0705revd - Contents, SVC Man, Passport V PDF
0705revd - Contents, SVC Man, Passport V PDF
0705revd - Contents, SVC Man, Passport V PDF
Datascope
Passport®
Copyright © Mindray DS USA, Inc., 2009. All rights reserved. Contents of this publication may not be reproduced in any
form without permission of Mindray DS USA, Inc.
Foreword ....................................................................................................................................................... v
Warnings, Cautions, and Notes ....................................................................................................................... v
Warnings ...................................................................................................................................................... v
Cautions ........................................................................................................................................................ v
Notes ............................................................................................................................................................ vi
Theory of Operation ......................................................................................................... 1 - 1
Introduction ....................................................................................................................................................1 - 1
System Connections ........................................................................................................................................1 - 2
Mounting the Patient Monitor ....................................................................................................................1 - 2
Connectors for Peripheral Devices .............................................................................................................1 - 2
Main Unit ......................................................................................................................................................1 - 3
Input System ...........................................................................................................................................1 - 4
Output System.........................................................................................................................................1 - 4
Processing and Communications System.....................................................................................................1 - 6
Power Management System ......................................................................................................................1 - 6
Equipment Interface System.......................................................................................................................1 - 8
Parameter modules ..................................................................................................................................1 - 10
Block Diagrams ................................................................................................................ 2 - 1
Introduction ....................................................................................................................................................2 - 1
Block Diagram................................................................................................................................................2 - 2
Repair Information ........................................................................................................... 3 - 1
Introduction ....................................................................................................................................................3 - 1
Safety Precautions...........................................................................................................................................3 - 1
Troubleshooting Guidelines ..............................................................................................................................3 - 2
Special Tools Required ....................................................................................................................................3 - 2
Disassembly Instructions...................................................................................................................................3 - 2
Removal of the Key Panel and Keys ...........................................................................................................3 - 3
Removal of the Front Housing Assembly .....................................................................................................3 - 4
Removal of the Main Board ......................................................................................................................3 - 5
Removal of the Inverter .............................................................................................................................3 - 6
Removal of the LCD Panel .........................................................................................................................3 - 7
Removal of the Keyboard .........................................................................................................................3 - 8
Removal of the Alarm LED Board ...............................................................................................................3 - 9
Removal of the Encoder............................................................................................................................3 - 9
Removal of the Multi-parameter Board Assembly .........................................................................................3 - 10
Removal of the Parameter Front Panel Assembly ..........................................................................................3 - 12
Removal of the Multi-parameter board........................................................................................................3 - 13
Removal of the CO2 Module.....................................................................................................................3 - 13
Removal of the Masimo SpO2 Module .......................................................................................................3 - 14
Removal of the Nellcor SpO2 Module ........................................................................................................3 - 14
Removal of the NIBP Assembly ..................................................................................................................3 - 15
Removal of the Local Printer Assembly ........................................................................................................3 - 15
Removal of the Local Printer Cover (if needed).............................................................................................3 - 16
Removal of the Main Frame and Multi-parameter Board Assembly .................................................................3 - 16
Removal of the Speaker Assembly .............................................................................................................3 - 17
Removal of the Fan Assembly....................................................................................................................3 - 18
Removal of the CF Card Assembly .............................................................................................................3 - 19
Removal of the Power Board .....................................................................................................................3 - 19
Removal of the Li-ion Battery Interface Board Assembly.................................................................................3 - 21
Removal of the Interface Board Assembly ...................................................................................................3 - 23
Removal of the Wireless AP ......................................................................................................................3 - 25
Nurse Call Cable............................................................................................................................................3 - 27
Foreword
The Passport V Service Manual is intended as a guide for technically qualified personnel
during repair and calibration procedures. This publication may have been updated to reflect
product design changes and/or manual improvements.
A WARNING is provided to alert the user to potential serious outcomes (death, injury, or
serious adverse events) to the patient or the user.
A CAUTION is provided to alert the user to use special care necessary for the safe and
effective use of the device. They may include actions to be taken to avoid effects on patients
or users that may not be potentially life threatening or result in serious injury, but about which
the user should be aware. Cautions are also provided to alert the user to adverse effects on
this device of use or misuse and the care necessary to avoid such effects.
Warnings
WARNING: The Passport V operates on line voltages. Therefore, an
electric shock hazard may exist when the instrument covers
are removed. Repair and calibration procedures should only
be performed by qualified personnel who proceed with care
and follow proper servicing techniques. Warnings are given
in various chapters, as well as in other appropriate
locations.
WARNING: Internal Electrical Shock Hazard - This unit does not contain
any user-serviceable parts. Do not remove instrument
covers. Refer Servicing to qualified personnel.
Cautions
CAUTION: Calibration is not to be performed while monitoring a
patient.
CAUTION: Using dark colored soaks may stain the cuffs. Test a single
cuff to ensure that no damage will occur.
CAUTION: The internal sampling system of the Gas Module does not
need to be cleaned or sterilized. There is no reverse flow
back to the patient. If the internal sampling system is
suspected to be clogged or dirty, the module should be
serviced by an authorized service person only.
