enter System
Service Screen, select Serial
Port---Parameters to enter Service Port Baud Rate:9600

Parameters Screen menu. Parity:EVEN

Apollo
Stop Bits:1
2. Set Protocol to MEDIBUS.
Data Bits:8
3.Serial port adapting cable between ID

adapter and monitor: Type C.

4-38
4.10.3 Installation and Test Report
Basic Information
Hospital Department
Serial number of ID
Name of external device
adapter
ID of the external
Type of serial port adapting cable
device
Software version and other information of
the external device
Checking the connection Test Result (Yes/No)
Can the patient monitor and the external device be assembled together using
designated accessories?
Does the green indicator of corresponding port on the BeneLink module
illuminate while the other indicators are not?
Are there numerics or characters displayed on the Devices Integrated screen of
the patient monitor?
Are the device type and parameter values displayed correctly on the Devices
Integrated screen of the patient monitor when the external device just enters
working mode?
Is the ventilation mode correctly displayed on the patient monitor? Does it
change correctly when the ventilation mode on the external device is changed?
Checking the parameters
Parameters on the Parameters on the patient
Value Value
external device monitor
PEEP PEEP
Pmean Pmean
Ppeak Ppeak
f (RR) f (RR)
VTe VTe

Checking the alarms

Alarm messages displayed on Alarm messages displayed in the

Alarm
the external device alarm list of the patient monitor
RR Too High
Apnea
Patient Disconnected
Other information

4-39
 4.11 Battery Check
Tools required:

 None.

Function Test

1. Verify that the patient monitor works properly when running on AC power.

2. Remove the AC power cord and verify that the patient monitor still works properly.

Performance Test

Perform the test procedure in the Battery section in the Operator's Manual and verify the operating time of the
battery meets the product specification.

4.12 Mounting Check

Tools required:

 None.

4.12.1 Safety check

Check the mounting of Patient Monitor is safe.

4.12.2 Overall Test and Check of Installed System

Implement installation test:
The following tests and checks need to be performed after a patient monitor is installed, or reinstalled after
being disassembled and repaired:

 Check that the screws fastening the bracket and guide rail are not loose.

 Check that the five installation screws on the bottom side of the N12 monitor are not loose.(six installation
screws for N15 and N17)

 Check that the four installation screws on the transfer metal and monitor bottom side are not loose.

 Check that it can be installed in place and locked when N12 monitor use fast lock installed way

 Check that it can be installed in place and locked when the monitor use on the cart installed way

 Check that the modules can be normally and securely inserted into the module rack.

 Check that the trim strip is properly installed after the display is disassembled and repaired.

 Check that the monitor handle is not loose.

 Check that the VHM bracket can place the monitor at any height as required.

4-40
 4
4.13 Facto
ory Main
ntenance
e
4.13.1
1 Accessin
ng Factory
y Mainten
nance Men
nu
Selecct Main Menu → Maintena
ance (input the
e correct passw
word) → Fac
ctory Maintenaance to open the
t Factory
Main
ntenance menu
u.

4.13.2
2 Monitor Informatio
on
You ccan view the information ab
bout the patien
nt monitor and export the log
g to a USB dissk.

4-41
4.13.3 Production Test
This tab page lists the basic functions of major hardware interfaces of the monitor. Production test can be
classified into auto test and single test. If auto test is selected, the system will automatically complete all the
tests in sequence; for single test, users can select a specific test as required. The test interface is shown in the
following figure.

4.13.4 Setup
This tab page supports the settings relevant to ECG alarms and other configurations.

 Neonate ST analysis switch: Switch it on to enable the neonate ST analysis function; switch it off to disable
relevant functions of neonate ST analysis.

 HR/PR alarm off switch: Switch it on to set the HR/PR alarm switch; switch it off to disable the setting of
HR/PR alarm switch.

 HR alarm delay switch: Switch it on to enable the HR alarm affected by the setting of alarm delay; switch it
off to prevent the HR alarm from being affected by the setting of alarm delay.

 ESN: Enter the electronic serial number.

 Wireless setting: Provide Wi-Fi regulation test procedure and settings.

 Update ID Module: Provide interface for burning device integration ID. Users should confirm the BeneLink
port and device ID before burning.

4-42
4.13.5
5 Debug
This tab page provvides settings related to the debug mode,, which is only
y applicable to testing.

4.13.6
6 Power In
nfo
This tab page disp
plays information about pow
wer supply.

4.13.7
7 ClinicalD
Data
This tab page provvides settings related to clin
nical data colle
ection.

4-43
  Clinical Data Location: Supports the settings of data storage location. (None indicates not stored; Local
indicates saving locally; and Udisk indicates saving in a USB disk.)

 Each parameter module provides independent parameter collection switch.

NOTE
 The recorder is disabled if Recorder is switched off in the Factory Maintenance menu.

4.13.8 Transferring Clinical Data

In the Factory Maintenance page, select Clinical Data Transfer. Select data you want to transfer.

4.13.9 Software Version

In the Factory Maintenance menu, select Software Version to show software version information.

4.13.10 Monitor Information

In the Factory Maintenance menu, select Monitor Information to show the status of the patient monitor.

Maintenance and Test Report

(See the above sections for detailed test procedures and contents)
Customer name
Customer address
Servicing person
Servicing company
Equipment under test
(EUT)
Model of EUT
SN of EUT
Hardware version
Software version
Test equipment Model/No. Effective date of calibration

Test Test
Test items
records results(Pass/Fail/NA)
Visual Inspection
The case, display screen, buttons, handle, SMR, modules,
power cord, wall-mount bracket and accessories have no
obvious signs of damage.

4-44
The external connecting cables are not frayed and the
connector pins are not loose and bent.
The external connectors are not loose or their pins are not
bent.
The safety labels and data plate are clearly legible.
Power on test
The power-on test is passed. The power indicator and alarm
system work correctly and the monitor start up properly.
Performance test
ECG performance test
ECG waves are displayed correctly without noise and the HR
value is within 60±1 bpm.
ECG Lead Off alarm behaves correctly.
Paced signals are detected and pace pulse marks are
displayed when Paced is set to Yes.
The difference between the amplitude of the ECG calibration
square wave and that of the wave scale is not greater than
5%.
Resp test
The Resp wave is not distorted and the Resp value is within
20±1 rpm.
SpO2 test
Measure SpO2 on a healthy person's finger and a Pleth wave
and PR value are displayed. The displayed SpO2 value is
within 95%-100%.
SpO2 Sensor Off alarm behaves correctly.
NIBP test
The difference is within ±3 mm when 0, 50 or 200 mmHg is set
for NIBP accuracy test.
There is no leakage with NIBP, or the manual leakage test
result does not exceed 6mmHg/min.
Temp test
The value displayed for each Temp channel of the monitor is
within 37±0.1ºC.
IBP test
The static pressure value displayed for each IBP channel is
within 200±2 mmHg.
The ART and LV waves for each IBP channel are displayed
correctly.
C.O. test
The TB value displayed on the monitor is within 37±0.1ºC.
The displayed C.O. value is within 5±0.25 L/min.
Mainstream CO2 test
The mainstream CO2 is zeroed successfully and the waveform
baseline recovers to zero.

4-45
CO2 Apnea alarm behaves correctly.
The displayed CO2 value is 45±2 mmHg.
Sidestream CO2 test
Block the gas inlet of the module or watertrap. The sidestream
CO2 flowrate is slower than 10ml/min and an alarm of CO2
CO2 Airway Occluded is given. It indicates that there is
no leakage.
The displayed CO2 value is 6±0.05%.
The displayed O2 value is within ±2% (when O2≤80%) or ±3%
(80%≤O2≤100%)
Microstream CO2 test
Block the gas inlet of the module or watertrap for about 30
seconds. An alarm of CO2 Airway Occluded is given. It
indicates that there is no leakage.
The displayed CO2 value is 45±2 mmHg.
AG test
When AG flowrate is slower than 10ml/min, an alarm of AG
Airway Occluded is given. It indicates that there is no leakage.
The measurement accuracy of CO2, N2O, O2 and AA (AA
represents an anesthetic agent) meets the product
specifications in the Operator's Manual.
EEG test (you can select either method to perform the test)
Method 1: The EEG wave is displayed on the monitor.
Method 2: All the leads are green then pass in the EEG
module resistance test.
Method 3: The resistance values displayed on the monitor are
1kΩ
BIS test (you can select either method to perform the test)
Method 1: The BIS value measured on healthy, wide-awake
adult is within 80-100.
Method 2: The result of impedance check for each electrode is
passed.
Method 3: The EMG value range is from 65 to 75, and SQI
value is 100 displayed on [Graphic Trends]
RM test(you can select either method to perform the test)
Method 1: The RM airway pressure is 58.2~61.8 cmH2O.
Method 2: The difference is within ±3% of reading when -20,
0, 10, 60, 120cmH2O is set for RM airway pressure accuracy
test.
CCO/SvO2 test
The CCO/SvO2 numerics displayed on the patient monitor and
Vigilance monitor are consistent.
The waves (at the ECG signal output port) displayed on the
oscilloscope are consistent with the ECG calibration waves
displayed on the monitor screen.

4-46
The amplitude of electrical level at the signal output port of
MAP, CVP and SpO2 are 5±0.25 V, 5±0.25 V and 10±0.5 V
respectively.
PiCCO test(you can select either method to perform the test)
The pArt value displayed on the monitor is within 200±4
mmHg, and the pCVP value is within 20±1 mmHg.
The waveforms of pArt and pCVP are displayed correctly.
Method 1: The BT value is 37±0.1ºC.
The value of CatheterType is PV2015L20
The C.O. value is displayed on the monitor
Method 2: The BT value is 37±0.1ºC.
The value of CatheterType is PV2015L20
The TI value is from 0 to 30ºC
NMT test(you can select either method to perform the test)
Method 1: The voltage change is detected by the multimeter
and the output of NMT stimulation is normal
Method 2: The pulse width is range from 180 to 220us, and
the calculated Stimulation Current is range from 33 to 37mA
The sensor check is pass.
Nurse call relay performance test
The relay contacts are close when an alarm occurs.
Analog output performance test
The waves displayed on the oscilloscope are identical with
those displayed on the monitor.
Electrical safety test
The Power Plug and cord check is passed.
The Visual Inspection of Device Enclosure and Accessories is
passed.
The Contextual Inspection of Device Enclosure and
Accessories is passed.
the Main unit label and Integrated warning labels are present
and legible
The Protective Earth Resistance test is passed
The Earth Leakage Test is passed
The Patient Leakage Current test is passed
The Mains on Applied Part Leakage test is passed
The Patient Auxiliary Current test is passed
Recorder check
The recorder can print ECG waves correctly and the printout
is clear.
Set the recorder to some problems such as out of paper, etc.
the patient monitor should give corresponding prompt
messages. After the problem is removed, the recorder should
be able to work correctly.
Automatic alarm recording for each parameter functions

4-47
 correctly when parameter alarms occur.
Network print test
The output of the printer's test page is normal.
Device integration check
Devices Integrated window can display the type of the
external device, ventilation mode, and corresponding
parameters normally.
Battery check
The monitor can operates correctly from battery power when
an AC power failure accidentally occurs.
The operating time of the battery meets the product
specification.
Mounting Check
The screws fastening the bracket and guide rail are not loose
The five installation screws on the bottom side of the N12
monitor are not loose.(six installation screws for N15 and N17)
The four installation screws on the transfer metal and monitor
bottom side are not loose
It can be installed in place and locked when N12 monitor use
fast lock installed way
The modules can be normally and securely inserted into the
module rack
The trim strip is properly installed after the display is
disassembled and repaired
The VHM bracket can place the monitor at any height as
required

Conclusion:
Qualified or not: (Yes No)

Signature of tester: Date:

4-48
5 Troubleshooting
5.1 Introduction
This chapter lists the problems that may occur during use of the monitor and recommended
measures. Refer to the table in this chapter to check the monitor, and confirm and fix these problems.
For more information about the troubleshooting, please contact the after-sales service department of
Mindray.

5.2 Part Replacement

For the monitor, the PCB, main parts and components can be replaced. For the LCD or touch screen
fault, only the front case assembly can be replaced. Once the faulty PCB is confirmed, replace the
PCB according to the operation guide in Chapter 7 Repair and Disassembly. Then, confirm that
the monitor can operate normally and has passed all the performance tests. For the information
about replaceable parts, refer to Chapter 8 Parts.

5.3 Check before Powering on the Monitor

After the AC power supply is connected, check whether the AC indicator is turned on. If not, confirm
whether the AC cable is connected to the socket and monitor reliably. If both the AC external power
supply and power cord are connected normally, but the AC indicator is off, the AC-DC power module
or main control board of the main unit may be damaged. Now, you need to insert a battery to see
whether the monitor can be powered on. If it cannot be powered on, the main control board may be
damaged or the internal board is abnormal, resulting in power supply protection. If the monitor can
be powered on, the AC-DC power module is damaged.

