SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray)
owns the intellectual property rights to this product and this manual.
This manual may refer to information protected by copyrights or patents and does not
convey any license under the patent rights of Mindray, nor the rights of others. Mindray
does not assume any liability arising out of any infringements of patents or other rights of
third parties.
owned by Mindray in China and other countries.
, , and are the registered trademarks or trademarks
Revision History
This manual has a revision number. This revision number changes whenever the manual is
updated due to software or technical specification change. Contents of this manual are
subject to change without prior notice. The version information of this manual is as follows:
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.
This manual is based on the maximum configuration and therefore some contents may not
apply to your product. If you have any question, please contact our Customer Service
Department.
Observance of the manual is a prerequisite for proper equipment maintenance and prevents
equipment damage and personnel injury.
Intended Audience
This manual is for biomedical engineers, authorized technicians or service representatives
responsible for troubleshooting, repairing and maintaining the equipment.
1.1 Information of This Manual...................................................................................................................... 1-1
2.2 Connectors for Peripheral Devices........................................................................................................2-1
2.3 Main Unit ........................................................................................................................................................2-2
2.4 Front Housing Assembly...........................................................................................................................2-3
3.1 Unpacking the Equipment....................................................................................................................... 3-1
3.2 Preparation for Installation......................................................................................................................3-1
3.2.1 Preparation for Installation Site ................................................................................................ 3-1
3.4 Preparation for Power on..........................................................................................................................3-3
4 Testing and Maintenance...................................................................................................... 4-1
4.1.1 Test Equipment ...............................................................................................................................4-1
4.1.2 Test Report........................................................................................................................................4-1
4.4.2 NIBP Test ............................................................................................................................................4-4
4.5 Electric safety tests...................................................................................................................................... 4-8
5.2 Parts Replacement ......................................................................................................................................5-1
7.2 Main Unit ........................................................................................................................................................7-1
7.2.2 Parts List............................................................................................................................................. 7-2
7.3 Front Housing Assembly...........................................................................................................................7-3
7.3.2 Parts List............................................................................................................................................. 7-3
7.4 Main Bracket Assembly .............................................................................................................................7-4
7.4.2 Parts List............................................................................................................................................. 7-5
7.5 Power Management Board Assembly .................................................................................................7-6
7.5.2 Parts List............................................................................................................................................. 7-6
7.6.2 Parts List............................................................................................................................................. 7-7
7.7.2 Parts List............................................................................................................................................. 7-8
8 Hardware and Software Upgrade......................................................................................... 8-1
A Electrical Safety Inspection ..................................................................................................A-1
A.1 Power Cord Plug........................................................................................................................................ A-1
A.2 Device Enclosure and Accessories...................................................................................................... A-2
A.7 Mains on Applied Part Leakage ........................................................................................................... A-7
3
FOR YOUR NOTES
4
1 Introduction
1.1 Information of This Manual
A detailed revision history of this manual is recorded in the table below:
Version Revision History
1.0 New
1.2 Safety Information
DANGER
z Indicates an imminent hazard that, if not avoided, will result in death or serious
injury.
WAR NIN G
z Indicates a potential hazard or unsafe practice that, if not avoided, will result in
death or serious injury.
CAUTION
z Indicates a potential hazard or unsafe practice that, if not avoided, could result in
minor personal injury or product/property damage.
NOTE
z Provides application tips or other useful information to ensure that you get the
most from your product.
1.2.1 Dangers
There are no dangers that refer to the product in general. Specific “Danger” statements may
be given in the respective sections of this manual.
1-1
1.2.2 Warnings
WAR NIN G
z All installation operations, expansions, changes, modifications and repairs of this
product are conducted by Mindray authorized personnel.
z There is high voltage inside the equipment. Never disassemble the equipment
before it is disconnected from the AC power source or the battery.
z When you disassemble/reassemble a parameter module, a patient leakage
current test must be performed before it is used again for monitoring.
z The equipment must be connected to a properly installed power outlet with
protective earth contacts only. If the installation does not provide for a protective
earth conductor, disconnect it from the power line and operate it on battery
power, if possible.
z Disposal of the packaging material should observe the applicable waste control
regulations and keeping it out of children’s reach.
1.2.3 Cautions
CAUTION
z Make sure that no electromagnetic radiation interferes with the performance of
the equipment when preparing to carry out performance tests. Mobile phone,
X-ray equipment or MRI devices are a possible source of interference as they may
emit higher levels of electromagnetic radiation.
z Before connecting the receiver to the power line, check that the voltage and
frequency ratings of the power line are the same as those indicated on the unit’s
label or in this manual.
z Protect the equipment from damage caused by drop, impact, strong vibration or
other mechanical force during servicing.