CAUTION: Never pull the local printer paper with force when a
recording is in process; it may cause damage to the local
printer.
CAUTION: Do not leave the local printer door open unless reloading
paper or troubleshooting.
Notes
NOTE: Unauthorized servicing may void the remainder of the
warranty. Check with the factory or with a local authorized
representative to determine the warranty status of a
particular instrument.
1.1 Introduction
This patient monitor is intended to be used for monitoring, displaying, reviewing, storing,
and transferring of multiple physiological parameters including: ECG, respiration (Resp),
temperature (Temp), SpO2, pulse rate (PR), non-invasive blood pressure (NIBP), invasive
blood pressure (IBP), End tidal CO2 value (EtCO2) and anesthetic gas (AG) of single adult,
pediatric, and neonatal patients.
1. Auxiliary Output
A standard BNC connector, through which defibrillator synchronization signals, analog
output signals, and nurse call signals can be outputted, depending on how the monitor is
configured.
2. SB Connector
A connector for an external storage device.
3. VGA Connector
A connector for a standard SVGA color monitor.
4. Network Connector
An RJ45 connector, through which an Ethernet network or a PC can be connected.
5. RS232 serial port
A DB9 connector, used to connect a PC for data or a Gas Module 3, depending on how
the monitor is configured.
6. RS232 serial port
A DB9 connector, used to connect a PC for data or a Gas Module 3, depending on how
the monitor is configured.
7. AC Power Connector
A connector for an AC power source (100 to 240 VAC, 50/60Hz).
8. Equipotential lug
A connector for common ground with other equipment.
• Input system:
keypad, knob, and power switch.
• Output system:
LCD panel, alarm LED board, local printer, speaker, AC/battery status LEDs).
• Processing and communications system:
CPU board, Power management and interface board.
• Power management system:
battery, battery interface board, power board (AC/DC), Power management and
interface board.
• Equipment interface system:
power management and interface board, Ethernet-wireless adapter.
• Parameter modules:
multi-parameter board, CO2 module, OEM SpO2 module, NIBP module.
Additionally, the patient monitor can also connect a DPM SB storage device, a Gas
Module 3, or a PC for data transfer.
Knob
The knob can be pressed, or rotated either clockwise or counter-clockwise. It connects to the
keypad.
Power switch
The power switch, located at the right side of the monitor, is a single-throw rocker switch.
Pressing it will power the monitor on or off. The power switch’s status is detected by the
power management and interface board.
Alarm Lamp
The monitor has an alarm lamp on the front panel. The alarm LED board converts the electric
signals into visual signals and then sends the visual signals to the alarm lamp through a light
pipe. The alarm lamp illuminates either red or yellow, depending on how the alarm is
configured.
Local Printer
The local printer receives data coming from the CPU board through a UART and then sends
them to the thermal print head for printing. The local printer has a hard key (starting/
stopping recordings) and a green LED on its front. It connects to the power management and
interface board.
LOCAL
LOCAL PRINTER
PRINTER
MAIN BOARD KEY BOARD
KEY BOARD
POWER
SUPPLY SIGNAL KEY & LED
INTERFACE INTERFACE INTERFACE
POWER DRIVE
CPU
MODULE POWER CIRCUIT
MOTOR
SUPPLY CONTROL
CONTROL
FPC INTERFACE
MODULE DESCRIPTION
Power supply interface Introduces a DC from the CPU board.
Power module Converts the input power into voltages that fit each module and
then forwards them to each module.
CPU Controls the communications between modules.
Signal interface Controls the communications between the CPU board and the
local printer CPU.
Drive circuit Receives control signals from the CPU and then forwards them to
the stepper motor.
Local Printer key board Sends key commands to the CPU and receives commands from
the CPU to control the LED on the local printer.
FPC interface Sends the thermal print head information to the CPU and
receives commands from the CPU to control the thermal print
head.
Speaker
The speaker provides sound for alarms, key strokes, heart beats, pulse, and so on. It is driven
directly by the CPU board.
The CPU board has a CPU system comprising the CPU, FLASH, memory, real-time clock,
EEPROM, FPGA, etc. Among them, FPGA deals with audio, video, and interfacing signals.
Also, it provides interfaces to other boards, modules, and devices.
Connections and communications with other components are implemented via the CPU
board, which provides interfaces to:
• A built-in display
• The power management and interface board. Between this board and the CPU board,
the signals of USB+Network+UART+SVGA+I2C+Speaker+GPIO are communicated.
Among them, UART signals finally go to the parameter boards.
• The keypad. Between the keypad and the CPU board, there are two signal wires: one is
the UART signal wire and another is the AC power and battery status signal wire.
• The alarm LED board
1. Auto-select the DC source between the power board and the two batteries.
2. Convert the DC source into 12V, 5V, and 3.3V DC and then output them to other boards
and modules.
3. Provide over-voltage and under-voltage protection for 12V, 5V, and 3.3V DC.
4. Detect the power switch status and control power on/off.
5. Detect the battery capacity and control battery charge/discharge.
6. Control the LED for battery and AC status.
7. Control the fan and detect its running status (the complex control algorithm is
implemented via the CPU board).
