MANUAL Cardiografo EDAN-3

I

About this Manual

P/N: 01.54.20055-21

Release Date: July 2011

Copyright EDAN INSTRUMENTS, INC. 2005-2011. All rights reserved.

Statement

This manual will help you understand the operation and maintenance of the product better. It is

reminded that the product shall be used strictly complying with this manual. Users operation

failing to comply with this manual may result in malfunction or accident for which EDAN

INSTRUMENTS, INC. (hereinafter called EDAN) can not be held liable.

EDAN owns the copyrights of this manual. Without prior written consent of EDAN, any

materials contained in this manual shall not be photocopied, reproduced or translated into other

languages.

Materials protected by the copyright law, including but not limited to confidential information

such as technical information and patent information are contained in this manual, the user shall

not disclose such information to any irrelevant third party.

The user shall understand that nothing in this manual grants him, expressly or implicitly, any

right or license to use any of the intellectual properties of EDAN.

EDAN holds the rights to modify, update, and ultimately explain this manual.

Responsibility of the Manufacturer

EDAN only considers itself responsible for any effect on safety, reliability and performance of

the equipment if:

Assembly operations, extensions, re-adjustments, modifications or repairs are carried out by

persons authorized by EDAN, and

The electrical installation of the relevant room complies with national standards, and

The instrument is used in accordance with the instructions for use.

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.

II

Terms Used in this Manual

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.

NOTE

A NOTE provides useful information regarding a function or a procedure.

III

Table of Contents

Chapter 1 Safety Guidance ....................................................................................................... 1 1.1 Intended Use ..................................................................................................................... 1 1.2 Warnings and Cautions ..................................................................................................... 1

1.2.1 Safety Warnings........................................................................................................ 1 1.2.2 Lithium Battery Care Warnings................................................................................ 4 1.2.3 General Cautions ...................................................................................................... 5 1.2.4 Cleaning & Disinfection Cautions............................................................................ 6

1.3 List of Symbols ................................................................................................................. 7 Chapter 2 Introduction............................................................................................................ 10

2.1 Top Panel ........................................................................................................................ 11 2.2 Control Panel and Keys .................................................................................................. 12 2.3 Patient Cable Socket and Signal Interface ...................................................................... 15 2.4 Mains Connection and Switch ........................................................................................ 17 2.5 Bottom Panel................................................................................................................... 18 2.6 Features........................................................................................................................... 20

Chapter 3 About SE-3 Application Interface......................................................................... 21 3.1 About the Main Interface (SE-3 Wide Screen) ............................................................... 21 3.2 About the Main Interface (SE-3 Narrow Screen) ........................................................... 22 3.3 About the System Setup Interface................................................................................... 23 3.4 About the Recall Window ............................................................................................... 24

Chapter 4 Operation Preparations......................................................................................... 26 4.1 Power and Earthing......................................................................................................... 26 4.2 Loading/Replacing Recorder Paper ................................................................................ 27 4.3 Preparing the Patient ....................................................................................................... 29

4.3.1 Instructing the Patient ............................................................................................. 29 4.3.2 Preparing the Skin .................................................................................................. 29

4.4 Connecting the Patient Cable to the Electrocardiograph and Electrodes ....................... 30 4.5 Attaching Electrodes to the Patient ................................................................................. 30

4.5.1 Reusable Electrodes................................................................................................ 31 4.5.2 Disposable Electrodes............................................................................................. 33

4.6 Inspection Before Power On........................................................................................... 35 Chapter 5 Switching on the Electrocardiograph................................................................... 37 Chapter 6 Sampling and Printing ECG ................................................................................. 38

6.1 Entering Patient Information .......................................................................................... 38 6.2 Printing ECG Reports ..................................................................................................... 40

6.2.1 AUTO Mode ........................................................................................................... 40

IV

6.2.2 MANUAL Mode .................................................................................................... 41 6.2.3 RHYTHM mode ..................................................................................................... 42 6.2.4 USBPRT mode........................................................................................................ 42

6.3 Transmitting ECG Data to the PC................................................................................... 43 6.3.1 Transmitting ECG Data Through the Serial Port.................................................... 43 6.3.2 Transmitting ECG Data Through the Net Port (Optional, Only for Net Type) ...... 44

6.4 ECG Reports ................................................................................................................... 48 6.4.1 ECG Reports in the AUTO Mode........................................................................... 48 6.4.2 ECG Reports in the RHYTHM Mode .................................................................... 50 6.4.3 ECG Reports in the USBPRT Mode....................................................................... 52

Chapter 7 Managing ECG Records........................................................................................ 54 7.1 Transmitting ECG Records to the PC ............................................................................. 54

7.1.1 Transmitting ECG Records Through the Serial Port .............................................. 54 7.1.2 Transmitting ECG Records Through the Net Port (Optional, Only for Net Type). 56

7.2 Copying ECG Records Between SE-3 and the U Disk .................................................. 57 7.3 Deleting Patient Records ................................................................................................ 59 7.4 Printing a Patient Record in the Recall Window ............................................................ 60 7.5 ECG Copy....................................................................................................................... 61

Chapter 8 Settings (SE-3 Wide Screen).................................................................................. 62 8.1 Login Settings ................................................................................................................. 62 8.2 Recording Settings .......................................................................................................... 63

8.2.1 Lead Settings .......................................................................................................... 63 8.2.2 Pacemaker Detection Sensitivity Settings (Optional, with DE12 ECG Board) ..... 64 8.2.3 Sampling Mode Settings......................................................................................... 64 8.2.4 USB Printer Settings............................................................................................... 64 8.2.5 Recording Settings.................................................................................................. 65 8.2.6 Measurement and Interpretation............................................................................. 66 8.2.7 Parameter Options .................................................................................................. 67

8.3 General Settings.............................................................................................................. 68 8.3.1 Filter Settings.......................................................................................................... 68 8.3.2 External Input/Output Settings ............................................................................... 69 8.3.3 Key Beep & QRS Beep Settings ............................................................................ 69 8.3.4 IP Settings (Optional, Only for Net Type) .............................................................. 69 8.3.5 Save Option Settings .............................................................................................. 69 8.3.6 Transmission Settings ............................................................................................. 70 8.3.7 Parameter Options .................................................................................................. 70

8.4 System Settings............................................................................................................... 71 8.4.1 Display Mode Settings............................................................................................ 71

V

8.4.2 Parameter Options .................................................................................................. 73 Chapter 9 Settings (SE-3 Narrow Screen) ............................................................................. 74 Chapter 10 Switching off the Electrocardiograph ................................................................ 76 Chapter 11 Hint Information .................................................................................................. 77 Chapter 12 Troubleshooting.................................................................................................... 78 Chapter 13 Cleaning, Care and Maintenance ....................................................................... 81

13.1 Cleaning ........................................................................................................................ 81 13.1.1 Cleaning the Main Unit and the Patient Cable ..................................................... 81 13.1.2 Cleaning the Electrodes ........................................................................................ 81 13.1.3 Cleaning the Print Head........................................................................................ 81

13.2 Disinfection................................................................................................................... 82 13.3 Care and Maintenance .................................................................................................. 82

13.3.1 Recharge and Replacement of Battery ................................................................. 82 13.3.2 Recorder Paper ..................................................................................................... 83 13.3.3 Maintenance of the Main Unit, the Patient Cable and Electrodes........................ 84

Chapter 14 Accessories ............................................................................................................ 86 Chapter 15 Warranty and Service.......................................................................................... 88

15.1 Warranty........................................................................................................................ 88 15.2 Contact information ...................................................................................................... 88

Appendix 1 Technical Specifications ...................................................................................... 89 A1.1 Safety Specifications.................................................................................................... 89 A1.2 Environment Specifications ......................................................................................... 90 A1.3 Physical Specifications ................................................................................................ 90 A1.4 Power Supply Specifications ....................................................................................... 90 A1.5 Performance Specifications ......................................................................................... 91

Appendix 2 EMC Information................................................................................................ 93 Appendix 3 Abbreviation......................................................................................................... 97

SE-3 Electrocardiograph User Manual Safety Guidance

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Chapter 1 Safety Guidance This chapter provides important safety information related to the use of the 3-Channel Electrocardiograph.

