Edan Instruments, Inc: Manual Ver: V1.0 Release Date: Aug. 2008 Part Number: MS1R-109399-V1.0
Edan Instruments, Inc: Manual Ver: V1.0 Release Date: Aug. 2008 Part Number: MS1R-109399-V1.0
Edan Instruments, Inc: Manual Ver: V1.0 Release Date: Aug. 2008 Part Number: MS1R-109399-V1.0
Statement
EDAN INSTRUMENTS INC. (hereinafter called EDAN) owns all rights to this unpublished
work and intends to maintain this work as confidential. EDAN may also seek to maintain this
work as an unpublished copyright. This publication is to be used solely for the purposes of
reference, operation, maintenance, or repair of our equipment. No part of this work can be
disseminated for other purposes.
In the event of inadvertent or deliberate publication, EDAN intends to enforce its rights to this
work under copyright laws as a published work. Those having access to this work may not copy,
use, or disclose the information in this work unless expressly authorized by our company to do
so.
All information contained in this publication is believed to be correct. EDAN shall not be liable
for errors contained herein nor for incidental or consequential damages in connection with the
furnishing, performance, or use of this material. This publication may refer to information and
protected by copyrights or patents and does not convey any license under the patent rights of
EDAN, nor the rights of others. EDAN does not assume any liability arising out of any
infringements of patents or other rights of third parties.
Content of this manual is subject to changes without prior notice.
NOTE:
This equipment is not intended for family usage.
WARNING :
This monitor is not a device for treatment purpose.
I
Using This Label Guide
This guide is designed to give key concepts on safety precautions.
WARNING
A WARNING label advises against certain actions or situations that could result in
personal injury or death.
CAUTION
A CAUTION label advises against actions or situations that could damage equipment,
produce inaccurate data, or invalidate a procedure.
Revision History
This service manual shall be revised whenever changes in regulatory requirements dictate.
II
Table of Contents
1 Introduction................................................................................................................. 1
1.1 General Information................................................................................................ 1
1.2 Screen Display ....................................................................................................... 2
1.3 Button Functions..................................................................................................... 5
1.4 Interfaces................................................................................................................ 7
1.5 Built-in Rechargeable Battery ................................................................................. 9
2 Principle .................................................................................................................... 12
2.1 General Parts .................................................................................................... 12
2.1.1 Parameter Measuring Part ............................................................................. 12
2.1.2 Main Control Part ........................................................................................... 13
2.1.3 Interface Part ................................................................................................. 13
2.1.4 Power Supply Part ......................................................................................... 13
2.1.5 Other Auxiliary Parts ...................................................................................... 13
2.2 Hardware Functional Principle .......................................................................... 13
2.2.1 Power Module ................................................................................................ 14
2.2.2 Main Control Board ........................................................................................ 16
2.2.3 Keyboard........................................................................................................ 17
2.2.4 Recorder Module ........................................................................................... 18
2.3 Software Function Principle............................................................................... 19
2.3.1 System Software ............................................................................................ 19
2.3.2 System Software Function ............................................................................. 20
2.4 System Parameters........................................................................................... 21
2.4.1 General .......................................................................................................... 21
2.4.2 NIBP............................................................................................................... 22
2.4.3 SpO2............................................................................................................... 22
3 Installation of Monitor .............................................................................................. 24
3.1 Open the Package and Check.............................................................................. 24
3.2 Connect the Power Cables ................................................................................... 24
3.3 Power on the Monitor ........................................................................................... 24
3.4 Connect Sensor to Patient.................................................................................... 25
3.5 Check the Recorder.............................................................................................. 25
3.6 Other Notes .......................................................................................................... 25
III
4 Test and Calculation................................................................................................. 26
4.1 Check the Monitor ............................................................................................. 26