In addition, check the appearance for damages before powering on. Particularly, when the touch
screen of the screen assembly is damaged, stop using the monitor immediately.

5-1
5.4 Software Version Check
Some troubleshooting tasks may involve software version compatibility. For information about the
configuration and software version of your patient monitor, contact Mindray After-sales Service. To
check the software version, do as follows:

1. Select Main Menu → System >> → Version Information >>. In the displayed menu, you
can check the version information of the system software.
2. Select Main Menu → System >> → Maintenance >> → enter the user's maintenance
password → Version Information >>. In the displayed menu, you can check the version
information of the system software and modules.

5.5 Technical Alarm Check

Before troubleshooting the patient monitor, check for technical alarm message. If an alarm message
is presented, eliminate the technical alarm first. For detailed information on technical alarm
messages, possible causes and countermeasures, refer to the patient monitor’s Operation Manual.

5.6 Troubleshooting Guide

5.6.1 Power On/Off Failures
Failure Symptom Possible Cause Countermeasure
AC mains not
connected or  Verify the AC mains is properly connected.
insufficient battery  Verify the battery capacity is sufficient and the
power or battery batter is not damaged.
damaged

 Verify the cable connecting the power-on/off

Cable defective or button board to the main control board.
improperly connected  Verify the connecting cable connectors and

Power on failure corresponding sockets are not damaged.

Power switch and

indicator board Replace the power switch and indicator board.
damaged

Power module
Replace the power module.
defective

Main control board

Replace the main control board.
failure

Power supply  If the main unit connects to other devices such

5-2
Failure Symptom Possible Cause Countermeasure
protection as the module, external module rack, mouse,
keyboard, USB disk, and scanning gun, first
disconnect these devices from the main unit.
If the monitor can be started after the
disconnection, an external device may fail,
leading to power supply protection.
 If the main unit is not connected to other
devices, check whether there is any short
circuit fault in the internal module rack COM
board or main control board and it leads to
protection of the power output.

5.6.2 Display Failures

Failure Description Possible Cause Troubleshooting
The display screen Cable defective or  Verify the cables (screen cable and backlight
does not function or improperly connected cable) connecting the display screen to the
the display is main control board are correctly connected.
abnormal, but the  Verify the connecting cable connectors and
main unit can corresponding sockets are not damaged.
operate
LCD screen defective Replace the front case assembly.

Main control board Upgrade the software of the main control board.
software abnormal

Backlight driver Replace the main control board.

defective

Display driver Replace the main control board.

defective

The touch screen Cable defective or  Verify the cable connecting the touch screen
does not respond improperly connected to the main control board is properly
connected.
 Verify the connecting cable connectors and
corresponding sockets are not damaged.

Touch screen Replace the front case assembly.

defective

Main control board Upgrade the software of the main control board.
software abnormal

Main control board Replace the main control board.

failure

Touch controller’s Touch the screen stably for 20 seconds, if the

firmware is running touch screen still does not work, please restart the

5-3
 wrong. monitor. If the touch screen could not work yet,
replace the front case assembly

5.6.3 Module Rack Failures

Failure Description Possible Cause Troubleshooting
SMR

 The cable connecting SMR and the main

unit of the monitor is not connected
properly or already damaged. Verify the
External cable
connecting cables and connectors are not
defective or poorly
damaged.
connected
 Verify that contact screws on SMR or
module are tightly fastened and well
connected.

Replace the malfunctioning parameter module

with a known good module. If the patient
Defective parameter
monitor identifies the replacement module and
module
can start measurement, it indicates that the
original module is faulty.

Wrong communication Upgrade the module and/or the SMR software

board software version to a compatible level.

 Check whether the SMR interface output

voltage of the main unit is 12 V. If it is
SMR cannot identify abnormal, the internal module rack COM
parameter modules SMR power supply board or main control board fails.
abnormal  Check whether the contact screw output
voltage of the external module rack is 12 V.
If it is abnormal, the communication
module on the SMR fails.

8-slot Module rack

Replace 8-slot the module rack communication
communication board
board.
defective

 Verify the cable between the module rack

interface board and the communication
Internal cable defective
board is properly connected.
or poorly connected
 Verify the connecting cables and
connectors are not damaged.

Internal module rack

Replace the internal module rack COM board.
COM board defective

Logic version error of

Upgrade the logic version of the internal
the internal module
module rack COM board.
rack COM board

5-4
 Main control board
Replace the main control board.
failure

Internal module rack

Replace the malfunctioning parameter module

with a known good module. If the patient
Defective parameter
monitor identifies the replacement module and
module
can start measurement, it indicates that the
original module is faulty.

 Verify the cable connecting the internal

Cable defective from
module rack COM board to the main
the main control board
control board is connected reliably.
to the internal module
 Verify the connecting cables and
rack COM board
connectors are not damaged.
The parameter module
Version inconsistency
does not respond
between the module
communication board Upgrade the module or internal module rack
and the internal COM board software.
module rack COM
board

Power supply to the The internal module rack COM board or main
internal module rack is control board may fail, and 12 V cannot be
not correct output.

Main control board

Replace the main control board.
failure

5.6.4 Alarm Failures

Failure Description Possible Cause Troubleshooting
 Verify the cable connecting the alarm LED
board to the main control board is properly
Cable defective or
connected.
Alarm LED off or cannot improperly connected
 Verify the connecting cables and
be turned off while the
connectors are not damaged.
audible alarm is
Alarm LED board
sounding Replace the alarm LED board.
failure

Main control board

Replace the main control board.
failure

Check whether the audible alarm is muted.

No audible alarm Select Main Menu → System >> →
Audible alarm
sounds emitted while Maintenance >> → enter the required
disabled
the alarm LED is normal maintenance password → Alarm>>, and then
in the popup menu, set Minimum Alarm

5-5
Failure Description Possible Cause Troubleshooting
Volume to a proper value. Select Alarm →
Setup, and set the alarm volume to a proper
value.

Speaker failure Replace the speaker.

Cable defective or Verify the cable connecting the speaker to the

improperly connected main control board is properly connected.

Main control board

Replace the main control board.
failure

5.6.5 Recorder Failures

Failure Description Possible Cause Troubleshooting
Verify the recorder status LED is lit.
Recorder module
If it is lit, recover its function in "Factory
disabled
Maintenance".

Printing paper jam Reinstall the paper roll properly.

 Verify the cable connecting the recorder

and the main control board is properly
No printout Cable defective or
connected.
improperly connected
 Verify the connecting cables and
connectors are not damaged.

Recorder failure Replace the recorder.

Main control board

Replace the main control board.
failure

Printing paper thermal

Replace the printing paper.
coating failure
Poor printing effect
Thermal head dirty Clean the thermal head.

Recorder failure Replace the recorder.

5.6.6 Output Interface Failures

Failure Description Possible Cause Troubleshooting
Internal module rack
Replace the internal module rack COM board.
COM board defective

Main control board

No output for the nurse Replace the main control board.
defective
call signal
 Verify the cable connecting the main
Cable defective or
control board to the internal module rack
improperly connected
COM board is connected reliably.

5-6
Failure Description Possible Cause Troubleshooting
 Verify the connecting cables and
connectors are not damaged.

Logic exception of the

Upgrade the logic of the internal module rack
internal module rack
COM board.
COM board

Main control board

USB Device Unusable. Replace the main control board.
failure

Network interface Main control board

Replace the main control board.
failure failure

Display not matched

with the DVI interface Use the recommended display.
DVI interface failure time sequence

Main control board

Replace the main control board.
defective

External display model

Use the display model recommended in the
not specified in the
user manual.
manual

Touch pad damage of

Touch screen failure of Replace the display.
the external display
the external display
Touch pad firmware of
the external display Contact the display manufacturer to fix the
inconsistent with the problem.
system software

5.6.7 Power Supply Failures

Failure Description Possible Cause Troubleshooting
Battery damaged Replace the battery.

 Verify the cable connecting the main

Battery cannot supply control board to the battery interface board
Cable defective or
power is correctly connected.
improperly connected
 Verify the connecting cables and
connectors are not damaged.

Battery damaged Battery change

 Verify the cable connecting the main

control board to the battery interface board
Battery cannot be Cable defective or
is correctly connected.
recharged or cannot be improperly connected
 Verify the connecting cables and
fully recharged
connectors are not damaged.

Main control board

Replace the main control board.
failure

5-7
 5.6.8 Network Related Problems
Failure Description Possible Cause Troubleshooting
Verify the network cables and connectors
are intact, the network interface connection
No connection to the LAN
is reliable, and the hub or switch setting is
correct.

Start the monitor. The "beep" sound should

be heard during startup. After the iView
The patient monitor
assembly starts, the iView interface can be
cannot be connected
displayed in the main unit.
to iView system
If neither of the above two conditions
iView assembly failure
cannot be reached, check whether the
power supply for the iView assembly is
normal. If it is not normal, the main control
board may be damaged; if the power supply
is normal, the iView assembly is damaged.

Check for network cable connection and

length (which should not exceed 50 m), or
Improper network cable
check whether the laid network cable is too
connection
Frequent dropouts near to the power supply for large power
equipment.

Check for IP conflict in the network. If

Incorrect network settings
conflict is found, reset the network.

Check for network cable connection and

length (which should not exceed 50 m), or
Improper network cable
check whether the laid network cable is too
The patient monitor is connection
near to the power supply for large power
connected to a equipment.
network but cannot
Too many simultaneous Confirm the maximum number of
view other patients in
requests for viewing the simultaneously connected monitors
the View Others mode
patient monitor according to the user manual.

Check for IP conflict in the network. If

Incorrect network settings
conflict is found, reset the network.

Verify the wireless network settings are

Incorrect network settings
correct.

Verify the antenna for the wireless network

Failure to connect to a Antenna not installed
card is connected to the wireless module
wireless network properly
reliably.

Wireless module damaged Replace the wireless module.

Main control board failure Replace the main control board.

5-9
Failure Description Possible Cause Troubleshooting
Antenna not installed Verify the antenna for the MPAN module is
properly installed properly.

MPAN module damaged Replace the MPAN module.

 Verify the cable connecting the MPAN

MPAN module not
module to the internal module rack
connected to the internal
COM board is connected properly.
MPAN failure module rack COM board
 Verify the connecting cables and
properly
connectors are not damaged.

Internal module rack COM

Replace the module rack COM board.
board defective

Wrong software version for

Upgrade the MPAN module software.
the MPAN module

5.6.9 Software Upgrade Problems

Failure Description Possible Cause Troubleshooting
 Verify the network connector, NOT the
iView network connector, on the patient
monitor is being used.
Incorrect connection
 Ensure the normal operation of the
network hub or switch, and verify the
hub cable is properly connected.
Program upgrade fails Please select the corresponding correct
Wrong upgrade package
wrong upgrade package.

Configure a fixed IP address in range C as

specified for the patient monitor. We
Incorrect IP address
recommend not to upgrade a program
configuration for the PC
when the patient monitor is connected to a
network with multiple PCs.

5-10
 5.6.10 Device Integration Failures
Failure Description Possible Cause Troubleshooting
The ID adapter is not  Replace the ID adapter.
compatible with the external  Upgrade the ID of the ID adapter in
device "Factory Maintenance" menu.
The "Devices
The serial port adapter cable
Integrated" window
not compatible with the Replace the serial port adapter cable.
displays nothing after
external device
connection
Wrong software version or
Verify the protocol version and software
wrong protocol version of the
version are supported by the ID adapter.
external device

Generate the alarm: The BeneLink module Upgrade or update the software
"BeneLink Comm application software is application of the BeneLink module with
Stop" corrupted the network upgrading tool.

The patient monitor The BeneLink module Upgrade or update the software
has no response application software is application of the BeneLink module with
when loading the ID corrupted the network upgrading tool.
adapter BeneLink module damaged Replace the module.

5-11
6 Upgrade

6.1 Overview

This monitor supports upgrade of the monitoring parameter function modules, upgrade of the
functional assemblies, and network upgrade of software.

NOTE
 For function upgrade involving disassembly of the monitor, eliminate static electricity
before the disassembly. When removing some parts with the electrostatic sensitive
mark, wear protective devices such as electrostatic ring or anti-electrostatic gloves, lest
the parts would be damaged.

 Properly connect and route the cables and wires when reassembling the equipment to
avoid pinched hoses and electrical short circuits.

 Use specified screws to reassemble the equipment. If the incorrect screws are forcefully
tightened, the equipment may be damaged and the screws or part may fall off during use,
causing unpredictable equipment damage or human injury.

 Be sure to follow the correct sequence when disassembling the monitor.

 Before removing assemblies, make sure that all the connection lines have been
unplugged. During removal, note to avoid breaking the connection line by pulling or
damaging the connector.