8. Detect the internal temperature of the patient monitor.
On this board there are four sub-boards: 3.3V and 5V DC board, 12V DC board, and two
battery charge boards. The 3.3V and 5V DC board converts the DC source into 5V and
3.3V. The 12V DC board converts the DC source into 12V DC. Both of them have an over-
current protection mechanism. Each of the two battery charge boards controls the charging
of a battery.
Power Battery
board interface
(AC/DC) board
16.8V 11.1V
Power management
and interface board DC source
auto-select
16.8V/11.1V
3.3V 5V 12V
DC/DC DC/DC DC/DC
3.3V 5V 12V
Backlight
LCD digital Local Wireless CO2 board
circuit Printer Adapter module
A USB HUB is located at the board. It receives USB signals from the CPU and then distributes
them to three USB ports, of which two connect the USB sockets, and the other connects the
CF control board.
This board provides connections for both wired network and wireless adapter. In the figure
below, switch 2 always stays off during normal use. The operator can switch between wired
network and wireless adapter through the software UI. Then, the CPU applies the operator’s
selection by controlling switch 1. In configuration mode, the CPU turns off switch 1 and then
turns on switch 2 so that the operator can connect a PC to the wired network to configure the
wireless adapter.
The CPU generates analog signals by controlling the DAC chip on the power management
and interface board via the I2C bus. The analog signals are transmitted to the BNC socket
via the amplifier circuit.
The signal r_flag from the multi-parameter board goes to the power management and
interface board. The CPU can select the source of defibrillator synchronization signals by
controlling the output of the DAC. The signal r_flag also goes to the CPU for a self-test.
Two UART interfaces (serial port 1 and serial port 2) from the CPU board are extended as
two RS232-level ports via the power management and interface board. Both interfaces can
be configured to accommodate a PC for data or an AG module.
• The multi-parameter board employs a high-speed DSP, making digital filtering, arrhythmia
analysis, and ST analysis faster and more effective.
• The DSP is in charge of 3- and 5-lead ECG monitoring, arrhythmia and ST analysis, RESP
monitoring, and communicating with the CPU board.
• The multi-parameter board also employs an MCU, which supports 1-channel temperature
measurement, DPM SpO2, and 2-channel IBP measurement. The MCU transfers all the
measurement data to the DSP.
• Respiration rate is monitored using the impedance method and can only be measured
with two ECG leads.
• The multi-parameter board integrates the DPM SpO2 circuit. If a monitor is configured
with an OEM SpO2 module, then DPM SpO2 functions are overridden.
CO2 Module
• There are two types of CO2 modules: DPM CO2 and Microstream CO2.
• The DPM CO2 module measures the CO2 concentration using the NDIR technology. It
performs a zero calibration periodically to ensure accurate measurements for a long
period of time. An appropriate compensation can be applied according to the patient
environment, thus preventing measurements from being influenced by interfering gases.
• The Microstream CO2 module ensures that measurements will not be affected by other
gases and the accuracy can be maintained without any gas compensation. Additionally,
the module has a very low sample flow rate, reducing its effect on the patient and the
environment to a minimum.
An isolation power board is attached to each of them and used to isolate the DC power and
the UART signal of the OEM SpO2 modules from other circuits in the main unit. The UART
signal comes from the CPU board and passes through the power management and interface
board.
NIBP Module
The figure below shows the NIBP module parameter board diagram.
PRESSURE OVER
PRESSURE SIGNAL PRESSURE
CUFF AMPLIFIER
SENSOR PROTECT
FOR CIRCUITS CIRCUIT ASYCHRONOUS
PROTECT FOR SERIAL
PROTECT COMMUNICATION
WATCHDOG
CPU
PRESSURE PRESSURE
PRESSURE SIGNAL SIGNAL
A/D
SENSOR AMPLIFIER CONVERTER
CIRCUITS
MOTOR CONTROL
FEEDBACK SIGNAL
MANIFOLD
PUMP AND
VALVE
VALVES FLASH DRAM
CONTROL
AND PUMP
CIRCUIT
The Passport V calculates NIBP values using the oscillometric method of noninvasive blood
pressure measurement. These measurements correspond to comparisons with auscultatory
values, measured using the fifth Korotkoff sound within ANSI/AAMI SP10 standards for
accuracy.
2.1 Introduction
The Block Diagrams indicate the internal organization of the instrument. The block diagrams are used to
gain both familiarity with the instrument and to locate malfunctioning PC boards as readily as possible.
NOTE: See Isometric Drawings and Parts List for a complete list of
Part Numbers.
3.1 Introduction
This chapter provides the necessary technical information to perform repairs on the
Passport V. The most important prerequisites for effective troubleshooting are a thorough
understanding of the instrument functions as well as understanding the theory of operation.
WARNING: Internal Electrical Shock Hazard - This unit does not contain
any user-serviceable parts. Do not remove instrument
covers. Refer Servicing to qualified personnel.
3. Release the key panel’s four clips from the bottom of the unit with a flat-bladed
screwdriver.
FIGURE 3-3 Remove the screws from the rear of the unit
3. Turn the unit over and carefully separate the front housing assembly and rear housing
assembly.