4.2 NIBP Calibration................................................................................................ 26
5 Disassembly Graph .................................................................................................. 28
5.1 Disassembly Graph........................................................................................... 28
5.2 Front Shuck Assembly ...................................................................................... 28
5.3 Rear Shuck Assembly....................................................................................... 30
5.4 Bracket Assembly ............................................................................................. 30
6 Troubleshooting........................................................................................................ 32
6.1 Device Failures ................................................................................................. 32
6.2 Display Failures................................................................................................. 33
6.3 Operation, Recording, Network Linking Failures ............................................... 33
6.4 Power Board Failures........................................................................................ 34
6.5 Parameter Failures............................................................................................ 34
7 Maintenance and Cleaning ...................................................................................... 36
7.1 General Cleaning .............................................................................................. 36
7.1.1 Cuff Maintenance and Cleaning ..................................................................... 37
7.1.2 SpO2 Sensor Maintenance and Cleaning....................................................... 38
7.2 Maintenance Menu............................................................................................ 39
8 Accessories and Ordering Information................................................................... 41
9 Warranty and Service ............................................................................................... 43
AppendixⅠProduct Specification .............................................................................. 46
A1.1 Classification ...................................................................................................... 46
A1.2 Specifications ..................................................................................................... 46
A1.2.1 Size and Weight ........................................................................................... 46
A1.2.2 Environment ................................................................................................. 46
A1.2.3 Display ......................................................................................................... 46
A1.2.4 Battery.......................................................................................................... 47
A1.2.5 Recorder ...................................................................................................... 47
A1.2.6 Review ......................................................................................................... 47
A1.2.7 NIBP............................................................................................................. 47
A1.2.8 SpO2............................................................................................................. 48
IV
M3 Vital Signs Monitor Service Manual
1 Introduction
■ General Information
■ Screen Display
■ Button Functions
■ Interfaces
■ Built-in Chargeable Battery
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②
③
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Heart beat
ID Current patient ID
NIBP:
SYS, MAP, DIA (Unit: mmHg or kPa)
Information Area (③ ④)
The Information Area is at the bottom and right part of the screen, displaying operating state of
the monitor and status of the patient.
The information area contains following data:
Patient type and ID;
NIBP measuring mode;
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⑧
⑨
① ② ③ ④
Figure1-4 Buttons
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① ON/OFF When the monitor is off, press this button to turn on it.
When the monitor is on, press this button and hold for 3s
to turn off the monitor; Or press this button for less than
1s, the monitor will enter Sleep mode.
② SILENCE Press this button for less than 2s to pause audio alarm for
④ TREND/WAVEFORM Press this button to change the display screen for data list.
⑤ RECORD Press to print out current displayed trend list or alarm list.
OK
DOWN
Above the ON/OFF button are the charge indicator ⑧ and power indicator ⑨.
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1.4 Interfaces
For the convenience of operator, interfaces of different function are in different sites of the
monitor.
② ③
Figure1-5 Left Panel
WARNING
Only connect the device to EDAN supplied or recommended accessories.
Rear Panel
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M3 Vital Signs Monitor Service Manual
This symbol indicates that the instrument is IEC/EN60601-1 Type BF equipment. The unit
displaying this symbol contains an F-Type isolated (floating) patient applied part providing a high
degree of protection against shock, and is suitable for use during defibrillation.
①
③
②
Bottom panel
There are battery compartment and fuse box at the bottom panel.
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Battery
compartment
cover
Fuse
box
If the monitor is off, you can see recharging status from the charger indicator. Battery status light
is yellow when recharging, off when full.
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For recharging, the battery is 90% to 100% charged after 300min of recharging.
Replace Battery
During monitoring state or communication state, when the electric energy of battery is low or
empty, the battery state icon will display and flash.
When the lifespan of battery is over, or foul odor and leakage has been detected, please contact
with manufacturer or local distributor for replacement of battery.
WARNING
Do not take off the battery when monitoring.
The unexpected power supply off can not impact the monitor normal working, for it has
battery for standby.