1.1 Intended Use

The intended use of the 3-Channel Electrocardiograph is to acquire ECG signals from adult and pediatric patients through body surface ECG electrodes. The electrocardiograph is intended to be used only in hospitals or healthcare facilities by doctors and trained healthcare professionals. The cardiogram recorded by the 3-Channel Electrocardiograph can help users to analyze and diagnose heart disease. However the ECG with measurements and interpretive statements is offered to clinicians on an advisory basis only.

1.2 Warnings and Cautions

In order to use the electrocardiograph safely and effectively, and avoid possible dangers caused by improper operations, please read through the user manual and be sure to be familiar with all functions of the equipment and proper operation procedures before use.

Please pay more attention to the following warning and caution information.

NOTE:

1. This device is not intended for home use.

2. The pictures and interfaces in this manual are for reference only.

1.2.1 Safety Warnings

WARNING

1. The electrocardiograph is provided for the use of qualified physicians or personnel professionally trained. They should be familiar with the contents of this user manual before operation.

2. Only qualified service engineers can install this equipment, and only service engineers authorized by the manufacturer can open the shell.


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WARNING

3. Only qualified installation or service engineers can shift the mains supply shift switch (100V-115V~/220V-240V~) according to local mains supply specifications.

4. The results given by the equipment should be examined based on the overall clinical condition of the patient, and it can not substitute for regular checking.

5. This device is not intended for treatment or monitoring.

6. The EQUIPMENT is protected against malfunction caused by electrosurgery according to the clause 36.202.101 in the IEC60601-2-25.

7. Electrodes of dissimilar metals should not be used; it may cause a high polarization voltage.

8. EXPLOSION HAZARD - Do not use the electrocardiograph in the presence of flammable anesthetic mixture with oxygen or other flammable agents.

9. SHOCK HAZARD - The power receptacle must be a hospital grade grounded outlet. Never try to adapt the three-prong plug to fit a two-slot outlet.

10. If the integrity of the external protective conductor is in doubt, the equipment should be operated by using the built-in rechargeable battery.

11. Do not use this equipment in the presence of high static electricity or high voltage equipment which may generate sparks.

12. This equipment is not designed for direct cardiac application.

13. Only the patient cable and other accessories supplied by the manufacturer can be used. Or else, the performance and electric shock protection can not be guaranteed.

14. Make sure that all electrodes are connected to the patient correctly before operation.

15. Ensure that the conductive parts of electrodes and associated connectors, including neutral electrode, do not come into contact with earth or any other conducting objects.

16. Electrodes with defibrillator protection should be used while defibrillating. To avoid a polarization or DC offset voltage, use non-polarizing electrodes(which will not form a DC offset voltage when subjected to a DC current) such as silver/silver-chloride types if there is a situation where there is a likelihood that a defibrillation procedure will be necessary.


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WARNING

17. There is no danger for patients with pacemakers. However, if a pacemaker is used, the results given by the equipment may be invalid, or lose the clinical significance.

18. Do not touch the patient, bed, table or the equipment while using the ECG together with a defibrillator.

19. In order to avoid being burned, please keep the electrodes far away from the radio knife while using electrosurgical equipment.

20. If reusable electrodes with electrode gel are used during defibrillation, ECG recovery will take more than 10 seconds. The manufacturer recommends the use of disposable electrodes at all times.

21. Accessory equipment connected to the analog and digital interfaces must be certified according to the respective IEC/EN standards (e.g. IEC/EN 60950 for data processing equipment and IEC/EN 60601-1 for medical equipment). Furthermore all configurations shall comply with the valid version of the standard IEC/EN 60601-1-1. Therefore anybody, who connects additional equipment to the signal input or output connector to configure a medical system, must make sure that it complies with the requirements of the valid version of the system standard IEC/EN 60601-1-1. If in doubt, consult our technical service department or your local distributor.

22. The summation of leakage current should never exceed leakage current limits while several other units are used at the same time; otherwise, electric shock may happen.

23. The potential equalization conductor can be connected to that of other equipment when necessary, to make sure that all these devices are connected to the potential equalization bus bar of the electrical installation.

24. If the wireless AP technology is used, in order to maintain compliance with the FCC RF exposure guidelines, the wireless AP should be installed and operated with a minimum distance of 20cm between the radiator and the human body. Use the supplied antenna only. There should be no shield in or around the room where the wireless AP is used.

25. Fix attention on the examination to avoid missing important ECG waves.

26. The disposable electrodes can only be used for one time.

27. We recommend that the electrocardiograph should be working on AC power supply at least 8 hours per month to avoid DATE&TIME missing.


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1.2.2 Lithium Battery Care Warnings

WARNING

1. Improper operation may cause the lithium battery (hereinafter called battery) to be hot, ignited or exploded, and it may lead to the declination of the battery capacity. It is necessary to read the user manual carefully and pay more attention to warning messages.

2. Only qualified service engineer authorized by the manufacturer can open the battery compartment and replace the battery. The battery of the same model and specification provided by the manufacturer should be used.

3. Danger of explosion -- Do not reverse the anode and the cathode when installing the battery.

4. Do not heat or splash the battery or throw it into fire or water.

5. When leakage or foul smell is found, stop using the battery immediately. If your skin or cloth comes into contact with the leakage liquid, cleanse it with clean water at once. If the leakage liquid splashes into your eyes, do not wipe them. Irrigate them with clean water first and go to see a doctor immediately.

6. The device and accessories are to be disposed of according to local regulations after their useful lives. Alternatively, they can be returned to the dealer or the manufacturer for recycling or proper disposal. Batteries are hazardous waste. Do NOT dispose of them together with house-hold garbage. At the end of their lives hand the batteries over to the applicable collection points for the recycling of waste batteries. For more detailed information about recycling of this product or the battery, please contact your local Civic Office, or the shop where you purchased the product.

7. Remove the battery from the electrocardiograph when the electrocardiograph is not used for a long time.

8. If the battery is stored alone and not used for a long time, we recommend that the battery should be charged at least once every 6 months to prevent overdischarge.


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1.2.3 General Cautions

CAUTION

1. Federal (U.S.) law restricts this device to sale by or on the order of a physician.

2. Avoid liquid splash and excessive temperature. The temperature must be kept between 5 C and 40 C during operation, and it should be kept between -20 C and 55 C during transportation and storage.

3. Do not use the equipment in a dusty environment with bad ventilation or in the presence of corrosive.

4. Make sure that there is no intense electromagnetic interference source around the equipment, such as radio transmitters, mobile phones etc. Attention: large medical electrical equipment such as electrosurgical equipment, radiological equipment and magnetic resonance imaging equipment is likely to bring electromagnetic interference.

5. Before use, the equipment, the patient cable and electrodes etc. should be checked. Replacement should be taken if there is any evident defectiveness or aging symptom which may impair the safety or the performance.

6. The following safety checks should be performed at least every 24 months by a qualified person who has adequate training, knowledge, and practical experience to perform these tests.

a) Inspect the equipment and accessories for mechanical and functional damage.

b) Inspect the safety related labels for legibility.

c) Inspect the fuse to verify compliance with rated current and breaking characteristics.

d) Verify the device functions properly as described in the instructions for use.

e) Test the protection earth resistance according to IEC/EN 60601-1: Limit: 0.1ohm.

f) Test the earth leakage current according to IEC/EN 60601-1: Limit: NC 500 A, SFC 1000A.

g) Test the enclosure leakage current according to IEC/EN 60601-1: Limit: NC 100A, SFC 500A.


