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Copyright
Copyright EDAN INSTRUMENTS, INC. 2008. All rights reserved.
Statement
Edan Instruments, Inc. (hereinafter called EDAN) makes no warranty of any kind with regard to
this material, including, but not limited to the implied warranties of merchantability and fitness
for a particular purpose. EDAN assumes no responsibility for any error that may appear in this
document, or for incidental or consequential damage in connection with the furnishing,
performance or use of this material.
No part of this document may be photocopied, reproduced or translated to another language
without prior written consent of EDAN.
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
this company, nor the rights of others. This company does not assume any liability arising out of
any infringements of patents or other rights of third parties.
The information contained in this document is subject to change without notice.
Upon request, EDAN may provide, with compensation, necessary circuit diagrams, and other
information to help qualified technician to maintain and repair some parts, which EDAN may
define as user serviceable.
-I-
-II-
Table of Contents
Chapter 1 General ...................................................................................................................... 1
1.1 Function Features ............................................................................................................ 1
1.2 Environment Requirement .............................................................................................. 2
1.3 Power Supply Requirement............................................................................................. 2
Chapter 2 Appearance Views .................................................................................................... 3
2.1 Top Panel......................................................................................................................... 3
2.2 Patient Cable Socket and Signal Interface ...................................................................... 3
2.3 Mains Connection and Switch......................................................................................... 5
2.4 Bottom Panel ................................................................................................................... 5
Chapter 3 Principle .................................................................................................................... 6
3.1 Abstract of theory of ECG operation............................................................................... 6
3.2 Composition of ECG....................................................................................................... 6
3.3 Lead................................................................................................................................. 7
3.4 Hardware Design Principle Description.......................................................................... 9
3.4.1 ECG Board description ....................................................................................... 10
3.4.2 Main control part description .............................................................................. 11
3.4.3 Power control part description ............................................................................ 12
Chapter 4 Tests ......................................................................................................................... 13
4.1 System Tests .................................................................................................................. 13
4.2 Application System Tests .............................................................................................. 13
4.3 Safety Tests.................................................................................................................... 15
Chapter 5 Electrocardiograph Servicing ............................................................................... 16
5.1 Disassembly Steps......................................................................................................... 16
5.2 Internal Boards and Interfaces....................................................................................... 19
5.3 Troubleshooting............................................................................................................. 23
Chapter 6 Electrocardiograph Installation............................................................................ 27
-III-
-IV-
Chapter 1 General
SE-3 is 3-channel electrocardiographs with 12 leads gathered simultaneously, visual display of
operation menu, ECG parameters as well as electrocardiogram.
3-channel ECG can be viewed on the LCD (liquid crystal display) screen of SE-3 simultaneously.
And it can be recorded by high-quality thermal recorder.
Manual, automatic, rhythm recording mode and USB print mode can be chosen conveniently.
Either mains supply or built-in rechargeable Lithium battery can be used as power.
With a high resolution thermal printer, 32-bit processor and huge capacity memorizer, SE-3 has
advanced performance and high reliability. And the compact size makes it suitable for clinic,
hospital and ambulance use.
Configurations: Main unit and accessories (power cord, earth wire, patient cable, electrodes and
thermal recording paper)
Note: It is not designed for internal use and direct cardiac application.
Automatic mode, manual mode, rhythm mode and USB print mode optional
Hint information for lead off, lack of paper and low battery capacity etc.
-1-
Working
Temperature:
-20~+55
5~40
Relative
Humidity:
Atmospheric
Pressure:
25%~93%
(Non-Condensing)
25%~80%
(Non-Condensing)
700hPa~1060hPa
860hPa~1060hPa
100V~115V/220V~240V
Rated frequency:
50Hz/60Hz
35VA
14.8V
3) Power Consumption:
35VA
4) Fuse Specification:
T200mA 250V 520 (for 220V~240V)
T400mA 250V 520 (for 100V~115V)
-2-
Recorder
External
Control Panel
Input/Output
Socket
RS232 Socket
Patient Cable Socket
Figure 2-1 Main Unit (320240 dot single color LCD Screen)
-3-
Signal
Pin
Signal
Pin
Signal
C2 (input)
SH
11
F (input)
C3 (input)
NC
12
NC
C4 (input)
NC
13
C1(input)
C5 (input)
R (input)
14
NC
C6 (input)
10
L (input)
15
N or RF (input)
2) RS232 Socket
WARNING
RS232 interface is 1500V AC isolated intensity and the maximum voltage applied
should not exceed +15V DC.