WARNING
Stop using the battery if abnormal heat, odor, discoloration, deformation or abnormal
condition is detected during use, recharge, or storage. Keep it away from the monitor.
WARNING
Make sure the monitor is used in the appointed range of voltage, the effect of power
supply can be not noticeable.
WARNING
Before using the rechargeable battery, be sure to read the user manual and safety
precautions thoroughly.
WARNING
Do not place battery in the monitor with the (+) and (-) in the wrong way around.
WARNING
Do not connect the positive (+) and negative (-) terminals with metal objects, and do not
put the battery together with metal object, which can result in short circuit.
WARNING
Do not heat or throw battery into a fire.
Do not use, leave battery close to fire or other places where temperature may be above
60℃.
WARNING
Do not immerse, throw, and wet battery in water/seawater.
WARNING
Do not destroy the battery: Do not pierce battery with a sharp object such as a needle;
do not hit with a hammer, step on or throw or drop to cause strong shock; do not
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WARNING
Before transporting, the battery should be taken off from monitor.
WARNING
Please take out the battery before storing the monitor for more than 1 month.
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2 Principle
Interface part
Main
control
part Power supply
part
Parameter
measuring part
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Speaker Alarm
Battery board
Fan
LCD backlight
LCD data
Power Keyboard
module
Slave keyboard
Air pump,
2410 NIBP module Valve, Cuff
Main control
USB board Wireless
RJ45
board module
Port Network board
Nurse call
Recorder
NOTE:
The Nurse call board and the Network board are optional configuration, they can not be
installed at the same time. If you want to use the Nurse call function, you should install
the Nurse call board, otherwise you should install the Network board.
Schematic Diagram
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Battery
Fan
Power board
Power
control board
Principle Introduction
This module converts 220V AC mains power supply or battery power into 5V, 12V and -12V DC
supplies to power other boards. If AC mains and battery coexist, the former take the priority to
power the system and charge the latter at the same time.
AC/DC
Converts high-voltage AC supply into low-voltage DC supply to power subsequent circuits and
charge the battery.
5V DC/DC
Convert the DC supply from the previous circuit into stable 5V DC supply to power other boards.
12V/-12V DC/DC
Convert the DC supply from the previous circuit into stable 12V/-12V DC supply to power other
boards.
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TFT/VGA driver
CPLD driver
Watchdog
FLASH
Audio driver
slave chip2
Serial port
Serial port
slave chip
Serial port
USB port
0-2
Printer port
COM7
COM8
COM3
COM4
COM5
COM6
CPU System
CPU is the kernel of ARM9, it is the core part of the Main control board. CPU connects with other
periphery modules by bus and I/O cable, it can realize data communication, data processing,
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RTC
RTC can offer second, minute, hour, day, month, year and other calendar information. CPU can
gain such calendar information from RTC, it also can rewrite the data in RTC.
Ethernet Controller
Ethernet controller supports IEEE 802.3/IEEE 802.3u Ethernet standard, supports 10Mbpsdata
transmission rate. CPU exchanges data with Ethernet via Ethernet controller.
LCD Controller
LCD controller can control LCD display.
2.2.3 Keyboard
This module acts as the man-machine interface.
Schematic Diagram
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Principle Introduction
This module detects key and encoder input signals, converts them into codes and sends to Main
control board. Main control board sends command to the keyboard and the latter accordingly
control indicator and audio process circuit to realize audio and visual alarm.
CPU
Detect key and encoder input signals;
Control LED status;
Regularly zero Watchdog Timer;
Communicate with Main control board.
Watchdog
After power-on, supply Reset signal to CPU;
Provide functions of Waterdog Timer Output and voltage detection.
Schematic Diagram
Principle Introduction
This module receives printing data from Main control board. At the same time of converting the
data into dot matrix data and sending them to the thermal recorder, it also drives the recorder to
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CPU System
Process printing data;
Control recorder and step motor;
Collect recorder status information and realize corresponding control;
Communicate with Main control board.