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CAUTION

h) Test the patient leakage current according to IEC/EN 60601-1: Limit: NC a.c. 10A, d.c. 10A; SFC a.c. 50A, d.c. 50A.

i) Test the patient auxiliary current according to IEC/EN 60601-1: Limit: NC a.c. 10A, d.c. 10A; SFC a.c. 50A, d.c. 50A.

j) Test the patient leakage current under single fault condition with mains voltage on the applied part according to IEC/EN 60601-1: Limit: 50A (CF).

The data should be recorded in an equipment log. If the device is not functioning properly or fails any of the above tests, the device has to be repaired.

7. Ruptured fuse must only be replaced with that of the same type and rating as the original.

1.2.4 Cleaning & Disinfection Cautions

CAUTION

1. Turn off the power before cleaning and disinfection. If the mains supply is used, the power cord should be dragged out of the outlet. Prevent the detergent from seeping into the equipment during cleaning.

2. Do not immerse the unit or the patient cable into liquid under any circumstances.

3. Do not clean the unit and accessories with abrasive fabric and avoid scratching the electrodes.

4. Any remainder of detergent should be removed from the unit and the patient cable after cleaning.

5. Do not use chloric disinfectant such as chloride, sodium hypochlorite etc.


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1.3 List of Symbols

External output

External input

Equipment or part of CF type with defibrillator proof

Caution

Consult Instructions for Use

Potential equalization

Mains supply

On (mains supply)

Off (mains supply)

Battery indicator

Battery recharging indicator

Sensitivity switch key

Recall key


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1mV calibration key& Copy key

Mode/RST switch key

Lead switch key

ON/OFF key

Menu key

Up arrow/Down arrow key

Left arrow/ Right arrow key

Print/Stop key

Recycle

Part Number

Serial Number

Date of Manufacture

Manufacturer

Authorized Representative in the European Community


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The symbol indicates that the device complies with the European Council Directive 93/42/EEC concerning medical devices.

It indicates that the device should be sent to the special agencies according to local regulations for separate collection after its useful life

Rx only (U.S.) Federal (U.S.) law restricts this device to sale by or on the order of a physician

SE-3 Electrocardiograph User Manual Introduction

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Chapter 2 Introduction SE-3 3-channel electrocardiograph gathers ECG signals of 12 leads simultaneously. It displays the operation menu, ECG parameters as well as electrocardiograms.

3-channel ECG waves can be viewed on the LCD screen and printed out by using a high-quality thermal recorder.

The auto, manual, rhythm, USB print and off modes can be chosen freely.

SE-3 can be powered by the mains supply or a built-in rechargeable lithium battery. Basic type and Net type are optional for each model, only the Net type electrocardiograph can support network transmission function. The DE12 ECG board is optional for all the models. With the DE12 ECG board, SE-3 can support full-scale pacemaker detection function.

With a high resolution thermal recorder, a 32-bit processor and a large-capacity memorizer, SE-3 has advanced performance and high reliability. The compact size makes it suitable for clinic, hospital and ambulance use.

Configuration: main unit, power cord, earth wire, patient cable, electrodes, thermal recorder paper, fuses and lithium battery

WARNING

1. This equipment is intended for use on adult and pediatric patients only.

2. This equipment is not designed for direct cardiac application.

3. The results given by the equipment should be examined based on the overall clinical condition of the patient, and it can not substitute for regular checking.


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2.1 Top Panel

Figure 2-1 SE-3 (320240 dot single color LCD screen, hereinafter called SE-3 Wide screen)

Figure 2-2 SE-3 (19264 dot single color LCD screen, hereinafter called SE-3 Narrow screen)

LCD Screen

Patient Cable Socket

EDAN SE-3

Recorder Paper

RS232 Socket

Recorder

Control Panel External Input/Output Socket

USB Interface

LCD Screen

Patient Cable Socket

EDAN SE-3

Recorder Paper

RS232 Socket

Recorder

Control Panel

External Input/Output Socket

USB Interface


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2.2 Control Panel and Keys

SE-3 Control Panel and Keys

1) Indicator Lamp

Mains supply indicator lamp: when the device is powered by the mains supply, the lamp will be lit.

Battery indicator lamp: when the device is powered by a built-in rechargeable lithium battery, the lamp will be lit.

Battery recharging indicator lamp: when the battery is being recharged, this lamp will be lit.

2) Sensitivity Switch Key

The sensitivity switch order: 10 mm/mV 20 mm/mV AGC (Auto Gain Control) 2.5 mm/mV 5 mm/mV.

3) Recall Key

Press the RECALL key to open the recall window. For details, see chapter 7, Managing ECG Records.


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4) 1mV/COPY Key

In the Manual mode, press this key to print a 1mV calibration mark while printing ECG reports.

In the AUTO mode, once the hint information COPY appears on the LCD screen, pressing the 1mV/Copy key can print the ECG report which was printed out last time.

5) MODE/RST Key

Press this key to select a printing mode among AUTO, MANUAL, RHYTHM, USBPRT and OFF.

The switch order of lead groups in each mode is listed in Table 2-1.

In the MANUAL mode, press this key to reset the waveform quickly while printing ECG reports.

WARNING

When using the device with a defibrillator, after the defibrillator discharges, you should press the MODE/RST key to reset the waveform quickly.

Note: The detailed information of the automatic mode can be set on the system setup interface.

Table 2-1 Switch Order of Lead Groups in Different Modes

Mode Switch Order (from Left to Right)

AUTO(Standard) // aVR/aVL/aVF V1/V2/V3 V4/V5/V6 AUTO(Cabrera) aVL/ I /-aVR II /aVF/ III V1/V2/V3 V4/V5/V6

MANUAL

In this mode, you need to press the Lead switch key to change the lead groups, the lead switch order can be that of AUTO (Standard) or AUTO (Cabrera), which is determined by settings of lead sequence and printing format on the system setup interface.


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6) LEAD Switch Key

In the MANUAL mode, press this key to switch the lead groups.

For SE-3 Narrow screen, press this key to switch to the prev or next page of the system setup interface, or press this key to switch to the prev or next page of records in the recall window.

7) PRINT/STOP Key

Press this key to begin or stop printing ECG reports.

8) ON/OFF Key

Press this key to turn on or off the device.

9) MENU Key

Press this key to open the system setup interface.

10) Up Arrow/Down Arrow Key

Press the Up or Down arrow to select an item on the main interface and the system setup interface.

11) Left Arrow/ Right Arrow Key

Press the Left or Right arrow to set the selected item.


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2.3 Patient Cable Socket and Signal Interface

As Figure 2-1 and Figure 2-2 show, on the right side of the main unit are the patient cable socket, the RS232 socket, the external input/output socket and the USB interface.

The net port (optional, only for Net type) is on the back of the main unit shown in the following figure. Only the electrocardiograph with net port can support network transmission function.

1) Patient Cable Socket

: Applied part of type CF with defibrillator proof

: Caution

Definitions of corresponding pins:

Pin Signal Pin Signal Pin Signal

1 C2 (input) 6 SH 11 F (input)

2 C3 (input) 7 NC 12 C1(input)/ NC

3 C4 (input) 8 NC 13 C1(input)

4 C5 (input) 9 R (input) 14 RF (or called N) (input)/ NC

5 C6 (input) 10 L (input) 15 RF (or called N) (input)

Net Port


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2) RS232 Socket


Pin Signal Pin Signal Pin Signal

1 NC 4 NC 7 NC

2 RxD (input) 5 GND 8 NC

3 TxD (output) 6 NC 9 NC

3) External Input/Output Socket


Pin Signal Pin Signal

1 GND 4 GND

2 GND 5 ECG Signal (input)

3 GND 6 ECG Signal (output)

4) USB Interface

WARNING

Only the USB equipment recommended by the manufacturer can be connected to the USB interface.