 Place the removed screws and other parts separately by category so that they can be
used in the re-installation. Do not drop, contaminate or lose them.

6-1
 6.2 Upgrade of Parameter Function Modules
You can upgrade the following parameter modules:

Monitoring
PN Name and Specification Remarks
Parameter Module

MPM module MPM-1 Module (MR Spo2/3/5

115-038696-00
lead/IBP)

MPM-3 Module (NC Spo2/3/5

115-038697-00
lead/IBP)

MPM-7 Module (MR Spo2/3/5lead/No

115-044666-00
IBP)

MPM-9 Module (NC Spo2/3/5lead/No

115-044667-00
IBP)

MPM-13 (MR
115-038698-00
SpO2/12lead/IBP/Analog)

MPM-14 (NC
115-038699-00
SpO2/12lead/IBP/Analog)

MPM-13 (MR
115-038700-00
SpO2/12lead/IBP/Analog)

MPM-14 (NC
115-038701-00
SpO2/12lead/IBP/Analog)

IBP module 6800-30-50850 IBP Module (Package/no accessory)

C.O. module CO Module kit (M03B V2.0) No

115-015238-00
accessory

CO2 module CAPNOSTAT CO2 (Package/no

115-013200-00
accessory)

ORIDION CO2 (Package/no

115-013201-00
accessory)

CO2+O2 Module (package/ Adu

115-034095-00
accessory)

6-2
 Monitoring
PN Name and Specification Remarks
Parameter Module

115-037385-00 One-slot CO2_O2 module

AG module 115-034108-00 AG Module (package/no accessory)

AG Module (O2/package/no
115-034109-00
accessory)

AG Module (BIS/package/no
115-034110-00
accessory)

AG Module (O2/BIS/package/no
115-034111-00
accessory)

ICG module 115-034123-00 ICG Module (package/ no accessory)

BIS module 115-013194-00 BIS Module (Package/no accessory)

RM module 115-034114-00 RM Module (package/no accessory)

SPO2 module SPO2 Module (MS-2013，No

115-015015-00
accessory)

SPO2 Module NC (package/ no

115-034088-00
accessory)

SPO2 Module (9008 V2.0, No

115-015016-00
accessory)

CCO/SvO2 module CCO/SvO2 Module (Package/no

115-013196-00
accessory)

PiCCO module PiCCO Module (Package/no

115-013196-00
accessory)

ScvO2 module SCVO2 Module (Package/no

115-013199-00
accessory)

EEG module EEG Module (Package/without

115-018353-00
accessory)

6-3
 Monitoring
PN Name and Specification Remarks
Parameter Module

NMT module 115-020916-00 NMT Module (Package/no accessory)

Benelink module Benelink Module International

115-038771-00
(Package)

rSO2 module 115-037264-00 rSO2module

TEMP module 115-039492-00 Temp module (package/no accessory)

Infrared ear Temp Infrared ear Temp (no

115-044684-00
module accessory/package)

You can insert and remove all the parameter modules during patient monitoring. Refer to the
BeneVision N Series Patient Monitor Operator's Manual (P/N: 046-009995-00) for the use of
parameter modules.

6-4
 6.3 Upgrade of Functional Assemblies
NOTE
 When upgrading the wireless network, analog output and CIS function for a patient
monitor with standard configuration, you have to replace old PCBAs in the patient
monitor with corresponding PCBAs included in the upgrade kit and remove the covers of
related connectors in addition to installing the corresponding functional assemblies in
the monitor.

You can upgrade the following functional assemblies for this monitor: the satellite module rack
(SMR), wireless network functional assembly, MPAN, recorder, independent display assembly, iView
system functional assembly, etc.

Functional Rem
PN Name and Specification
Assembly arks

SMR material package (2m/without

115-037384-00
handle and hook)

SMR material package (2m/with

SMR 115-033887-00
handle and hook)

SMR material package (10m/with

115-033888-00
handle and hook)

Recorder 115-044523-00 Recorder upgrade package

Wifi 115-044521-00 2.4G/5G Wifi upgrade package

MPAN 115-044522-00 MPAN upgrade package

iView upgrade package (Without

115-044553-00
MainBoard)
iView
iView upgrade package
115-044578-00
(MainBoard)

ID upgrade package (Without

115-044554-00
MainBoard)
Independent Display

115-044579-00 ID upgrade package (MainBoard)

6-5
 Functional Rem
PN Name
N and Spe
ecification
Asse
embly arks
s

N12 Upgrade
Upgrade
U packa
age
packkage 115-044508--00
(DVI&
&TDS&BNC)
(DVI&TDS&BNC)
This monitor is configured with
w wireless n
network functio
ons and can be
b connected tto network thrrough
wireless AP. To
T upgrade wirreless function el of our comppany to connect
ns, ask authorrized personne
and set up the
e wireless netw
work, and the n carry out the
e performance
e test.

6.3
3.1 Upgra
ading SMR
R
The SMR can
n be connected
d to the patien
nt monitor thro
ough the SMR
R connector viaa a powered USB
U
cable.

For details, se
ee BeneVision
n N Series Pattient Monitor Operator's
O Manual (P/N: 0466-009995-00).

6.3
3.2 Upgra
ading Wire
eless Netw
work Functions
 Installati on
o method: Re
efer to the corrresponding se
ection of this manual
m to instaall the wireless
s
network functional
f assembly in your patient monitor. Pleases install the assem
mbly as show
wn in
the follow
wing pictures.

 How to usse WiFi functions: See Ben eVision N Serries Patient Monitor Operatoor's Manual (P
P/N:
046-0099
995-00).

The wireless signal

s will be affected
a by ina
accuracy insta
allation locatio
on of the antennna.

6.3
3.3 Upgra
ading Reco
order
 Installati on
o method: Re
efer to the corrresponding se
ection of this manual
m to instaall the recorde
er in
your patie
ent monitor.

 How to usse the recorde

er: See BeneV
Vision N Serie
es Patient Mon
nitor Operator''s Manual (P/N
N:
046-0099
995-00).

6-6
6.3
3.4 Upgra
ading iView
w System
 Installati on
o method: Re
efer to the corrresponding se
ection of this manual
m to instaall the related
boards off the iView upgrade packag
ge in your patie
ent monitor.

 How to usse iView syste

em functions: See BeneVisiion N Series Patient
P Monito r Operator's
Manual (P/N: 046-0099
995-00).

NOTE
 During in
nstallation, us
se a blade to cut off the se
eals for the USB,
U DVI and network interface
at the rear case so th
hat the interfa
ace can stretc
ch out from th
he rear case.

6.3
3.5 Upgra
ading Independent D
Display Fu
unction
 Installati on
o method: Re
efer to the corrresponding se
ection of this manual
m to instaall the related
boards off the independ
dent display u pgrade packa
age in your pattient monitor.

 How to usse the independent display function: See

e BeneVision N Series Patieent Monitor
Operatorr's Manual (P/N
N: 046-009995
5-00).

NOTE
 During in
nstallation, us
se a blade to cut off the DV
VI seal at the rear case so
o that the interface
can strettch out from the rear case
e.

6-7
 6.4 Upgrading Software
This monitor supports network upgrade through a PC or upgrade through a USB disk to complete
the update function for the monitor and peripheral related firmware.

 You can upgrade the software with the System Update Tool (PN: 110-005042-00 PC Upgrade
Tool) through network. This tool can directly run on a PC. Through network or by connecting the
patient monitor to a PC via a crossover network cable, you can upgrade the following programs.

 The programs of this monitor can also be upgraded through a specially authorized USB disk
(which contains the USB disk upgrade BIOS program PN:110-004854-00) or the following
programs of the monitor can also be upgraded.

Software PN Name and Specification Remarks

System
software / Large N12N15N17 system package /
package

/ Bluetooth firmware function program /

Module rack
software
/ FPGA write software /

/ M51C module DSP(BF70X) software /

/ M51C module M0 software /

Mindray monitoring algorithm package ECG

MPM modules / (extended ARR 12-lead ST configuration
Glasgow12-lead resting) software

ECG
Mindray monitoring algorithm package
/ configuration
(full function configuration) BF512
software

IBP module / M03B module write software /

CO module / M03B module write software /

6-8
6.4
4.1 Desc
cription of Network U
Upgrade Tool
T
6.4.1.1 Tool
T Softwa
are Installattion Method
d

1. Click the executive pro

ogram “System
mUpdateTool.e
exe” of the sys
stem upgrade tool software to

display th
he related prompt interface.. Click to enter
e the inputt interface of the

information about SN.

2. Enter e SN informatio
the on, and click to enter prrogram installaation location

interface. Select the co

orresponding ffolder for insta
allation, and click to

e installation according
complete a to th
he installation prompt.

Appendix: Re
eference Table of Multiple La
anguages:
La
anguage (Eng
glish) Lang
guage (Chine
ese) Remarkss
EN
NGLISH 英语
语 /

SIIM.CHINESE 简体
体中文 /

FR
RENCH 法语
语 /

GERMAN 德语
语 /

ITA
TALIAN 意大
大利语 /

PO
OLISH 波兰
兰语 /

SP
PANISH 西班
班牙语 /

PO
ORTUGUESE
E 葡萄
萄牙语 /

RU
USSIAN 俄语
语 /

CZ
ZECH 捷克
克语 /

TU
URKISH 土耳
耳其语 /

HU
UNGARIAN 匈牙
牙利语 /

Da
anish 丹麦
麦语 /

Du
utch 荷兰
兰语 /

Finnish 芬兰
兰语 /

6-9
Language (English) Language (Chinese) Remarks
Norwegian 挪威语 /

Swedish 瑞典语 /

Romanian 罗马尼亚 /

Serbian 塞尔维亚 /

GREEK 希腊语 /

TRA.CHINESE 繁体中文 /

Japanese 日语 /

6.4.1.2 PC and Monitor Connection Method

Make sure that at least one network card is installed on the PC, and the PC is connected to the
monitor through the network card.

1. PC connected to the monitor through the hub

 PC connected to the hub through a network cable: Connect one end of the network cable to
the network card slot of the PC and the other end to the hub slot.

 Hub connected to the monitor through a network cable: The connection method is the
same as the above method. The hub has multiple slots, so multiple (at least 5) monitors
can be connected in this case and upgraded at the same time.

2. Changing the IP address of PC network card

NOTE
 To ensure correct upgrade, the IP address set using the following rule must be used
before running the upgrade program. The IP address must be set to 77.77.1.xx, but there
are no special requirements for the gateway and DNS. For example, the IP address is
77.77.1.13, and the subnet mask is “255.255.255.0”.

How to enter the upgrade mode:

 Connect the monitor to the USB keyboard. When starting the monitor, constantly click ' F4+F5'
or '*' at the same time to enter the upgrade mode to perform upgrade;

 When starting the monitor, use two or more fingers to continuously and rapidly tap the screen to
enter the upgrade mode to perform upgrade.

6-10
 6.4.1.3 Software Too
ol Upgrade
e Operations
s

The software upgrade pack

kage of each p
product needs
s to be set acc
cording to the aabove
configuration requirements.. The software
e upgrade pac
ckage can only
y be set by thee administrator and
is also specia
ally managed by
b the adminisstrator. System
m software upg
grade settingss:

1. Do wnload
d the large software packag
ge of N12/N15
5/N17 system (the storage loocation is the
ackage path), run the installled system (network) upgra
model pa ade tool softwaare, click Sele
ect A
odel Package, select the "Me
New Mo erak.Tool" mo
odel package, click Open, annd then click OK,
O
as show
wn in the follow
wing figures:

6-11
 2. On the diisplayed mach
hine type selecction interface
e, select the machine
m type "M
Merak".

The following interface is diisplayed on th

he PC:

6.4
4.2 Guide to Softwa
are Upgrad
de Operattions
6.4.2.1 System Softw
ware Upgra
ading Metho
od

1. Enter the
e main interfac
ce for downloa
ading of system
m upgrade, an
nd click .
2. Select the
e prepared sy
ystem software
e upgrade pac ugh browsing,, check to ens
ckage file throu sure
that the selected
s down
nloading conte
ent (including the
t information such as the upgrade item
m,
check su
um, version an
nd description)) is correct, an
nd then click OK.
O

Now, the
e Start hot key
y of the main m
menu is enable
ed.

6-12
3. Confirm t
that the downloading netwo
ork cable is con
nnected correctly, make surre that the mo
onitor
n powered off, and click the Start hot key of the upgrade tool to enterr the download
has been ding
procedurre of software..

6.4.2.2 Upgrading Module

M Rac k Software

1. F irst conn
nect the SMR connection lin N15/N17 main unit
ne to the multii-function interrface of N12/N
(the syste
em software has
h been upgrraded, and the
e main unit is off),
o connect thhe downloadin
ng
network cable
c to the N12/N15/N17 m
main unit (the same as the connecting
c meethod for upgrrade
of the N12/N15/N17 main unit), and confirm that all
a the connecttion lines are cconnected
correctly..