4. Disconnect the 50-pin ribbon cable from the front housing assembly.
FIGURE 3-4 Disconnect the ribbon cable from the front housing assembly
3. Carefully remove the knob with a pair of pliers that have protection on the jaws. Some
pliers may damage the knob.
4. Remove the nut that secures the encoder.
5. Remove the encoder carefully.
5. Remove the four screws that secure the assembly to the rear housing and main frame.
6. Disconnect the CO2 tubing and cable from the multi-parameter board assembly (if CO2
module is configured).
7. Remove the multi-parameter board assembly carefully.
3. Unfasten the two screws that secure the SpO2 connector and then remove the connector
(if Masimo or Nellcor SpO2 module is configured).
4. Remove the three screws that secure the parameter front panel.
5. Remove the parameter front panel.
4. Remove the water trap connector assembly or microstream CO2 connector fixture
assembly from the parameter front panel assembly (if necessary).
FIGURE 3-27 Remove the screws and cables from the main frame
5. Remove the two screws that secure the main frame from the bottom.
6. Remove the main frame and multi-parameter board assembly.
FIGURE 3-28 Remove the main frame and multi-parameter board assembly
FIGURE 3-29 Disconnect the speaker cable from the interface board
FIGURE 3-31 Disconnect the fan cable from the interface board
FIGURE 3-34 Remove the screws securing the local printer connecting board
3. Disconnect the power board connecting cable from the interface board.
4. Remove the three screws that secure the power socket support from the back of the main
frame.
5. Remove the screw that secures the grounding wire.
FIGURE 3-36 Remove the screws that secure the power socket
FIGURE 3-38 Remove the screws securing the local printer connecting board
4. Disconnect the Li-ion battery interface board cable from the interface board.
5. Remove the four nuts that secure the Li-ion battery interface board assembly.
6. Remove the Li-ion battery interface board assembly.
5. Remove the two screws that secure the main frame from the bottom.
6. Remove the main frame assembly and place to the side.
7. Disconnect the Li-ion battery interface board cable from the interface board.
8. Disconnect the power cable from the interface board.
9. Disconnect the local printer cable from the interface board.
14. Remove the two screws that secure the interface board assembly to the main frame.
15. Remove the interface board assembly.
5. Remove the two screws that secure the main frame from the bottom.
6. Remove the main frame assembly.
7. Remove the nut that secures the wireless AP to the main frame.
FIGURE 3-48 Remove the nut securing the wireless AP to the main frame
DESCRIPTION DASH #
10 24", snap, 5-lead set, Domestic -02
11 24", snap, 3-lead set, Domestic -05
12 24", snap, 5-lead set, International -11
13 24", snap, 3-lead set, International -14
FIGURE 3-66 5-pin Temp Cable for 400 Series Disposable Sensor
FIGURE 3-68 5-pin Temp Cable for MRS Disposable Sensor (5.5 DC Jack)
NOTE: Respiration
monitoring via the
ECG electrodes will
not be available
when using an ESIS
ECG cable.
Muscle Noise 1 Inadequate skin 1 Repeat skin preparation
preparation prior to and electrode location
application of electrode, procedures.
tremors, tense subject, 2 Apply fresh, moist
and/or poor electrode electrodes.
placement. 3 Avoid areas of the torso
that are very muscular.
Excessive alarms: heart rate, 1 Electrodes dry 1 Re-prep skin and apply
lead fault 2 Alarm limits set too close fresh, moist electrodes.
to patient's normal heart 2 Readjust.
rate. 3 Must have a higher
3 R-wave wrong size. amplitude than the other
4 Excessive patient ECG waves, like the P
movement or muscle and T waves.
tremor. 4 Reposition electrodes and
secure with tape, if
necessary.
ECG Noise 1 External interference. 1 Check patient.
2 Patient movement. 2 Check electrode contacts
/reposition electrodes/
cable.
3 Check environment for
source of interference.
No ECG Waveform 1 Gain set too low. 1 Readjust as required (Set
2 Lead wires and patient via the Size key).
cable not fully or properly 2 Check for proper
inserted. insertion.
3 Cable or lead wires 3 Check with lead
damaged. continuity tester.
The following items are set through the Installation Mode menu: Language, Date Format,
Time Format, NIBP Timeout, Temperature Units, Weight Units, Height Units, CO2 Units, ECG
Standard, Notch Filter, ESU Filter, SpO2 Sensor Off Audio, SpO2 Tones, Enable Arrhythmia
All Off Selection, Apnea Latch, Enable Silence All Permanent Selection, Auxiliary Output,
Nurse Call Mode, Set up Serial Port 1, Set up Serial Port 2, Copy Monitor Defaults to
Storage Device, Copy Monitor defaults from Storage Device, Reboot in demo mode, Restore
factory defaults, Advanced Installation Setup, Change Password, and Options.
1. Enter Installation Mode by pressing and holding the Discharge key while powering on
the monitor.
2. Set each item as necessary. The operation of the menu is the same as that of the normal
operating mode. To save all of the selected settings, choose Save Current before exiting
this menu. To access the normal operation screen, power the unit OFF and ON again.