1.2.4 Notes
NOTE
z Refer to Operator's Manual for detailed operation and other information.
1-2
1.3 Equipment Symbols
NOTE
z Not all the symbols listed below are applied to your equipment.
The following definition of the WEEE label applies to EU member states
only.
This symbol indicates that this product should not be treated as
household waste. By ensuring that this product is disposed of correctly,
you will help prevent bringing potential negative consequences to the
environment and human health. For more detailed information with
regard to returning and recycling this product, please consult the
distributor from whom you purchased it.
* For system products, this label may be attached to the main unit only.
Pediatric
Adult
Equipotentiality
Input/Output
Date of manufacture
Manufacturer
Insertion Direction
Protection against fluid
ingress
1-3
2 Theory of Operation
2.1 Overview
The monitor is intended for spot-check monitoring physiologic parameters, including SpO2,
PR, NIBP and TEMP, on adult, pediatric, and neonatal patients in healthcare facilities by
clinical physicians or appropriate medical staff under the direction of physicians.
2.2 Connectors for Peripheral Devices
1
2
3
1. Input/Output connect (RS-232 connector)
This connector is used for software upgrade and DIAP communication.
2. AC power input
3. Equipotential grounding terminal:
When the equipment and other devices are to be used together, their equipotential
grounding terminals should be connected together to eliminate the potential
difference between them.
2-1
2.3 Main Unit
The main unit of the vital signs monitor consists of three parts:
Front housing assembly, consisting of main board, segment-code display, and Power
On/Off keypad;
Rear housing assembly: power module (AC/DC), power management and interface
board (including SpO
(including three types of configuration, i.e. Mindray, Masimo, and Nellcor); and,
External module: Temp module.
The following figure shows the main unit architecture of the vital signs monitor.
Front Housing Assembly
Segment-code
display
Rear Housing Assembly
2600mAh
battery
isolation power), battery, NIBP module, and SpO2 board
2
I2C
Main board
Backlight
Power
management
and interface
board
Pump
SpO
(Mindray standard,
2
isolation power
NIBP module
SpO2board
OEM optional)
Power On/Off keypad
(indicator)
NIBP
receptacle
SpO
receptacle
2
External module
15V
AC-DC power
module
AC-IN
External connector
Only RS232 port (for
upgrade, screened for
end users)
Temp module
Temp probe
2-2
2.4 Front Housing Assembly
Main Board
Keypad
Main Board
The main board is the control center of the equipment. It provides communication and
display functions, including:
Communication with SpO
parameter measurement, and reading measured results;
Communication with Predictive/IR (Infrared Radiation) Temp module through serial
ports;
Communication with power management board through serial ports;
Extending an RS232 serial port;
Control over the Segment-code LCD display through I2C;
Providing backlight drive for segment-code display;
Recognition of keypad actions, and providing corresponding response;
Control over the beeper through IO port; and,
Providing 24 hour timing via the inner RTC.
board, and NIBP module through serial ports, starting
2
Keypad
The keypad consists of elements like keypad and AC/Battery indicator etc.
2-3
2.5 Rear Housing Assembly
Power management
and interface board
AC/DC power
module
SpO2 board
Battery
compartment
NIBP module
Rear housing assembly consists of power module (AC/DC), power management and
interface board (including SpO
board (including three types of configuration, i.e. Mindray, Masimo, and Nellcor).
SpO
2
isolation power), battery compartment, NIBP module, and
2
AC/DC Power Module
The AC/DC power board transforms the input AC into DC power, which is the power source
for all voltages in the equipment.
Power management and interface board
The power management interface board mainly provides the following functions:
Charge and discharge of battery and charge detection;
DC/DC conversion: outputs 12V and 5V DC power;
Control over power On/Off key and AC, BAT indicator;
Communication transmission among parameter modules;
2-4
Providing isolation power for Mindray/OEM SpO
module; and,
2
Providing external connectors, and also filter and protection for these connectors.
NIBP Module
The NIBP module consists of blood pressure measurement board and pump and valve
assembly, providing measurement acquisition of blood pressure data. The main functions of
the NIBP module are:
NIBP measurement; and,
Data exchange with the main board through the serial ports.
SpO2 board
The independently developed Mindray SpO2 board provides SpO2 measurement as good as
other boards but with smaller size and lower consumption. The power management and
interface board is also compatible with Nellcor NELL-1 SpO
board.
SpO
2
board and Masimo MS-2013
2
The SpO
board collects SpO2 signals, processes SpO2 algorithm and sends measurement
2
results to the main board. The power management interface board provides isolation power
for it.
2.6 External Module
An external Temp module can be extended on the monitor.
The independently developed Mindray Temp module consists of an isolation power board,
Temp measurement board, and probes. The Temp measurement board collects Temp signals,
processes algorithm and sends measurement results to the main board.
