Professional Documents
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BeneVision N12/BeneVision
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N12C
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Patient Monitor
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Service Manual
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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..
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,, and are the registtered tradema
arks or tradem
marks owned by
b
hina and otherr countries.
Mindray in Ch
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Re
evisio
on His
story
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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.
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Version n
number 3.0
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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.
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Observance of the manual is a prerequisite for proper equipment maintenance and prevents
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equipment damage and personnel injury.
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Intended Audience
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This manual is for biomedical engineers, authorized technicians or service representatives
responsible for troubleshooting, repairing and maintaining the monitors
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Passwords PI
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A password may be required to access different modes. The passwords are listed below:
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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
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1.1.4 Notes.............................................................................................................................1-3
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2 Operation Theory .......................................................................................................................2-1
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2.1 Overview ..................................................................................................................................2-1
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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
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2.2.3 Power Architecture ........................................................................................................2-4
2.2.4 Independent Display Board (for the N17 Only) .............................................................2-5
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2.2.5 iView Module (for the N17 Only) ...................................................................................2-5
2.2.6 Alarm LAMP Board........................................................................................................2-5
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2.2.7 Power Switch Board ......................................................................................................2-5
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2.3 Data Logic Flow .......................................................................................................................2-5
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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
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4.4.3 SpO2 Test .................................................................................................................... 4-13
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4.4.5 Temp Test .................................................................................................................... 4-14
4.4.6 IBP Tests ..................................................................................................................... 4-14
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4.4.7 C.O. Test ..................................................................................................................... 4-16
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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
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4.4.11 EEG Test ................................................................................................................... 4-18
4.4.12 BIS Test..................................................................................................................... 4-19
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4.4.13 RM Test ..................................................................................................................... 4-20
4.4.14 CCO/SvO2 Tests ........................................................................................................ 4-21
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4.4.15 PiCCO Test ............................................................................................................... 4-22
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4.4.16 NMT Tests ................................................................................................................. 4-25
4.5 Nurse Call Relay Performance Test .......................................................................................4-26
4.6 Analog Output Performance Test ...........................................................................................4-26
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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
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5.4 Software Version Check ..........................................................................................................5-2
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5.6 Troubleshooting Guide .............................................................................................................5-2
5.6.1 Power On/Off Failures...................................................................................................5-2
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5.6.2 Display Failures ............................................................................................................5-3
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5.6.3 Module Rack Failures ...................................................................................................5-4
5.6.4 Alarm Failures ...............................................................................................................5-5
5.6.5 Recorder Failures .........................................................................................................5-6
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5.6.6 Output Interface Failures...............................................................................................5-6
5.6.7 Power Supply Failures ..................................................................................................5-7
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5.6.8 Network Related Problems ...........................................................................................5-9
5.6.9 Software Upgrade Problems .......................................................................................5-10
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5.6.10 Device Integration Failures ....................................................................................... 5-11
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6 Upgrade ......................................................................................................................................6-1
6.1 Overview ..................................................................................................................................6-1
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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
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7.5.4 Removing the WiFi Module .........................................................................................7-13
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7.5.6 Removing the Main Support Assembly ....................................................................... 7-18
7.5.7 Removing the iView Board Assembly (N17 Series)..................................................... 7-22
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7.5.8 Removing the Independent Display Board Assembly (N17 Series) ............................7-24
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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
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7.8 Disassembling the M51C Module ..........................................................................................7-29
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8 Parts ............................................................................................................................................8-1
8.1 N12 Parts .................................................................................................................................8-1
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8.1.1 N12 Whole Unit .............................................................................................................8-1
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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
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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
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A.3 Device Labeling ...................................................................................................................... A-2
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A.5 Earth Leakage Test ................................................................................................................ A-4
A.6 Patient Leakage Current ........................................................................................................ A-6
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A.7 Mains on Applied Part Leakage .............................................................................................. A-7
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A.8 Patient Auxiliary Current ......................................................................................................... A-9
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FOR YOUR NOTES
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1 Safetyy
1.1 Safety Informat
I ion
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DAN GER
Indicates
s an imminen
nt hazard thatt, if not avoid
ded, will resullt in death or serious injurry.
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WA RNING
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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.
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CAUT
TION
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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.
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NOTE
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Provides
s application tips or other useful inform
mation to ensure that you get the most from
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your pro
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1.1.1 Dange
ers
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1-1
1.1.2 Warnings
WARN
NING
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disconne
ected from th
he AC power source.
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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
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d to a properrly installed power
The equiipment must be connected p outlet w
with protectiv
ve
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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.
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keeping it out of child
dren’s reach..
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1.1.3 Cautio
ons
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CAUT
TION
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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
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netic radiatio n.
levels off electromagn
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
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mechaniical force durring servicing
g.
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1-2
1.1.4 Notes
NOTE
Refer to Operation Ma
anual for deta
ailed operatio
on and other information..
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1.2
2 Equipm
ment Sym
mbols
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Sym
mbol D
Description Symbol Description
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Refer to instruuction
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General warning sign
manual/bookleet
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Serial number Catalogue Nuumber
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Date of manuffacture Manufacturer
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B
Battery indicattor Direct currentt
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Equipotentialit
ty Alternating
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D
DEFIBRILLAT
TION-PROOF TYPE DEFIBRILLAT
TION-PROOF
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CF P TYPE
T BF APP
PLIED PART
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Stop USB Zero
Z key
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Calibrate key
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NIBP start/stop key
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Setup menu ke
ey Main menu keey
1-3
Symbol Description Symbol Description
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Output Input
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Dispose of in accordance to your Authorised representative in the
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country’s requirements European Community
The product bears CE mark indicating its conformity with the provisions of the Council
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Directive 93/42/EEC concerning medical devices and fulfils the essential requirements
of Annex I of this directive.
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Note: The product complies with the Council Directive 2011/65/EU.
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1-4
2 Operation Theory
2.1 Overview
As a bedside workstation for multi-parameter monitoring, the N series can provide the complete
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patient management, abundant physiological parameter monitoring and physiological alarm
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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
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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
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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.
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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
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and keyboard to operate the monitor. The N series can connect to multiple display screens to
function as mirror screens or extension screens.
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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
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application of patients.
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In comparison with the BeneView T series products, the N series boast better human-computer
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interaction design and clinical applicability, more complete IT solution capability of hospitals, and
more abundant CDS applications.
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The N12 main unit uses the 12.1” TFT WXGA display screen.
The N15 main unit uses the 15.6” TFT FHD display screen.
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The N17 main unit uses the 18.5”TFT FHD display screen.
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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.
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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.
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Two models of internal module rack COM boards are available. The N12 uses the 4-slot COM board,
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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
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corresponding power circuit are also provided on the internal module rack COM board.
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2-3
2.2.3 Power Architecture
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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
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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
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15V, and the AC power supply and battery power supply can be switched according to AC on-line
detection.
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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.
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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
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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
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power-off mode. In the case of battery power supply, the iView module cannot start.
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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.
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As an embedded computer module, it provides the following external interfaces: the network
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interface, DVI interface, and the USB interface. It can connect to the keyboard, mouse, network
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cable, and display independently. The configuration of the iView module is mutually exclusive with
that of the independent display module.
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2.2.6 Alarm LAMP Board
The LED alarm lamp and light sensor are provided on the board. The light sensor implements the
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ambient light detection and is used to adjust brightness of the LCD background light.
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
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3 WLAN Installation
3.1 Introduction
This chapter describes how to install Mindray patient monitors using WLAN.
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3.2 Network Deployment Process
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If the hospital has built its WLAN, the installation process is illustrated as follows:
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Mindray/agent A0 Provide network
marketing or sales requirements
personnel
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Mindray A1 Communicate with
headquarters
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the hospital about
intention to order
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Mindray/agent
service personnel A2 Communicate with the
hospital about network
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requirements and ask the
hospital to perform
corresponding setting and
adjustment
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A3 Do site survey
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Pass or fail
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Pass
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
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Network
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Requirements
A3 Netw ork acceptance Confirm that the customer Wireless
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report network meets requirements Network
of Mindray patient monitors by Acceptance
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means of questionnaire and Table in 3.4.3
measurement. Network
Verification
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Process
A5 Installation confirmation Confirm the actual operation Patient Monitor
report
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of the Mindray patient Installation
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monitors after installation. Confirmation
Table in 3.5
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Network
Coverage
Assessment
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with Patient
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Monitors
If the hospital plans to build a new WLAN for the Mindray patient monitors, make sure
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that there is at least one idle wifi channel that is not in use. Otherwise, you can’t make
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co-channel interference meet Mindray patient monitors’ requirement after the new WLAN
is built. The installation process is illustrated as follows:
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Mindray/agent A0 Provide network
marketing or sales requirements
personnel
Mindray/agent
service personnel A2 Do site survey and
design network
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A3 Sign the contract
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A4 Install network
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A5 Install the device
and confirm system
operation
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Figure 3-2 Installation Process for a New WLAN PI
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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
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A2 Network design / /
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document,
Bill of material
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A5 Installation Confirm the actual operation of the Patient Monitor
confirmation Mindray patient monitors after
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Installation
report installation. Confirmation Table
in 3.5 Network
Coverage
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Assessment with
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NOTE
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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.
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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
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devices).
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WLAN features
1 AP channel width Set the channel width to 20MHz, don’t use HT40 or even HT80.
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2 802.11 protocol WLAN can't use protocols that Mindray patient monitor can’t
support, e.g 802.11ac
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patient monitor can’t support.
WPA2-PSK is highly recommended.
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WPA2-Enterprise may increase probability of
offline when roaming, so not be recommended.
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4 Dedicated The patient monitors need to work on a dedicated
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VLAN VLAN.
Using VLAN can minimize Broadcast or multicast data which can
affect patient monitors’ stability.
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Important settings
1 DHCP The DHCP server reserves a sufficient number of
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snooping
3 Multicast If patient monitors use multicast, the multicast
function of network should be enabled.
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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.
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NOTE
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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
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some third party for help.
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3.4.2 Wi-Fi Signal Calibration
Before a wireless network survey tool (running on laptop computer) is used to test
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network coverage, follow this procedure to calibrate the RSSI of wireless network survey
tool with a patient monitor
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1. Keep the patient monitor and wireless network survey tool close. The distance
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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
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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.
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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).
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This part is completed through two ways: First the hospital completes items requiring
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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
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completes the Network Acceptance Table. If any item is found incompliant during
network Verification test, adjustment should be made before the patient monitors
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installation.
When in test, the wifi network SSID broadcast needs to be enabled to ensure that the wifi
SSID can be scanned.
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N Item Content of Verification Method Check Results
o. Requirements
Wireless coverage requirements
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expected coverage
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areas such as
ward, corridor,
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toilet, stairs, and
elevator are tested.
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2 Co-chann -20dB Service person
el performs the test by
interferen using network
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ce survey tool.
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Make sure that all
expected coverage
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areas such as
ward, corridor,
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–t –l 32 –w 1000
IPaddress-of -cellphone” for
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10 minutes.
4. Run“ ctrl+c”.
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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
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simultaneously must be
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more than 32.
2. The AP can create
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several SSIDs.
2 Device The maximum number of Check with hospital IT if this
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density devices connected to one requirement is met or not.
AP simultaneously is 12
(including patient monitors
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and other devices).
WLAN features
1 AP Set the channel width to
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Check with hospital IT if this
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channel 20MHz, don’t use HT40 or requirement is met or not.
width even HT80.
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WPA2-PSK is
highly
recommended.