2. Enter the
e main interfac
ce for downloa
ading of system
m upgrade, click " ", and
d

select the
e Rack.pkg file
e in the large ssoftware pack
kage of N12/N15/N17 system
m:

3. Upgrade the SMR upgrade program by referring to

o “System Sofftware Upgradding Method”.

4. If the upg
grade fails, che
eck whether a
all the wires arre connected correctly,
c and then perform
upgrade again.

6-13
 6.4.2.3 Upgrading Module Software

Upgrade the module program file by referring to “System Software Upgrading Method”. When the
upgrade is completed, click the Stop button on the upgrade menu to stop the upgrade, remove the
network cable, turn off the monitor, and then restart it.

For the detailed operations of network program upgrade, refer to the help and instructions included in
the System Update Tool, or consult your service personnel.

6.4.3 Guide to Upgrade through a USB Disk

6.4.3.1 Directory Structure Preparation for Upgrade through a USB Disk

Required tools:

 USB disk: a common USB disk in the FAT format (e.g., the USB disk of Kingston, Netac or other
models with a memory of 2GB or above);

1. Create the following content under the root directory of the USB disk: UPGRADE_AMP\Merak;

2. Copy the upgrade BIOS program Merak_Installer.pkg (do not change this file name) to the
UPGRADE_AMP\Merak directory;

3. Copy the upgrade file (PKG or MPKG) to the UPGRADE_AMP\Merak directory.

6.4.3.2 Inserting the USB Disk into the USB port of the Monitor

Insert the prepared USB disk into anyone of the four (4) USB ports of the main control board. Do not
insert the USB disk into the USB port of the iView board.

6.4.3.3 Entering Upgrade through the USB Disk

 Method 1: As pressing the on/off button of the monitor to start the monitor, use two or more
fingers to continuously and rapidly tap the touch screen to enter the upgrade mode.

 Method 2: Connect the USB keyboard, and constantly click 'F2+F3' or 'F4+F5' or '*' at the same
time to power on the monitor and enable it to enter the upgrade mode; in this way, the user's
upgrade file selection interface can be accessed.

6-14
 6.4.3.4 Selecting the
e File for Up
pgrade thro
ough the US
SB Disk

 O nly one upgrade pack

kage file is ava
ailable at pres
sent. It is selec
cted by defaullt. If multiple
upgrade packages exis
st, they are dissplayed in the
e left and right columns, andd a maximum of
o 16
upgrade packages can d. This upper limit cannot be
n be displayed The up, down, left
e exceeded. T
and right keys can be used
u to switch
h and select th
he desired upg
grade packagee.

 T ap the area on the to

ouch screen to pgrade prograam downward; or
o select the up
press the
e “” direction
n key on the ke
eyboard to sellect it;

 T ap the area on the ttouch screen to select the upgrade

u progra
ram upward; or
o
press the
e “” direction
n key on the ke
eyboard to sellect it;

 T ap the area on the ttouch screen to

t select the upgrade prograam leftward; or
o

press the
e “” direction
n key on the ke
eyboard to select it;

 T ap the area on the touch screen to select the upgrade

u progrram rghtward; or
press the
e “” direction
n key on the ke
eyboard to select it;

6-15
 T ap the area on the ttouch screen to
t confirm the selected upgrrade program; or
e Enter key on
press the n the keyboard
d to confirm it.

6.4.3.5 Upgrade Com

mpleted thrrough the USB
U Disk

When the inte

erface below is
s displayed, th
he current upg
grade is completed. The upggrade takes efffect
after the monitor is powered
d off and resta
arted.

CAUT
TION
 Disconnect the patien
nt monitor fro
om the patien
nt and make sure
s that imp
portant data are
a
saved be
efore upgrade
e.

 Do not shut down or power off the

e equipment when upgrad
ding the BIOS
S program an
nd
FPGA prrogram. Otherwise, the eq
quipment may
y break down
n.

 Program
m upgrade sho
ould be perfo
ormed by qua
alified service
e personnel o
only. Indicates a
potential hazard or unsafe practic
ce that, if not avoided, cou minor personal
uld result in m
injury orr product/property damage
e.

NOTE
 After upg
grading the BIOS
B program
m, you have to upgrade sy
ystem progra m and other
program
ms to ensure their
t compatiibility.

 Make sure the version of the upgrrade package

e is your desired one. If yo
ou want to ob
btain
the lates
st upgrade pa
ackage, conta
act Mindray Customer
C Serrvice Departm
ment.

6-16
 6.5 Upgrading CAA license function
To upgrade the monitor to have CAA functions, you need to buy the licenses. Provide the following
information when you order the licenses:

 Order number (contents CAA license function requirement )

 Product Model (for example, BeneVision N17)

 Monitor serial number (for example, F2-6C000031)

 MID number/MAC address (for example: 000F140839AE). To get the MID number, select :
Main Menu → License (in the System column).

 Customer's email (for receiving license key file)

Refer to the following instructions to upgrade the licenses

1. Unzip the PMLS.zip file. Then you would get a folder named PMLS.

2. Copy the folder to a USB disk.

NOTE
 The U disk should be FAT32 format.

 The PMLS folder should be in the root directory.

3. Plug the USB disk into the BeneVision N series patient monitor.

4. In the interface of BeneVision monitor, choose Main Menu → License (in the System column)
→ External, and then click the Install button.

6-17
FOR YOUR NOTES

6-18
7 Repaiir and Disassem
D mbly

7.1 Tools
During disasssembly and rep
pair, the follow
wing tools may
y be required:

 Phillips screwdrivers

 Small flatt-bladed screw

wdriver (speciffication 101 orr 102)

 Contact spanner
s (6800
0-J95)

 Tweezerss

 Needle nose pliers

 M3 sleevve

7.2
2 Prepara
ations fo
or Disass
sembly
Before disasssembling the monitor,
m make following prep
parations:

 Stop mon
nitoring the pa
atient, turn off tthe monitor an
nd disconnect all the accesssories and
periphera
al devices.

 Disconne
ect the AC pow
wer supply and
d take out all the
t batteries.

 Remove all the parame

eter modules iin the integral module rack;

 if the SMR is connecte

ed, disconnect the SMR from
m the monitor and then remoove all the
paramete
er modules in it.

CAUT
TION
 Eliminate
e static electricity before tthe disassem
mbly. When re
emoving som
me parts with the
electrosttatic sensitive mark, wearr protective devices
d such as electrostaatic ring or
anti-elec
ctrostatic glov
ves, lest the p
parts would be
b damaged.

 Properly
y connect and
d route the ca ssembling th e equipment to
ables and wirres when reas
avoid pin
nched hoses and electrica
al short circu
uits.

 Use spec
cified screws
s to reassemb
ble the equipment. If the in
ncorrect screews are force
efully
tightened, the equipm
ment may be d
damaged and
d the screws or part may ffall off during
g use,
causing unpredictablle equipmentt damage or human
h injury.

 Be sure to
t follow the correct sequ
uence when disassemblin
d g the monito
or.

 Before re
emoving asse
emblies, mak
ke sure that all
a the connec
ction lines haave been
unplugged. During re
emoval, note to avoid brea nnection line by pulling orr
aking the con
damagin
ng the connec
ctor.

7-1
 CAUT
TION
 Place the
e removed sc
crews and oth
her parts sep
parately by ca
ategory so th at they can be
b
used in the
t re-installa
ation. Do not drop, contam
minate or lose them.

7.3
3 Whole Unit
U Disa
assembly
y
7.3
3.1 Basic Disassem
mbly
NOTE
 Be sure to
t disassemb
ble the base ffirst before proceeding wiith other partts.

1. Remove the power plug anti-pull hookk from the rearr case of the monitor.
m

ezer to pry up the four screw

2. Use a twee w covers at the
e four corners of the rear caase and loosen
n and
remove the fo
our M3×8 scre
ews under them
m.

(Screw cover)) (Screw)

(

7-2
7.3.2 Disconnecting the Base
NOTE
 Be sure to place the monitor face up when disconnecting the base. To lay the monitor
face down, make sure that the surface is non-abrasive and static-free, lest the touch
screen would be scratched. Be sure to remove the base first before proceeding with
other parts.

1. As shown in the figure below, place the monitor face up, unscrew the M4×8 screws (5 for the
N12 series and 6 for the N15N17 series) from the bottom case;

2. Pull out the base.

 For the N12 series machines, the base assembly can be removed when the base is pulled
out.

7-3
  For the
t N15N17 se
eries machine
es, the base as
ssembly can be
b removed whhen the conne
ection
line connected
c to the
t battery intterface board of main board is pulled out.

J24

J20

NOTE
 Be sure to
t pull out the base with p
proper force, without dam
maging the caables and
connecto
ors.

7.3
3.3 Separa
ating the Front
F and Rear Halff of the Mo
onitor
1. After the base assemb
bly is removed , carefully plac
ce the monitor face down.

NOTE
 Before placing
p the monitor face do
own, make sure that the desktop
d is flaat, without forreign
matters, lest the scre
een would be damaged.

 Release the clip (if an nnection line

ny) on the con e socket before disconneccting the
connectiion line. Be sure
s to pull ou
ut the base with
w orce, without damaging the
proper fo
cables and
a connectors.

 For the
t N12 series
s machines, re
emove the con
nnection line for the LCD sccreen and the
conn
nection line forr the small boa
ard of front ca
ase.

7-4
  For the N15N17 series machines, remove the connection line for the touch screen,
connection line for the LCD screen and the connection line for the small board of front case.

2. Lift the rear case assembly to separate it from the front case assembly.

NOTE
 As shown in the above figure, there are two types of front case assemblies (NLT and
SHARP), which are different in the cabling way.

 N12

(N12 rear case assembly)

7-5
(N12-NLT fron
nt case assem
mbly) (N12-SHARP front case asssembly)

7-6
  N15

(N15 rear casse assembly)

(N15-NLT fron
nt case assem
mbly) (N
N15-SHARP frront case asse
embly)

 N17

(N17 rear casse assembly)

(N17-NLT fron
nt case assem
mbly) (N17-SHARP
( front case asssembly)

7-7
7.4
4 Furtherr Disasse
embly off the Fron
nt Case Assembl
A ly
7.4
4.1 Remov
ving the PowerSwit
P tch Board
1. Remove the connection line on the po
owerswitch boa
ard.

2. Remove the two PT3×8 screws and ta

ake out the powerswitch boa
ard.

2PCS
S

NOTE
 Use pro
oper force to
o remove the
e cable care
efully lest it would
w be brokken.

 During in
nstallation, press the boarrd to the silic
cone keypad direction by aaligning with
h the
front cas
se board positioning rib.

 Note to control
c the to
orsion when ttightening the
e twoPT3×8 screws
s again,, avoiding sc
crew
sliding.

7.4
4.2 Remov
ving the Alarm
A Lam
mp and Lig
ght Sensor Board
1. Remove the connection line on the ala
arm lamp and light sensor b oard.

2. Remove the two PT3×8 screws and ta

ake out the ala
arm lamp and light sensor board.
b

2PCS PT3
3 X8

Connnec
tionn line
k t

7-8
 NOTE
 Use prop
per force to re
emove the ca
able carefully
y lest it would
d be broken.

 During in
nstallation, press the boarrd to the alarrm lamp shad
de direction b
by aligning wiith
the frontt case board positioning rrib.

 Note to control
c the to
orsion when ttightening the
e two PT3×8 screws
s again
n, avoiding sc
crew
sliding.

7.4
4.3 Remov
ving the Screen
S Ass
sembly Connection
n Line
1. Cut off the cable time used
u to tie the connection lin
nes, and remo
ove the connecction line conn
nector
connecte
ed to the displa
ay screen and
d touch screen
n control board
d. All the connnection lines ca
an be
removed
d by releasing the buckling p
position for cla
amping cable on
o the front caase.

C
Cabl

(N12-NLT) (N12-SHARP)

Cab

(N15-NLT) HARP)
(N15-SH

Ca

(N17-NLT) (N17-SHARP)

7-9
 CAUT
TION
 Prevent pressure on the front face
e of display screen
s during
g disassemblyy.

 Remove the LCD scre

een assembly
y in an enviro
onment as du
ust-free as po
ossible; the
display screen
s and to
ouch screen a
are integrated materials and
a cannot bee disassemblled.
s a potential hazard or un safe practice
Indicates e that, if not avoided,
a coul d result in minor
personal injury or pro
oduct/properrty damage.

7.5
5 Furtherr Disasse
embly off the Rea
ar Case Assembly
A y
7.5.1 Remov
ving the Recorder
R
1. First open the
t recorder door
d on the rig
ght of the mach
hine, and then
n unscrew the two M3×6 screws.