Signal
Pin
Signal
Pin
Signal
NC
NC
NC
RxD (input)
GND
NC
TxD (output)
NC
NC
Signal
Pin
GND
GND
GND
GND
-4-
Signal
4) USB Interface
Signal
Pin
VBUS
D+
D-
GND
WARNING
Signal
Battery Compartment
Fuse
Fuse Label
Label
-5-
Chapter 3 Principle
3.1 Abstract of theory of ECG operation
The heart is a power organ of the body blood circulation. Before the systole or diastole, a cardiac
impulse happens in the heart muscle, and a faint bioelectric current signal is thus generated. The
bioelectric current signal is transmitted through the whole body, and the electric potential
difference is generated on the different skin surfaces because of the different distances from the
heart.
The cardiogram is a record of the amplification of the electric potential distribution on the body
skin surface. The electric potential difference is sampled by the electrodes, and is amplified and
processed by the electrocardiograph, and at last it is recorded on the paper. From it the doctor can
detect if the heart has a disease. The Electrocardiograph is just a kind of medical electrical
equipment intended for producing cardiograms for diagnostic purposes with 10 associated
electrodes at certain specific locations on the body. They only record the heart's electrical activity.
They do not produce any electricity of their own. The test does not hurt and has no known side
effects. It does not require any preparation (except for possibly shaving chest hair to get a better
recording). The recording itself takes only a few seconds.
There has been more than one hundred years since the electrocardiograph was applied in clinical
diagnosis. It is an important measure in clinical diagnosis of heart-disease. This instrument has
been equipped in almost every hospital and clinic.
-6-
P wave: the sequential activation (depolarization) of the right and left atria
QRS complex: right and left ventricular depolarization (normally the ventricles are
activated simultaneously)
ST-T wave: ventricular repolarization
U wave: origin for this wave is not clear - but probably represents
"after-depolarizations" in the ventricles.
PR interval: time interval from onset of atria depolarization (P wave) to onset of
ventricular depolarization (QRS complex)
QRS duration: duration of ventricular muscle depolarization
QT interval: duration of ventricular depolarization and repolarization
RR interval: duration of ventricular cardiac cycle (an indicator of ventricular rate)
PP interval: duration of atria cycle (an indicator or atria rate)
3.3 Lead
It is important to remember that the 12-lead ECG provides spatial information about the
heart's electrical activity in 3 approximately orthogonal directions:
Right
Left
Superior
Inferior
Anterior
Posterior
-7-
Each of the 12 leads represents a particular orientation in space, as indicated below (RA =
right arm; LA = left arm, LL = left leg):
Bipolar limb leads (frontal plane):
Lead I: RA (-) to LA (+) (Right Left, or lateral)
Lead II: RA (-) to LL (+) (Superior Inferior)
Lead III: LA (-) to LL (+) (Superior Inferior)
Augmented unipolar limb leads (frontal plane):
Lead aVR: RA (+) to [LA & LL] (-) (Rightward)
Lead aVL: LA (+) to [RA & LL] (-) (Leftward)
Lead aVF: LL (+) to [RA & LA] (-) (Inferior)
Unipolar (+) chest leads (horizontal plane):
Leads V1, V2, V3: (Posterior Anterior)
Leads V4, V5, V6:(Right Left, or lateral)
2)
Front_end module including signal acquisition, digital filter and the amplifier;
3)
4)
5)
6)
-9-
This module is a 12-channel ECG signal sampling and processing module. It can realize the
amplification and pre-processing of patient ECG signal in every channel, and the detection of
lead situations, as well as sending data to ARM9 MCU. This module is connected to ARM9MCU
through UART port.
The standard 12-lead electrocardiograph has 10 lead cables, including 9 lead signal input and 1
Right Foot electrode as the float ground. The ECG signals pass through the defibrillator
protection circuit, buffering circuit (U1~U3), and enter the difference amplifier circuit. And then
they continue to pass through the pacemaker pulse restraining, high-pass filter, low-pass filter,
channel switch, second level amplification, and are sent to the A/D sampling port of
MSP430F147.
Because the ECG system must meet the safety requirement of the photo-electricity isolation, the
serial signals will be sent to the photo-electricity component.
The system uses ARM9 (S3C2410) (U1) as the control MCU, and the peripheral equipments are
connected to the MCU ports. The MCU controls the peripheral equipments by several kinds of
methods. The system expands 64M external SDRAM (U6, U7), 64M FLASH (U2), LAN
-11-
-12-
Chapter 4 Tests
4.1 System Tests
1. Unit appearance and assembly examinations
1) Clean appearance, firm assembly, no remainder in the unit when shaking it.