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WPA2-Enterprise
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may increase
probability of offline
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when roaming, so
not be
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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.
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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.
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2 IGMP If patient monitors use Check with hospital IT if this
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snooping multicast, enable IGMP requirement is met or not.
snooping
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3 Multicast If patient monitors use Check with hospital IT if this
multicast. The multicast requirement is met or not.
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function of network should
be enabled.
4 Beacon & AP DTIM = 1, Beacon = Check with hospital IT if this
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DTIM 100ms requirement is met or not.
Service
port
Refer to Mindray Patient
Monitoring Network PI
Check with hospital IT if this
requirement is met or not.
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Whitepaper; patient
monitors need some certain
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TCP/UDP ports to be
opened
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To confirm coverage, perform coverage test in the areas where patients often go.
C
Check whether coverage meets requirements by observing the signal strength (RSSI)
showing on Patient monitor, and by observing whether an offline event occurs.
A
When necessary, adjust locations of APs or add APs to ensure the overage effect.
PI
Do as follows:
1. Set the patient monitor to access to CMS.
O
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
C
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.
A
Ping the patient monitor from the CMS and make
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PI
sure that the mean delay is less than 250 ms and the
packet lost rate shall be less than 1%.
O
Hold the patient monitor and walk in the scope of
C
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.
A
In the location where coverage is the poorest,
signal strength displayed on the screen is higher than
-65dBm.
PI
O
C
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.
A
PI
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.
A
2.4G = only use 2.4GHz band
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PI
Auto = use both 2.4GHz and 5GHz bands(5GHz
takes priority)
O
AUT. Server Type ACS Options are: ACS and SBR.
C
ACS means Cisco Access Control Server.
SBR means another server different from ACS.
This only applies if the security type is Enterprise.
A
BG Channel Specified Options are: All, Specified, None.
Specifying the channels improves stability and
PI
roaming performance by restricting the channels
scanned to only those specified. For example, on a
O
2.4GHz network set channels 1, 6, and 11.
C
BG channel settings on the monitor must match the
WLAN AP channel settings.
A Channel Specified Options are: All, Specified, None.
A
Management
Local / Display the existing EAP certificates in a
PI
patient monitor
USB Drive / Display the existing EAP certificate in the
O
USB drive
C
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
A
trigger, the period of the probe request is
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5s.
PI
Patient monitor support the following security modes:
O
Menu Basic Authentication Mode Encryption CCKM
C
Selection Algorithm Support
WPA WPA PSK TKIP/RC4 No
PSK
A
WPA2 WPA2 PSK CCMP/AES No
PSK
WPA
PSK AES
WPA PSK PI CCMP/AES No
O
WPA WPA EAP TKIP/RC4 No
C
TKIP
WPA2 WPA2 EAP CCMP/AES No
AES
A
AES
A
PI
O
C
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
A
V2
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PI
PEAP-G Y O Y Y N N N
TC
O
PEAP-T Y O Y Y Y N N
LS
C
TTLS Y O Y Y N N N
TLS Y N Y Y Y N N
FAST Y O Y N N Y Y
A
LEAP Y N Y N N N N
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.
A
Identity: user identity, it is the user name in the AD, LDAP or local user management
PI
PAC Certificate: When the EAP-FAST is selected, choose the PAC certificate from
PI
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
O
and password.
C
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
A
Wi-Fi signal icon indicated on the monitor is larger than –65 dBm.
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PI
on the monitor. Ensure that the intra-frequency interference
meets the requirement.
O
The SSID, IP address Configure the information again by referring to
acquisition mode, and security this manual.
C
mode are not correctly
configured on the monitor.
The monitor fails. Check whether another monitor can get online. If
A
yes, restart the monitor and ensure that the
PI
configurations of the two monitors are
consistent. If the monitor still cannot get online,
O
return the monitor to Mindray for repair.
The monitor can The monitor is not admitted on Admit the monitor on the CMS.
C
pool on the DHCP server are If the problem cannot be solved, contact the IT
used up. department.
O
The network link fails. Check whether the CMS can be pinged by
PI
using PC or cell-phone.
If the problem cannot be solved, contact the IT
O
department.
The services required by the Check whether the services required by the
C
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.
A
Check whether an IP address is assigned to
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PI
more than one device.
Multiple monitors The APs in some areas are Ensure that the APs are turned on and run
O
become damaged. properly.
disconnected The interference is intense in Check whether the interference is intense by
C
intermittently certain areas. using a network survey tool and remove obvious
interference sources or adjust WLAN
deployment to meet the requirements of
A
Mindray.
The signal coverage is
insufficient in some areas. PI
Check the signal coverage by using network
survey tool. If signal coverage is insufficient in
O
any area, adjust the position of the AP or add an
AP.
C
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
A
Mindray.
A
PI
O
C
3-15
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C
O
PI
A
FOR YOUR NOTES
C
O
PI
A
3-16
C
O
PI
A
C
O
PI
A
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
A
moniitor with recom nd frequency. The service personnel shouuld perform the testing
mmended test equipment an
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PI
and m
maintenance procedures
p as
s required and
d use appropriate test equipment.
O
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
C
repla
acement must be done to co
orrect the prob
blem. If the pro s, contact our Customer Service
oblem persists
Depa
artment.
A
CAUTION
N
A
All tests shou
PI
uld be perforrmed by qualiified service personnel on
nly.
O
C
Care should be taken whe i Maintenan
en changing tthe settings in nce and Connfiguration menus
m to
C
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.
A
PI
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
A
and AG modules, once a year.
tests Calibration
4. AG leakage test should be performed before AG
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PI
Performance test
AG tests measurement.
Calibration
O
Performance Tests
Performance test
C
ECG tests
Calibration
Resp performance test
A
SpO2 test
Pressure check
NIBP test
Leakage test
PI
O
Temp test
Performance test
C
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
A
measurement.
Leakage test
C
BIS test
RM test
PI
Interconnecting function
CCO/SvO2 tests
O
Output calibration
Performance test
C
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.
A
Recorder check Following any repair or replacement of the recorder.
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PI
1. When first installed.
Network print test
2. Whenever the printer is serviced or replaced.
O
1. When first installed.
Device integration check
2. Following any repair or replacement of the external device.
C
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
A
Performance test
significantly.
Mounting check
PI
1. When first installed.
2. At least every two years or as required.
O
Note: Performance test is not required for the ICG, rSO2, Tympanic Temp and ScvO2 modules, because the first
C
three modules perform self tests, and the last one needs to be calibrated prior to use.
A
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:
C
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.
A
Inspect the power cord, bracket and module accessories for obvious signs of damage.
PI
Inspect all external connections for loose connectors, bent pins or frayed cables.
Inspect all connectors on the equipment for loose connectors or bent pins.
O
Make sure that safety labels and data plates on the equipment are clearly legible.
C
4-3
4.2.2 NIBP Tests
NIBP Accuracy Test
Tools required:
T-shape connector
Tubing
Squeeze bulb
A
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PI
Follow this procedure to perform the test:
O
1. Connect the equipment as shown below.
C
Monitor Manometer
A
Tubing
NIBP connector
PI
O
C
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.
PI
3. Select Main Menu → Maintenance → enter the required password → Module → NIBP → NIBP
Accuracy Test.
O
4. Check the reading of the manometer and the reading of the patient monitor. Both should be 0 mmHg.
C
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
A
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.
O
C
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:
Tubing
Cylinder
A
1. Set Patient Category to Adult.
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PI
2. Connect the NIBP cuff to the NIBP connector on the patient monitor.
O
C
Cylinder
Monitor
Hose
Cuff
A
NIBP
4. PI
Select Main Menu → Maintenance → enter the required password → Module → NIBP → NIBP
O
Leakage Test. The message NIBP Leakage Test is displayed in the NIBP parameter area.
C
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,
A
verify the connections and make sure that the NIBP cuff, hose, and connectors are not leaking. Then,
perform the test again.
PI
O
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.
A
3. Record the current pressure value and meanwhile count time with a timer. Then, record the pressure value
after counting to 60 seconds.
PI
4. Compare the two values and make sure the difference is not greater than 6 mmHg.
O
C
4-5
NIBP Overpressure Protection Circuit Test
Tools required:
T-shape connector
Approprating tubing
Balloon pump
A
Reference manometer (calibrated with accuracy equal to or greater than 1 mmHg)
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PI
Follow this procedure to perform a NIBP calibration:
O
2. Select [Main Menu]→ [Maintenance ]→enter the required password →[Factory Maintenance]→ [NIBP].
C
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
A
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
PI
160-165 mmHg. After the pressure value is stabilized, select [Test] to start a calibration. and the [NIBP]
O
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].
C
Leakage Test
PI
2. Wait until CO2 warmup is finished and then completely block the gas inlet of the module or water trap (by
O
using your finger or other objects). The sidestream and microstream CO2 modules will behave as follows:
C
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
A
Occluded will appear on the screen. Block the gas inlet for another 60 seconds. Select Main Menu →
PI
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
O
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.
C
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:
T
T-shape conn
nector
T
Tubing
A
Flowmeter
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PI
1. P
Plug the modu
ule into the mo
odule rack.
O
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
C
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:
A
Flowmeter PI
O
C
Tubing
Relief valve
A
Monitor
PI
T-shape con
nnector
O
Gas cyylinder
C
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.
A
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
PI
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
A stteel gas cylind
der with >40% O2 and balan
nce gas N2 (ap
pplicable to sid
destream CO22 module with O2
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PI
dule equipped)
mod
T-sh
hape connecto
or
O
Tub
bing
C
Flow
wmeter
A
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 PI
d password → Module → CO2.
er the required
O
4. he CO2 menu, select Zero.
In th
C
5. Afte shed successffully, connect the equipment as follows:
er the zero caliibration is finis
A
er
Flowmete
PI
O
Tu
ubing
C
Relief valvve
Mon
nitor
T-shape con
nnector
A
PI
Gas cylind
der
O
6. Ope
en the relief va
alve, and adjus
st it until the fllowmeter has a stable readiing between
C
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.
A
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PI
4.2.4 AG Tests
Leakage Test
O
1. Plug the AG module into the module rack.
C
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.
A
3. Block the gas inlet for another 60 seconds. Select Main Menu → Maintenance → enter the required
PI
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.
O
If the alarm message disappears, or the flow rate is greater than or equal to 10 ml/min, it indicates that the
C
module leaks.
A
Accuracy Test
PI
Tools required:
O
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
C
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
A
Tubing
PI
Flowmeter
O
2. Wait at least 10 min and then perform a leakage test to make sure that the airway has no leakage.
4-9
Flowmetter
Tubing
Relief vallve
A
Monitor
T-shape cconnector
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PI
der
Gas cylind
O
C
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.
A
Calibration
PI
O
Tools req
quired:
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
A
T-sh
hape connecto
or
Tub
bing
O
Flow
wmeter
C
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
A
2. Che
eck the airwayy and make sure that there a
are no occlusio
ons or leaks.
PI
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.
C
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
A
Monitor
M
T sh ape connector
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PI
Gas ccylinder
O
C
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.
A
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
PI
e gas for calib
bration, set othher gases' con
ncentration
O
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.
C
7. S
Select Calibra
ate to start a ca
alibration.
CAUTION
N
C
C
Calibrate the O2 module, if it has been transported for long dista
ance.
A
4
4.3 Powerr On Tes
st
PI
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:
1. Connect the patient simulator with the ECG module using an ECG cable.
A
2. Set the patient simulator as follows: ECG sinus rhythm, HR = 60 bpm with the amplitude as 1 mV.
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PI
3. Verify that the ECG waves are displayed correctly without noise and the displayed HR value is within 60±1
bpm.