Parameter Parameter
Para. Display Display
data alarm screen
Data output
Parameter analyse
analyse
measuring
Parameter
Module
Classify/
process
Recorder Recorder
output
Alarm
control LUNIX
Core Network
LUNIX
Core
Network
data Alarm
Send out indicator/
speaker
User
input GUI Interface
responsion output/
control Analog
Analog output
output
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It indicates software system inner the frame above, on the left of frame is software system input,
and on right is software system output; parameter measuring module exchanges data with
software system by serial ports, while user communicates with system by keyboard; among the
output devices, recorder and alarm devices receive data via serial ports, the analogue output
apparatus is MBUS, screen and network controller are controlled directly by CPU.
Once after
1 System initialization System initialization task
POST
Have record
7 Recorder task Accomplish output all the records
task
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2.4.1 General
Parameter module is the basic unit to acquire signals for monitoring parameters in monitor. The
results are transmitted to Main control board by keyset to finally accomplish processing and
displaying of data and waveforms. Main control board commends and module status messages can
also be transmitted via keyset. The keyset can also realize power switching and conversion. The
whole system structure is show in the figure below:
Medical staff
NIBP SpO2
Patient
As shown in the above figure, the two parameter modules execute real-time monitoring of NIBP,
SpO2 respectively through using cuff and measuring cables, the results can send to Main control
board for processing and displaying, and they can also be sent to recorder for output and printing.
Hereinafter the function details of parameter monitor will be explained.
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2.4.2 NIBP
Blood pressure monitors commonly measure arterial pressure, which is produced by the
contraction of the heart and constantly changes over the course of cardiac cycle. Three blood
pressure values, expressed in millimeters of mercury above atmospheric pressure, are typical
obtained. The systolic pressure is the maximum cycle pressure; which occurs during ventricular
contraction. The diastolic pressure is the minimum cycle pressure, occurring during the
ventricle’s filling stage between contractions. The means arterial pressure (MAP) is the mean
value of the blood pressure over the cardiac cycle.
The monitor measures non-invasive blood pressure using the oscillometric method. Following are
detailed measurement procedures. Inflate the cuff encircled the upper arm until the pressure in the
cuff blocking the blood flow in the artery of the upper arm. Then deflate the cuff gradually
according to the requirement of certain arithmetic. With the decreasing of the pressure in the cuff,
the artery blood will palpitate with the pulse, which results in palpitation in the cuff. Through the
pressure sensor connected with the inflating pipe of the cuff, a palpitation signal palpitating with
the pulse will be generated. After being filtered by a high-pass filter (about 1Hz), this signal
becomes pulsating signal and is amplified. Then the amplified signal is converted into digital
signal by A/D. After using the singlechip to process this digital signal, we may obtain systolic
pressure, diastolic pressure and mean pressure. Be careful to choose appropriate cuffs for
neonatal, pediatric and adult patients so as to avoid generating measurement error. NIBP module
also has protection circuit to prevent the cuff from being inflated to a very high pressure.
Following are the main operating modes of NIBP.
a. Adult/pediatric/neonate: select according to the patient shape, weight and age.
b. Manual measurement/auto measurement/continuous measurement: Manual measurement
is also called single measurement. It means the monitor performs only one measurement
for each time. Auto measurement means to perform one measurement within selected
cycle. Time interval can be set up as 1, 2, 3, 4, 5, 10, 15, 30, 60, 90, 120, 240 and 480
minutes. Continuous measurement means after being activated, the monitor will perform
quick measurement continuously within 5 minutes. Continuous measurement is effective
in monitoring changes in blood pressure.
2.4.3 SpO2
SpO2 is based on the absorption of pulse blood oxygen to red and infrared light by means of
finger sensor and SpO2 measuring unit. The light-electronic transducer in finger sensor converts
the pulse red and infrared light modulated by pulse blood oxygen into electrical signal, the signal
is processed by hardware and software of the unit. The PLETH curve and numeral value of SpO2
will be obtained.