2) Keys feel well when pressing.
3) Labels are full and correct.
4) Standard configurations are full; Sockets are installed firmly.
5) Vibration test should be done before doing the following tests.
2. Switch on
After turned on, the electrocardiograph runs well and LCD screen displays well.
Model
ECG emulator
FLUKE MPS450
system will be shifted to the main interface automatically. And then enter the corresponding
interfaces of the System Setup window to set the current time and change some menu options and
exit.
Turn off the electrocardiograph, and turn on it five seconds later. When the electrocardiograph is
ready for examination and recording, observe if the time displayed on the LCD screen is the
current time. And enter the corresponding interfaces of the System Setup window to see if these
menus keep the changed options. Then restore these menus to the default values and turn off the
electrocardiograph. Five seconds later, turn on the electrocardiograph again. When the
electrocardiograph is ready for examination and recording, observe if the menus are still the
default options.
6. Heart Rate display tests
Set the heart rate output from the ECG emulator as different values, and the error of Heart Rate
values displayed on the LCD screen of electrocardiograph should be within 1bpm. When the
heart rate output from the ECG emulator is 240bpm, the electrocardiograph will give the hint
information of Heart Rate exceeding the limit and make an alarm sound.
7. Recording tests
1) Set the following values:
The heart rate output of ECG emulator is 80bpm, the work mode of electrocardiograph is auto,
the speed is 25mm/s, the AC Filter is off, the Lowpass Filter is 150Hz and all the options in the
Record Setting menu are on. Install the recording paper and press PRINT/STOP key to begin to
record. Examine whether the recording content are integrated and consistent with the information
displayed on the LCD screen.
2) Make the ECG detector output the sine wave with 2mV and 10Hz. Press PRINT/STOP key to
begin to record. Examine whether the recording content are integrated and consistent with the
information displayed on the LCD screen. The amplitude of ECG waveform of Lead I should not
be less than 25mm.
3) The ECG record includes: Date and time, ID, Name, Sex, Age, Sensitivity, Paper speed, filter,
Lead, 1mV calibration mark, ECG waveform, Heart Rate etc. Meanwhile, before recording ECG
wave, 1mV Calibration mark and lead names will be recorded. Recorded characters and
waveforms are clear.
4) Open the casing of recorder and remove paper, the hint information of Paper? should be
displayed. Install the paper again and close the casing of recorder, the hint information of
Paper? should disappear.
-14-
-15-
3. Disassembly steps of the upper unit (Configuration A--19264 dot single color LCD
screen)
The upper unit of the electrocardiograph (19264 dot single color LCD screen) includes the
-16-
lower casing of the displaying box, filmy switch panel, LCD screen, rotation base etc.
The disassembly steps:
Remove the cables between LCD screen , filmy switch panel and transfer board
.Remove the five crosshead panhead screws (M36), and dismantle the transfer board
Remove the four crosshead panhead screws (M38), and dismantle the upper casing of
the displaying box to show the LCD screen and rotation base fixed on the lower casing of
the displaying box. Remove the screws used to fix the LCD screen and dismantle the LCD
screen. Remove the two crosshead sunk screws (M320) to dismantle the lower casing of
the displaying box Remove the four crosshead sunk screws (M36) to dismantle the
rotation base .
The label (11) and filmy switch panel are sticked to the upper unit , and can be torn off.
Note: The LCD screen should be protected from being damaged when disassembling it.
4. Disassembly steps of the upper unit (Configuration B--320240 dot single color LCD
screen)
The difference between disassembling Configuration A and B is that the LCD screen of
Configuration B is embedded in the upper casing of the displaying box, while the LCD screen of
Configuration A is fixed in the lower casing of the displaying box by screws.
The following picture shows: crosshead panhead screws M36, transfer board, the
upper unit, rotation base, crosshead panhead screws M38, the lower casing of the
displaying box, crosshead sunk screws M36, crosshead sunk screws M320, LCD
screen, filmy switch panel, (11) the upper casing of the displaying box, (12) label, (13)
protection screen.
-17-
-18-
-19-
Pin
1
Description
Digital signal (output)
RxD (input)
Pin
Description
GND
TxD (output)
+5V
-20-
CON11-- Socket connected to ECG board. Please refer to P2 socket of ECG board for pin
information.