O
4. Disconnect each of the leads in turn and observe the corresponding lead off message displayed on the
C
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.
A
ECG Verification PI
O
Tools required:
C
Vernier caliper
3. Select Calibrate ECG. A square wave appears on the screen and the message ECG Calibrating is
displayed.
O
4. Compare the amplitude of the square wave with the wave scale. The difference should be within 5%.
C
If necessary, you can print out the square wave and wave scale through the recorder and then measure the
A
difference.
PI
O
C
4-12
4.4.2 Resp Performance Test
Tools required:
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
A
impedance as 1 Ω, respiration rate as 20 rpm.
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PI
3. Verify that the Resp wave is displayed without any distortion and the displayed Resp value is within 20±1
rpm.
O
C
4.4.3 SpO2 Test
Tools required:
None.
A
1. PI
Connect SpO2 sensor to the SpO2 connector of the monitor. Set Patient Category to Adult and PR Source
O
to SpO2 on the monitor.
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.
A
PI
blood sample reference measured with a CO-oximeter. Pulse oximeter measurements are statistically
C
distributed and about two-thirds of the measurements are expected to come within the specified accuracy range
compared to CO-oximeter measurements.
NOTE
A
PI
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
O
4-13
4.4.5 Temp Test
Tools required:
1. Connect the two pins of any Temp connector of a module to the two ends of the resistance box using two
wires.
A
3. Verify each Temp channel of the monitor and make sure that the displayed value is within 37±0.1ºC.
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PI
O
4.4.6 IBP Tests
Performance Test
C
Tools required:
A
Dedicated IBP adapter cable (300B, P/N 00-002199-00) (use P/N 00-002198-00, if the simulator is
MPS450)
PI
O
1. Connect the patient simulator to the monitor's IBP connector.
C
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.
O
7. Make the patient simulator outputs 120/80 mmHg ART signals and 120/0 mmHg LV signals respectively to
C
each IBP channel and check that the IBP wave is displayed correctly.
Pressure Calibration
A
Method 1:
PI
Tools required:
O
Dedicated IBP adapter cable (300B, P/N 00-002199-00) (use P/N 00-002198-00, if the simulator is
C
MPS450)
4-14
1. C
Connect the patient
p simulattor to the mon itor's IBP conn
nector.
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.
A
7. IIf the calibratio
on is complete ge Calibration Completed! w
ed successfullly, the messag will be displaye
ed.
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PI
O
Otherwise, a corresponding
c g message wil l be displayed
d.
O
Meth
hod 2:
C
Toolss required:
S
Standard sphyygmomanome
eter
S
Squeeze bulb
b
A
T
Tubing
T
T-shape conn
nector
PI
O
1. C
Connect the 3-way
3 momanometer and the squee
stopcock, the sphygm eze bulb throuugh a T-shape
e connector,
C
a
as shown belo
ow.
2. Z
Zero the transsducer, and then open the sstopcock to the
e sphygmoma
anometer.
A
PI
Pressure
e transducer
O
3-w
way stopcock
C
Pre
essure adapter cable
A
IBP
T-shape co
onnector
PI
module
Sphygmoman
nometer
O
3. S
Select Main Menu→
M Mainte nter the requirred password → Module → IBP. In the displayed
enance → en
C
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.
A
1. Connect the patient simulator to the C.O. module using a C.O. main cable.
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PI
2. Set the blood temperature (BT) to 37ºC on the patient simulator and check the temperature value is
37±0.1ºC.
O
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.
C
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.
A
6. Verify that the C.O. value is 5±0.25 L/min.
PI
O
4.4.8 Mainstream CO2 Tests
C
NOTE
Make sure that the barometric pressure set in Main Menu → Maintenance → en ter
A
the required password → Other accords with the local barometric pressure before
performing mainstream CO2 tests.
PI
O
Tools required:
C
T-shape connector
A
Tubing
PI
Flowmeter
O
C
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.
A
5. C
Connect the te
est system as follows:
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PI
O
C
Relief valve
v Flowmeter
A
T-shape
e
connecto
or
T-sha
ape connector
PI Monittor
O
R
Relief valve
C
C 2 gas cylinder
CO
A
PI
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.
O
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.
C
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.
A
PI
4.4.9 Sidestrea
am and Mic
crostream
m CO2 Testts
See ssection 4.2.3S
Sidestream an
nd Microstrea
am CO2 Testts.
O
C
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:
A
1. Connect pins of EEG lead wires to an ECG simulator.
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Set the ECG simulator to output Sine wave and frequency to between 0.5 and 30Hz. The range is 2mV. The
PI
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.
O
2. Open the EEG setting menu on monitor, Set the Scale of EEG to be 2000uV. Then you can find a Sine
C
wave on screen of Patient Monitor.
Method 2:
A
Tools required:
None.
PI
O
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.
C
Method 3:
Tools required:
A
Resistance box
PI
Multimeter
O
1. Connect the EEG module/cable to the EEG simulator and the monitor.
C
3. Adjust the resistance box to 1 kΩ, verify the resistance value displayed on the monitor is 1kΩ.
A
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.
PI
O
C
4-18
BIPOLAR
RA = 10 K A+
RA = 10 K A-
RA = 10 K PGND
MONOPOLAR
RA = 10 K A
A
RA = 10 K NE
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PI
PGND
O
RA = 10 K
C
4.4.12 BIS Test
A
You can choose either of the following methods to perform the test:
Method 1:
Tools required:
PI
O
None.
C
1. Connect the BIS sensor to a healthy, wide-awake adult as directed in the Operator's Manual.
A
2. Check the EEG wave and BIS numerics displayed on the screen and make sure the BIS value is within 80
and 100.
PI
O
Method 2:
Tools required:
C
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.
PI
2. After the cyclic impedance check is finished, check that the result for each electrode is passed.
O
Method 3:
C
Tools:
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.
4. Verify the EMG value range from 65 to 75, and SQI value should be 100 displayed on Graphic Trends.
A
4.4.13 RM Test
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Method 1:
PI
Tools required:
O
T-shape connector
Tubing
C
Squeeze bulb
A
Reference manometer (calibrated with accuracy equal to or greater than 1 mmHg)
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.
A
PI
Monitor Reference
O
manometer
RM sensor
C
RM connector
A
PI
Method 2:
C
Tools required:
Tubing
1. Connect the module, RM sensor, air pump and pressure gauge according to picture below.
A
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PI
O
C
A
4.4.14 CCO/SvO2 Tests
Interconnecting Function
Tools required: PI
O
None.
C
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.
A
3. Verify that the CCO/SvO2 numerics displayed on the patient monitor and Vigilance II monitor are consistent.
PI
O
Output Performance
C
Tools required:
Multimeter
1. Connect the signal output end of the connecting cables of the CCO/SvO2 module to the oscilloscope.
A
2. Select CCO Setup → Signal Output Setup and then select Simulated High Value from the pop-up menu.
PI
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.
O
C
4-21
4.4.15 PiCCO Test
Performance Test
Tools required:
1. Connect the patient simulator, the PiCCO IBP test cable and the PiCCO module.
A
2. Let the patient simulator outputs 0 mmHg respectively to the pArt channel and the pCVP channel.
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PI
3. Select the pArt parameter interface to access the pArt Setup menu, and then select Zero.
O
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.
C
6. The pArt value displayed on the monitor should be within 200±4 mmHg, and pCVP value within 20±1
mmHg.
A
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
8.
sensor.
PI
Let the patient simulator output ART signal to the pArt channel and CVP signal to the pCVP channel, check
O
whether the IBP waveform is correctly displayed.
C
Pressure Calibration
A
Method 1:
PI
Tools required:
1. Connect the patient simulator, the PiCCO IBP test cable and the PiCCO module.
A
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.
PI
4. Select the pCVP parameter interface to access the pCVP Setup menu, and then select Zero.
O
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
A
ssphygmomano
ometer.
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PI
O
Pressure transducer
C
3-way sto
opcock
A
PI
Connector cable of pressure trransducer
O
IBP
T-shape connector
c
module
C
Sphyg
gmomanomete
er
A
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
PI
4. IInflate using th
he squeeze bu eading of sphy
ulb until the re ygmomanometer approximaates the preset calibration
O
vvalue.
4-23
C.O. Test
Method 1:
Tools required:
A
1. Connect the patient simulator and the C.O. module using a C.O. trunk cable and a C.O. adapter box.
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PI
2. Set the blood temperature (BT) to 37ºC on the patient simulator and check the temperature value is
O
37±0.1ºC.
3. Select CCO parameter interface to access the C.O. Measure interface. Then, select Setup to check
C
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.
A
5. In the C.O. Measurement window, select Start to start C.O. measurement. As soon as the prompt Inject
PI
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.
O
6. Verify that the C.O. value displayed on the monitor is correct.
C
Method 2:
Tools required:
A
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.
A
3. Select CCO parameter interface to access the C.O. Measure interface. Then, select Setup to check
PI
4. Turn the injectate temperature (TI) knob on the C.O. adapter box to check whether the value of the TI is
O
from 0 to 30ºC.
C
4-24
4.4.16 NMT Tests
Performance Test
Method 1:
Tools required:
Resistance box
Multimeter
A
1. Set the resistance value to 1kOhm. Connect the stimulation electrodes to the two wiring terminals.
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PI
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.
O
3. Insert the NMT module into the module rack of the monitor. Select the NMT parameter area of the monitor
C
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.
A
Method 2:
Tools required: PI
O
Resistance box (0~9999.9 Ω)
C
Oscilloscope (Agilent DS0-X3014A)
1. Set resistance box to 1kOhm, connect stimulation electrodes to the resistance box.
A
2. Insert the NMT module to monitor. Set [Stimulation current] to [Supra (35mA)], [Pulse width] to 200μs.
PI
3. Measure the voltage wave of the resistance box by oscilloscope, verify the pulse width is range from 180 to
O
220us, and calculate the Stimulation Current according stimulation voltage should be range from 33 to
C
37mA.
A
Sensor Check
PI
Tools required:
None.
O
C
2. Select Main Menu → Maintenance → enter the required password → Module → NMT.
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
A
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PI
4.5 Nurse Call Relay Performance Test
O
C
Tools required:
Multimeter
A
1. Connect the nurse call cable to the Nurse Call Connector of the patient monitor.
2.
PI
Enter Demo mode. Then, select Main Menu → Maintenance >> → enter the required password →
Alarm to access the Nurse Call setup menu.
O
3. In Nurse Call menu, select all options of Alarm Priority and Alarm Type. and set Contact Type to Normally
C
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
A
an alarm.
PI
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)
O
Tools required:
PI
Patient simulator
Oscilloscope
O
C
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
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
A
o
of these piec
ces of test equipment, and
d be familiar with
w their usa
age.
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PI
Electrical saffety tests sha
all comply witth the followiing standards
s: IEC 60601--1 and
A
ANSI/AAMI ES60601-1.
E
O
In case of oth
her stipulatio
ons in local la
aws and regulations, imple
ement electriical safety
C
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
A
m
must be impllemented in accordance
a w
with the test interval of the
e patient mon
nitor.
NOT
TE
A
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
C
pressure).
Appendix A Electrical
E Saffety Inspectio
PI
O
C
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
A
prompt messages. After the problem is removed, the recorder should be able to work correctly.
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PI
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.