By tracing the pulse waveform in the fingertip, using specified arithmetic and consulting the
clinical data table, we can obtain the SpO2 value. The SpO2 sensor consists of two LED and a
photodetector. The two LED are respectively red diode and infrared diode, which are lighted on
according to certain time sequence. When the capillary vessel of the fingertip congests repeatedly,
the light of the LED is absorbed by blood vessels and organs and then projected onto the
photodetector. The photodetector can detect the light intensity varying with pulse changes and
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M3 Vital Signs Monitor Service Manual
display the changing light intensity in the form of changing electronic signals. The ratio between
the DC and AC of the two types of signals for light is the proportion of oxygen in the blood. Then
we can calculate correct SpO2 value by using specified arithmetic and also calculate pulse rate
according to the SpO2 waveform.
The SpO2 module mainly consists of following four parts: sensor, signal processing, control unit
of LED driving sequence, singlechip.
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M3 Vital Signs Monitor Service Manual
3 Installation of Monitor
NOTE:
When the battery configuration is provided, after the monitor is transported or stored, the
battery must be charged. Powering on without connecting AC power supply may cause
the monitor out of work. Switch on AC power supply can charge the battery no matter if
the monitor is powered on.
NOTE:
Check all the functions that may be used to monitor and make sure that the monitor is in
good status.
NOTE:
If chargeable batteries are provided, charge them after using the monitor every time to
ensure the electric power is enough.
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NOTE:
For information on correct connection, refer to related chapters in User manual.
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M3 Vital Signs Monitor Service Manual
First check the device appearance and installation, and be sure that:
1) The shell of the device is clean and has no scratches. The installation is stable. When shaking
the device, these is no inside leftovers.
2) Buttons are smooth and free for operation.
3) Labels are complete and sufficient and correct in delivering information.
4) Standard configuration is complete, the sockets are installed safely. All the outer cables,
inserted modules and accessories are in good condition.
5) There is any mechanical damage.
If you find any damage on the monitor, stop using the monitor on patient, and contact the
biomedical engineer of the hospital or our company service personnel immediately.
Connect all the cables well, then turn on the monitor,the POST (Power-On-Self-Test) is
performed automatically. After successfully POST, the EDAN logo will display, then enter the
main interface.
Check if all the monitoring functions of the monitor can work normally so as to make sure that
the monitor is in good condition.
Routine Check
The overall check of the monitor, including the functional safety check, must be performed by
qualified personnel once every 6 to 12 month or each time after fixing up. All checks that need to
open the monitor enclosure must be performed by qualified service personnel.
WARNING
If the hospital or agency does not follow a satisfactory maintenance schedule when
using monitor, the monitor may become invalid, and the human health may be
endangered.
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M3 Vital Signs Monitor Service Manual
authorized by EDAN.
NOTE:
The calibration of NIBP is just a method for checking the measuring result, it will not
change the measuring standard.
Calibration procedure:
1. Connect air way as indicated in figure 4-1;
T-connector
Thermometer
Monitor
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M3 Vital Signs Monitor Service Manual
5 Disassembly Graph
This chapter introduces the inner structure and parts of the monitor, including disassembly graph,
front shuck assembly, rear shuck assembly and main bracket assembly.