MENU TITLE ON
SCREEN ACTIONS/
MENU CHOICES DEFAULT COMMENTS
Save Current Select to save current
settings as defaults.
Select Language English, French, English Select to change
German, Italian, language.
Spanish, Portuguese,
Russian, Dutch
Date Format M/D/Y, D/M/Y, Y/ M/D/Y Select to change date
M/D format.
Time Format 12 hour, 24 hour 12 hour Select to change time
format.
NIBP Timeout 15min, 30min, 15min Selects time old and
45min, 60min data is removed from
screen.
Temperature Units ºC, ºF ºF Select to change
temperature units.
Weight Units kg, lbs lbs Select to change
weight units.
Height Units cm, Ft/inches inches Select to change
height units.
CO2 Units mmHg, %, kPa mmHg Select to change CO2
units.
ECG Standard AHA, IEC AHA Select to change ECG
lead standard.
Notch Filter 50Hz, 60Hz 60Hz Select to change notch
filter frequency.
ESU Filter Auto, Disable Auto Select to change ESU
Filter setting.
SpO2 Sensor Off Off, Once, Repeat Off Select to change
Audio SpO2 Sensor Off
Audio.
SpO2 Tones Standard Tones, Standard Tones Select to change the
Alternative Tones SpO2 tones.
Enable Arrhythmia All Yes, No No Select to enable or
Off Selection disable the Arrhythmia
All Off menu
selection.
Apnea Latch On, Off On Select to turn apnea
alarm latching on or
off.
Enable Silence All Yes, No No Select to enable or
Permanent Selection disable the Permanent
Audio Off menu
selection.
Auxiliary Output Nurse Call, Analog Nurse Call Select to change the
Output, Defib Sync Auxiliary Output.
Nurse Call Mode Normally Open, Normally Open Select to change
Normally Close Nurse Call Mode.
Set up Serial Port 1 None, DIAP, Gas None Select to set up a
Module serial output protocol
port.
MENU TITLE ON
ACTIONS/
SCREEN
MENU CHOICES DEFAULT COMMENTS
Set up Serial Port 2 None, DIAP, Gas None Select to set up a
Module serial output protocol
port.
Copy Monitor Defaults Select to copy the
to Storage Device monitor defaults and
settings to the DPM SB
storage device.
Copy Monitor Defaults Select to copy the
from Storage Device monitor defaults and
settings from the DPM
SB storage device.
Re-boot in demo mode Yes, No No Set to YES to start the
monitor in demo mode
on next power-up.
Normal monitoring
will resume after
cycling power in
demo mode.
Restore factory Select to restore
defaults factory defaults.
Advanced Setup Select to view/edit
Advanced Setup.
Change Password Select to change
password.
Options Select to view/edit
options.
1. Insert the DPM SB storage device into the SB slot of the source monitor.
2. Access the Installation menu by pressing and holding the Discharge key while
powering on the monitor.
3. Select Copy Monitor Defaults to Storage Device. A status message will report completion
of the transfer.
4. Remove the DPM SB storage device and insert it into the SB slot of the receiving monitor.
5. Enter Installation Mode on the receiving monitor by pressing and holding the
Discharge key while powering on the monitor.
6. Select Copy Monitor Defaults from Storage Device. A status message will report
completion of the transfer.
7. Select Save Current and power-cycle the receiving monitor to enter normal monitoring
mode.
This menu is accessed by selecting Advanced Installation Setup from the Installation Menu.
Select each letter using the Navigator Knob. When finished, rotate to Previous Menu and
select using the Navigator Knob.
MENU TITLE ON
SCREEN MENU CHOICES DEFAULT TEXT STRINGS
DIAP Baud Rate 9600, 19200 9600 Select to change the
DIAP baud rate.
Enable Network Wired, Wireless Wired Select to change
network.
IP Address [0,255] 192.168.0.100 Select to set up IP
Address.
Subnet Mask ID [0,255] 255.255.255.0 Select to set up Subnet
Mask ID.
Configure Wireless Select to configure
AP wireless AP.
Search Printer Select to search
printer.
Paper Size A4, Letter A4 Select to change
paper size.
Device ID
Select Update Monitor From Storage Device from Options Menu to update the monitor via
DPM SB storage device. Updating via DPM SB storage device can only be used to enable
certain system functions.
The Update button only appears on the left of an item not yet updated (with “/” on the right)
after Update Monitor From Storage Device is selected and license file verification is passed.
When Update is selected, updating will begin. When update is complete, Permanent will be
displayed in Expiration column. If Update is selected again before the update is completed,
updating will be cancelled and “/” will be displayed.
Patient information and trend data stored in the CF card will be available if the monitor
restarts within one hour after being powered off. Otherwise, the data will be deleted.
The PC Software Upgrade Tool can create a network update package and license only when
the software is installed through the administrator’s serial number. The user can use the
upgrade package to upgrade the patient monitor.
To access the update mode, press the panel key Trends while powering up the monitor. If an
update signal from the same network is detected, the monitor starts to update software.
The monitor screen will indicate the BIOS version, Host software version, module version,
and corresponding status message. The status message “Upgrade is successful! Disconnect
the network cable, and reboot the monitor.” will display after download is complete.