O
C
4.9 Network Print Test
NOTE
A
HP LaserJet Pro M202dw laser printer is recommended for BeneVision patient monitor
series
PI
O
C
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:
A
BeneVis Network
PI
ion printer
O
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
A
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.
O
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:
ID adapter tha
at matches the
e external devvice
A
RJ45 connectting cable
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PI
S
Serial port ada
apting cable th
hat matching tthe external device
O
Conn
nect an extern
nal device as shown
s below. T
The figure bellow is for referrence only.
C
BeneLink module RJ45
5 connecting ccable ID
D adapter
A
Label
PI External
device
O
C
A
PI
O
Serial p
port adapting cable
c (optional)
C
2. C
Connect the ID
D adapter thatt matches the external device to the Bene
eLink module with a RJ45 connecting
c
A
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
PI
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..
O
4. A
Attach a label indicating dev
vice name to tthe RJ45 conn
necting cable at the end clos
oser to the Ben
neLink
C
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.
A
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PI
Type of serial port adapting
External Device ID for ID adapter
cable
O
No need to use the adapting cable;
the ID adapter can be plugged into
C
Mindray Wato 20/30/55/65 4D52B2AE
the serial port of the external device
directly.
Newport E360 4E50B1B0 Type B
A
SNDF: 5042AFBE
No need to use the adapting cable;
4434BBCC Type B
dura/Evita 4/Evita XL
PI
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
A
GE Engstrom Carestation 4F45B0BB Type B
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PI
Maquet Servo-U 4d55B2AB Type B
HUL Leoni Plus 4849B7B7 Type C
O
HUL Leon Plus 4850B7B0 Type C
HUL Leon 484CB7B4 Type C
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
A
directly.
directly.
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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:
A
Gas source(tube or gas cylinder), including air or O2 at least, and N2O or other anesthesia gases are
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optional
O
Test lung and a matching Y-pipe, or other accessories
C
4.10.2.2 Procedure and Items to Be Checked
A
Follow the steps below:
1.
PI
Connect the BeneLink module to the ventilator or the anesthesia machine. Please see Device Connection
and Setup for more details.
O
2. Connect the gas supply and test lungs to the ventilator or anesthesia machine, turn on the device, and
C
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.
A
3. Make sure the ID adapter is correctly configured, and the green indicator of corresponding port on the
PI
4. Access Integrated Devices screen on the patient monitor. Check that the device type (ventilator or
anesthesia machine) and ventilation mode are correctly displayed.
C
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.
A
6. Re-configure the above parameters on the ventilator or the anesthesia machine and check if the parameter
PI
7. Trigger alarms MV Too Low, Airway Pressure Too High, PAW Too High, Peak Too High, and No Gas
O
Supply (no Air or O2) on the ventilator or the anesthesia machine. Check whether these alarm messages
C
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.
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Serial Port Configuration List
A
Module in standby mode and
tick the corresponding module.
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The following information is for
further reference: Baud Rate:
O
Maquet Servo-i 9600 bps
Not required.
C
Maquet Servo-s Word Length: 8 bits
Parity: even
Stop Bits: 1
A
Channel A: Not required;
Channel B:
Draeger Evita 2
Protocol: Medibus
Baud rate: 19200
PI /
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Parity: even
C
Stop Bits: 1
Protocol: Medibus
Draeger Evita 2 Baud Rate: 19200
A
XL Stop Bits: 1
Interval: --- (Evita 2 dura)
O
Parity: NONE
Stop Bits: 1
PI
A
Baud Rate: 19200 bps
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Ohmeda Word Length: 7 bits
Not required.
Avance/Aisys Parity: odd
O
Stop Bits: 1
Baud Rate: 19200 bps
C
Ohmeda Aestiva Word Length: 7 bits
Not required.
7100 /7900 Parity: odd
Stop Bits: 1
A
1. Access the repair mode;
Drager Fabius
2. Protocol: Medibus;
3. Baud Rate: 9600 bps PI /
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GS/Plus/Tiro Word Length: 7 bits
Parity: even
C
Stop Bits: 1
1. Access the repair mode;
2. Protocol: Medibus;
A
Stop Bits: 1
Baud Rate: 9600 bps
C
Stop Bits: 1
1. Access the Savina maintenance menu and
C
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External Device Setup Remark
A
1. Access Diagnosis mode and select baud
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rate.
To access Diagnosis mode, do as follows:
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1) Turn off V60.
2) Press and hold the confirm button (a "√"
C
symbol on the hardkey) in the right upper
part of the touchscreen, and then press the
power-on button.
A
3) A message indicating whether V60 enters
PI
the Diagnosis mode is displayed on upper
side of the touchscreen. Release the Confirm
O
Philips V60 button and click it again to access the Baud Rate: 19200 bps
diagnosis mode.
C
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External Device Setup Remark
A
Baud Rate: 38400 bps
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1. Serial port adapting cable between ID Word Length: 8 bits
Maquet Servo-U
adapter and monitor: Type B Parity: even
O
Stop Bits: 1
1. Access the Standby mode. Use the
C
interface switch button to access the Service
interface. Select Login and set User to
Baud Rate: 19200 bps
Service Engineer (password: 0002). Then,
A
Word Length: 8 bits
HUL Leoni Plus select Connections from the left. In Serial
Parity: NONE
Engineer (password: 0002). Then, select the Baud Rate: 19200 bps
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External Device Setup Remark
A
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O
1.Access the Standby mode through
C
“Biomed service”, input maintenance
password.
2.Select “Medibus setup” menu and select
A
Baud rate = 9600
COM1 as example for configuation.: set
Draeger ZeusIE Parity = Even
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“ Commands to Medibus device” to “On” ; set
“Medibus version” to “SW4.n; set “ Port” to
Stop bits = 1
O
“On” , Then press “Activate” button.
3. Serial port adapting cable between ID
C
4-37
External Device Setup Remark
A
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O
C
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
A
Parameters Screen menu. Parity:EVEN
Apollo
2. Set Protocol to MEDIBUS.
PI Stop Bits:1
Data Bits:8
O
3.Serial port adapting cable between ID
C
adapter and monitor: Type C.
A
PI
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C
A
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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
A
the external device
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Checking the connection Test Result (Yes/No)
Can the patient monitor and the external device be assembled together using
O
designated accessories?
Does the green indicator of corresponding port on the BeneLink module
C
illuminate while the other indicators are not?
Are there numerics or characters displayed on the Devices Integrated screen of
the patient monitor?
A
Are the device type and parameter values displayed correctly on the Devices
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Integrated screen of the patient monitor when the external device just enters
working mode?
O
Is the ventilation mode correctly displayed on the patient monitor? Does it
C
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
A
PEEP PEEP
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Pmean Pmean
Ppeak Ppeak
O
f (RR) f (RR)
C
VTe VTe
RR Too High
Apnea
O
Patient Disconnected
Other information
C
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4.11 Battery Check
Tools required:
None.
Function Test
1. Verify that the patient monitor works properly when running on AC power.
A
2. Remove the AC power cord and verify that the patient monitor still works properly.
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O
Performance Test
C
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.
A
4.12 Mounting Check
Tools required:
PI
O
None.
C
Check that the screws fastening the bracket and guide rail are not loose.
A
Check that the five installation screws on the bottom side of the N12 monitor are not loose.(six installation
screws for N15 and N17)
PI
Check that the four installation screws on the transfer metal and monitor bottom side are not loose.
O
Check that it can be installed in place and locked when N12 monitor use fast lock installed way
C
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 VHM bracket can place the monitor at any height as required.
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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.
A
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O
C
A
PI
O
C
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.
A
PI
O
C
A
PI
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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.
A
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O
C
A
PI
O
C
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
A
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.
O
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.
C
Update ID Module: Provide interface for burning device integration ID. Users should confirm the BeneLink
port and device ID before burning.
PI
O
C
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4.13.5
5 Debug
This tab page provvides settings related to the debug mode,, which is only
y applicable to testing.
A
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O
C
A
PI
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4.13.6
6 Power In
nfo
C
This tab page disp
plays information about pow
wer supply.
A
4.13.7
7 ClinicalD
Data
This tab page provvides settings related to clin
nical data colle
ection.
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C
A
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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.)
NOTE
The recorder is disabled if Recorder is switched off in the Factory Maintenance menu.
A
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4.13.8 Transferring Clinical Data
In the Factory Maintenance page, select Clinical Data Transfer. Select data you want to transfer.
O
C
4.13.9 Software Version
In the Factory Maintenance menu, select Software Version to show software version information.
A
4.13.10 Monitor Information
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In the Factory Maintenance menu, select Monitor Information to show the status of the patient monitor.
O
Maintenance and Test Report
C
(See the above sections for detailed test procedures and contents)
Customer name
Customer address
A
Servicing person
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Servicing company
Equipment under test
O
(EUT)
Model of EUT
C
SN of EUT
Hardware version
Software version
A
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
A
ECG performance test
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ECG waves are displayed correctly without noise and the HR
value is within 60±1 bpm.
O
ECG Lead Off alarm behaves correctly.
Paced signals are detected and pace pulse marks are
C
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
A
5%.
Resp test
The Resp wave is not distorted and the Resp value is within PI
O
20±1 rpm.
SpO2 test
C
NIBP test
The difference is within ±3 mm when 0, 50 or 200 mmHg is set
O
within 37±0.1ºC.
PI
IBP test
The static pressure value displayed for each IBP channel is
O
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%
A
(80%≤O2≤100%)
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Microstream CO2 test
Block the gas inlet of the module or watertrap for about 30
O
seconds. An alarm of CO2 Airway Occluded is given. It
indicates that there is no leakage.
C
The displayed CO2 value is 45±2 mmHg.
AG test
When AG flowrate is slower than 10ml/min, an alarm of AG
A
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 PI
O
specifications in the Operator's Manual.
EEG test (you can select either method to perform the test)
C
1kΩ
BIS test (you can select either method to perform the test)
O
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
A
The C.O. value is displayed on the monitor
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Method 2: The BT value is 37±0.1ºC.
The value of CatheterType is PV2015L20
O
The TI value is from 0 to 30ºC
NMT test(you can select either method to perform the test)
C
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
A
the calculated Stimulation Current is range from 33 to 37mA
The sensor check is pass.
Nurse call relay performance test PI
O
The relay contacts are close when an alarm occurs.
Analog output performance test
C
the Main unit label and Integrated warning labels are present
and legible
The Protective Earth Resistance test is passed
A
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
A
an AC power failure accidentally occurs.
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The operating time of the battery meets the product
specification.
O
Mounting Check
The screws fastening the bracket and guide rail are not loose
C
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
A
bottom side are not loose
It can be installed in place and locked when N12 monitor use
fast lock installed way PI
O
The modules can be normally and securely inserted into the
module rack
C
required
PI
Conclusion:
O
4-48
5 Troubleshooting
5.1 Introduction
This chapter lists the problems that may occur during use of the monitor and recommended
A
measures. Refer to the table in this chapter to check the monitor, and confirm and fix these problems.
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For more information about the troubleshooting, please contact the after-sales service department of
Mindray.
O
C
5.2 Part Replacement
For the monitor, the PCB, main parts and components can be replaced. For the LCD or touch screen
A
fault, only the front case assembly can be replaced. Once the faulty PCB is confirmed, replace the
PI
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
O
about replaceable parts, refer to Chapter 8 Parts.
C
After the AC power supply is connected, check whether the AC indicator is turned on. If not, confirm
PI
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
O
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
C
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.
A
In addition, check the appearance for damages before powering on. Particularly, when the touch
PI
screen of the screen assembly is damaged, stop using the monitor immediately.