2. Pull the two

o clips in as in e figure below to separate it from the rear case, and pull out
ndicated in the
the recorrder at the sam
me time.

3. After the re
ecorder is pulle own the recorrder connection line from thee positioning rib,
ed out, take do r
and pull out
o the sockett respectively. Then, the rec
corder can be removed.

M3 Positioning

Cli

NOTE
 Use prop
per force to re
emove the ca
able carefully
y lest it would
d be broken.

7-10
7.5.2 Furthe
er Disasse
embly of th
he Record
der
1. First remove one PT2X
X6 screw, and take down the grounding piece
p at the saame time.

2. Release the
t two clips backward
b and take out the recorder
r drive board. Pay atttention to the snap
in the fro
ont.

Sn

3. First pull up the pressin

ng buckle by a
about 1 mm to
o remove the flexible
f cable; remove the
connection line from th
he drive board
d to the button
n board; unscrew one PT2×66 screw, and
remove the
t ground cable of the drivve board. Rem
move the recorrder drive boarrd.

Pressingg

7-11
 4. Remove the other PT2
2×6 screw and
d take out the thermal
t printhead.

5. Loosen and
a remove the two PT2×6 sscrews and re
emove the button board of re
recorder.

Reecorder button
n

Thhermal print

NOTE
 Use proper force to remove
r the ca
able carefully
y lest it would
d be broken.

7.5.3 Remov
ving the MPAN
M Boa
ard
1. Pull out th
he MPAN boa
ard connection
n line at the end of internal module
m rackCO
OM board; then pull
out the MPAN
M antenna
a connector in
nserted on the
e MPAN board; unscrew onee M3×6 screw
w to
remove the
t MPAN boa
ard.

7-12
 2. Tear the MPAN antenn
na fixing piece
e. Then, the MPAN
M antenna can be removved.

NOTE
 Use proper force to remove
r the ca
able carefully
y lest it would
d be broken.

7.5.4 Remov
ving the WiFi
W Modu
ule
1. Press the
e clips at two sides
s of the W
WiFi socket, an
nd take out the
e WiFi modulee from the sock
ket.

2. Remove the adhesive tape fixing the

e antenna, and
d tear off the WiFi
W sticker anntenna.

7-13
 3. Pull out th
he WiFi anten
nna plug from tthe board; uns
screw the thre
ee M2X4 screw
ws, and separrate
the WiFi module from the WiFi supp
port board.

WiFi

WiFi
support

NOTE
 Use proper force to remove
r the ca y lest it would
able carefully d be broken.

 Use pro
oper force to
o separate th
he board ca
arefully, lestt the board ssocket and
golden finger part would be da
amaged. Pro
ovides applic
cation tips or other useful
information to ensurre that you ma
aintain your product bette
er.

7.5.5 Remov
ving the In
nternal Mo
odule Rac
ck Assemb
bly
NOTE
 Release the clips on the
t connectio
on line socke
et before disconnecting thee connection
n line,
lest the cable
c would be
b broken.

7-14
 N12

1. Remove the connection line of batte

ery interface bo
oard from the main board ennd, and then take
t
out the connection
c line
e of internal mo
odule rack CO
OM board; uns
screw the four M3X6 screws
s, and
force upw
ward to take out
o the batteryy cavity assem
mbly as indicated in the figurre.

Conn
nection line off battery interfa
ace

J10

J20

Connectionn line of
internal moodule rack
COM boarrd

2. Loosen and
a remove the two M3X6 sscrews, and re
emove the batttery interface board.

3. Loosen and
a remove the five M3X6 sscrews, and fo
orce upward ve
ertically to rem
move the intern
nal
module rack
r assembly
y as indicated in the figure.

7-15
4. Place the
e face of the re
emoved modu
ule rack assem
mbly board up.. First unscrew
w the two M2.5
5X6
screws on
o the SMR intterface, the tw
wo PT3X8 scre
ews, and the six M3X6 screw
ws in turn, and
d then
take dow
wn the internal module rack COM board.

M3X6
6

M2.5

SMR innterface shee

et

PT3X

5. Turn over the removed

d internal mod ule rack COM
M board, and ta
ake down the ffour POGO PIN
ases.
silicon ca

 N15N17

1. First remove the conne

ection line of in
nternal module rack COM board;
b unscrew
w the four M3X
X6
screws according
a to th
he positions sh
hown below, and
a loosen one
e captive screew; force upwa
ard
verticallyy to remove the
e module rackk assembly as
s indicated in the figure.

Conne
ection line of i nternal modulle rack COM
board

One ca
aptive

7-16
2. Place the
e face of the re
emoved modu
ule rack assem
mbly board up.. First unscrew
w the two M2.5
5X6
screws on
o the SMR intterface, the tw
wo PT3X8 scre
ews, and the seven
s M3X6 sscrews in turn,, and
then take
e down the internal module rack COM board.

M2.5

PT3X

M3X6

3. Turn over the removed

d internal mod ule rack COM
M board, and ta
ake down the six POGO PIN
N
ases.
silicon ca

7-17
7.5.6 Remov
ving the Main
M Supp
port Assem
mbly
 N12

1. Pull out th
he speaker co
onnection line,, unscrew the two M3X6 scrrews, and takee down the spe
eaker
assemblyy.

Speakerr

2. a remove the five M3X6 sscrews, and ve

Loosen and o the main suupport assembly.
ertically take out

3. As shown
n in the figure below, place tthe face of the
e removed ma
ain board of maain support up
p, pull
out the connection
c line
e from the maiin control boarrd to the ACDC and insert itt in the main board
b
end, unscrew the two DVI stud screw
ws and four M3X6
M screws, and then takee out the main
control board.

7-18
Connection line
from the main
control board to
DVI stud
4. Turn over the main support with the main control board removed, and place its face up; remove
the connection line from the main control board to the ACDC, and insert it into the ACDC power
supply end; remove the power cord from the AC input to the ACDC, and insert it into the ACDC
power supply end; unscrew four M3X6 screws, and take down the power board.

5. Loosen and remove two M3X6 screws, and take out the recorder cover; unscrew one M3X6
screw, and take out the power cord from the AC input to ACDC.

Recorder

Power cord from the AC

input to ACDC

7-19
 N15N17

1. he speaker co
Pull out th onnection line,, loosen and remove the two
o M3X6 screw
ws, and take down
the speaker assembly.

Speaker

2. As shown
n below, for th
he N15 series machine, loos
sen and remov
ve the five M33X6 screws, an
nd
verticallyy take out the main
m support a
assembly.

(N15)

As shown below, for the N17

N series ma
achine, loosen
n and remove the six M3X6 screws, and
vertically take out the main
m support a
assembly.

(N17)

7-20
3. As shown
n in the figure below, place tthe face of the
e removed ma
ain board of maain support up
p, pull
out the connection
c line
e from the maiin control boarrd to the ACDC and insert itt in the main board
b
end, loossen and remov VI stud screws and four M3X
ve the two DV X6 screws, andd then take ou
ut the
main con
ntrol board.

Connection
n line from the
main contro
ol board to the
e

4. Turn over the main sup

pport with the main control board
b removed, and place itts face up; rem
move
the connection line from the main co
ontrol board to
o the ACDC, and
a insert it intto the ACDC power
p
supply en
nd; remove the power cord from the AC input to the AC
CDC, and inseert it into the ACDC
A
power su
upply end; loos
sen and remo
ove four M3X6
6 screws, and take down thee power board
d.

Connecti on line from th

he
main conntrol board to the
t

Power

AC
A input to AC
CDC power

5. Cut off th
he cable tie on the connectio
on line, loosen
n and remove the two M3X66 screws, and take
out the re
ecorder cover; loosen and rremove one M3X6
M screw, and take out thhe power cord from
the AC in
nput to ACDC.

7-21
 Cable

NOTE
 Do not injure the cable when cutting the cable tie.

7.5.7 Removing the iView Board Assembly (N17 Series)

1. First screw out the two DVI stud screws.

2. Remove the two iView board connection lines and the internal module rack connection line,
loosen and remove the four M3X6 screws, and then take out the iView board assembly.

7-22
 Two iView boaard connection

3. Place the
e face of the re
emoved iView
w board assem
mbly board up, and take dow
wn the SSD ha
ard
disk by pressing
p the SSD
S hard disk clips; loosen and remove th
he four M3X6 screws, and take
t
down the
e iView board..

SSD ha
ard

4. As shown
n below, place
e up the face o
of the iView bo
oard side with the computerr module, loos
sen
and remo
ove the four M2X6
M screws, and separate the computerr module from the iView sup
pport
board.

Comput
er

iView
support

7-23
7.5.8 Remov
ving the In
ndepende
ent Display
y Board Assembly
A ((N17 Serie
es)
1. First scre
ew out the two DVI stud scre
ews.

2. Remove the independe ard connection line and the internal moduule rack conne
ent display boa ection
line, loossen and remov 3X6 screws, and then take out
ve the four M3 o the indepeendent display
y
board asssembly.

3. Loosen and
a remove the four M3X6 sscrews, and ta
ake down the independent ddisplay board.

7-24
 7.5.9 Removing the Handle
1. Place the face of the rear case handle down, loosen and remove the two PT 3X8 screws,
forcibly release the four clips on the top cover of rear case, and push down to take out the top
cover of rear case.

2. Pry open the two handle positioning pins to the middle direction, and take out the handle.

7.6 Further Disassembly of the Base Assembly

 N12

Take out the battery door connecting belt from the through hole, and remove the battery door.

7-25
  N15N17

1. Loosen and
a remove the two M3X6 sscrews, and re
emove the batttery interface board.

2. As shown
n below, open the battery do
oor, insert a a piece of cloth
h into the gap between the
battery door
d and the base, and force wn to take out the battery dooor.
edly press dow

7.7
7 Disasse
embling the Mod
dule Rack
k
1. Removing the handle and
a hooks

 As shown in the fo
ollowing figure
e, loosen and remove
r the eig
ght M3X10 crooss recessed
coun
ntersunk head screws, and remove the ho
ooks.

7-26
 M3X10

 As shown in the fo
ollowing figure
e, loosen and remove
r the three M3×8 crosss recessed
coun
ntersunk head screws, and remove the ha
andle.

M3X
X8

2. Removing the rear cas

se of module ra
rack

As shown ng figure, use a tweezer to take

n in the followin t out the six screw coverrs on the rear case,
loosen an
nd remove the d pan head screw, and sepaarate the front case
e six M3X16 ccross recessed
from the rear case.

Screw

7-27
 M3X16

3. Removing the module rack interface

e board

Loosen and e two M3X8 c ross recessed

a remove the d pan head scrrews, pull out the connection line
e internal module rack COM board, and thhen take out th
between the interface board and the he
interface board.

M3X8

Connec
ction line from
m the interface
board of
o external moodule rack to
the 8-slot board

4. Removing the internal module rack C

COM board.

Pull out th
he connection
n line between
n the module rack antenna and
a the internaal module rack
k
COM boa
ard, loosen an
nd remove the
e seven M3X8 cross recesse
ed pan head sscrews on the
internal module
m rack COM
C board, an
nd take down the
t eight POG
GO PIN siliconn cases of mod
dule
rack.

Modu
ule rack

7-28
 M3X6
M screw

POGO PIN
N silicon
cases of m
module rack

7.8
8 Disasse
embling the M51C
C Module
1. Removing the front pan
nel assembly

 As shown in the fig

gure, use a co
ontact wrench to remove the
e screw for thee back end terrminal
of the module; use
e a small flat-b
bladed screwd
driver to remov
ve the wrenchh; use a Phillip
ps
screw
wdriver to rem
move the front panel screw. Then, the fron
nt panel of moodule can be pulled
p
out.

Use a co
ontact wrench Remove the Remoove the
to removve the termina
al

 As shown in the fo
ollowing figure
e, loosen and remove
r crew between the front pane
the sc el and
the bracket,
b and unplug the air ttube at the air nozzle. Then the front paneel can be removed.

7-29
 R
Remove the
brracket screw

2. Remove the parameter board

As shown in the
t following figure, loosen a he board screw
and remove th ws, pull out thhe pump and valve
v
connection lin
ne and NIBP air
a tube. Then,, the paramete
er board can be
b removed.

Parrameter board
scre
ews and connection

Pu
ull out along th
his

3. Removing the blood ox

xygen board

ygen board screws, and thenn pull out the blood

As shown in the following figure, remove the blood oxy
oxygen board
d.

Remove the screws

4. Removing the infrared board

As shown in the
t following fiigure, remove
e the infrared board
b connection line, and tthen remove th
he
infrared board
d.

Pull out from thiss

7-30
5. Removi ng
g the pump an
nd valve

 As sh
hown in the fo
ollowing figure , cut off the ca
able tie, unplug
g the pump poower line and NIBP
ube, and then remove the p
air tu pump.