To update by DPM SB storage device, select Options in installation mode. The update button
only appears after Update Monitor From Storage Device is selected and license file
verification is passed.
When Update is selected, updating will begin. When update is complete, Permanent will be
displayed in the Expiration column. If Update is selected again before update is complete,
updating will be cancelled and “/” will be displayed.
Updating by DPM SB storage device can only be used to enable certain system functions.
4.1 Introduction
This chapter provides information necessary to identify the replacement parts and assemblies
of instruments.
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5.1 Introduction
The following procedures are provided to verify the proper operation of the Passport V
Monitor. Service Diagnostics provides the capability of diagnosing problems within the
Passport V hardware. A menu driven interface, similar to that of the Passport V user
interface, is used to execute all tests.
5.4 Services
To enter the Service mode:
NOTE: The reference pressure can be set from 240 mmHg to 260
mmHg. The default pressure is 250 mmHg and the input
step is 1 mmHg.
5. When the pressure viewed on the manometer matches the reference pressure, select
Accept to accept the calibrated result. The measured pressure will replace the reference
pressure to complete the calibration.
5. Make sure the CO2 tubing is vented before flowing the gas. CO2 readings will appear
during the calibration.
6. After the measured CO2 concentration becomes stable, select Calibrate to calibrate the
CO2 module. Continue to steadily flow gas until a calibration message appears at the
bottom of the calibration tile.
7. If the calibration is successful, the message “Calibration Completed Successfully”
appears. Otherwise, the message “Calibration Failure” appears. If so, another
calibration is required.
6. The message “Feed Calibration Gas” will be displayed. At this time, vent the desired
standard gas or gas mixture to the tubing opening the gas valve. Gas values will appear
in the window as the Gas Module samples the calibration gas.
7. When the calibration is completed, the message “Feed Calibration Gas” will disappear
and the message “Complete” will be displayed next to each value that was successfully
measured. If at least one gas was successfully measured, the Accept menu choice will
become available. If the values are acceptable, select Accept. To cancel the calibration
and restore the previous calibration data, select Abort.
NOTE: For Gas Module 3, if any input data is corrupt or if there are
any other errors, a Calibration Error message will appear
after the Accept button is selected. The Gas Module 3 will
not accept span calibration with errors in any channel.
1. Select the Monitor Log using the NavigatorTM Knob to enter the Monitor Log Menu.
2. Errors log will appear on screen. Each error is time stamped and dated.
3. Use the NavigatorTM Knob to move the cursor within the list of errors.
4. To clear all data from the error log, use the NavigatorTM Knob to select Clear.
5.5 Verification
5.5.1 Initial Set-up
1. Using a patient simulator, connect the ECG, IBP1, IBP2 and temperature cables to the
left side connector panel. Set the ECG simulator for 60 bpms, 1mv QRS signal.
2. Set up the Patient Menu for Adult (Patient Size) as follows:
A. Monitor Setup
1. Display Setup – 3 Waveforms
2. ECG Speed – 25 mm/sec
3. IBP Speed – 25 mm/sec (optional)
4. Respiration / Gas Speed – 12.5 mm/sec
B. Print Setup
1. Waveform 1 – ECG 1
2. Waveform 2 – ECG 2
3. Select Printer – Local
C. Parameters
1. ECG
a. ECG 1 – II
b. ECG 2 – I
c. ECG 3 – III
d. ECG 1 thru 6 Size - 1 cm/mV
e. ECG 1 - I
f. ECG 2 - II
g. ECG 3 - III
h. ECG 4 - AVR
i. ECG 5 - AVL
j. ECG 6 – AVF
k. ECG 7 – V
2. NIBP
a. Set Start Pressure – 180 mmHg
Interval – 5 minutes
5. Respiration
a. Resp lead – II
b. Apnea Delay – 60
c. Resp source – Auto
d. Scale – 3
6. Gases (optional)
a. Select agent – Auto
b. O2 scale - 100%
c. Agent scale– 10%
5.5.2 ECG
5.5.2.1 Initialization
1. Observe that the trace display sweeps across the waveform 1 screen in six (6) seconds.
There should be six (6) complete ECG cycles. The same display and timing should be
seen on the Waveform 2 screen.
2. Check the following sweep speeds for the appropriate displays:
12.5 mm/sec – 12 second sweep/window
Heart Rate
1. Set the ECG simulator to ECG QRS Waveform. Set the rate to 250 bpm.
2. Verify the Rate display is 250 ± 5 bpm.
3. Decrease the rate to 30 bpm and allow signal to stabilize. Verify that the rate display is
30 bpm ± 3 bpm.
Alarms
1. Set the simulator to 1mv ECG QRS signal, rate set to 60 bpm.
2. Set to Print on Alarm, install paper in the local printer, and set the Low HR alarm to 50
bpm, and High alarm to 120 bpm.
1. Set the Simulator to 37° C. Connect to the monitor using a 400 series probe.
2. Verify the temperature is 37° ± 0.1°C.
Specifications: Verify the current reading of the test is less than 100 µA under normal
operating conditions Less than 300 µA under a single fault condition for 120 VAC and less
than 500 µA under a single fault condition for 230 VAC
Patient Leakage
1. Lead to ground: Sink Current Patient circuit (Test V, Model 431 Dempsey; patient
leakage with line voltage on leads).