6 7
1 2 3 4 5
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M3 Vital Signs Monitor Service Manual
29 30
28
16 19 20 24 25 27
14 15 17 18 21 22 23 26
31
32
33
34
11
1 2 3 4 5 6 7 8 9 10 12 13
1, 5, 7: Cross recessed pan head screw M3×6; 2: Main control board; 3: M3 Main control
board Insulated gasket; 4: M3 Screen bracket; 6: 5.7 inches LCD; 8, 21, 26: Cross
recessed pan head self-tapping screw ST3×8; 9: Main control keyboard; 10: M3 Main
control keyboard pressure plate; 11: M3 Main control keyboard silica gel button;12: M6
hexagon head nut and Φ6 washer; 13: M14 hexagon head nut; 14: Cross recessed pan
head self-tapping screw ST3×15 plain; 15: Cross recessed pan head screw M3×4 (iron);
16: M3 alarm light fixed board; 17: Alarm light board; 18: Cross recessed pan head
screw M2×3; 19: M3 short sponge bar 91.6×9×2.5; 20: M3 long sponge bar 136×9×2.5;
22: Insulated plain washer Φ10.3MM (red); 23: Slave keyboard; 24: M3 slave keyboard
pressure plate; 25: M3 slave keyboard silica gel button; 27: M3 copper grounding sets;
28: USB board; 29: M3 USB silica gel seal cover; 30: M3 alarm lampshade; 31: 5.7
inches LCD screen protection/Homochromy; 32: NIBP connector; 33: SpO 2 connector;
34: M3 front shuck and seal Φ2.0×160MM.
Figure5-2 Front shuck assembly
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10
7 8 9 - 11
12
6
13
14
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12
11 13 14
15
10
9 16
17
4 18
3 19
20 21
22 23 24 25
1: Label on M3 rear board; 2: Cross recessed countersunk head screw M3×6; 3: M3 rear
board; 4: M3 grounding wire pole; 5, 18: Nut M4; 6: AC power supply interface board; 7,
8, 12, 14, 16, 25: Cross recessed pan head screw M3×6; 9: Power board; 10: M3 power
module insulated gasket; 11: Lithium battery box connector components; 13: M3 main
bracket; 15: SpO2 module; 17: NIBP module; 19: M3 baffle; 20: Lithium battery; 21:
Network interface board; 22: M3 battery baffle; 23: M3 battery baffle torsion spring; 24:
M3 battery baffle fixed nut.
Figure5-4 Support assembly
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M3 Vital Signs Monitor Service Manual
6 Troubleshooting
In transportation, storage and use of monitor, various factors such as unstable network voltage,
changing environmental temperature, falling-down or impact, component aging may all result in
monitor failures and therefore affect normal application of the device. In failure conditions,
professional personnel with the experience of repairing electronic medical devices should
perform component-level upkeep for the failure classification listed in the table below.
Component-level upkeep means based on analyzing, replacing or trial-operating the component,
we can pinpoint the failure on a certain component of the device, such as power board, Main
control board, LCD assembly, measuring cable or parameter module, etc. Repair of only some
components means component-level repair. The repair operation must be conducted by a service
engineer with abundant experience and with the assistance of special equipment and in specific
environment and conditions.
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WARNING
Turn off the power and disconnect the line power before cleaning the monitor or the
sensor/probe.
CAUTION
Pay special attention to avoid damaging the monitor:
1) Avoid using ammonia-based or acetone-based cleaners such as acetone.
2) Most cleaning agents must be diluted before use. Dilute the cleaning agent as the
manufacturer's direction.
3) Do not use the grinding material, such as steel wool, etc.
4) Do not let the cleaning agent enter the monitor. Do not immerse any part of the
system into liquid.
5) Do not leave the cleaning agents at any part of the equipment.
CAUTION
1) Follow the manufacturer’s instruction to dilute the solution, or adopt the lowest
possible density.
2) Do not let liquid enter the monitor.
3) No part of this monitor can be subjected to immersion in liquid.
4) Do not pour liquid onto the monitor during sterilization.
5) Use a moistened cloth to wipe off any agent remained on the monitor.
CAUTION
Do not use EtO gas or formaldehyde to disinfect the monitor.
c. Hydrogen Peroxide 3%
d. Alcohol
e. Isopropanol
■ Sterilization
To avoid extended damage to the equipment, sterilization is only recommended when stipulated
as necessary in the Hospital Maintenance Schedule. Sterilization facilities should be cleaned first.