 As shown in the fig

gure, unplug tthe valve powe
er line and NIB
BP air tube, usse a flat-blade
ed
screw
wdriver to pok
ke the slots at two sides of the
t valve, and then remove the valve
asse
embly.

7-31
FOR YOUR NOTES

7-32
8 Parts
This chapter lists the explod
ded views and
d material cod
des of the parts
s including thee monitor's ma
ain
unit, SMR and
d parameter module.
m It help
ps the enginee
er to identify th
he parts duringg disassembly
y of
the patient mo
onitor and spa
are parts repla
acement.

8.1 N12 Parrts

8.1.1 N12 Whole
W Unit
Exploded View

8-1
Parts List

No. Name and Specification Qty Material Code

1 N12-NLT front housing assembly (FRU) 1 115-044502-00

N12rear housing assembly (with TDS/BNC, with

2 1 /
DVI)

3 N12 screw cover / 049-001226-00

Cross recessed pan head screw GB/T818-2000

4 / /
M4X30 plated with green color zinc

5 AC inlet hook 1 9211-20-87369

8-2
 8.1.2 N12-NLT Front Housing
H A
Assembly
Exploded View

Partts List

No. N
Name and Spe
ecification Qty
Q M
Material Code
e

1 N
N12-NLT front housing asse
embly (FRU) 1 1115-044502-00
0

2 S
Screen clip 2 0033-000636-00
0

3 L
Light guild pilla
ar 1 0043-007582-00
0

4 M hood
MK 1 0049-001214-00
0

5 M alarm cap
MK 1 0049-001135-00
0

6 A
Alarm LED and
d Light Sensorr Board PCBA
A 1 0051-002693-00
0

8-3
 Cross recessed pan head thread-cutting
7 tapping screws PT3X8 plated with green color 4 /
zinc

8 N12 front shell plate cable 1 009-006396-00

9 N12 Mainboard to LCD cable (NLT) 1 009-006410-00

10 Power Switch and Indicate LED Board PCBA 1 051-002711-00

11 MK POWER BUTTON (P+R) 1 043-007956-00

12 Conductive cloth pad 0.08m /

13 Earth plate (N12) 1 042-018667-00

8-4
 8.1.3 N12-SHARP Fro
ont Housin
ng Assembly
Exploded View

Partts List

No. N
Name and Spe
ecification Qty
Q M
Material Code
e

1 N
N12-SHARP fro
ont housing asssembly (FRU) 1 1115-044503-00
0

2 S
Screen clip 2 0033-000636-00
0

3 Light guild pillarr 1 0043-007582-00

0

4 M hood
MK 1 0049-001214-00
0

5 M alarm cap
MK 1 0049-001135-00
0

6 A
Alarm LED and Light Sensor B
Board PCBA 1 0051-002693-00
0

C
Cross recessed pan head thre
ead-cutting tapping
7 4 /
screws PT3X8 plated
p with gre
een color zinc

8-5
 No. N
Name and Spe
ecification Qty
Q M
Material Code
e

8 N front shell plate

N12 p cable 1 0009-006396-00
0

9 N Mainboard to LCD cable (NLT)

N12 1 0009-006409-00
0

10 P
Power Switch and Indicate LE
ED Board PCBA
A 1 0051-002711-00
0

11 M POWER BU
MK UTTON (P+R) 1 0043-007956-00
0

12 E
Earth plate (N12
2) 1 0042-018667-00
0

13 C
Conductive cloth pad 0.08m
0 /

14 C
CORE O.D=21.5mmI.D=9.5m
mm 1 /

8.1.4 N12 Rear Housing

Exploded View

8-6
Parts List

No. Name and Specification Qty Material Code

1 N12 handle 1
115-044501-00
2 Cushion pad /

3 N12 top cover 1 043-007578-00

4 Waterproof strip N12 1 048-006308-00

5 Handle Left Damping Block, N12 1 /

6 N12 rear housing (silk screen) 1 043-008005-00

7 N12 internal module rack assembly (with TDS/BNC) 1 /

8 Speaker bracket 1 115-044509-00

9 Speaker 2W 4ohm 500Hz 1

10 MK speaker foam 1

11 Small cross recessed pan head GB9074.5-88 M3X6 / /

with pad and plated with green color zinc

12 N12 main bracket assembly (with DVI) 1 /

13 TR6F recorder 1 /

14 Handle Right Damping Block, N12 1 /

15 Self-Clinching Pilot Pins.TPS-3-18 / /

16 Screw cap 2(T8) / 049-000650-00

17 Cross recessed pan head thread-cutting tapping / /

screws PT3X8 plated with green color zinc

18 Conductive foam 2.0*7.0mm / /

8-7
 8.1.5 N12 Rear Housing Assem
mbly (FRU)(115-0444
499-00)
Exploded View

8-8
Partts List

No. N
Name and Spe
ecification Qty
Q M
Material Code
e

1 N rear housin
N12 ng (silk screen)) 1 0043-008005-00
0

2 H
Handle Right Da
amping Block, N12 1 0049-001250-00
0

3 S
Screw cap 2(T8
8) 3 /

4 W
Waterproof strip
p N12 1 0048-006308-00
0

5 H
Handle Left Dam
mping Block, N
N12 1 0049-001249-00
0

6 C
Conductive foam
m 2.0*7.0 mm 0.11m
0 /

8.1.6 N12 Battery Cav

vity Assem
mbly (FRU
U)(115-044
4504-00)
Exploded View

8-9
Partts List

No. N
Name and Sp
pecification Qty Maaterial Code

1 N battery cav
N12 vity 1 /

C
Cross recessed
d pan head scrrew GB/T818-2
2000
2 1 /
M
M4X30 plated with
w green colo
or zinc

3 B
Battery bar 1 92211-20-87256

4 B
Battery bar slee
eve 1 /

C
Cushion pad.Bumpon SJ5302
2, white and
5 1 /
transparent

8.1.7 N12 Module

M Rac
ck Body A
Assembly (FRU) (115-044507--00)
Exploded View

8-10
Partts List

No. N
Name and Sp
pecification Qty Maaterial Code

1 N module rac
N12 ck (four slots) 1 /

2 Infrared lens 4 0447-005213-00

3 C
Contact screw 8 68800-21-51100

4 C
Contact spring 8 68800-20-50261

5 S
Spring 8 68800-20-50388

F washer-Grade A GB/T97 .1-2002 3 plate

Flat ed with
6 8 /
g
green color zinc
c

H nut and tap

Hex per lock washe
er assembly M3
3
7 8 /
p
plated with gree
en color zinc

8.2
2 N 15 Pa
arts
8.2
2.1 N15 Whole
W Unit
Exploded View

8-11
Partts List

No. N
Name and Spe
ecification Qty M
Material Code
e

1 N
N15-NLT front housing asse
embly (FRU) 1 1 15-044544-00
0

2 N rear housing assembly (with SMR/BN

N15 NC) 1 /

3 N base asse
N15 embly (FRU) 1 1 15-044543-00
0

4 S
Screw / /

8.2
2.2 N15-NLT Front Housing
H A
Assembly
Exploded View

8-12
Parts List

No. Name and Specification Qty Material Code

1 N15-NLT Front Housing Assembly (FRU) 1 115-044544-00

2 Screen clip 4 033-000636-00

3 Light guild pillar 1 043-007582-00

4 MK alarm cap 1 049-001135-00

5 MK hood 1 049-001214-00

6 Alarm LED and Light Sensor Board PCBA 1 051-002693-00

Cross recessed pan head thread-cutting

7 tapping screws PT3X8 plated with green color 4 /
zinc

8 N15N17 front shell plate cable 1 009-006736-00

9 CORE O.D=21.5mmI.D=9.5mm 1 1 /

10 N15 Mainboard to LCD cable (NLT) 1 009-006408-00

11 N15N17 touch screen cable (NLT) 1 009-006397-00

12 Power Switch and Indicate LED Board PCBA 1 051-002711-00

13 MK POWER BUTTON (P+R) 1 043-007956-00

14 Conductive cloth pad 0.08m /

15 Earth plate (NLT) 1 042-017398-00

8-13
 8.2
2.3 N15-SHARP Fro
ont Housin
ng
Exploded View

8-14
Parts List

No. Name and Specification Qty Material Code

1 N15-SHARP front housing assembly (FRU) 1 115-044545-00

2 Screen clip 4 033-000636-00

3 Light guild pillar 1 043-007582-00

4 MK alarm cap 1 049-001135-00

5 MK hood 1 049-001214-00

6 Alarm LED and Light Sensor Board PCBA 1 051-002693-00

Cross recessed pan head thread-cutting tapping

7 4 /
screws PT3X8 plated with green color zinc

8 N15N17 front shell plate cable 1 009-006736-00

9 CORE O.D=21.5mmI.D=9.5mm 1 1 /

10 N15 Mainboard to LCD cable (SHARP) 1 009-006407-00

11 N15N17 touch screen cable (SHARP) 1 009-006730-00

12 Power Switch and Indicate LED Board PCBA 1 051-002711-00

13 MK POWER BUTTON (P+R) 1 043-007956-00

14 Conductive cloth pad 0.08m /

15 Earth plate (N15-SHARP) 1 042-018592-00

8-15
 8.2
2.4 N15 Rear Housing
Exploded View

8-16
Parts List

No. Name and Specification Qty Material Code

1 N15 rear housing 1 043-008003-00

2 Handle left damping block, N15 1 /

3 N15 top cover 1 043-007566-00

4 N15 handle 1

5 Cushion pad 1 115-044542-00

6 Blind rivet hole BSO-3.5M3-28 ZC 2

7 Handle right damping block, N15 1 /

8 Cross recessed pan head thread-cutting tapping / /

screws PT3X8 plated with green color zinc

9 Recorder door 1 043-000184-00

10 MK speaker foam 1 115-044547-00

11 Speaker 2W 4ohm 500Hz 1

12 Speaker bracket 1

13 N 15 main bracket assembly (with DVI) 1 /

14 N15N17 module rack assembly (with SMR/BNC) 1 /

15 Screw / /

16 Conductive foam 2.0*7.0mm / /

8-17
 8.2
2.5 N15 Rear Housing Assem
mbly (FRU) (115-044
4541-00)
Exploded View

Partts List

No. N
Name and Spe
ecification Qty M
Material Code
e

1 N rear housin
N15 ng (silk screen)) 1 0043-008003-00

2 W
Waterproof foam
m (N15) 1 0048-006291-00

3 N Handle Rig
N15 ght Damp 1 0049-001283-00

4 N Handle Lefft Damp

N15 1 0049-001284-00

5 C
Conductive foam
m 2.0*7.0 mm 3 /

8-18
 8.2
2.6 N15 Base Assem
mbly (FRU
U)(115-044
4543-00)
Exploded View

Partts List

No. Name and Sp

pecification Qty M
Material Code

1 N15 bottom ca
ase 1 /

2 N15 Battery Door (Tether) 1 0443-007966-00

3 Rubber foot pa
ad 4 /

8-19
 8.2
2.7 N15N1
17 Module
e Rack Bod
dy Assem
mbly (FRU)) (115-0445546-00)
Exploded View

Partts List

No. N
Name and Spe
ecification Qty M
Material Code
e

H nut and tap

Hex per lock washe r assembly M3
3 plated
1 12 /
w green colorr zinc
with

F washer-Gra
Flat ade A GB/T97. 1-2002 3 plate
ed with
2 12 /
green color zinc
c

3 S
Spring 12 66800-20-50388

4 N module rac
N15 ck (six slots) 1 /

5 In
nfrared lens 12 04
047-005213-00

6 C
Contact screw 12 66800-21-51100

7 C
Contact spring 12 66800-20-50261

8 C
Captive screw M3X10
M 1 /

8-20
8.3
3 N17 Parrts
8.3
3.1 N17 Whole
W Unit
Exploded View

Partts List

No. N
Name and Spe
ecification Qty M
Material Code
e

1 N front housin
N17 ng assembly 1 1 15-044551-00

2 N rear housin
N17 ng assembly 1 /

3 S
Screw / /

4 N screw cove
N17 er / 0049-001210-00

5 N base assem
N17 mbly (FRU) 1 1 15-044550-00

8-21
 8.3
3.2 N17-NLT Front Housing
H A
Assembly
Exploded View

Partts List

No. N
Name and Spe
ecification Qty
Q M
Material Code
e

1 N
N17-NLT front housing
h assem
mbly (FRU) 1 1115-044551-00
0

2 Light guild pillarr 1 0043-007582-00

0

3 M alarm cap
MK 1 0049-001135-00
0

4 M hood
MK 1 0049-001214-00
0

5 A
Alarm LED and Light Sensor B
Board PCBA 1 0051-002693-00
0

C
Cross recessed pan head thre
ead-cutting tapping
6 4 /
screws PT 3X8 plated with gre
een color zinc