CON12-- Interface connected to recorder.
Pin
Description
Draw to GND
2, 15
+5V
Paper Detection
16
Temperature Detection
4, 5, 24
NC
6, 7, 25, 26
+8V
Data Output
Clock Output
GND
Description
1, 2, 3, 4
H: DISPLAY ON
6, 7, 8, 9, 21
10, 40
+3V
GND
NC
13
14
Restoration Signal
36
37, 39
38
Description
1, 2, 23, 24
NC
GND
+5V
5, 6
7, 8, 11, 12, 21
Restoration Signal
10, 13~20
36
37, 39
38
-22-
5.3 Troubleshooting
The electrocardiograph is a complicated electrical device and it is difficult for even an
experienced person to repair the internal hardware failure. The manufacture does not recommend
the user to repair it. Always call the representative of the manufacture for service if the device
failed to work.
This troubleshooting guide introduces the suitable actions for correcting the problems or
replacing the accessory or calling the service person. It can also help the user to have more exact
descriptions of the fault symptoms when call for service, which greatly makes the service fast and
efficient.
1. Troubles of the whole machine
Fault symptoms
Can not turn on the
electrocardiograph with mains
supply.
Can not turn on the
electrocardiograph with
battery.
Possible cause
Fuse failure
Interface board failure
Key panel failure
Battery failure
Interface board failure
Key panel failure
-23-
Correction action
Change fuse
Change interface board
Change key panel
Change battery
Change interface board
Change key panel
strong interference of
electric networks
ARM9 board failure
Out of work
Power supply or
plug-in unit on the master
control board failure
The power supply or
Fuse is burned when turning on
other component is
the electrocardiograph.
short-circuited.
Fuse is burned when
This component is
connecting a certain
short-circuited.
component.
2. Display troubles
Fault symptoms
Possible cause
Correction action
3. Transmission troubles
Fault symptoms
Possible cause
Correction action
-24-
4. Operation troubles
Fault symptoms
Possible cause
Correction action
Key failure
Buzzer failure
Change buzzer
Recording is illegible
-25-
Clean print-head
Change print-head
Clean the stain on the
detecting position of the
print-head
Change print-head
Change main board
5. Parameter troubles
Fault symptoms
Possible cause
Correction action
Install electrode clamp
again or clean electrode area
on body surface with alcohol
connect the patient cable
with the unit
Change ECG board
Install electrode clamp
again or clean electrode area
on body surface with alcohol
Change patient cable
Change ECG board
Waveform measuring
failure
Adjust connections
-26-
Before use, the equipment, patient cable and electrodes should be checked. Replace it if
there is any evident defectiveness or aging which may impair the safety or performance.
And be sure that the equipment is in proper working condition.
100V~115V or 220V~240V
50Hz/60Hz
35VA
Make sure the mains supply meets the above requirements before power on. And then press the
mains power switch to power on the unit. Then the mains supply indicator lamp ( ) will be lit.
If the built-in rechargeable battery is weak when mains supply used, it will be recharged
automatically at the same time. And both the mains supply indicator lamp (
recharging indicator lamp (
) will be lit.
) will be lit.
during storage and transport, the capacity of battery may not be full. If the symbol
and the
hint information BAT WEAK are displayed, which means the battery capacity is weak, please
-27-
Casing
Paper Tray
Paper Roller
Printer Platen
Groove
Place fingers under the flange of the recorder casing, pull upwards directly to release
the casing;
2)
Take out the paper roller, and remove remain paper from the left of roller if necessary;
3)
Take off the wrapper of thermal paper roll, and then put through the roller from the left
with the papers grid side facing downward;
-28-
4)
Place the paper and roller gently in the recorder with the roller pin on the rollers left
side facing to the groove;
5)
Pull about 2cm of paper out, and put down the recorder casing;
6)
Place fingers under the flange of the recorder casing, pull upwards directly to release
the casing;
2)
3)
Take off the wrapper of folded thermal paper, and then put it in the Paper Tray with the
papers grid side facing the thermal print head while put the free end of paper upright;
4)
Pull about 2cm of paper out, and put down the recorder casing;
5)
Patient cable includes two parts, main cable and lead wires with associated connectors, which
can be distinguished from the color and identifier on the connectors.
Main Cable
Lead Wires
Screw
Electrode Connectors
Connector
-29-
Suction Bulb
Electrode
Metal Cup
Limb Electrode:
Electrode
Reed
Clamp
The identifier and color code of electrodes used complies with IEC/EN requirements. In order
to avoid incorrect connections, the electrode identifier and color code is specified in Table 4-1.