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Pin Signal Pin Signal

1 VBUS 3 D+

2 D- 4 GND

WARNING

1. Accessory equipment connected to the analog and digital interfaces must be certified according to the respective IEC/EN standards (e.g. IEC/EN 60950 for data processing equipment and IEC/EN 60601-1 for medical equipment). Furthermore all configurations shall comply with the valid version of the standard IEC/EN 60601-1-1. Therefore anybody, who connects additional equipment to the input or output connector to configure a medical system, must make sure that it complies with the requirements of the valid version of the system standard IEC/EN 60601-1-1. If in doubt, consult our technical service department or your local distributor.

2. The summation of leakage current should never exceed the leakage current limit while several other units are used at the same time.

2.4 Mains Connection and Switch

Mains Switch

Potential EqualizationTerminal

Mains Socket


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1) Potential Equalization Terminal

The potential equalization conductor provides a connection between the unit and the potential equalization bus bar of the electrical installation.

2) Mains Socket

AC SOURCE: alternating current supply socket

3) Mains Switch

: On

: Off

2.5 Bottom Panel

1) Battery Compartment

The battery label indicates the rated voltage and the rated capacity of the rechargeable

lithium battery.

Rated voltage: 14.8V, Rated capacity: 2200mAh.

Caution

WARNING

1. Improper operation may cause the battery to be hot, ignited or exploded, and it may lead to the decrease of the battery capacity. Therefore, it is necessary to read the user manual carefully and pay more attention to warning messages.

Mains Supply Shift Switch

Fuse Label

Battery Compartment

Label

Fuse


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WARNING

2. When leakage or foul smell is found, stop using the battery immediately. If your skin or cloth comes into contact with the leakage liquid, cleanse it with clean water at once. If the leakage liquid splashes into your eyes, do not wipe them. Irrigate them with clean water first and go to see a doctor immediately.

3. Only qualified service engineer authorized by the manufacturer can open the battery compartment and replace the battery. The battery of the same model and specification provided by the manufacturer must be used.

2) Mains Supply Shift Switch

Mains supply with rated input voltage 230V (220-240V) or 115V (100-115V) can be chosen by using the shift switch according to local mains supply specifications.

WARNING

Only qualified installation or service engineer can shift the mains supply shift switch according to local mains supply specifications.

3) Fuse

There are two fuses of the same specifications installed on the bottom of the main unit. The specifications are shown on the fuse label: 220V-240V: T200mA; 100V -115V: T400mA; 520.

WARNING

Ruptured fuses must only be replaced with those of the same type and rating as the original.


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2.6 Features

Low weight and compact size High resolution thermal recorder, recording frequency response 150Hz ECG signals of 12 leads are gathered and amplified simultaneously, 3-channel waves

are displayed and recorded simultaneously

The auto, manual, rhythm, USB print and off modes are optional Measurement function and interpretation function are optional System setup interface for parameter settings Built-in rechargeable lithium battery with large capacity Hint information for lead off, lack of paper, low battery capacity etc. Automatic adjustment of baseline for optimal printing Standard input/output interface and RS232 communication interface ECG data can be transmitted to the PC software through the serial cable, net cable

(optional, only for net type), or wireless AP (optional).

SE-3 Electrocardiograph User Manual About SE-3 Application Interface

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Chapter 3 About SE-3 Application Interface The following sections provide an overview of the main functions in the SE-3 application. After

you turn on the device, the main interface pops up. Then you can press the MENU key to open

the system setup interface. Or press the RECALL key to open the recall window.

3.1 About the Main Interface (SE-3 Wide Screen)

ID: 210605-1812 Female Age 30 AUTO 11:01:43

60

R L F C1 C2 C3

C4 C5 C6 10mm/mV

25mm/s

AC ON

EMG OFF

Figure 3-1 Main Interface (SE-3 Wide Screen)

The main interface includes:

Top Row (from left to right):

Patient ID(generated automatically according to the examination date and time) Sex (Male/Female) Age Printing mode(AUTO, MANUAL, RHYTHM, USBPRT or OFF) Current time and the battery capacity symbol (The battery capacity symbol appears

only when the built-in battery is used.)


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Right Row (from top to bottom):

Heart rate Electrode identifiers (The highlighted electrode identifiers show the status of Lead

Off, which means electrodes fall off the patient or the patient cable falls off the unit.)

Sensitivity (2.5mm/mV, 5mm/mV, 10mm/mV, 20mm/mV, AGC) Printing speed (5mm/s, 6.25mm/s, 10mm/s, 12.5mm/s, 25mm/s, 50mm/s) AC filter (AC ON, AC OFF) EMG filter (EMG OFF, EMG 25Hz, EMG 35Hz, EMG 45Hz) Hint information (Paper?, Printing, Sampling, Bat Weak etc.)

Press the Up or Down arrow to select the ID, sex, age, speed, AC filter or EMG filter item, and then press the Left or Right arrow to set the selected item.

Press the MODE/RST key to select a printing mode among AUTO, MANUAL, RHYTHM, USBPRT and OFF.

Press the SENS key to switch the sensitivity.

Note: When modifying the printing mode or the sensitivity on the main interface, you should press MENU twice to save these modifications to the system. After that, you will see these modifications on the main interface when you turn on the electrocardiograph next time.

3.2 About the Main Interface (SE-3 Narrow Screen)

Figure 3-2 Main Interface (SE-3 Narrow Screen)

The main interface:

First Row (from left to right):

Printing mode(AUTO, MANUAL, RHYTHM, USBPRT or OFF) Hint information (Paper?, Printing, Sampling, Bat Weak etc.) Sex (Male/Female) Age

AUTO Paper? M 35YI II III 10mm/mV 60


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Second Row (from left to right):

Current sampling lead group Sensitivity (2.5mm/mV, 5mm/mV, 10mm/mV, 20mm/mV, AGC) Heart rate Battery capacity symbol (The battery capacity symbol appears only when the built-in

battery is used.)

Third Row:

ECG waves Press the Up or Down arrow to select the sex or age item, and then press the Left or Right arrow to set the selected item.

Press the MODE/RST key to select a printing mode among AUTO, MANUAL, RHYTHM, USBPRT and OFF.

Press the SENS key to switch the sensitivity.

Note: When modifying the printing mode or the sensitivity on the main interface, you should press MENU twice to save these modifications to the system. After that, you will see these modifications on the main interface when you turn on the electrocardiograph next time.

3.3 About the System Setup Interface

Figure 3-3 System Setup Interface (SE-3 Wide Screen)

There are four tabs on the system setup interface of SE-3 Wide screen: LOGIN, RECORD, GENERAL and SYSTEM.

GENERALLOGIN RECORD SYSTEM

ID : 161105-1723 HEIGHT: 170 NAME : WEIGHT: 60 AGE : 30 BP : 80/120 SEX : Male HOSPITAL : DOCTOR :

ABCDEFGHIJKLM NOPQRSTUVWXYZ0123456789_-

DEL OK Next

Prev


- 24 -

Press the Up or Down arrow to select the Prev or Next button, and then press the Left or Right arrow to switch among these tabs.

Figure 3-4 System Setup Interface (SE-3 Narrow screen)

Press the Lead switch key to switch to the prev or next page of the system setup interface.

Press the Up or Down arrow to select an item, and then press the Left or Right arrow to set the selected item.