7 S
Screen clip 4 0033-000636-00
0

8 N
N15N17 front sh
hell plate cable
e 1 0009-006736-00
0

9 C
CORE O.D=21.5mmI.D=9.5m
mm 1 1 /

8-22
 No. N
Name and Spe
ecification Qty
Q M
Material Code
e

10 N Mainboard to LCD cable (NLT)

N17 1 0009-006732-00
0

11 N
N15N17 touch screen
s cable (N
NLT) 1 0009-006397-00
0

12 P
Power Switch and Indicate LE
ED Board PCBA
A 1 0051-002711-00
0

13 M POWER BU
MK UTTON (P+R) 1 0043-007956-00
0

14 C
Conductive cloth pad 0.08m
0 /

15 E
Earth plate (NLT
T) 1 0042-017398-00
0

8.3
3.3 N17-SHARP Fro
ont Housin
ng
Exploded View

8-23
Parts List

No. Name and Specification Qty Material Code

1 N17-SHARP front housing assembly (FRU) 1 115-044552-00

2 Light guild pillar 1 043-007582-00

3 MK alarm cap 1 049-001135-00

4 MK hood 1 049-001214-00

5 Alarm LED and Light Sensor Board PCBA 1 051-002693-00

Cross recessed pan head thread-cutting tapping

6 4 /
screws PT 3X8 plated with green color zinc

7 Screen clip 4 033-000636-00

8 N15N17 front shell plate cable 1 009-006736-00

9 CORE O.D=21.5mmI.D=9.5mm 1 1 /

10 N17 Mainboard to LCD cable (SHARP) 1 009-006398-00

11 N15N17 touch screen cable (SHARP) 1 009-006730-00

12 Power Switch and Indicate LED Board PCBA 1 051-002711-00

13 MK POWER BUTTON (P+R) 1 043-007956-00

14 Conductive cloth pad 0.08m /

15 Earth plate (N17-SHARP) 1 042-018593-00

8-24
 8.3
3.4 N17 Rear Housing
Exploded View

Partts List

No. N
Name and Spe
ecification Qty M
Material Code
e

1 N
N15N17 module
e rack assemb ly (with SMR/B
BNC) 1 /

S
Small cross recessed pan hea
ad GB9074.5-8
88 M3X6
2 / /
w pad and pla
with ated with green
n color zinc

N main brack
N17 ket asembly (iV
View or indepen
ndent
3 1 /
display)

4 C
Conductive foam
m 3.2*6.4mm / /

5 S
Speaker bracke
et 1
1 15-044547-00
6 S
Speaker 2W 40hm 1

8-25
No. Name and Specification Qty Material Code

7 MK speaker foam 1

8 Cross recessed pan head thread-cutting tapping / /

screws PT3X8 plated with green color zinc

9 TR6F recorder 1 /

10 AC inlet hook 1 9211-20-87369

11 N17 rear housing (silk screen) 1 043-007458-00

12 Waterproof foam (N17) 1 048-006292-00

13 Handle right damping block, N17 1 /

14 Blind rivet hole BSO-3.5M3-35 ZC / /

15 Handle left damping block, N17 1 /

16 N17 top cover 1 043-007661-00

17 Cushion pad 2 115-044549-00

18 N17 handle 1

8-26
 8.3
3.5 N17 Rear Housing Assem
mbly (FRU)( 115-044
4548-00)
Exploded View

Partts List

No. N
Name and Spe
ecification Qty
Q M
Material Code
e

1 N rear housin
N17 ng (silk screen)) 1 0043-007458-00
0

2 C
Conductive foam
m 3.2*6.4mm 0.11m
0 /

3 N Handle Lefft Damp

N17 1 0049-001285-00
0

4 W
Waterproof foam
m (N17) 1 0048-006292-00
0

5 N Handle Rig
N17 ght Damp 1 0049-001286-00
0

8-27
 8.3
3.6 N17 Base Assem
mbly (FRU
U)( 115-044
4550-00)
Exploded View

Partts List

No. N
Name and Spe
ecification Qty M
Material Code
e

1 N bottom cas
N17 se 1 /

2 R
Rubber foot pad
d 4 /

3 N Battery Door (Tether)

N15 1 0043-007966-00

8-28
 8.3
3.7 Indepe
endent Dis
splay Upg
grade Pack
kage (With
hout Main
nboard)
(115-0445544-00)
Exploded View

Partts List

Material
No. N
Name and Spe
ecification Qty
Code

1 In
ndependent dis
splay assemblyy 1 /

S
Small cross rece
essed pan hea
ad GB9074.5-88 M3X6 with
2 4 /
pad and plated with green colo
or zinc

8-29
 8.3
3.8 Indepe
endent Dis
splay Upg
grade Pack
kage (With
h Mainboaard)
(115-0445799-00)
Exploded View

Partts List

No. N
Name and Spe
ecification Qty M
Material Code
e

1 N Main board
N17 d (FRU/SW/iVie
ew&ID) 1 0051-002718-00-00

2 In
ndependent dis
splay assemblyy 1 1 15-044586-00

S
Small cross recessed pan hea
ad GB9074.5-8
88 M3X6
3 4 /
w pad and pla
with ated with green
n color zinc

8-30
 8.3
3.9 Indepe
endent Dis
splay Ass
sembly
Exploded View

Partts List

Material
No. N
Name and Spe
ecification Qty
Code

1 N heat sink (iView or indepe

N17 endent display) 1 041-026485-00

2 In
ndependent Dis
splay Board PC
CBA 1 051-002712-00

S
Small cross recessed pan hea
ad GB9074.5-8
88 M3X6
3 4 /
w pad and pla
with ated with green
n color zinc

8-31
 8.3
3.10 iView
w Module Assembly
y
Exploded View

8-32
Parts List

N Q
o Name and Specification t Material Code
. y

1 N17 heat sink (iView or independent display) 1 041-026485-00

2 IVIEW CPU heat conducting pad 1 /

3 IVIEW memory heat conducting pad 5 /

Cross recessed pan head screw GB/T818-2000 M2X6

4 4 /
plated with green color zinc

0
.
0
5 Conductive foam 2.0*7.0mm /
4
6
m

6 Computer module Celeron J1900 1 023-001083-00

7 iView support board PCBA 1 051-002739-00

Small cross recessed pan head GB9074.5-88 M3X6 with

8 4 /
pad and plated with green color zinc

9 SSD 128GB MLC mSata 1 023-001329-00

8-33
8.4
4 Externa
al Satellitte Modulle Rack (SMR)
(
Exploded View

Partts List

No. N
Name and Spe
ecification Qty M
Material Code
e

1 F
Front housing silkscreen of mo
odule rack 1 0043-006301-00

2 8-slot PCBA of external modu le rack 1 1 15-037493-00

3 In
nterface board fixing sheet m etal 1 /

4 In
nterface board PCBA of exterrnal module rac
ck 1 0051-001908-00

5 M
Module rack cufff bracket 1 1 15-033914-00

6 R
Rear housing silkscreen of mo
odule rack 1 0043-006300-00

C
Cross recessed pan head scre
ew GB/T818-2000
7 1 /
M
M3X16 plated with
w green colo r zinc

9 M
Module rack cab
ble hook 1 1 15-033911-00

8-34
8.5
5 M51C Module
M
Exploded View

8-35
Parts List

No. Name and Specification Qty Material Code

M51C-LE, 5L5P, MR-SPO2, IBP, MPM I/F 051-002481-00

M51C-ME, 5L5P, MR/NC-SPO2, IBP, MPM 1

051-002482-00
1 I/F selected

M51C-FF (Ext Arr /12 Lead ST /Glasgow_12) from 4 051-002483-00-00

M51C-FF(Mindray:Hr /Glasgow_12) 051-002483-00-01

Stainless steel cross recessed pan head

2 4 /
screw GB/T818-2000 M2X4

3 M51C-9008V3.0 SPO2 PCBA 1 051-002353-00

4 Hex nut and taper lock washer assembly M3 2 /

5 M51C module back plane (with IBP/FRU) 1 051-002383-00

6 Fixing base 2 /

Cross recessed countersunk head screw

7 2 /
GB/T819.1-2000 M3X6

8 Spanner (T8) 2 /

9 Dual module rear housing (M51C) 1 /

10 Terminal screw 2 /

11 Infrared lens 1 /

12 Standard spring washer GB/T93-1987 3 2 /

13 Barcode serial number label 1 (for module) 1 /

14 High-end Mindray patent label (English) 1 /

15 Pump shock pad 1 /

Air valve. Dual air valve (custom) 12VDC

16 2 082-000864-00
normally-open line, 125 mm long

17 Pump. 12VDC with 120 wire and connector 1 082-000862-00

18 Filter. Inline Filter43um 1/8”I.D.Tubing 2 /

19 630F flow restrictor 1 /

20 Silicone tube 11 /

21 Bracket (T8) 1 043-001964-02

21 Module waterproof pad (M51C) 1 /

8-36
No. Name and Specification Qty Material Code

22 MPM(M51C) front panel

M51C front panel maintenance package

115-044668-00
(Mindray SpO2/no IBP FRU)

M51C front panel maintenance package

115-044669-00
(Nellcor SpO2/no IBP FRU)

M51C front panel maintenance package

1 115-044670-00
(Mindray SpO2/IBP FRU)
23 selected
M51C front panel maintenance package
from 6 115-044671-00
(Nellcor SpO2/IBP FRU)

M51C front panel maintenance package

115-044672-00
(Mindray /IBP analog FRU)

M51C front panel maintenance package

115-044673-00
(Nellcor /IBP analog FRU)

8-37
FOR YOUR NOTES

8-38
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. 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

A.1.1 The Power Plug
Test Item Acceptance Criteria

The power plug pins No broken or bent pin. No discolored pins.

The plug body No physical damage to the plug body.

The power plug No physical damage to the strain relief. No plug
The strain relief
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.

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.

No physical damage to meters, switches,

connectors, etc.
The enclosure and 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 smells (e.g., burning or smoky smells,

The enclosure and accessories
particularly from ventilation holes).

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 Protective Earth Resistance

Protective Earth Resistance is measured using the RED test lead attached to the DUT Protective
Earth terminal or enclosure. Select the test current by pressing SOFT KEY 3 to toggle between
1AMP, 10AMP, and 25AMP. The front panel outlet power is turned off for this test.

A-2
The following conditions ap
pply: L1 and L2
2 Open.

Preparatio
on
1. First sele
ect the test currrent that will b
be used for pe
erforming the Protective
P Earrth Resistance
e test
by pressiing AMPERES
S (SOFT KEY 3).

2. Connect the test lead(s

s) between the
e RED input ja
ack and the GREEN input jaack.

3. Press CA
AL LEADS. The 601PRO willl measure the
e lead resistan
nce, and if lesss than 0.150 Ohms,
O
it will storre the reading and subtract it from all eartth resistance readings
r takenn at the calibrated
current.

If the calibration fails, the previously store

ed readings will
w be used until a passing ccalibration has
s
occurred.:

WAR
RNING
 During Earth Resistance testing,, the DUT must be plugged into the 6011PRO front
outlet. If the DUT faiils Earth Resiistance, discontinue tests
s and label th
he device
defectiv
ve.

To Perform
m the Test
1. From the MAIN MENU, or with the o
outlet unpowerred, plug the DUT
D into the 6601PRO front panel
outlet.

2. ED input lead tto the device’s

Attach the 601PRO RE s Protective Earth terminal oor an exposed
d
ea.
metal are

3. Press sho
ortcut key 3. The
T Protective
e Earth Resista
ance test is displayed.

4. Press SO
OFT KEY 3 to select a test ccurrent (1AMP
P, 10AMP, or 25AMP).
2 The sselected test
current iss displayed in the upper righ
ht corner of the
e display.

A-3
 5. Press START TEST to start the test. The test current is applied while resistance and current
readings are taken. This takes approximately 5 seconds.

6. Press the print data key at any time to generate a printout of the latest measurement(s).

NOTE

 When "Over" is displayed for Ohms, this signifies that a valid measurement was not
obtained because either an open connection was detected or that the measurement
was not within range. Readings greater than 9.999 Ohms will be displayed as Over.

In Case of Failure
Once it reaches the limitation, stop using and inform the Customer Service Engineer for analysis and
disposal.

LIMITS
ALL COUNTRIES R = 0.2 Ω Maximum

A.5 Earth Leakage Test

Run an Earth Leakage test on the device being tested before performing any other leakage tests.

Leakage current is measured the following ways:

 Earth Leakage Current, leakage current measured through DUT outlet Earth

 Earth Leakage Current AP-EARTH (ALL Applied Parts connected to Earth), leakage current
measured through DUT outlet Earth

There is no need to attach a test lead; the 601PRO automatically connects the measuring device
internally.

To Perform the Test

1. From the MAIN MENU, or with the outlet unpowered, plug the DUT into the 601PRO front panel
outlet, and turn on the device.