Recommended sterilization material:
1 Ethylate: 70% alcohol, 70% isopropanol
2 Acetaldehyde
■ Disinfection
To avoid extended damage to the equipment, disinfection is only recommended when stipulated
as necessary in the Hospital Maintenance Schedule. Disinfection facilities should be cleaned first.
WARNING
■ Do not squeeze the rubber tube on the cuff.
■ Do not allow liquid to enter the connector socket at the front of the monitor.
■ Do not wipe the inner part of the connector socket when cleaning the monitor.
■ When the reusable cuff is not connected with the monitor, or being cleaned, always
place the cover on the rubber tube to avoid liquid permeation.
The cuff can be sterilized by means of conventional autoclaving, gas, or radiation sterilization in
hot air ovens or disinfected by immersion in decontamination solutions, but remember to remove
the rubber bag if you use this method. The cuff should not be dry-cleaned.
The cuff can also be machine-washed or hand-washed, the latter method may prolong the service
life of the cuff. Before washing, remove the latex rubber bag, and for machine-washing, close the
Velcro fastening. Allow the cuff to dry thoroughly after washing. Then reinsert the rubber bag.
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To replace the rubber bag in the cuff, first place the bag on top of the cuff so that the rubber tubes
line up with the large opening on the long side of the cuff. Now roll the bag lengthwise and insert
it into the opening on the long side of the cuff. Hold the tubes and the cuff and shake the
complete cuff until the bag is in position. Thread the rubber tubes from inside the cuff, and out
through the small hole under the internal flap.
NOTE:
For protecting environment, the disposable blood pressure cuffs must be recycled or
disposed of properly.
WARNING
Before cleaning the monitor or the sensor, make sure that the equipment is switched off
and disconnected from the power line.
WARNING
Do not subject the sensor to autoclaving.
Do not immerse the sensor into any liquid.
Do not use any sensor or cable that may be damaged or deteriorated.
For cleaning:
n Use a cotton ball or a soft mull moistened with hospital-grade ethanol to wipe the surface of
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M3 Vital Signs Monitor Service Manual
the sensor, and then dry it with a cloth. This cleaning method can also be applied to the
luminotron and receiving unit.
n The cable can be cleaned with 3% hydrogen dioxide, 7% isopropanol, or other active reagent.
However, connector of the sensor shall not be subjected to such solution.
User Maintain
Input the password 9 9 8 1 in the USER KEY box and press OK button, the USER MAINTAIN
menu will pop up, in which you can set up following items.
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M3 Vital Signs Monitor Service Manual
NOTE:
Please restart the monitor after changing the language.
n ALM SOUND: You can set alarm sound to ON or OFF. For more details refer to Chapter
Alarm.
n NURSE CALL: turn on or off the nurse call. When the parameter alarm occurs, the monitor
gives 3s nurse call alarm prompt; if the audio alarm or the audio system is off, the monitor
can also give the nurse call alarm in abnormal condition.
n EXIT: exit the menu.
Factory Maintain
Factory maintenance function is only available for the service engineers of EDAN or
representative authorized by EDAN.
Enter factory maintain through password 9 9 8 0.
Set SpO2 and NIBP module by SPO2 DEV (SpO2 device) and NIBP DEV (NIBP device).
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NOTE:
For using neonatal disposable cuff, one NIBP Tube, one connecting tube and one
neonatal disposable cuff are necessary.
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EDAN on time. We will, at this option, dispatch the replace one(s) with confirmed shipping
invoice.
NOTE:
(1) Both Return Material Authorization Form and Declaration Form are offered
by EDAN service department once the SCF is confirmed by service
engineer.
(2) Customer is responsible for freight & insurance charges when the
equipment is shipped to EDAN for service including custom charges. EDAN
is responsible for the freight, insurance & custom charges from EDAN to
customer.