Press the MENU key again to exit the system setup interface.

3.4 About the Recall Window

Figure 3-5 Recall Window (a) (SE-3 Wide screen)

Press the Up or Down arrow to select the TRANS ALL button, and then press the MENU or PRINT/STOP key to transmit all the patient records to the PC.

Press the Up or Down arrow to select the ALL to USB button, and then press the MENU or PRINT/STOP key to transmit all the patient records to the U disk.

Press the Up or Down arrow to select the USB to ECG button, and then press the MENU or PRINT/STOP key to transmit the patient records in the U disk to the electrocardiograph.

Press the Up or Down arrow to select the DEL ALL button, and then press the MENU or PRINT/STOP key to delete all the patient records.

AC Filter :On EMG Filter : Off DFT Filter :0.15Hz Lowpass Filter : 100Hz

0610051702

0610051718

0610051725

TRANS ALL DEL ALL

0710051230

ALL to USB USB to ECG


- 25 -

Press the Up, Down, Left or Right arrow to select a patient record, and then press the MENU or PRINT/STOP key to open the recall window (b).

Figure 3-6 Recall Window (b) (SE-3 Wide screen)

Press the Up or Down arrow to select the DELETE button, and then press the MENU or PRINT/STOP key to delete the patient record.

Press the Up or Down arrow to select the TRANSMIT button, and then press the MENU or PRINT/STOP key to transmit the patient record to the PC.

Press the Up or Down arrow to select the TO USB button, and then press the MENU or PRINT/STOP key to transmit the patient record to the U disk.

Press the Up or Down arrow to select the RECORD button, and then press the MENU or PRINT/STOP key to print out the patient record.

Press the Up or Down arrow to select the BACK button, and then press the MENU or PRINT/STOP key to return to the recall window (a).

Press the RECALL key again to return to the main interface.

For SE-3 Narrow screen, press the Lead switch key to switch to the prev or next page of records in the recall window. Press the Left or Right arrow to switch among the TRANS ALL, ALL to USB, USB to ECG, DEL ALL, DELETE, TRANSMIT, TO USB, and RECORD buttons.

For details on managing patient records, please refer to chapter 7, Managing ECG Records.

0610051702

0610051725

DELETE

0710051230

TRANSMIT RECORD BACKTo USB

SE-3 Electrocardiograph User Manual Operation Preparations

- 26 -

Chapter 4 Operation Preparations

WARNING

Before use, the equipment, the patient cable and electrodes should be checked. Replace them if there is any evident defectiveness or aging which may impair the safety or the performance. Make sure that the equipment is in proper working condition.

4.1 Power and Earthing

WARNING

If the integrity of the external protective conductor is in doubt, the equipment should be powered by the built-in rechargeable lithium battery.

Power Supply

The electrocardiograph can be powered either by the mains supply or a built-in rechargeable lithium battery.

Mains supply The mains socket is on the left side of the unit. If the mains supply is used, connect the power cord to the socket first, and then connect the power cord to the hospital grade outlet.

Operating voltage: 100V-115V~ / 220V-240V~

Operating frequency: 50Hz / 60Hz

Input power: 35VA

Make sure the mains supply meets the above requirements before power-on, and then press the mains switch. Then the mains supply indicator lamp ( ) will be lit.

If the built-in rechargeable battery is weak when the mains supply is used, it will be recharged automatically at the same time. Then both the mains supply indicator lamp ( ) and the battery recharging indicator lamp ( ) will be lit. The 3-channel electrocardiograph can not be recharged when it is printing reports, and the battery recharging indicator is black; when the 3-channel electrocardiograph is switched off, the battery recharging indicator lamp ( ) is black if the battery is fully recharged.


- 27 -

Built-in rechargeable battery When the built-in rechargeable lithium battery is used, turn on the unit by pressing the ON/OFF key on the control panel directly. Then the battery indicator lamp ( ) will be

lit and the battery symbol will be displayed on the LCD screen. Because of the

consumption during the storage and transport course, the battery capacity may not be full. If the symbol and the Hint information BAT WEAK are displayed, which means the battery capacity is low, please recharge the battery first.

Please refer to the maintenance section for how to recharge the battery. When the battery is being recharged, SE-3 can be powered by the mains supply at the same time.

WARNING

The potential equalization conductor of the unit should be connected to the potential equalization bus bar of the electrical installation when necessary.

4.2 Loading/Replacing Recorder Paper

There are two kinds of recorder paper. One is the rolled thermal paper with the width of 80mm, and the other is the folded thermal paper with the width of 80mm.

Note: When the folded thermal paper is used, the paper roller is unnecessary and must be taken out.

When the recorder paper runs out or is not loaded, warning message Paper? will appear on the screen. Then you should load or replace the recorder paper immediately.

Paper Roller

Groove

Casing

Printer Platen

Paper Tray

Thermal Print Head


- 28 -

Loading/Replacing Process of Rolled Thermal Paper:

1) Place fingers under the two flanges of the recorder casing, pull them upwards directly to release the casing.

2) Take out the paper roller, and remove remainder paper from the roller if necessary.

3) Take off the wrapper of the new thermal paper roll, and then put the paper roll through the roller.

4) Place the paper and the roller gently in the recorder with the roller pin clicking into the groove.

5) Pull about 2 cm of paper out with the grid side of the paper facing the thermal print head, and shut the recorder casing.

6) Press down the recorder casing firmly.

Loading/Replacing Process of Folded Thermal Paper:

1) Place fingers under the two flanges of the recorder casing, pull them upwards directly to release the casing.

2) Remove remainder paper in the paper tray if necessary.

3) Take off the wrapper of the new folded thermal paper, and then put it in the paper tray.


- 29 -

4) Pull about 2 cm of paper out with the grid side of the paper facing the thermal print head, and shut the recorder casing.

5) Press down the recorder casing firmly.

4.3 Preparing the Patient

4.3.1 Instructing the Patient

Before attaching the electrodes, greet the patient and explain the procedure. Explaining the

procedure decreases the patients anxiety. Reassure the patient that the procedure is painless.

Privacy is important for relaxation. When possible, prepare the patient in a quiet room or area

where others cant see the patient. Make sure that the patient is comfortable. The more relaxed

the patient is, the less the ECG will be affected by noise.

4.3.2 Preparing the Skin

Thorough skin preparation is very important. The skin is a poor conductor of electricity and

frequently creates artifact that distorts the ECG signal. By performing methodical skin

preparation, you can greatly reduce the possibility of the noise caused by muscle tremor and

baseline drift, ensuring high-quality ECG waves. There is natural resistance on the skin surface

due to dry, dead epidermal cells, oils and dirt.

To prepare the skin

1. Shave hair from electrode sites, if necessary. Excessive hair prevents a good connection.

2. Wash the area thoroughly with soap and water.

3. Dry the skin with a gauze pad to increase capillary blood flow to the tissues and to remove the

dead, dry skin cells and oils.


- 30 -

4.4 Connecting the Patient Cable to the

Electrocardiograph and Electrodes

WARNING

The performance and electric shock protection can be guaranteed only if original patient cable and electrodes of the manufacturer are used.

The patient cable includes main cable and lead wires which can be connected to electrodes according to the colors and identifiers.

1. Connecting the Patient Cable to the Electrocardiograph

Connect the patient cable to the patient cable socket on the right side of the main unit, and then secure them with two screws.

2. Connecting the Patient Cable to Electrodes

Align all lead wires of the patient cable to avoid twisting, and connect the lead wires to the corresponding electrodes according to the colors and identifiers. Firmly attach them.