O
C
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
A
can check the version information of the system software.
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2. Select Main Menu → System >> → Maintenance >> → enter the user's maintenance
password → Version Information >>. In the displayed menu, you can check the version
O
information of the system software and modules.
C
5.5 Technical Alarm Check
A
Before troubleshooting the patient monitor, check for technical alarm message. If an alarm message
PI
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.
O
C
AC mains not
connected or Verify the AC mains is properly connected.
O
damaged
Power module
Replace the power module.
defective
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
A
devices, check whether there is any short
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circuit fault in the internal module rack COM
board or main control board and it leads to
O
protection of the power output.
C
5.6.2 Display Failures
Failure Description Possible Cause Troubleshooting
A
The display screen Cable defective or Verify the cables (screen cable and backlight
does not function or
the display is
improperly connected
PI
cable) connecting the display screen to the
main control board are correctly connected.
O
abnormal, but the Verify the connecting cable connectors and
main unit can corresponding sockets are not damaged.
C
operate
LCD screen defective Replace the front case assembly.
Main control board Upgrade the software of the main control board.
A
software abnormal
PI
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.
A
defective
C
Main control board Upgrade the software of the main control board.
software abnormal
5-3
wrong. monitor. If the touch screen could not work yet,
replace the front case assembly
A
properly or already damaged. Verify the
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External cable
PI
connecting cables and connectors are not
defective or poorly
damaged.
O
connected
Verify that contact screws on SMR or
C
module are tightly fastened and well
connected.
A
with a known good module. If the patient
Defective parameter
monitor identifies the replacement module and
module
PI
can start measurement, it indicates that the
original module is faulty.
O
Wrong communication Upgrade the module and/or the SMR software
C
board software version to a compatible level.
parameter modules SMR power supply board or main control board fails.
abnormal Check whether the contact screw output
O
board.
defective
PI
5-4
Main control board
Replace the main control board.
failure
A
Verify the cable connecting the internal
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Cable defective from
module rack COM board to the main
the main control board
control board is connected reliably.
O
to the internal module
Verify the connecting cables and
rack COM board
C
connectors are not damaged.
The parameter module
Version inconsistency
does not respond
between the module
A
communication board Upgrade the module or internal module rack
and the internal COM board software.
module rack COM PI
O
board
Power supply to the The internal module rack COM board or main
C
connected.
Alarm LED off or cannot improperly connected
Verify the connecting cables and
PI
5-5
Failure Description Possible Cause Troubleshooting
Volume to a proper value. Select Alarm →
Setup, and set the alarm volume to a proper
value.
A
Main control board
Replace the main control board.
failure
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O
5.6.5 Recorder Failures
C
Failure Description Possible Cause Troubleshooting
Verify the recorder status LED is lit.
Recorder module
If it is lit, recover its function in "Factory
disabled
A
Maintenance".
improperly connected
Verify the connecting cables and
connectors are not damaged.
A
5-6
Failure Description Possible Cause Troubleshooting
Verify the connecting cables and
connectors are not damaged.
A
Network interface Main control board
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PI
Replace the main control board.
failure failure
O
with the DVI interface Use the recommended display.
C
DVI interface failure time sequence
A
External display model
Use the display model recommended in the
not specified in the
manual PI
user manual.
O
Touch pad damage of
Touch screen failure of Replace the display.
the external display
C
Cable defective or
power is correctly connected.
improperly connected
PI
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.
A
be heard during startup. After the iView
The patient monitor
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assembly starts, the iView interface can be
cannot be connected
displayed in the main unit.
to iView system
O
If neither of the above two conditions
iView assembly failure
cannot be reached, check whether the
C
power supply for the iView assembly is
normal. If it is not normal, the main control
board may be damaged; if the power supply
A
is normal, the iView assembly is damaged.
PI
Check for network cable connection and
length (which should not exceed 50 m), or
O
Improper network cable
check whether the laid network cable is too
connection
C
Frequent dropouts near to the power supply for large power
equipment.
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
A
correct.
5-9
Failure Description Possible Cause Troubleshooting
Antenna not installed Verify the antenna for the MPAN module is
properly installed properly.
A
properly
connectors are not damaged.
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Internal module rack COM
Replace the module rack COM board.
board defective
O
Wrong software version for
C
Upgrade the MPAN module software.
the MPAN module
A
5.6.9 Software Upgrade Problems
Failure Description Possible Cause
PI
Troubleshooting
Verify the network connector, NOT the
O
iView network connector, on the patient
monitor is being used.
C
Incorrect connection
Ensure the normal operation of the
network hub or switch, and verify the
hub cable is properly connected.
A
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.
A
displays nothing after
external device
connection
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Wrong software version or
Verify the protocol version and software
wrong protocol version of the
O
version are supported by the ID adapter.
external device
C
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.
A
The patient monitor The BeneLink module Upgrade or update the software
has no response
when loading the ID
application software is
corrupted PI
application of the BeneLink module with
the network upgrading tool.
O
adapter BeneLink module damaged Replace the module.
C
A
PI
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C
A
PI
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C
5-11
6 Upgrade
6.1 Overview
A
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This monitor supports upgrade of the monitoring parameter function modules, upgrade of the
functional assemblies, and network upgrade of software.
O
C
NOTE
For function upgrade involving disassembly of the monitor, eliminate static electricity
before the disassembly. When removing some parts with the electrostatic sensitive
A
mark, wear protective devices such as electrostatic ring or anti-electrostatic gloves, lest
the parts would be damaged.
PI
Properly connect and route the cables and wires when reassembling the equipment to
O
avoid pinched hoses and electrical short circuits.
Use specified screws to reassemble the equipment. If the incorrect screws are forcefully
C
tightened, the equipment may be damaged and the screws or part may fall off during use,
causing unpredictable equipment damage or human injury.
A
Before removing assemblies, make sure that all the connection lines have been
PI
unplugged. During removal, note to avoid breaking the connection line by pulling or
damaging the connector.
O
Place the removed screws and other parts separately by category so that they can be
C
6-1
6.2 Upgrade of Parameter Function Modules
You can upgrade the following parameter modules:
Monitoring
PN Name and Specification Remarks
Parameter Module
A
lead/IBP)
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MPM-3 Module (NC Spo2/3/5
115-038697-00
O
lead/IBP)
C
MPM-7 Module (MR Spo2/3/5lead/No
115-044666-00
IBP)
A
MPM-9 Module (NC Spo2/3/5lead/No
115-044667-00
IBP)
PI
O
MPM-13 (MR
115-038698-00
SpO2/12lead/IBP/Analog)
C
MPM-14 (NC
115-038699-00
SpO2/12lead/IBP/Analog)
A
PI
MPM-13 (MR
115-038700-00
SpO2/12lead/IBP/Analog)
O
MPM-14 (NC
C
115-038701-00
SpO2/12lead/IBP/Analog)
115-013200-00
accessory)
6-2
Monitoring
PN Name and Specification Remarks
Parameter Module
A
AG Module (O2/package/no
115-034109-00
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accessory)
PI
O
AG Module (BIS/package/no
115-034110-00
accessory)
C
AG Module (O2/BIS/package/no
115-034111-00
accessory)
A
ICG module 115-034123-00
PI
ICG Module (package/ no accessory)
O
BIS module 115-013194-00 BIS Module (Package/no accessory)
C
accessory)
PI
accessory)
C
accessory)
O
6-3
Monitoring
PN Name and Specification Remarks
Parameter Module
A
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PI
O
TEMP module 115-039492-00 Temp module (package/no accessory)
C
Infrared ear Temp Infrared ear Temp (no
115-044684-00
module accessory/package)
A
You can insert and remove all the parameter modules during patient monitoring. Refer to the
PI
BeneVision N Series Patient Monitor Operator's Manual (P/N: 046-009995-00) for the use of
parameter modules.
O
C
A
PI
O
C
A
PI
O
C
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
A
the monitor.
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PI
You can upgrade the following functional assemblies for this monitor: the satellite module rack
O
(SMR), wireless network functional assembly, MPAN, recorder, independent display assembly, iView
system functional assembly, etc.
C
Functional Rem
PN Name and Specification
Assembly arks
A
115-037384-00
PI
SMR material package (2m/without
handle and hook)
O
SMR material package (2m/with
C
SMR 115-033887-00
handle and hook)
115-033888-00
handle and hook)
PI
MainBoard)
iView
O
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
A
wireless AP. To
T upgrade wirreless function el of our comppany to connect
ns, ask authorrized personne
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PI
6.3
3.1 Upgra
ading SMR
R
O
The SMR can
n be connected
d to the patien
nt monitor thro
ough the SMR
R connector viaa a powered USB
U
C
cable.
For details, se
ee BeneVision
n N Series Pattient Monitor Operator's
O Manual (P/N: 0466-009995-00).
A
6.3
3.2 Upgra
ading Wire
eless Netw
work Functions PI
O
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
C
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).
A
PI
O
C
A
PI
O
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.
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.
NOTE
A
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.
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PI
O
C
A
PI
O
C
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.
A
NOTE
C
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.
A
PI
O
C
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.
A
The programs of this monitor can also be upgraded through a specially authorized USB disk
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PI
(which contains the USB disk upgrade BIOS program PN:110-004854-00) or the following
programs of the monitor can also be upgraded.
O
C
Software PN Name and Specification Remarks
System
software / Large N12N15N17 system package /
A
package
Module rack
software
/
/
O
/ M51C module DSP(BF70X) software /
C
ECG
O
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
display th
he related prompt interface.. Click to enter
e the inputt interface of the
A
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PI
O
C
A
2. Enter e SN informatio
the on, and click
PI
to enter prrogram installaation location
O
interface. Select the co
orresponding ffolder for insta
allation, and click to
C
e installation according
complete a to th
he installation prompt.
Appendix: Re
eference Table of Multiple La
anguages:
A
La
anguage (Eng
glish) Lang
guage (Chine
ese) Remarkss
PI
EN
NGLISH 英语
语 /
SIIM.CHINESE 简体
体中文 /
O
FR
RENCH 法语
语 /
C
GERMAN 德语
语 /
ITA
TALIAN 意大
大利语 /
PO
OLISH 波兰
兰语 /
A
SP
PANISH 西班
班牙语 /
PI
PO
ORTUGUESE
E 葡萄
萄牙语 /
RU
USSIAN 俄语
语 /
O
CZ
ZECH 捷克
克语 /
C
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 /
A
Japanese 日语 /
All rights reserved - Mindray Medical Colombia
PI
O
6.4.1.2 PC and Monitor Connection Method
C
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.
A
PC connected to the hub through a network cable: Connect one end of the network cable to
PI
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
O
same as the above method. The hub has multiple slots, so multiple (at least 5) monitors
C
can be connected in this case and upgraded at the same time.
NOTE
PI
To ensure correct upgrade, the IP address set using the following rule must be used
O
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
C
Connect the monitor to the USB keyboard. When starting the monitor, constantly click ' F4+F5'
PI
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
O
6-10
6.4.1.3 Software Too
ol Upgrade
e Operations
s
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
A
as show
wn in the follow
wing figures:
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PI
O
C
A
PI
O
C
3
A
PI
O
2
C
A
PI
O
C
6-11
2. On the diisplayed mach
hine type selecction interface
e, select the machine
m type "M
Merak".
A
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PI
The following interface is diisplayed on th
he PC:
O
C
A
PI
O
C
A
PI
6.4
4.2 Guide to Softwa
are Upgrad
de Operattions
6.4.2.1 System Softw
ware Upgra
ading Metho
od
O
C
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,
A
check su
um, version an
nd description)) is correct, an
nd then click OK.