Out of Warranty:
After receiving the RMA from service department, customer sends defective parts to EDAN
in advance. We will analyze the problems and discuss with customer about either repairing or
replacing the part(s). Once the maintenance fee is invoiced and paid, we will make sure to
dispatch good part(s) to confirmed address.
NOTE: Customer is responsible for any freight & insurance charge for the
returned product.
(3) Obtain RMA Form.
Before the shipment of the materials, customer must obtain a RMA form from our service
department, in which the RMA number, description of returning parts and shipping
instruction are included. The RMA number should be indicated on the outside of the shipping
container.
NOTE: EDAN should not have any obligation to end-user or customer who
returns the goods without the notification by EDAN’s service department. The
sender takes the whole responsibility of accounted fee.
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Contact Information
If you have any question about maintenance, technical specifications or malfunctions of devices,
do not hesitate to contact us.
EDAN Instruments, Inc.
TEL: +86-755-26898321, 26899221
FAX: +86-755-26882223, 26898330
E-mail: [email protected]
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M3 Vital Signs Monitor Service Manual
AppendixⅠProduct Specification
A1.1 Classification
Anti-electroshock type ClassⅠequipment and internal powered equipment
EMC type Class A
Anti-electroshock degree SpO2, NIBP BF Defibrillation type
Ingress Protection IPX1
Working system Continuous running equipment (less than 7 days)
A1.2 Specifications
A1.2.2 Environment
Temperature
Working 5 ~ 40 °C
Transport and Storage -20 ~ 55 °C
Humidity
Working 25% ~ 80%(no coagulate)
Transport and Storage 25% ~ 93%(no coagulate)
Atmospheric pressure
Working 860 hPa ~ 1060 hPa
Transport and Storage 700 hPa ~ 1060 hPa
A1.2.3 Display
Device
5.7 inch, Monochrome LCD,
Resolution 320×240, LED backlight
Messages
1 Power Indicator LED (Green)
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A1.2.4 Battery
Quantity 1
Type Li battery
Power-off delay 5 ~ 15min
Voltage 14.8 VDC
Capacitance 4, 400 mAh
Working period >290min (at 25℃, continuous SpO2 measuring and
NIBP automatic measuring mode)
Rechargeable period <300min
A1.2.5 Recorder
Record Width 48 mm
Paper Speed 25mm/s
Recording types
Current displayed parameter list recording
Current displayed alarm list recording
A1.2.6 Review
A1.2.7 NIBP
Method Oscillometric
Mode Manual, Auto, Continuous
Measuring Interval in Auto Mode
1/2/3/4/5/10/15/30/60/90/120/240/480 min
Continuous 5min, 5s measuring interval
Measuring Type Systolic Pressure, Diastolic Pressure, Mean Pressure
Measuring Rang
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M3 Vital Signs Monitor Service Manual
Adult Mode
SYS 30~270mmHg
DIA 10~220mmHg
MAP 20~235mmHg
Pediatric Mode
SYS 30~235mmHg
DIA 10~220mmHg
MAP 20~225mmHg
Neonatal Mode
SYS 30~135mmHg
DIA 10~110mmHg
MAP 20~125mmHg
Cuff Pressure measuring Range 0~280mmHg
Pressure Resolution 1mmHg
Pressure Accuracy ±3 mmHg
Mean error ±5 mmHg
Maximum Standard deviation ≤8 mmHg
Entire Measuring Period 20~45s typical (depend on HR/motion disturbance)
Overvoltage protection Dual Overvoltage protection
Adult 297±3mmHg
Pediatric 240±3mmHg
Neonatal 145±3mmHg
A1.2.8 SpO2
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EDAN INSTRUMENTS, INC.
Addr: 3/F-B, Nanshan Medical Equipments Park, Nanhai Rd 1019#, shekou,
Nanshan Shenzhen, 518067 P.R. China
Tel: +86-755-26882220 Fax: +86-755-26882223