2-5
FOR YOUR NOTES
2-6
3 Equipment Installation
3.1 Unpacking the Equipment
Open the package and take out the packing list. Check that all the articles included in the
packing list are available and the quantity and specification are correct. Make sure that:
All the optional parts purchased by the customer shall also be checked.
Notify the supplier if provided components are not correct as compared to the packing
list.
In case of damage during transportation, keep the packing material and notify the
supplier immediately.
Keep the packing material till new equipment is accepted.
3.2 Preparation for Installation
3.2.1 Preparation for Installation Site
1. Ensure that the site meets all safety, environmental and power requirements.
2. Check that required power sockets are available.
3. Check that a network connector is available if the equipment needs to be connected to
network.
3.2.2 Environmental Requirements
To avoid explosion hazard, do not use the equipment in the presence of flammable
anesthetics, vapors or liquids. The environment where the equipment will be used should be
reasonably free from vibration, dust and corrosive substances. If these conditions are not
met, the system may not function normally.
The environmental specification is as follows:
Main Unit
Item
Operating
environment
Storage
environment
Temperature (℃)
0 to 40 (without Temp module)
5 to 40 (with Temp module)
-30 to 70 10% to 95% 16.0 to 107.4
Relative humidity
(noncondensing)
15% to 95% 57.0 to 107.4
Altitude (kPa)
3-1
NOTE
z The environmental specifications of unspecified parameters are the same as those
of the main unit.
3.2.3 Electrical Requirements
Check that the system cables, power cords, and power plugs are not damaged, and that
the pins are not loose. In case of any damage, remove it from use.
WARNI NG
z Only power sockets with protective grounding can be used.
z Use the supplied power cord only!
z If you doubt the completeness of the installation and cabling of the external
protective cables, disconnect the equipment from the power line and operate it
on battery. Otherwise, patient or operator might be shocked.
Voltage 100 to 240V AC
Current 0.9 to 0.5A
Frequency 50/60 Hz
3.3 Equipment Installation
Follow the procedure below to install the equipment:
1. Check the quantity of equipment and accessories as per the packing list.
2. Check for mechanical damages on the equipment and accessories.
3. Install the battery (optional). For detailed operations, please refer to the Operator's
Manual of the vital signs monitor.
4. Connect AC power.
5. Connect the accessories.
The vital signs monitor can be mounted on a wall bracket or on a trolley support. The wall
bracket or trolley support can be ordered optionally. Each type of mounting bracket is
delivered with a complete set of mounting hardware and instructions. For detailed
installation information, please refer to Wall- moun t Bra cket Instruc tions for Use (PN: 0010-20-42933) and Rollstand Instructions for Use (PN: 0010-20-42934).
3-2
CAUTION
z Use mounting brackets we supply or approve. If other compatible mounting
bracket is used, be sure it can be safely used on the vital signs monitor.
z The mounting bracket should be installed by our qualified service personnel, or
engineers who have adequate knowledge on it.
z If other mounting solution is used, the installation personnel and the customer
should verify if it can be safely used on the equipment, and the customer assume
the responsibility for any risk resulting from that.
3.4 Preparation for Power on
1. Before you start to make measurements, check the equipment for any mechanical
damage and make sure that all external cables, plug-ins and accessories are properly
connected.
2. Plug the power cord into the AC power source. If you run the equipment on battery
power, ensure that the battery is sufficiently charged.
3. Press the
button on the front panel to turn on the equipment.
3-3
FOR YOUR NOTES
3-4
4 Testing and Maintenance
4.1 Introduction
To ensure the equipment always functions normally, qualified service personnel should
perform regular inspection, maintenance and test. This chapter provides a checklist of the
testing procedures for the equipment with recommended test equipments and frequency.
The service personnel should perform the testing and maintenance procedures as required
and use appropriate test equipments.
The testing procedures provided in this chapter are intended to verify that the equipment
meets the performance specifications. If the equipment or a module fails to perform as
specified in any test, repairs or replacements must be done to correct the problem. If you
have any question, contact our Customer Service Department.
CAUTION
z All tests should be performed by qualified service personnel only.
z Service personnel should acquaint themselves with the test tools and make sure
that test tools and cables are applicable.
4.1.1 Test Equ i p ment
See the following sections.
4.1.2 Test Rep o r t
Upon the completion of the tests, the table of preventative maintenance test reports and
the table of maintenance test reports in this chapter should be kept properly.
4.1.3 Preventative Maintenance
Below are preventative maintenance tests which need to be performed on the monitor. The
recommended frequency of preventative maintenance is at least once per year. See the
following sections for detailed maintenance procedures.
Visual Inspection
NIBP test and calibration
4-1
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