2. Connect the ground wire from the safety analyzer to the equipotential lug of the monitor.
3. Connect the ECG cable from the Analyzer to the monitor.
4. On the safety analyzer depress the Apply 115 VAC button and note the reading.
5. Repeat the test for normal and open ground polarity combinations.
Specifications: Verify the current readings of the test are below 50µA under a single fault
condition.
1. Inspect outer case, line cords, rolling stands, wall mounts, modular accessories and
interconnecting cables.
2. Inspect patient interface connections (ECG, IBP, SpO2, Temp, CO2, and NIBP).
The equipment should be cleaned regularly. Please consult your hospital’s policy for the
recommended frequency for cleaning and disinfecting equipment.
The exterior surfaces of the equipment may be cleaned with a clean and soft cloth, sponge or
cotton ball, dampened with either of the following cleaning solutions:
1. Check sensors and cables daily for signs of damage. Replace as required.
2. Sensors should be cleaned before and after each new patient.
3. Wipe the patient contact area using a soft cloth with mild soap and water solution or
isopropyl alcohol. Hydrogen peroxide can be used to remove dried blood.
4. Allow the sensor to completely dry before using.
Cleaning
The cuff can be hand washed or machine washed in warm water or with mild detergent. The
bladder can be cleaned with a damp cloth. Air dry the cuff thoroughly after washing.
NOTE: Machine washing may shorten the service life of the cuff.
Disinfection
Disinfect the cuff with a damp cloth with 70% ethanol or 70% isopropanol or with ultraviolet.
Disinfect the bladder only with ultraviolet.
Replace the bladder after cleaning and disinfecting the cuff, as follows:
1. Place the bladder on the top of the cuff, as the figure shows.
2. Roll the bladder lengthwise and insert it into the large opening. See the figures below.
3. Hold the hose and the cuff and shake the complete cuff until the bladder is in position.
4. Thread the hose from inside the cuff, and out through the small hole under the internal
flap.
NIBP cuffs can be sterilized with gamma sterilization without affecting the repeated
performance of the cuff. Steam sterilization is not recommended. Use of a washing liquid
containing bleach is not recommended because chlorine will chemically break down the
urethane on the inside of the cuff.
Antimicrobial Definition
Bladderless cuffs are treated with an antimicrobial coating. Antimicrobial technology
effectively controls a broad spectrum of bacteria, fungi, algae and yeasts on a wide variety
of treated substrates.
CAUTION: The internal sampling system of the Gas Module does not
need to be cleaned or sterilized. There is no reverse flow
back to the patient. If the internal sampling system is
suspected to be clogged or dirty, the module should be
serviced by an authorized service person only.
1. The Water Trap Reservoir must be checked and emptied whenever changing patients or
if it is more than half full.
• To remove the water trap, push the water trap latch to the right. The water trap is
spring loaded and will pop out. An Air Leak message will be displayed. The monitor
will suspend sampling.
• Detach the reservoir from the water trap assembly by pulling it down carefully.
• Empty the reservoir and rinse with water only.
• Re-attach the reservoir to the assembly tightly.
• Re-install the whole unit into the Gas Module making sure the latch is set. Check that
the Air Leak message disappears and monitoring resumes.
Lithium-Ion
Storage of the lithium-ion batteries depends on temperature, time period and the degree of
cell charging state. After one month of storage at 23 degree, fully charged lithium-ion
batteries have a retention capacity of 96%.
1. Take measures against static electricity such as wearing a Disposable Wrist Strap for the
work.
2. Open the local printer door and remove the paper.
3. Gently wipe around the printhead using cotton swabs dampened with alcohol.
4. After the alcohol has been dried completely, reload the paper and close the local printer
door.
CAUTION: Do not use anything that may destroy the thermal element.
1. Use the latch at the upper right corner of the local printer door to pull the door open.
2. Remove the empty paper spool.
3. Insert a new paper roll so that it fits snugly into its housing and the sensitive side of the
paper faces the print head at the top of the local printer (paper feeding off of the spool
from the bottom).
4. Pull out approximately 4 inches of paper.
5. Align the paper across the top of the roller.
6. Holding the paper in place, close the local printer door.
7. To ensure that the paper is aligned properly and has not been pinched in the door, pull
the loose edge out a couple of inches. If the paper jams, open the door and return to
step 5.
CAUTION: Never pull the local printer paper with force when a
recording is in process. Otherwise, it may cause damage to
the local printer.
CAUTION: Do not leave the local printer door open unless you reload
paper or remove troubles.
• Ultraviolet Light
We recommend storing the recordings in a filing cabinet within a few days of printing.
Long term exposure to natural or artificial U.V. sources is detrimental.
• Storage Temperature and Humidity
Keep the recordings in a cool and dry area for a longer lasting image. Extreme
temperature and humidity (above 80° F/26° C and 80% humidity) should be avoided.