2. Attach the device's applied parts to the 601PRO applied part terminals if applicable.

3. Press shortcut key 4.The Earth Leakage test appears on the display, and the test begins
immediately:

A-4
  SOFT KE
EY 1 toggles th
he DUT outlett Polarity from Normal to Offf to Reverse.

 SOFT KE
EY 2 toggles th
he DUT outlett from Earth to
o No Earth.

 SOFT KE
EY 3 toggles th
he DUT outlett from L2 to No
o L2.

 SOFT KE
EY 4 toggles th h to No AP to Earth.
he AP to Earth

4. e print data key at any time to generate a printout of the

Press the e latest measuurement.

In Case of Failurre

 Check an
ny broken of th
he enclosure. Replace any defective part.

 Inspect wiring
w for bad crimps,
c poor cconnections, or
o damage.

 Test the wall ded and is free of other wiring abnormalitties. Notify the
w outlet; verify it is ground e user
or owner to correct any
y deviations. A
As a work arou e other outlets to see if they could
und, check the
be used instead.
i

 Change another
a probe to confirm if tthe fail is caus
sed by console
e.

 If the leakkage current measurement

m tests fail on a new unit and if situation caan not be corre
ected,
submit a Safety Failure
e Report to do
ocument the sy
ystem problem
m. Remove unnit from operattion.

 If all else fails, stop using and inform

m the Custome
er Service Eng
gineer for anallysis and dispo
osal.

LIMIITS

For IEC60601
1-1,

 5mA
A in Normal Co
ondition

 10mA
A in Single Fa
ault Condition

A-5
A.6
6 Patientt Leakage
e Curren
nt
Patient leakag
ge currents arre measured b
between a sele
ected applied part and mainns earth. All
measurementts have a true RMS only ressponse.

Prep
paration

Perform a calibration from the

t Mains on A
Applied Part menu.
m

The following outlet conditio

ons apply whe
en performing this test:

 Normal Polarity,
P Earth Open, Outlet ON Norma
al Polarity, Ou
utlet ON

 Normal Polarity,
P L2 Op
pen, Outlet ON
N Reverrsed Polarity, Outlet ON

 Reversed
d Polarity, Earrth Open, Outl et ON Reverrsed Polarity, L2 Open, Outtlet ON

WAR
RNING
 If all of the applied parts
p corresp
pond to the in
nstrument typ
pe, the applieed parts will be
b
tied tog ne reading wiill be taken. Iff any of the applied parts differ from th
gether and on he
instrum
ment type, all applied parts
s will be teste
ed individually, based on the type of
applied
d part. This ap
pplies to Auto
o and Step modes
m only.

To P
Perform the Test
T

1. From the MAIN MENU, or with the o

outlet unpowerred, plug the DUT
D into the 6601PRO front panel
outlet, an
nd turn on the device.

2. Attach the applied partts to the 601P RO's applied part terminals.

3. Press sho
ortcut key 6. The eakage test is displayed, and the test beggins immediate
T Patient Le ely.

4. Press AP
PPLIED PART
T (SOFT KEY 4
4) at any time to select the desired applieed part leakage
current.

5. Modify th
he configuratio
on of the front panel outlet by
b pressing the
e appropriate S n the
SOFT KEY on
601PRO..

6. e print data key at any time to generate a printout of the

Press the e latest measuurement.

A-6
In Case of Failurre

 Check an
ny broken of th
he enclosure. Replace any defective part.

 Inspect wiring
w for bad crimps,
c poor cconnections, or
o damage.

 Test the wall ded and is free of other wiring abnormalitties. Notify the
w outlet; verify it is ground e user
or owner to correct any
y deviations. A
As a work arou e other outlets to see if they could
und, check the
be used instead.
i

 Change another
a probe to confirm if tthe fail is caus
sed by console
e.

 If the leakkage current measurement

m tests fail on a new unit and if situation caan not be corre
ected,
submit a Safety Failure
e Report to do
ocument the sy
ystem problem
m. Remove unnit from operattion.

 If all else fails, stop using and inform

m the Custome
er Service Eng
gineer for anallysis and dispo
osal.

LIMIITS

For CF applied parts

 10μA
A in Normal Co
ondition

 50μA
A in Single Fault Condition

For BF applied parts

 100μ
μA in Normal Condition
C

 500μ
μA in Single Fa
ault Condition
n

A.7
7 Mains on
o Applied Part L
Leakage
The Mains on
n Applied Part test applies a test voltage, which is 110%
% of the mainss voltage, throu
ugh a
ance, to selected applied pa
limiting resista art terminals. Current
C measurements are then taken
between the selected
s applie
ed part and ea
arth. aken with the ttest voltage (1
Measurrements are ta 110%
of mains) to applied
a parts in
n the normal a
and reverse po
olarity conditio
ons as indicateed on the disp
play.

The following outlet conditio

ons apply whe
en performing the Mains on Applied Part ttest.

 Normal Polarity;
P

 Reversed
d Polarity

Prep
paration

To perform a calibration
c from the Mains o
on Applied Parrt test, press CAL
C (SOFT KE
EY 2).

1. Disconne
ect ALL patient leads, test le
eads, and DUT
T outlet conne
ections.

2. Press CA
AL to begin calibration, as sh
hown:

A-7
 If the calibrattion fails, the previously
p storred readings will
w be used un
ntil a passing calibration
n has
occurred. Also
o, the esc/stop
p key has no e
effect during calibration.
c

3. When the
e calibration is plied Part test will reappear..
s finished, the Mains on App

WAR
RNING
 A 2-bee
ep-per-second signal indic
cates high vo
oltage presen
nt at the appliied part
termina
als while a ca
alibration is b
being perform
med.

 High vo
oltage is pres
sent at applie
ed part termin
nals while measurements aare being tak
ken.

To P
Perform the Test
T

1. From the MAIN MENU, or with the o

outlet unpowerred, plug the DUT
D into the 6601

2. Attach the applied partts to the 601P RO applied pa

art terminals.

3. Attach the red terminall lead to a con

nductive part on
o the DUT en
nclosure.

4. Press sho
ortcut key 7. The
T Mains on A
Applied Part test
t is displaye
ed.

5. Select the
e desired outle
et configuratio
on and applied
d part to test using
u the appro
ropriate SOFT
KEYS:

6. Press ST
TART TEST (S
SOFT KEY 1) to begin the te
est.

7. Press the
e print data key to generate a printout of the
t latest mea
asurement.

NOTE

 If all of the applied parts

p corresp
pond to the in
nstrument typ
pe, the applieed parts will be
b
tied tog ne reading wiill be taken. Iff any of the applied parts differ from th
gether and on he
instrum
ment type, all applied parts
s will be teste
ed individually, based on the type of
applied
d part. This ap
pplies to Auto
o and Step modes
m only.

A-8
In Case of Failurre

 Check an
ny broken of th
he enclosure. Replace any defective part.

 Inspect wiring
w for bad crimps,
c poor cconnections, or
o damage.

 Test the wall ded and is free of other wiring abnormalitties. Notify the
w outlet; verify it is ground e user
or owner to correct any
y deviations. A
As a work arou e other outlets to see if they could
und, check the
be used instead.
i

 Change another
a probe to confirm if tthe fail is caus
sed by console
e.

 If the leakkage current measurement

m tests fail on a new unit and if situation caan not be corre
ected,
submit a Safety Failure
e Report to do
ocument the sy
ystem problem
m. Remove unnit from operattion.

 If all else fails, stop using and inform

m the Custome
er Service Eng
gineer for anallysis and dispo
osal.

LIMIITS

 For CF applied parts:

p 50 μA

 For BF applied parts:

p 5000 μA
A

A.8
8 Patientt Auxiliarry Curren
nt
Patient Auxilia
ary currents arre measured b
between any selected
s ECG jack and the rremaining selected
ECG jacks. All measurements may have a true RMS only
o response.

Prep
paration

1. From the MAIN MENU, or with the o

outlet unpowerred, plug the DUT
D into the 6601PRO front panel
outlet, an
nd turn on the device.

2. Attach the patient leads to the 601PR

RO ECG jacks
s.

3. Define the Lead Types

s from the View
w Settings Op
ption (refer to: Lead Type Deefinitions in Se
ection
5 of this chapter).
c

4. Press sho
ortcut key 8. The
T Patient Au
uxiliary Curren
nt test is displa
ayed, and the test begins
immediattely. Display values
v ntinuously updated until another test is se lected.
are con

A-9
 5. Press SO
OFT KEYS 1-4
4 to select leakkage tests

6. Press AP
PPLIED PART
T (SOFT KEY 4
4) at any time to select the desired applieed part leakage
current:

7. Modify th
he configuratio
on of the front panel outlet by
b pressing the
e appropriate S n the
SOFT KEY on
601PRO::

8. e print data key at any time to generate a printout of the

Press the e latest measuurement.

In Case of Failurre

 Check an
ny broken of th
he enclosure. Replace any defective part.

 Inspect wiring
w for bad crimps,
c poor cconnections, or
o damage.

 Test the wall ded and is free of other wiring abnormalitties. Notify the
w outlet; verify it is ground e user
or owner to correct any
y deviations. A
As a work arou e other outlets to see if they could
und, check the
be used instead.
i

 Change another
a probe to confirm if tthe fail is caus
sed by console
e.

 If the leakkage current measurement

m tests fail on a new unit and if situation caan not be corre
ected,
submit a Safety Failure
e Report to do
ocument the sy
ystem problem
m. Remove unnit from operattion.

 If all else fails, stop using and inform

m the Custome
er Service Eng
gineer for anallysis and dispo
osal.

LIMIITS

For CF a
applied parts,

 10μA
A in Normal Co
ondition

 50μA
A in Single Fault Condition

For BF a
applied parts,

 100μ
μA in Normal Condition
C

 500μ
μA in Single Fa
ault Condition
n

A-10
 ELECTRICAL SAFETY INSPECTION FORM

Overall assessment:

Scheduled inspection Test item: 1, 2, 3, 4, 5, 6, 7, 8

Location: Te chnician:

Equipment: Control Number:

Manufacturer: Mode l: SN:

Measurement equipment /SN: Date of Calibration:

Pass/Fa
INSPECTION AND TESTING Limit
il

1 Power Cord Plug

2 Device Enclosure and Accessories
3 Device Labeling
4 Protective Earth Resistance Ω Max 0.2 Ω

Normal
____μA
condition(NC) Max:
5 Earth Leakage NC: 5mA

Single Fault SFC: 10mA

____μA
condition(SFC)

□BF____μA
Normal Max:
Patient condition(NC) □CF____μA CF applied part:
6 Leakage NC:10μA, SFC: 50μA
□BF____μA
Current Single Fault BF applied part:
condition(SFC) □CF____μA NC:100μA, SFC: 500μA

□BF____μA
Max:
7 Mains on Applied Part Leakage CF applied part: 50μA
□CF____μA
BF applied part: 5000μA

□BF____μA
Max:
Normal condition(NC)
Patient □CF____μA CF applied part:
8 Auxiliary NC:10μA, SFC: 50μA
□BF____μA
Current Single Fault BF applied part:
condition(SFC) □CF____μA NC:100μA, SFC: 500μA

Name/ Signature: __________________________ Date:_____________________________

A-11
Unopened repair type Test item: 1, 2, 3

Opened repair type, not replace the power part Test item: 1, 2, 3, 4
including transformer or patient circuit board

Opened repair type, replace the power part Test item: 1, 2, 3, 4, 5

including transformer

Opened repair type, replace patient circuit board Test item: 1, 2, 3, 4, 6, 7, 8

Location: Te chnician:

Equipment: Control Number:

Manufacturer: Mode l: SN:

Measurement equipment /SN: Date of Calibration:

Pass/Fa
INSPECTION AND TESTING Limit
il

1 Power Cord Plug

2 Device Enclosure and Accessories
3 Device Labeling
4 Protective Earth Resistance Ω Max 0.2 Ω

Normal
____μA
condition(NC) Max:
5 Earth Leakage NC: 5mA

Single Fault SFC: 10mA

____μA
condition(SFC)

□BF____μA
Normal Max:
Patient condition(NC) □CF____μA CF applied part:
6 Leakage NC:10μA, SFC: 50μA
□BF____μA
Current Single Fault BF applied part:
condition(SFC) □CF____μA NC:100μA, SFC: 500μA

□BF____μA
Max:
7 Mains on Applied Part Leakage CF applied part: 50μA
□CF____μA
BF applied part: 5000μA

□BF____μA
Max:
Normal condition(NC)
Patient □CF____μA CF applied part:
8 Auxiliary NC:10μA, SFC: 50μA
□BF____μA
Current Single Fault BF applied part:
condition(SFC) □CF____μA NC:100μA, SFC: 500μA

Name/ Signature: __________________________ Date:_____________________________

A-12
PN: 046-010023-00 (3.0)