Moreover the equivalent code according to American requirements is given in Table 4-1 too.
Table 4-1 Electrodes and their identifier and color code
European
Electrodes
Identifier
American
Color code
Identifier
Color code
Right arm
Red
RA
White
Left arm
Yellow
LA
Black
Right leg
N or RF
Black
RL
Green
Green
LL
Red
Left leg
Chest 1
C1
Red
V1
Red
Chest 2
C2
Yellow
V2
Yellow
Chest 3
C3
Green
V3
Green
Chest 4
C4
Brown
V4
Blue
Chest 5
C5
Black
V5
Orange
Chest 6
C6
Violet
V6
Violet
As the following figure shows, the chest electrodes position on body surface is
-30-
C1
C4
C2
C6
C3
C5
The contacting resistance between the patient and the electrode will affect the quality of ECG
greatly. In order to get a high-quality ECG, the skin/electrode resistance must be minimized
while connecting electrodes.
WARNING
WARNING
2)
Align all lead wires of patient cable to avoid twisting, and connect the associated
electrode connectors with corresponding electrodes according to the color and
identifier;
3)
4)
Daub the round area of 25mm diameter on each electrode site with gel evenly;
5)
Place a small mount of gel on the brim of chest electrodes metal cup;
6)
Place the electrode on chest electrode site and squeeze the suction bulb. Unclench it and
-31-
then the electrode is adsorbed on chest. Attach all chest electrodes in the same way.
Limb electrodes connection:
1)
2)
Align lead wires of patient cable to avoid twisting, and connect the electrode connectors
to corresponding electrodes according to the color and identifier;
3)
Clean electrode area on a short distance above the ankle or wrist with alcohol;
4)
5)
Place a small amount of gel on the metal part of limb electrode clamp;
6)
Connect the electrode to limb, and be sure that the metal part be placed on the electrode
area above the ankle or wrist. Attach all limb electrodes in the same way.
Check and make sure that there is no electromagnetic interference source around the
equipment, especially large medical electrical equipment such as electrosurgical
equipment, radiological equipment and magnetic resonance imaging equipment etc.
Switch off these devices when necessary.
Keep the examination room warm to avoid muscle action voltages in ECG signal
caused by cold.
2) Power Supply:
If mains power used, please check whether the power cord has been connected to the
unit well. And the grounded three-phase outlet should be used.
-32-
3)
Recharge the battery first when the battery capacity is weak before use.
Patient Cable:
Check whether the patient cable has been connected to the unit firmly, and keep it far
away from the power cord.
4) Electrodes:
Check whether all electrodes have been connected to lead wires of patient cable
correctly according to the identifier and color.
Ensure that the chest electrodes havent contacted with each other.
5) Recorder Paper:
6) Patient:
The patient should not contact with conducting object such as earth, and metal part of
bed etc.
WARNING
-33-
Chapter 7 Cleaning
7.1 Clean
CAUTION
Turn off the power before cleaning and disinfection. Mains supply must be switch off
if it has been in use.
Prevent the detergent from seeping into the main unit while cleaning. Do not
immerse the unit or patient cable into liquid under any circumstances.
CAUTION
Do not clean the unit and accessories with abrasive fabric and avoid scratching the
electrodes.
-34-
7.2 Disinfection
To avoid permanent damage to the equipment, disinfection can be performed only when it has
been considered as necessary according to your hospitals regulations.
Before disinfection clean the equipment first. Then wipe the surface of the unit and patient
cable with hospital standard disinfectant.
CAUTION
Do not use chloric disinfectant such as chloride and sodium hypochlorite etc.
-35-
Chapter 8 Maintenance
8.1 Recharge and Replacement of Battery
1) Capacity Identification
Current capacity of the rechargeable battery can be identified according to the battery
symbol in the top right corner on LCD screen.
: Full capacity
: Capacity is limited, and recharge should be taken into account
: Battery is weak; and warning message BAT WEAK will be displayed on LCD screen.
The battery should be recharged immediately
2) Recharge
SE-3 is equipped with recharge control circuit together with built-in rechargeable lithium
battery. When connect with the mains supply, the battery will be recharged automatically.
And then the battery recharge indicator lamp (
will be lit at the same time. During the course of recharging, the symbol
will flash in
the top right corner of LCD screen. When the capacity of battery is full, the symbol
will stop flashing, and the battery recharge indicator lamp (
if SE-3 is power off, the lamp will still lit just because the equipment will not monitor the
recharge status; so you need to power on the device to verify the status.