• Solvent Reactions
Do not store the recordings in plastic bags, acetate sheet protectors, or similar items
made from petroleum products. These products emit a small amount of vapor which will,
over a period of time, deteriorate the image on the chart paper.
• Adhesive Tape
Never place adhesive tape over recordings. The reaction between the adhesive
compound and the chemical/thermal paper can destroy the image within hours.
• Archives
We recommend that if long term archives are required, make a photocopy of the
recordings as back-up. Under normal office filing conditions, the recordings should retain
acceptable image quality for about five years
Except as otherwise provided herein, the terms, conditions and limitations of Mindray DS
USA, Inc.’s standard warranty will remain in effect.
Mindray DS USA, Inc. will not be liable for any incidental, special, or consequential loss,
damage, or expense directly or indirectly arising from the use of its products, liability under
this warranty and the buyer’s exclusive remedy under this warranty is limited to servicing or
replacing at Mindray’s option at the factory or at an authorized Distributor, any product
which shall under normal use and service appear to the Company to have been defective in
material or workmanship.
No agent, employee, or representative of Mindray DS USA, Inc. has any authority to bind
Mindray DS USA, Inc. to any affirmation, representation, or warranty concerning its
products, and any affirmation, representation or warranty made by any agent, employee, or
representative shall not be enforceable by buyer.
This warranty is expressly in lieu of any other express or implied warranties, including any
implied warranty or merchantability or fitness, and of any other obligation on the part of the
seller.
Damage to any product or parts through misuse, neglect, accident, or by affixing any non-
standard accessory attachments or by any customer modification voids this warranty.
Mindray DS USA, Inc. makes no warranty whatever in regard to trade accessories, such
being subject to the warranty of their respective manufacturers.
A condition of this warranty is that this equipment or any accessories which are claimed to
be defective be returned when authorized by Mindray, freight prepaid to Mindray DS USA,
Inc., Mahwah, New Jersey 07430. Mindray DS USA, Inc. shall not have any responsibility
in the event of loss or damage in transit.
Calibration may be performed without the need to disassemble the instrument. It is the
responsibility of the purchaser to perform calibration as necessary, in accordance with the
instructions provided in this manual.
Mindray DS USA, Inc. shall not be liable for any incidental, special, or consequential loss,
damage, or expense directly or indirectly arising from the use of its products, liability under
this warranty and the buyer’s exclusive remedy under this warranty is limited to servicing or
replacing at Mindray’s option at the factory or at an authorized Distributor, any product
which shall under normal use and service appear to the Company to have been defective in
material or workmanship.
No agent, employee, or representative of Mindray DS USA, Inc. has any authority to bind
Mindray DS USA, Inc. to any affirmation, representation, or warranty concerning its
products, and any affirmation, representation or warranty made by any agent, employee, or
representative shall not be enforceable by buyer.
This warranty is expressly in lieu of any other express or implied warranties, including any
implied warranty or merchantability or fitness, and of any other obligation on the part of the
seller.
Damage to any product or parts through misuse, neglect, accident, or by affixing any non-
standard accessory attachments or by any customer modification voids this warranty.
Mindray DS USA, Inc. makes no warranty whatever in regard to trade accessories, such
being subject to the warranty of their respective manufacturers.
A condition of this warranty is that this equipment or any accessories which are claimed to
be defective be returned when authorized by Mindray, freight prepaid to Mindray DS USA,
Inc., Mahwah, New Jersey 07430. Mindray DS USA, Inc. shall not have any responsibility
in the event of loss or damage in transit.
Calibration may be performed without the need to disassemble the instrument. It is the
responsibility of the purchaser to perform calibration as necessary, in accordance with the
instructions provided in this manual.
Please include the instrument model number, the serial number, and a description of the
problem with all requests for service.
Any questions regarding the warranty should be directed to the closest authorized location.
A list of international offices, along with their phone numbers, is provided at the end of this
manual.
Mindray Medical Netherlands B.V.• Drs. W. van Royenstraat 8 • P.O. Box 26 • 3870 CA
Hoevelaken • The Netherlands • Tel: +31 33 25 44 911 • Fax: +31 33 25 37 621
Mindray (UK) Limited • 3 Percy Road • St. John’s Park • Huntingdon • Cambridgeshire PE29 6SZ •
United Kingdom • Tel: 01480 416840 • Fax: 01480 436588
Mindray Medical France SARL • Europarc Créteil •123, Chemin des Bassins •
94035 Créteil Cedex • France • Tel: (0)1.45.13.91.50 • Fax: (0)1.45.13.91.51
Mindray Medical Germany GmbH • Zwischen den Bächen 4 • 64625 Bensheim • Deutschland •
Tel: +49.6251.17524-0 • Fax: +49.6251.17524-20
Mindray Medical International Ltd. • 2813 Office Tower, Convention Plaza • No 1 Harbour Road •
Wanchai • Hong Kong • Tel: +852 2793 5596 • Fax: +852 2344 8824
Medstar Importação e Exportação Ltda • Av. Vereador José Diniz, 3300 • São Paulo, SP • CEP
04804-000 • Brazil • Tel: 55 11 2872-3385 • Fax: 55 11 2872-3385
0002-08-8918