4.5 Attaching Electrodes to the Patient There are two types of electrode for you to choose, one is the reusable electrodes, and the other is the disposable electrodes. The uses of the two types of electrode are as shown below:

Connecting to Electrocardiograph

Screw

Main Cable

Connecting to Electrodes

Lead Wires


- 31 -

4.5.1 Reusable Electrodes

Reusable Electrodes is divided into Limb electrode and Chest Electrode, as the following figure shows:

Chest Electrode

Limb Electrode

The identifiers and color codes of electrodes used comply with IEC/EN requirements. In order to avoid incorrect connections, the electrode identifiers and color codes are specified in Table 4-1. Moreover the equivalent codes according to American requirements are given in Table 4-1 too.

Table 4-1 Electrodes and Their identifiers and color codes

European American

Electrodes Identifier Color code Identifier Color code

Right arm R Red RA White

Left arm L Yellow LA Black

Right leg N or RF Black RL Green

Left leg F Green LL Red

Chest 1 C1 White/red V1 Brown/red

Chest 2 C2 White/yellow V2 Brown/yellow

Chest 3 C3 White/green V3 Brown/green

Chest 4 C4 White/brown V4 Brown/blue

Reed

Electrode

Clamp

Suction Bulb

Electrode Metal Cup


- 32 -

Chest 5 C5 White/black V5 Brown/orange

Chest 6 C6 White/violet V6 Brown/violet

As the following figure shows, the positions of chest electrodes on the body surface are

C1: Fourth intercostal space at the right border of the sternum

C2: Fourth intercostal space at the left border of the sternum

C3: Fifth rib between C2 and C4

C4: Fifth intercostal space on the left midclavicular line

C5: Left anterior axillary line at the horizontal level of C4

C6: Left midaxillary line at the horizontal level of C4

Chest Electrode Connection:

1) Ensure that the electrodes are clean;

2) Align all lead wires of the patient cable to avoid twisting, and connect the lead wires to the corresponding electrodes according to the colors and identifiers;

3) Clean the electrode area on the chest surface with 75% alcohol;

4) Daub the round area of 25mm in diameter on each electrode site with gel evenly;

5) Place a small amount of gel on the brim of chest electrodes metal cup;

6) Place the electrode on the chest electrode site and squeeze the suction bulb. Unclench it and the electrode is adsorbed on the chest;

7) Attach all chest electrodes in the same way.

C6

C1

C2

C5

C4

C3


- 33 -

Note: Long-time measurement with a strong negative pressure on the suction bulb may cause reddening of the skin. When using the electrode on small children or patients with delicate skin, squeeze the suction ball lightly.

Limb Electrode Connection:

1) Ensure that the electrodes are clean;

2) Align all lead wires of the patient cable to avoid twisting, and connect the lead wires to the corresponding electrodes according to the colors and identifiers;

3) Clean the electrode area which is a short distance above the ankle or the wrist with alcohol;

4) Daub the electrode area on the limb with gel evenly;

5) Place a small amount of gel on the metal part of the limb electrode clamp;

6) Connect the electrode to the limb, and make sure that the metal part is placed on the electrode area above the ankle or the wrist;

7) Attach all limb electrodes in the same way.

4.5.2 Disposable Electrodes

Disposable Electrode Alligator Clip

Disposable electrode must be used together with the alligator clip.


- 34 -

The electrodes positions on body surface are as the following table and figures:

American label

European label

Electrode placement

RA R Right deltoid

LA L Left deltoid

RL N or RF Above right ankle (Alternate placement, upper leg as close to torso as possible)

LL F Above left ankle (Alternate placement, upper leg as close to torso as possible)

V1 C1 Fourth intercostals space at right border of sternum

V2 C2 Fourth intercostals space at left border of sternum

V3 C3 Fifth rib between V2 and V4

V4 C4 Fifth intercostals space on left midclavicular line

V5 C5 Left anterior axillary line at the horizontal level of V4

V6 C6 Left midaxillary line at the horizontal level of V4

Disposable Electrode connection

1) Align all lead wires of the patient cable to avoid twisting, and connect the alligator clips to the lead wires.

2) Clean the electrode areas on the body surface with 75% alcohol.

3) Attach the disposable electrodes to the electrode positions on body surface.

4) Clip the disposable electrodes with the alligator clips.

The quality of ECG waveform will be affected by the contacting resistance between the patient and the electrode. In order to get a high-quality ECG, the skin-electrode resistance must be minimized when you attach electrodes to patients.

V6

V1

V2

V5

V4

V3


- 35 -

CAUTION

The disposable electrodes can only be used for one time.

WARNING

1. Make sure that all electrodes are connected to the patient correctly before operation.

2. Make sure that the conductive parts of electrodes and associated connectors, including neutral electrode, do not come in contact with earth or any other conducting objects.

4.6 Inspection Before Power On In order to avoid safety hazards and get good ECG records, the following inspection procedure is recommended before power-on and operation.

1) Environment:

Make sure that there is no electromagnetic interference source around the equipment, especially large medical electrical equipment such as electrosurgical equipment, radiological equipment, magnetic resonance imaging equipment etc. Switch off these devices when necessary.

Keep the examination room warm to avoid muscle action voltages in ECG signals caused by cold.

2) Power Supply:

If the mains supply is used, please check whether the power cord is connected to the unit well. The grounded three-phase outlet should be used.

When the battery capacity is low, recharge the battery before use. 3) Patient Cable:

Check whether the patient cable is connected to the unit firmly, and keep it far away from the power cord.

4) Electrodes:

Check whether all electrodes are connected to lead wires of the patient cable correctly.

Ensure that the chest electrodes do not contact. 5) Recorder Paper:

Ensure that there is enough recorder paper loaded correctly.


- 36 -

6) Patient:

The patient should not come into contact with conducting objects such as earth, metal parts etc.

Ensure the patient is warm and relaxed, and breathe calmly. WARNING

The electrocardiograph is provided for the use of qualified physicians or personnel professionally trained, and they should be familiar with the contents of this user manual before operation.

SE-3 Electrocardiograph User Manual Switching on the Electrocardiograph

- 37 -

Chapter 5 Switching on the Electrocardiograph When the mains supply is used, connect the power cord, press the mains switch on the left

side of the unit, and then the mains supply indicator lamp ( ) is lit. Then press the ON/OFF key on the control panel to turn on the unit. The equipment information such as the device name, the version number will be displayed on the LCD screen after self-test. Then SE-3 is ready for use.

When a built-in rechargeable lithium battery is used, press the ON/OFF key on the control panel directly to turn on the unit, and then the battery indicator ( ) is lit. The equipment information such as the device name, the version number will be displayed on the LCD screen after self-test. Then SE-3 is ready for use.

SE-3 Electrocardiograph User Manual Sampling and Printing ECG

- 38 -

Chapter 6 Sampling and Printing ECG

6.1 Entering Patient Information

After switched on, the electrocardiograph begins sampling ECG.

1. Enter the information of sex and age on the main interface.

1) Press the Up or Down arrow to select the sex or age item.

2) Press the Left or Right arrow to enter the information of patient sex or age

ID: 210605-1812 Female Age 30 AUTO 11:01:43

60

R L F C1 C2C3

C4 C5 C6 10mm/mV

25mm/s

AC ON

EMG OFF

Figure 6-1 Main Interface (SE-3 Wide screen)

Figure 6-2 Main Interface (SE-3 Narrow screen)

2. The system generates patient ID automatically according to the examination time. You can

also enter patient ID manually in the following ways.

1) Press the Up or Down arrow to select the ID item on the main interface, and then press

the Left or Right arrow to set the ID item. (Only for SE-3 Wide screen)

AUTO Paper? M 35YI II III 10mm/mV 60


- 39 -

2) Or press the MENU key to open the system setup interface. Press the Up or Down arrow

to select the ID item. Press the Left or Right arrow to set the ID item. (Only for SE-3

Narrow screen)

3. Or you can enter the detailed information about the patient and the doctor on the system

setup interface. (Only for SE-3 Wide screen)

Press the MENU key to open the system setup interface. Edit patient information on the login

setting interface.