Because of the capacity consumption during storage and transport, the capacity of battery is
not full while using at the first time. Battery recharge should be considered before first
usage.
3) Replacement
When the useful life of battery is over, or foul smell and leakage has been found, please
contact with manufacturer or local distributor for replacement of battery.
WARNING
Only qualified service engineer authorized by EDAN can open the battery
compartment and replace the battery. And the battery of same model and
specification provided by manufacturer must be used.
-36-
When the batterys useful life is over, contact with the manufacturer or local
distributor for disposal or dispose the battery according to local regulations.
Record paper should be stored in dry, dark and cool area, avoiding excessive
temperature, humidity and sunshine.
Do not overlap the recorded paper long time, or else the ECG record may trans-print
each other.
equipment log. If the device is not functioning properly or fails any of the above tests, the
device has to be repaired.
WARNING
Failure on the part of the responsible individual hospital or institution employing the use
of this equipment to implement a satisfactory maintenance schedule may cause undue
equipment failure and possible health hazards.
1) Main Unit
Put on the dustproof coat after use and prevent from shaking violently when moving it
to another place.
Prevent any liquid from seeping into the equipment, for it will affect the safety and
performance of electrocardiograph.
2) Patient Cable
Integrity of patient cable, including main cable and lead wires, should be checked
regularly. And be sure that it is conductible.
Do not drag or twist the patient cable with excessive stress while using. Hold the
connector plugs instead of the cable when connect or disconnect the patient cable.
Align the patient cable to avoid twisting, knotting or crooking in closed angle while
using.
Store the lead wires in bigger wheel to prevent any people from stumbling.
Once damage or aging of the cable patient has been found, replace it with a new one
immediately.
3) Electrodes
Electrodes must be cleansed after use and be sure there is no remainder gel on them.
Keep the suction bulb of chest electrode from sunshine and excessive temperature.
After long-term use, the surface of electrodes will be oxidized because of erosion and
other causes. By this time, electrodes should be replaced to achieve high-quality ECG.
CAUTION
The equipment should be sent to the special agencies according to local regulation for
separate collection after its useful life.
-38-
Standards
Classification
Anti-electric-shock type:
Anti-electric-shock degree:
Type CF
Ordinary
equipment
(Sealed
equipment without liquid proof)
Disinfection/sterilization method:
Working mode:
Continuous operation
EMC:
Group , type A
Dimensions
288mm210mm70mm
Weight
About 2.5kg
Display
Environment
Transport /Storage
Working
Temperature:
-20~55
5~40
Relative
25%~93%
25%~80%
Non-Condensing
Non-Condensing
700hPa ~1060hPa
860hPa ~1060hPa
Humidity:
Atmospheric
Pressure:
Power Supply
Pack:
Recording
Power Consumption:
35VA (max)
Fuse:
Recorder:
Record Paper:
Rolled thermal paper, 80mm width
Effective Width:
Paper Speed:
HR
Recognition
ECG Unit
72mm
5mm/s, 10mm/s, 12.5mm/s, 25mm/s, 50mm/s
3%
Accuracy of data:
5% (x-axis), 5%(y-axis)
Technique:
Peak-peak detection
HR Range:
Accuracy:
1BPM
Leads:
12 standard leads
Acquisition Mode:
simultaneously 12 leads
A/D Resolution:
12 bits
Time Constant:
3.2s
Frequency Response:
0.05Hz ~ 150Hz
Sensitivity:
Input Impedance:
50M (10Hz)
50nA
<5 mVpp
-40-
Calibration Voltage:
1mV3%
Noise:
<12.5 Vp-p
Multichannel crosstalk
0.5mm
AC Filter: On/Off
DFT Filter: 0.05/0.15/0.25/0.5
Filter
EMG Filter: 25Hz/35Hz/OFF
LOWPASS Filter:150Hz/100Hz/75Hz
CMRR
110dB
Sampling Frequency
1000Hz
<10 A (220V~240V)
<0.1 A (DC)
Dielectric Strength:
4000V rms
External
Input/Output
Input
(Optional)
Output
-41-
FAX: 86-755-26882223
EC REPRESENTATIVE
Shanghai International Holding Corp. GmbH (Europe)
Eiffestrasse 80, D-20537 Hamburg Germany
TEL: +49-40-2513175
FAX: +49-40-255726
E-mail: antonjin@yahoo.com.cn