O
PI
Now, the
e Start hot key
y of the main m
menu is enable
ed.
O
C
6-12
A
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PI
O
C
A
3. Confirm t
that the downloading netwo
ork cable is con PI
nnected correctly, make surre that the mo
onitor
O
n powered off, and click the Start hot key of the upgrade tool to enterr the download
has been ding
procedurre of software..
C
1. F irst conn
nect the SMR connection lin N15/N17 main unit
ne to the multii-function interrface of N12/N
PI
(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
O
correctly..
2. Enter the
e main interfac
ce for downloa
ading of system
m upgrade, click " ", and
d
A
select the
e Rack.pkg file
e in the large ssoftware pack
kage of N12/N15/N17 system
m:
PI
O
C
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
A
the System Update Tool, or consult your service personnel.
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PI
O
6.4.3 Guide to Upgrade through a USB Disk
C
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
A
models with a memory of 2GB or above);
1.
2.
PI
Create the following content under the root directory of the USB disk: UPGRADE_AMP\Merak;
Copy the upgrade BIOS program Merak_Installer.pkg (do not change this file name) to the
O
UPGRADE_AMP\Merak directory;
C
3. Copy the upgrade file (PKG or MPKG) to the UPGRADE_AMP\Merak directory.
A
6.4.3.2 Inserting the USB Disk into the USB port of the Monitor
PI
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.
O
C
Method 1: As pressing the on/off button of the monitor to start the monitor, use two or more
A
fingers to continuously and rapidly tap the touch screen to enter the upgrade mode.
PI
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
O
6-14
6.4.3.4 Selecting the
e File for Up
pgrade thro
ough the US
SB Disk
A
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PI
O
C
A
PI
O
C
A
PI
press the
e “” direction
n key on the ke
eyboard to sellect it;
PI
press the
e “” direction
n key on the ke
eyboard to sellect it;
C
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.
A
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PI
O
C
A
PI
O
C
CAUT
TION
A
saved be
efore upgrade
e.
FPGA prrogram. Otherwise, the eq
quipment may
y break down
n.
C
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.
A
PI
NOTE
O
After upg
grading the BIOS
B program
m, you have to upgrade sy
ystem progra m and other
C
program
ms to ensure their
t compatiibility.
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:
A
MID number/MAC address (for example: 000F140839AE). To get the MID number, select :
Main Menu → License (in the System column).
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PI
Customer's email (for receiving license key file)
O
Refer to the following instructions to upgrade the licenses
C
1. Unzip the PMLS.zip file. Then you would get a folder named PMLS.
NOTE
A
The U disk should be FAT32 format.
6-17
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C
O
PI
A
FOR YOUR NOTES
C
O
PI
A
6-18
C
O
PI
A
C
O
PI
A
7 Repaiir and Disassem
D mbly
7.1 Tools
During disasssembly and rep
pair, the follow
wing tools may
y be required:
A
Phillips screwdrivers
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PI
Small flatt-bladed screw
wdriver (speciffication 101 orr 102)
Contact spanner
s (6800
0-J95)
O
Tweezerss
C
Needle nose pliers
M3 sleevve
A
7.2
2 Prepara
ations fo
or Disass
sembly PI
O
Before disasssembling the monitor,
m make following prep
parations:
C
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.
A
CAUT
TION
Eliminate
e static electricity before tthe disassem
mbly. When re
emoving som
me parts with the
A
Properly
y connect and
d route the ca ssembling th e equipment to
ables and wirres when reas
O
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
C
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.
A
7.3
3 Whole Unit
U Disa
assembly
y
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PI
7.3
3.1 Basic Disassem
mbly
NOTE
O
Be sure to
t disassemb
ble the base ffirst before proceeding wiith other partts.
C
1. Remove the power plug anti-pull hookk from the rearr case of the monitor.
m
A
PI
O
C
remove the fo
our M3×8 scre
ews under them
m.
PI
O
C
A
PI
O
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.
A
1. As shown in the figure below, place the monitor face up, unscrew the M4×8 screws (5 for the
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PI
N12 series and 6 for the N15N17 series) from the bottom case;
O
C
A
PI
O
C
A
PI
O
C
A
For the N12 series machines, the base assembly can be removed when the base is pulled
out.
O
C
7-3
A
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PI
For the
t N15N17 se
eries machine
es, the base as
ssembly can be
b removed whhen the conne
ection
O
line connected
c to the
t battery intterface board of main board is pulled out.
C
J24
A
J20
PI
O
C
A
NOTE
PI
Be sure to
t pull out the base with p
proper force, without dam
maging the caables and
connecto
ors.
O
C
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.
A
NOTE
PI
Before placing
p the monitor face do
own, make sure that the desktop
d is flaat, without forreign
O
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
A
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PI
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.
O
C
A
PI
O
C
2. Lift the rear case assembly to separate it from the front case assembly.
NOTE
A
As shown in the above figure, there are two types of front case assemblies (NLT and
PI
N12
C
A
PI
O
C
7-5
A
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(N12-NLT fron
nt case assem
mbly) (N12-SHARP front case asssembly)
PI
O
C
A
PI
O
C
A
PI
O
C
A
PI
O
C
7-6
N15
A
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PI
(N15 rear casse assembly)
O
C
A
(N15-NLT fron
nt case assem
mbly) (N PI
N15-SHARP frront case asse
embly)
O
N17
C
A
PI
O
C
(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.
2PCS
S
A
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PI
O
C
NOTE
A
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
front cas
se board positioning rib.
PI
cone keypad direction by aaligning with
h the
O
Note to control
c the to
orsion when ttightening the
e twoPT3×8 screws
s again,, avoiding sc
crew
C
sliding.
A
7.4
4.2 Remov
ving the Alarm
A Lam
mp and Lig
ght Sensor Board
PI
2PCS PT3
3 X8
A
PI
Connnec
tionn line
O
k t
C
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.
A
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PI
7.4
4.3 Remov
ving the Screen
S Ass
sembly Connection
n Line
O
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
C
removed
d by releasing the buckling p
position for cla
amping cable on
o the front caase.
A
PI
O
C
C
Cabl
(N12-NLT) (N12-SHARP)
A
PI
O
C
Cab
A
(N15-NLT) HARP)
(N15-SH
PI
O
C
Ca
(N17-NLT) (N17-SHARP)
7-9
CAUT
TION
Prevent pressure on the front face
e of display screen
s during
g disassemblyy.
A
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PI
7.5
5 Furtherr Disasse
embly off the Rea
ar Case Assembly
A y
O
7.5.1 Remov
ving the Recorder
R
C
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.
A
the recorrder at the sam
me time.
3. After the re
ecorder is pulle
and pull out
own the recorrder connection line from thee positioning rib,
ed out, take do
o the sockett respectively. Then, the rec PI
corder can be removed.
r
O
C
M3 Positioning
A
PI
O
C
Cli
A
NOTE
PI
Use prop
per force to re
emove the ca
able carefully
y lest it would
d be broken.
O
C
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.
A
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PI
O
2. Release the
t two clips backward
b and take out the recorder
r drive board. Pay atttention to the snap
C
in the fro
ont.
Sn
A
PI
O
C
A
PI
remove the
t ground cable of the drivve board. Rem
move the recorrder drive boarrd.
C
A
PI
O
C
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
A
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PI
Thhermal print
O
C
NOTE
Use proper force to remove
r the ca
able carefully
y lest it would
d be broken.
A
7.5.3 Remov
1.
ving the MPAN
M
Pull out th
Boa
ard
he MPAN boa
ard connection
PI
n line at the end of internal module
m rackCO
OM board; then pull
O
out the MPAN
M antenna
a connector in
nserted on the
e MPAN board; unscrew onee M3×6 screw
w to
C
remove the
t MPAN boa
ard.
A
PI
O
C
A
PI
O
C
7-12
2. Tear the MPAN antenn
na fixing piece
e. Then, the MPAN
M antenna can be removved.
A
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PI
O
NOTE
Use proper force to remove
r the ca
able carefully
y lest it would
d be broken.
C
7.5.4 Remov
ving the WiFi
W Modu
ule
A
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.
PI
O
C
A
PI
O
C
A
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
A
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WiFi
PI
support
O
C
NOTE
A
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
golden finger part would be da
he board ca
amaged. Pro PI
arefully, lestt the board ssocket and
ovides applic
cation tips or other useful
O
information to ensurre that you ma
aintain your product bette
er.
C
7.5.5 Remov
ving the In
nternal Mo
odule Rac
ck Assemb
bly
NOTE
A
7-14
N12
Conn
nection line off battery interfa
ace
A
J10
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PI
J20
O
C
Connectionn line of
internal moodule rack
COM boarrd
A
PI
O
C
2. Loosen and
a remove the two M3X6 sscrews, and re
emove the batttery interface board.
A
PI
O
C
3. Loosen and
a remove the five M3X6 sscrews, and fo
orce upward ve
ertically to rem
move the intern
nal
A
module rack
r assembly
y as indicated in the figure.
PI
O
C
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
A
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PI
M2.5
O
C
SMR innterface shee
et
PT3X
A
5. Turn over the removed
ases.
silicon ca
d internal mod ule rack COM
PI
M board, and ta
ake down the ffour POGO PIN
O
C
A
PI
O
C
N15N17
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.
PI
O
Conne
ection line of i nternal modulle rack COM
C
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
A
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PI
PT3X
O
C
A
PI
M3X6
O
C
A
PI
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.
A
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PI
O
C
Speakerr
A
2. a remove the five M3X6 sscrews, and ve
Loosen and
PI o the main suupport assembly.
ertically take out
O
C
A
PI
O
C
A
3. As shown
n in the figure below, place tthe face of the
e removed ma
ain board of maain support up
p, pull
PI
7-18
Connection line
from the main
A
control board to
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PI
DVI stud
4. Turn over the main support with the main control board removed, and place its face up; remove
O
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
C
power supply end; unscrew four M3X6 screws, and take down the power board.
A
PI
O
C
A
5. Loosen and remove two M3X6 screws, and take out the recorder cover; unscrew one M3X6
PI
screw, and take out the power cord from the AC input to ACDC.
O
C
Recorder
A
PI
input to ACDC
C
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.
A
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PI
Speaker
O
C
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.
A
PI
O
C
A
PI
O
(N15)
C
(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
A
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PI
O
C
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
A
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
PI
6 screws, and take down thee power board
d.
O
Connecti on line from th
he
C
Power
PI
O
C
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
A
out the re
ecorder cover; loosen and rremove one M3X6
M screw, and take out thhe power cord from
PI
the AC in
nput to ACDC.
O
C
7-21
A
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PI
Cable
O
C
NOTE
Do not injure the cable when cutting the cable tie.
A
7.5.7 Removing the iView Board Assembly (N17 Series) PI
O
1. First screw out the two DVI stud screws.
C
A
PI
O
C
A
PI
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.
O
C
7-22
Two iView boaard connection
A
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PI
O
C
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..
A
PI
O
C
SSD ha
ard
A
PI
O
C
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
A
board.
PI
O
C
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.
A
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PI
O
C
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.
A
PI
O
C
A
PI
O
C
3. Loosen and
a remove the four M3X6 sscrews, and ta
ake down the independent ddisplay board.
A
PI
O
C
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.
A
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PI
O
C
A
PI
O
2. Pry open the two handle positioning pins to the middle direction, and take out the handle.
C
A
PI
O
C
A
PI
N12
Take out the battery door connecting belt from the through hole, and remove the battery door.