Note: The patient information can not be set or changed during the printing course.

To Enter Name:

1) Press the Up or Down arrow to select the NAME item, and a textbox appears after the

NAME item.

2) Press the Left or Right arrow and the textbox becomes highlighted. Then press the Up,

Down, Left or Right arrow to select a letter or a number on the soft keyboard. After that,

press the MENU key to add the selected letter or number to the textbox.

3) To delete wrong letters, firstly press the Up, Down, Left or Right arrow to select the DEL

button on the soft keyboard, and then press the MENU key to confirm.

4) Press the Up, Down, Left or Right arrow to select the OK button on the soft keyboard, and

then press the MENU key to confirm.

You can enter the hospital name and the doctor name in the same way.

GENERALLOGIN RECORD SYSTEM

ID : 161105-1723 HEIGHT: 170 NAME : WEIGHT: 60 AGE : 30 BP : 80/120 SEX : Male HOSPITAL : DOCTOR :

ABCDEFGHIJKLM NOPQRSTUVWXYZ0123456789_-

DEL OK Next

Prev


- 40 -

To Enter ID:

1) Press the Up or Down arrow to select the ID item.

2) Press the Left or Right arrow to set the ID item.

3) Press the MENU key to confirm.

You can enter age, BP, sex, height and weight in the same way.

6.2 Printing ECG Reports There are four modes to print ECG reports.

In the AUTO mode, the lead groups are switched in order automatically during the printing course. There is a blank area on the recorder paper before printing the ECG signals of the next lead group. Moreover, a 1mV calibration mark will be printed at the beginning of ECG reports. The switch orders of lead groups are listed in Table 2-1.

In the MANUAL mode, you should switch the lead group manually. You can determine the lead group to be printed and set the printing settings or other parameters for different lead groups.

In the RHYTHM mode, you can print 60s rhythm-lead ECG waveforms.

In the USBPRT mode, ECG reports can be printed out through a USB printer.

Note: The printing mode can not be changed during the printing course. Stop printing reports before changing the printing mode.

6.2.1 AUTO Mode

1) Press the MODE/RST key to select the AUTO mode, which will be displayed in the top right corner of the LCD screen.

2) Press the SENS key to set the sensitivity.

3) Set the gain, AC filter and EMG filter to get good ECG traces. Press the Up or Down arrow to select the gain, AC filter and EMG filter item. Then press the Left or Right arrow to set them. (Only for SE-3 Wide screen)

4) Or press the MENU key to open the system setup interface to set the detailed settings. Press the MENU key again to return to the main interface. For details about settings, please refer to chapter 8 Settings (SE-3 Wide screen) and chapter 9 Settings (SE-3 Narrow screen).

5) Press the Up or Down arrow to select the speed item. Then press the Left or Right arrow to set the speed.


- 41 -

6) Press the PRINT/STOP key to begin printing ECG reports. It will stop automatically after printing a complete ECG report of 12 leads. Or press the PRINT/STOP key again to stop printing reports.

Press PRINT/STOP during the printing course to stop printing ECG reports. Then when you begin printing ECG reports again, the system will print ECG reports from the first lead group, and the ID number will change automatically according to the current examination time. You can adjust the ID number manually. For details on setting the ID number, see section 6.1, Entering Patient Information.

6.2.2 MANUAL Mode

1) Press the MODE/RST key to select the MANUAL mode, which will be displayed in the top right corner of the LCD screen.




5) Press the Lead switch key to select the lead group to be printed.


7) Press the PRINT/STOP key to begin printing reports.

8) Press the 1mV/COPY key to print out 1mV mark in the ECG report. Press the Lead switch key to switch the lead group while printing ECG reports.

9) Press the PRINT/STOP key to stop printing ECG reports.

Press PRINT/STOP during the printing course to stop printing ECG reports. Then when you begin printing ECG reports again, the ID number will change automatically according to the current examination time. You can adjust the ID number manually. For details on setting the ID number, see section 6.1, Entering Patient Information.


- 42 -

6.2.3 RHYTHM mode

1) Press the MODE/RST key to select the RHYTHM mode; which will be displayed in the top right corner of the LCD screen.



4) Or press the MENU key to open the system setup interface to set the RHYTHM LEAD item or other settings. Press the MENU key again to return to the main interface. For details about settings, please refer to chapter 8 Settings (SE-3 Wide screen) and chapter 9 Settings (SE-3 Narrow screen).


6) Press the PRINT/STOP key, the hint information Sampling will be displayed on the main interface, and the sampling time will be counted. When the sampling time reaches 60s, it begins to print ECG reports.

7) It will stop automatically after printing a complete report of rhythm-lead ECG waveforms. Or press the PRINT/STOP key again to stop printing ECG reports.

Press PRINT/STOP during the printing course to stop printing ECG reports. Then when you begin printing ECG reports again, the ID number will change automatically according to the current examination time. You can adjust the ID number manually. For details on setting the ID number, see section 6.1, Entering Patient Information.

6.2.4 USBPRT mode

1) Connect SE-3 to the USB printer recommended by the manufacturer. Please refer to section 8.2.4 USB Printer Settings for details.

2) Press the MODE/RST key to select the USBPRT mode, which will be displayed in the top right corner of the LCD screen.


4) Set the gain, AC filter and EMG filter to get good ECG traces. Press the Up or Down arrow to select the gain, AC filter and EMG filter item. Then press the Left or Right arrow to set them. (Only for SE-3 Wide screen).


- 43 -



7) Press the PRINT/STOP key to begin printing reports. During the printing coursepressing the PRINT/STOP key again can not stop printing ECG reports. It will stop automatically after printing a complete ECG report.

6.3 Transmitting ECG Data to the PC

Note: To transmit ECG data to the PC, Smart ECG Viewer software of the manufacturer must be installed in the PC. You should log into the Smart ECG Viewer software before the transmission.

6.3.1 Transmitting ECG Data Through the Serial Port

1. Connect the RS232 socket of the PC to the RS232 socket of the electrocardiograph with a RS232 cable.

2. Or if the PC has no RS232 socket, connect the USB socket of the PC to the RS232 socket of the electrocardiograph by using the RS232-USB assembly.


- 44 -

Figure 6-3 RS232-USB Assembly

3. Press the MENU key to open the system setup interface.

For SE-3 Wide screen,

1) Press the Up or Down arrow to select the Next or Prev button, and then press the Left or Right arrow to select GENERAL tab to open the general setting interface.

2) Press the Up or Down arrow to select the AUTO TRANSFER item, and then press the Left or Right arrow to set the AUTO TRANSFER item to UART AUTO.

For SE-3 Narrow screen, press the Up or Down arrow to select the AUTO TRANSFER item, and then press the Left or Right arrow to set the AUTO TRANSFER item to UART AUTO.

Press the MENU key again to return to the main interface.

4. In the AUTO, OFF or USBPRT mode, ECG data can be transmitted through the UART port automatically after an ECG report is printed out.

6.3.2 Transmitting ECG Data Through the Net Port (Optional, Only

for Net Type)

1. Connect the PC to the electrocardiograph with an Ethernet cable recommended by the manufacturer. If the wireless AP transmission is used, connect the PC to one wireless AP, and connect the electrocardiograph to the other wireless AP. Only the wireless AP recommended by the manufacturer can be used.


- 45 -

Note:

1) For details on configuring the wireless AP, please refer to the user manual delivered with the wireless AP.

2) There should be no shield in or around the room where the wireless AP is used, or else the wireless transmission may fail.