7-25
A
N15N17
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PI
1. Loosen and
a remove the two M3X6 sscrews, and re
emove the batttery interface board.
O
C
A
PI
O
2. As shown
n below, open the battery do
oor, insert a a piece of cloth
h into the gap between the
C
battery door
d and the base, and force wn to take out the battery dooor.
edly press dow
A
PI
O
C
A
PI
O
C
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
A
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PI
O
C
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.
A
M3X
X8
PI
O
C
A
PI
loosen an
nd remove the d pan head screw, and sepaarate the front case
e six M3X16 ccross recessed
from the rear case.
A
PI
Screw
O
C
7-27
M3X16
A
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PI
3. Removing the module rack interface
e board
O
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
C
interface board.
A
PIM3X8
O
Connec
ction line from
m the interface
C
board of
o external moodule rack to
the 8-slot board
A
PI
Pull out th
he connection
n line between
n the module rack antenna and
a the internaal module rack
k
C
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.
A
PI
O
Modu
ule rack
C
7-28
M3X6
M screw
A
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PI
O
C
POGO PIN
N silicon
cases of m
module rack
A
7.8
8 Disasse
embling the M51C
C Module PI
O
1. Removing the front pan
nel assembly
C
out.
PI
O
C
A
PI
Use a co
ontact wrench Remove the Remoove the
O
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
A
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PI
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
O
connection lin
ne and NIBP air
a tube. Then,, the paramete
er board can be
b removed.
C
Parrameter board
A
scre
ews and connection
PI
O
Pu
ull out along th
his
C
oxygen board
d.
PI
O
C
As shown in the
t following fiigure, remove
e the infrared board
b connection line, and tthen remove th
he
infrared board
d.
O
C
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.
A
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PI
O
C
A
PI
O
C
A
PI
O
C
A
PI
O
C
7-31
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C
O
PI
A
FOR YOUR NOTES
C
O
PI
A
7-32
C
O
PI
A
C
O
PI
A
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.
A
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PI
8.1 N12 Parrts
O
8.1.1 N12 Whole
W Unit
C
Exploded View
A
PI
O
C
A
PI
O
C
A
PI
O
C
8-1
Parts List
A
3 N12 screw cover / 049-001226-00
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PI
Cross recessed pan head screw GB/T818-2000
4 / /
M4X30 plated with green color zinc
O
5 AC inlet hook 1 9211-20-87369
C
A
PI
O
C
A
PI
O
C
A
PI
O
C
8-2
8.1.2 N12-NLT Front Housing
H A
Assembly
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
C
Partts List
A
PI
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
O
2 S
Screen clip 2 0033-000636-00
0
C
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
A
11 MK POWER BUTTON (P+R) 1 043-007956-00
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PI
12 Conductive cloth pad 0.08m /
O
C
A
PI
O
C
A
PI
O
C
A
PI
O
C
8-4
8.1.3 N12-SHARP Fro
ont Housin
ng Assembly
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
C
Partts List
No. N
Name and Spe
ecification Qty
Q M
Material Code
e
A
1 N
N12-SHARP fro
ont housing asssembly (FRU) 1 1115-044503-00
0
PI
2 S
Screen clip 2 0033-000636-00
0
O
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
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
A
12 E
Earth plate (N12
2) 1 0042-018667-00
0
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PI
13 C
Conductive cloth pad 0.08m
0 /
14 C
CORE O.D=21.5mmI.D=9.5m
mm 1 /
O
C
8.1.4 N12 Rear Housing
Exploded View
A
PI
O
C
A
PI
O
C
A
PI
O
C
8-6
Parts List
1 N12 handle 1
115-044501-00
2 Cushion pad /
A
4 Waterproof strip N12 1 048-006308-00
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PI
5 Handle Left Damping Block, N12 1 /
O
6 N12 rear housing (silk screen) 1 043-008005-00
C
7 N12 internal module rack assembly (with TDS/BNC) 1 /
A
9 Speaker 2W 4ohm 500Hz 1
10
11
MK speaker foam
/ /
O
with pad and plated with green color zinc
C
13 TR6F recorder 1 /
A
8-7
8.1.5 N12 Rear Housing Assem
mbly (FRU)(115-0444
499-00)
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
C
A
PI
O
C
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 /
A
4 W
Waterproof strip
p N12 1 0048-006308-00
0
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PI
5 H
Handle Left Dam
mping Block, N
N12 1 0049-001249-00
0
O
6 C
Conductive foam
m 2.0*7.0 mm 0.11m
0 /
C
8.1.6 N12 Battery Cav
vity Assem
mbly (FRU
U)(115-044
4504-00)
A
Exploded View
PI
O
C
A
PI
O
C
A
PI
O
C
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
A
3 B
Battery bar 1 92211-20-87256
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PI
4 B
Battery bar slee
eve 1 /
O
C
Cushion pad.Bumpon SJ5302
2, white and
5 1 /
transparent
C
8.1.7 N12 Module
M Rac
ck Body A
Assembly (FRU) (115-044507--00)
A
Exploded View
PI
O
C
A
PI
O
C
A
PI
O
C
8-10
Partts List
No. N
Name and Sp
pecification Qty Maaterial Code
1 N module rac
N12 ck (four slots) 1 /
3 C
Contact screw 8 68800-21-51100
A
4 C
Contact spring 8 68800-20-50261
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PI
5 S
Spring 8 68800-20-50388
O
F washer-Grade A GB/T97 .1-2002 3 plate
Flat ed with
6 8 /
C
g
green color zinc
c
A
8.2
2 N 15 Pa
arts
8.2
2.1 N15 Whole
W Unit PI
O
Exploded View
C
A
PI
O
C
A
PI
O
C
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
3 N base asse
N15 embly (FRU) 1 1 15-044543-00
0
A
4 S
Screw / /
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PI
O
8.2
2.2 N15-NLT Front Housing
H A
Assembly
C
Exploded View
A
PI
O
C
A
PI
O
C
A
PI
O
C
8-12
Parts List
A
4 MK alarm cap 1 049-001135-00
All rights reserved - Mindray Medical Colombia
PI
5 MK hood 1 049-001214-00
O
6 Alarm LED and Light Sensor Board PCBA 1 051-002693-00
C
Cross recessed pan head thread-cutting
7 tapping screws PT3X8 plated with green color 4 /
zinc
A
8 N15N17 front shell plate cable 1 009-006736-00
9 CORE O.D=21.5mmI.D=9.5mm 1
PI 1 /
O
10 N15 Mainboard to LCD cable (NLT) 1 009-006408-00
C
11 N15N17 touch screen cable (NLT) 1 009-006397-00
8-13
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C
O 8.2
PI Exploded View
A
C
2.3 N15-SHARP Fro
O
ont Housin
PI
ng
8-14
C
O
PI
A
C
O
PI
A
Parts List
A
4 MK alarm cap 1 049-001135-00
All rights reserved - Mindray Medical Colombia
PI
5 MK hood 1 049-001214-00
O
6 Alarm LED and Light Sensor Board PCBA 1 051-002693-00
C
Cross recessed pan head thread-cutting tapping
7 4 /
screws PT3X8 plated with green color zinc
A
9 CORE O.D=21.5mmI.D=9.5mm 1 1 /
8-15
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C
O 8.2
PI Exploded View
A
C
O
2.4 N15 Rear Housing
PI
A
8-16
C
O
PI
A
C
O
PI
A
Parts List
A
4 N15 handle 1
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PI
5 Cushion pad 1 115-044542-00
O
6 Blind rivet hole BSO-3.5M3-28 ZC 2
C
7 Handle right damping block, N15 1 /
A
9 Recorder door 1 043-000184-00
10 MK speaker foam PI
1 115-044547-00
O
11 Speaker 2W 4ohm 500Hz 1
C
12 Speaker bracket 1
15 Screw / /
8-17
8.2
2.5 N15 Rear Housing Assem
mbly (FRU) (115-044
4541-00)
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
C
A
Partts List
PI
No. N
Name and Spe
ecification Qty M
Material Code
e
O
1 N rear housin
N15 ng (silk screen)) 1 0043-008003-00
C
2 W
Waterproof foam
m (N15) 1 0048-006291-00
3 N Handle Rig
N15 ght Damp 1 0049-001283-00
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
A
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PI
O
C
A
PI
O
C
A
PI
O
C
Partts List
A
1 N15 bottom ca
ase 1 /
O
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
A
All rights reserved - Mindray Medical Colombia
PI
O
C
A
PI
O
C
A
PI
O
Partts List
C
No. N
Name and Spe
ecification Qty M
Material Code
e
F washer-Gra
Flat ade A GB/T97. 1-2002 3 plate
ed with
2 12 /
green color zinc
c
O
3 S
Spring 12 66800-20-50388
C
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
A
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PI
O
C
A
PI
O
C
A
PI
O
C
Partts List
A
No. N
Name and Spe
ecification Qty M
Material Code
e
PI
1 N front housin
N17 ng assembly 1 1 15-044551-00
O
2 N rear housin
N17 ng assembly 1 /
C
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
A
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PI
O
C
A
PI
O
C
A
PI
Partts List
O
C
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
A
3 M alarm cap
MK 1 0049-001135-00
0
4 M hood
MK 1 0049-001214-00
0
O
5 A
Alarm LED and Light Sensor B
Board PCBA 1 0051-002693-00
0
C
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
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
A
14 C
Conductive cloth pad 0.08m
0 /
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PI
15 E
Earth plate (NLT
T) 1 0042-017398-00
0
O
8.3
3.3 N17-SHARP Fro
ont Housin
ng
C
Exploded View
A
PI
O
C
A
PI
O
C
A
PI
O
C
8-23
Parts List
A
4 MK hood 1 049-001214-00
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PI
5 Alarm LED and Light Sensor Board PCBA 1 051-002693-00
O
Cross recessed pan head thread-cutting tapping
6 4 /
C
screws PT 3X8 plated with green color zinc
A
9 CORE O.D=21.5mmI.D=9.5mm 1 1 /
8-24
8.3
3.4 N17 Rear Housing
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
C
Partts List
No. N
Name and Spe
ecification Qty M
Material Code
e
A
1 N
N15N17 module
e rack assemb ly (with SMR/B
BNC) 1 /
PI
S
Small cross recessed pan hea
ad GB9074.5-8
88 M3X6
2 / /
O
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
9 TR6F recorder 1 /
A
11 N17 rear housing (silk screen) 1 043-007458-00
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PI
12 Waterproof foam (N17) 1 048-006292-00
O
13 Handle right damping block, N17 1 /
C
14 Blind rivet hole BSO-3.5M3-35 ZC / /
A
16 N17 top cover 1 043-007661-00
17
18
Cushion pad
N17 handle
PI
2
1
115-044549-00
O
C
A
PI
O
C
A
PI
O
C
8-26
8.3
3.5 N17 Rear Housing Assem
mbly (FRU)( 115-044
4548-00)
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
C
A
Partts List
PI
No. N
Name and Spe
ecification Qty
Q M
Material Code
e
O
1 N rear housin
N17 ng (silk screen)) 1 0043-007458-00
0
C
2 C
Conductive foam
m 3.2*6.4mm 0.11m
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
A
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PI
O
C
A
PI
O
C
A
PI
O
Partts List
C
No. N
Name and Spe
ecification Qty M
Material Code
e
1 N bottom cas
N17 se 1 /
A
2 R
Rubber foot pad
d 4 /
PI
8-28
8.3
3.7 Indepe
endent Dis
splay Upg
grade Pack
kage (With
hout Main
nboard)
(115-0445544-00)
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
C
Partts List
A
Material
No. N
Name and Spe
ecification Qty
Code
PI
1 In
ndependent dis
splay assemblyy 1 /
O
S
Small cross rece
essed pan hea
ad GB9074.5-88 M3X6 with
2 4 /
C
8-29
8.3
3.8 Indepe
endent Dis
splay Upg
grade Pack
kage (With
h Mainboaard)
(115-0445799-00)
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
Partts List
C
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
A
2 In
ndependent dis
splay assemblyy 1 1 15-044586-00
PI
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
O
C
8-30
8.3
3.9 Indepe
endent Dis
splay Ass
sembly
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
O
C
A
PI
Partts List
O
Material
No. N
Name and Spe
ecification Qty
Code
C
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
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C
O 8.3
PI Exploded View
A
3.10 iView
C
O
w Module Assembly
y
PI
A
8-32
C
O
PI
A
C
O
PI
A
Parts List
N Q
o Name and Specification t Material Code
. y
A
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PI
Cross recessed pan head screw GB/T818-2000 M2X6
4 4 /
O
plated with green color zinc
C
0
.
0
5 Conductive foam 2.0*7.0mm /
A
4
6
PI m
O
6 Computer module Celeron J1900 1 023-001083-00
C
7 iView support board PCBA 1 051-002739-00
8-33
8.4
4 Externa
al Satellitte Modulle Rack (SMR)
(
Exploded View
A
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PI
O
C
A
PI
O
C
A
PI
Partts List
O
No. N
Name and Spe
ecification Qty M
Material Code
e
C
1 F
Front housing silkscreen of mo
odule rack 1 0043-006301-00
3 In
nterface board fixing sheet m etal 1 /
PI
4 In
nterface board PCBA of exterrnal module rac
ck 1 0051-001908-00
O
5 M
Module rack cufff bracket 1 1 15-033914-00
C
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
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C
O 8.5
PI Exploded View
A
M
5 M51C Module
C
O
PI
A
8-35
C
O
PI
A
C
O
PI
A
Parts List
A
M51C-FF (Ext Arr /12 Lead ST /Glasgow_12) from 4 051-002483-00-00
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PI
M51C-FF(Mindray:Hr /Glasgow_12) 051-002483-00-01
O
Stainless steel cross recessed pan head
2 4 /
screw GB/T818-2000 M2X4
C
3 M51C-9008V3.0 SPO2 PCBA 1 051-002353-00
A
5 M51C module back plane (with IBP/FRU) 1 051-002383-00
6 Fixing base
PI
2 /
O
Cross recessed countersunk head screw
7 2 /
GB/T819.1-2000 M3X6
C
8 Spanner (T8) 2 /
10 Terminal screw 2 /
PI
11 Infrared lens 1 /
O
20 Silicone tube 11 /
8-36
No. Name and Specification Qty Material Code
A
M51C front panel maintenance package
115-044670-00
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PI
(Mindray SpO2/IBP FRU)
23 selected
M51C front panel maintenance package
O
from 6 115-044671-00
(Nellcor SpO2/IBP FRU)
C
M51C front panel maintenance package
115-044672-00
(Mindray /IBP analog FRU)
A
115-044673-00
(Nellcor /IBP analog FRU)
PI
O
C
A
PI
O
C
A
PI
O
C
8-37
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C
O
PI
A
FOR YOUR NOTES
C
O
PI
A
8-38
C
O
PI
A
C
O
PI
A
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
A
local regulations.
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PI
All tests can be performed using commercially available safety analyzer test equipment. These
O
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,
C
or Gerb may require modifications to the procedure. Follow the instructions of the analyzer
manufacturer.
A
The consistent use of a safety analyzer as a routine step in closing a repair or upgrade is
PI
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
O
and grounding, as well as total current loads.
C
to the cord.
A-1
A.2 Device Enclosure and Accessories
A.2.1 Visual Inspection
Test Item Acceptance Criteria
A
No physical damage to meters, switches,
connectors, etc.
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PI
The enclosure and accessories
No residue of fluid spillage (e.g., water, coffee,
O
chemicals, etc.).
C
terminals, etc.).
A
A.2.2 Contextual Inspection
Test Item
PI
Acceptance Criteria
Check the labels provided by the manufacturer or the healthcare facility are present and legible.
C
Protective Earth Resistance is measured using the RED test lead attached to the DUT Protective
C
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).
3. Press CA
AL LEADS. The 601PRO willl measure the
e lead resistan
nce, and if lesss than 0.150 Ohms,
O
A
it will storre the reading and subtract it from all eartth resistance readings
r takenn at the calibrated
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PI
current.
O
C
A
If the calibration fails, the previously store
ed readings will
w be used until a passing ccalibration has
s
occurred.:
PI
O
C
WAR
RNING
During Earth Resistance testing,, the DUT must be plugged into the 6011PRO front
A
To Perform
m the Test
C
ea.
metal are
PI
3. Press sho
ortcut key 3. The
T Protective
e Earth Resista
ance test is displayed.
O
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.
C
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
A
was not within range. Readings greater than 9.999 Ohms will be displayed as Over.
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PI
O
In Case of Failure
Once it reaches the limitation, stop using and inform the Customer Service Engineer for analysis and
C
disposal.
A
LIMITS
ALL COUNTRIES R = 0.2 Ω Maximum
PI
O
A.5 Earth Leakage Test
C
Run an Earth Leakage test on the device being tested before performing any other leakage tests.
A
Earth Leakage Current, leakage current measured through DUT outlet Earth
Earth Leakage Current AP-EARTH (ALL Applied Parts connected to Earth), leakage current
O
There is no need to attach a test lead; the 601PRO automatically connects the measuring device
internally.
A
1. From the MAIN MENU, or with the outlet unpowered, plug the DUT into the 601PRO front panel
O
2. Attach the device's applied parts to the 601PRO applied part terminals if applicable.
C
3. Press shortcut key 4.The Earth Leakage test appears on the display, and the test begins
immediately:
A-4
A
SOFT KE
EY 1 toggles th
he DUT outlett Polarity from Normal to Offf to Reverse.
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PI
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.
O
SOFT KE
EY 4 toggles th h to No AP to Earth.
he AP to Earth
C
4. e print data key at any time to generate a printout of the
Press the e latest measuurement.
A
In Case of Failurre
Check an
ny broken of th
PI
he enclosure. Replace any defective part.
O
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
C
Change another
a probe to confirm if tthe fail is caus
sed by console
e.
A
LIMIITS
A
For IEC60601
1-1,
PI
5mA
A in Normal Co
ondition
10mA
A in Single Fa
ault Condition
O
C
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
A
The following outlet conditio
ons apply whe
en performing this test:
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PI
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
O
Reversed
d Polarity, Earrth Open, Outl et ON Reverrsed Polarity, L2 Open, Outtlet ON
C
A
WAR
RNING
If all of the applied parts
tied tog
p corresp
pond to the in
PI
nstrument typ
pe, the applieed parts will be
b
ne reading wiill be taken. Iff any of the applied parts differ from th
gether and on he
O
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.
C
A
To P
Perform the Test
T
PI
2. Attach the applied partts to the 601P RO's applied part terminals.
C
3. Press sho
ortcut key 6. The eakage test is displayed, and the test beggins immediate
T Patient Le ely.
A
PI
O
4. Press AP
PPLIED PART
T (SOFT KEY 4
4) at any time to select the desired applieed part leakage
C
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..
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.
A
If the leakkage current measurement
m tests fail on a new unit and if situation caan not be corre
ected,
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PI
submit a Safety Failure
e Report to do
ocument the sy
ystem problem
m. Remove unnit from operattion.
O
C
LIMIITS
A
For CF applied parts
10μA
A in Normal Co
50μA
ondition
100μ
μA in Normal Condition
C
500μ
μA in Single Fa
ault Condition
n
A
PI
A.7
7 Mains on
o Applied Part L
Leakage
O
The Mains on
n Applied Part test applies a test voltage, which is 110%
% of the mainss voltage, throu
ugh a
C
Normal Polarity;
P
O
Reversed
d Polarity
C
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
A
occurred. Also
o, the esc/stop
p key has no e
effect during calibration.
c
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PI
3. When the
e calibration is plied Part test will reappear..
s finished, the Mains on App
O
C
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.
A
High vo
oltage is pres
sent at applie
ed part termin
nals while measurements aare being tak
ken.
PI
O
To P
Perform the Test
T
C
4. Press sho
ortcut key 7. The
T Mains on A
Applied Part test
t is displaye
ed.
O
C
A
5. Select the
e desired outle
et configuratio
on and applied
d part to test using
u the appro
ropriate SOFT
PI
KEYS:
6. Press ST
TART TEST (S
SOFT KEY 1) to begin the te
est.
O
7. Press the
e print data key to generate a printout of the
t latest mea
asurement.
C
NOTE
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
A
Change another
a probe to confirm if tthe fail is caus
sed by console
e.
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PI
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.
O
If all else fails, stop using and inform
m the Custome
er Service Eng
gineer for anallysis and dispo
osal.
C
LIMIITS
A
For CF applied parts:
p 50 μA
A.8
8 Patientt Auxiliarry Curren
nt
Patient Auxilia
ary currents arre measured b
between any selected
s ECG jack and the rremaining selected
A
Prep
paration
C
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
O
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::
A
In Case of Failurre
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PI
Check an
ny broken of th
he enclosure. Replace any defective part.
O
Inspect wiring
w for bad crimps,
c poor cconnections, or
o damage.
C
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
A
Change another
a probe to confirm if tthe fail is caus
sed by console
e.
LIMIITS
A
For CF a
applied parts,
PI
10μA
A in Normal Co
ondition
O
50μA
A in Single Fault Condition
C
For BF a
applied parts,
100μ
μA in Normal Condition
C
A
500μ
μA in Single Fa
ault Condition
n
PI
O
C
A-10
ELECTRICAL SAFETY INSPECTION FORM
Overall assessment:
Location: Te chnician:
A
Equipment: Control Number:
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PI
Manufacturer: Mode l: SN:
O
Pass/Fa
INSPECTION AND TESTING Limit
C
il
A
3 Device Labeling
4 Protective Earth Resistance Ω
PI Max 0.2 Ω
O
Normal
____μA
condition(NC) Max:
C
□BF____μA
Normal Max:
Patient condition(NC) □CF____μA CF applied part:
O
□BF____μA
Max:
A
□CF____μA
BF applied part: 5000μA
O
□BF____μA
Max:
Normal condition(NC)
C
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
A
Location: Te chnician:
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PI
Equipment: Control Number:
O
Measurement equipment /SN: Date of Calibration:
C
Pass/Fa
INSPECTION AND TESTING Limit
il
A
1 Power Cord Plug
2
3
Device Enclosure and Accessories
Device Labeling PI
O
4 Protective Earth Resistance Ω Max 0.2 Ω
C
Normal
____μA
condition(NC) Max:
5 Earth Leakage NC: 5mA
A
condition(SFC)
□BF____μA
O
Normal Max:
Patient condition(NC) □CF____μA CF applied part:
C
□BF____μA
PI
Max:
7 Mains on Applied Part Leakage CF applied part: 50μA
□CF____μA
O
□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
A-12
All rights reserved - Mindray Medical Colombia
C
O
PI
A
C
O
PI
A
C
O
PI
A
C
O
PI
A
All rights reserved - Mindray Medical Colombia
C
O
PI
A
C
O
PI
A
C
O
PI
A
C
O