1) Press the Up or Down arrow to select the Next or Prev button, and then press the Left

or Right arrow to select GENERAL tab to open the general setting interface.

2) Press the Up or Down arrow to select the AUTO TRANSFER item, and then press the

Left or Right arrow to set the AUTO TRANSFER item to Net AUTO. Press the Up or

Down arrow to select the REMOTE IP item, and then press the Left or Right arrow to

set the REMOTE IP item to the local IP of Smart ECG Viewer. Press the Up or Down

arrow to select the LOCAL IP item, and then set the first three numbers of the

LOCAL IP item to the first three numbers of the local IP of Smart ECG Viewer. The

last number of the LOCAL IP item can be set at random, but it cant be the same as

the last number of the local IP of Smart ECG Viewer.

For example, view the local IP on the System Setting interface of the Smart ECG Viewer software.


- 46 -

Set the REMOTE IP item to the local IP of Smart ECG Viewer. Set the first three numbers of the LOCAL IP item to the first three numbers of the local IP of Smart ECG Viewer. The last number of the LOCAL IP item can be set at random, but it cant be the same as the last number of the local IP of Smart ECG Viewer.

For SE-3 Narrow screen, press the Up or Down arrow to select the AUTO TRANSFER item, and then press the Left or Right arrow to set the AUTO TRANSFER item to Net AUTO. Press the Up or Down arrow to select the REMOTE IP item, and then press the Left or Right arrow to set the REMOTE IP item to the local IP of Smart ECG Viewer. Press the Up or Down arrow to select the LOCAL IP item, and then set the first three numbers of the LOCAL IP item to the first three numbers of the local IP of Smart ECG Viewer. The last number of the LOCAL IP item can be set at random, but it cant be the same as the last number of the local IP of Smart ECG Viewer.

For example, view the local IP on the System Setting interface of the Smart ECG Viewer software.

GENERAL LOGIN RECORD SYSTEM

AC FILTER :On DFT FILTER :0.15Hz EMG FILTER :Off LOWPASS FILTER :150Hz EXTERN INP/OUTP :Off KEY BEEP :On QRS BEEP :Off REMOTE IP : 192.168.7.77 LOCAL IP : 192.168.7.21 AUTO TRANSFER : Net AUTO SAVE OPTION :On

Next

Prev


- 47 -

Set the REMOTE IP item to the local IP of Smart ECG Viewer. Set the first three numbers of the LOCAL IP item to the first three numbers of the local IP of Smart ECG Viewer. The last number of the LOCAL IP item can be set at random, but it cant be the same as the last number of the local IP of Smart ECG Viewer.


3. In the AUTO, OFF or USBPRT mode, ECG data can be transmitted through the net automatically after an ECG report is printed out.

SAVE OPTION :On AUTO TRANSFER : Net AUTO LOCAL IP : 192.168.7.21 REMOTE IP : 192.168.7.77


- 48 -

6.4 ECG Reports

6.4.1 ECG Reports in the AUTO Mode

(a)

(b)

(c)


- 49 -

Figure (a) shows the following contents:

10mm/mV----Sensitivity 0.15~100Hz----Filter Information

AC50----50Hz AC Filter 05-12-2007 10:06:26----Date and Time

----1mV Calibration Mark

I, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6----Lead Name

ECG waves of 12 leads in the format of 3Ch/3Ch

25mm/s----Paper speed

Figure (b) shows the average template when the AVERAGE TEMPLET item is set to 26+1R on the system setup interface.

Figure (c) shows the measurement and interpretation information when the MEASUREMENT and INTERPRETATION items are set to ON on the system setup interface. The measurement information includes:

ID, Name, Age, Sex, BP, Height, Weight, HR (Heart Rate)

P Dur----P wave duration: the average P-wave duration from several selected dominant beats PR int----P-R interval: the average P-R interval from several selected dominant beats; QRS Dur----QRS complex duration: the average QRS complex duration from several

selected dominant beats; QT/QTC int----Q-T interval / Normalized QT interval;

P/QRS/T axis----dominant direction of the average integrated ECG vectors;

RV5/SV1 amp----The maximum amplitude of R or R wave of one selected dominant beat from lead V5 / The maximum amplitude of S or S wave of one selected dominant beat from lead V1;

RV5+SV1 amp---- Sum of RV5 and SV1;

RV6/SV2 amp---- The maximum amplitude of R or R wave of one selected dominant beat from lead V6 / The maximum amplitude of S or S wave of one selected dominant beat from lead V2;

The interpretation information includes: Minnesota Code, Diagnosis Information and Report Confirmed by.

Note: In the AUTO or MANUAL mode, if the sensitivity is set to 20mm/mV, only one calibration mark will be printed in the ECG report.


- 50 -

6.4.2 ECG Reports in the RHYTHM Mode

(a)

(b)


- 51 -

Figure (a) shows the following contents:

10mm/mV (Sensitivity)

0.67~100Hz (Filter Information)

AC50 (50Hz AC Filter)

(1mV Calibration Mark)

II (Lead Name)

60s rhythm waveform of lead II

00:00, 00:20, 00:40 (Timer 25mm/s (Paper Speed

80 (Heart Rate Figure (b) shows RR analysis results, including RR interval measurement information, RR histogram and RR trend chart.

RR Interval measurement information includes the following contents:

Current Date & Current Time

Patient Information (ID, Name, Age, Sex, BP, Height, Weight)

Measure Time

Total R Num (Total R-wave number)

HR (Heart Rate)

RR Avg Interval (Average RR Interval)

RR Max Interval (Maximum RR Interval)

RR Min Interval (Minimum RR Interval)

Max/Min (Ratio of Maximum RR Interval to Minimum RR Interval)

SDNN (Standard Deviation of Normal to Normal Intervals)

RMSSD (The Root Mean Square of Successive Difference)


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6.4.3 ECG Reports in the USBPRT Mode


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As the above figure shows, the USBPRT mode report includes:

ID, Paper Speed, Sensitivity, Date and Time;

Name, Age, Sex, BP, Height, Weight;

Heart Rate, P Duration, PR Interval, QRS Duration, QT/QTC Interval, P/QRS/T Axis, RV5/SV1 Amplitude, RV5+SV1 Amplitude, RV6/SV2 Amplitude;

Minnesota Code;

Diagnosis Information;

Unconfirmed Report, Reviewed By;

ECG waveforms of 12 leads.

SE-3 Electrocardiograph User Manual Managing ECG Records

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Chapter 7 Managing ECG Records If you want to save the ECG records in the electrocardiograph, you should set the SAVE OPTION item to On. The default value is On. Then the ECG records will be saved in the recall window automatically.


2. For SE-3 Wide screen

1) Press the Up or Down arrow to select the Prev or Next button. Then press the Left or Right arrow to select the GENERAL tab.

2) Press the Up or Down arrow to select the SAVE OPTION item. Then press the Left or Right arrow to set the SAVE OPTION item to On.

3) Press the MENU key again to return to the main interface.

3. For SE-3 Narrow screen

1) Press the Up or Down arrow to select the SAVE OPTION item.

2) Press the Left or Right arrow to set the SAVE OPTION item to On.

3) Press the MENU key again to return to the main interface.

Press the RECALL key to open the recall window where patient records are saved. The recall window allows records to be stored, deleted, printed and transmitted. When there is no space for more records to be stored in the recall window, the message MemFull will be displayed.

7.1 Transmitting ECG Records to the PC

Note: To transmit ECG records to the PC, Smart ECG Viewer software of the manufacturer must be installed in the PC. You should log into the Smart ECG Viewer software before the transmission.

7.1.1 Transmitting ECG Records Through the Serial Port

1. Connect the RS232 socket of the PC to the RS232 socket of the electrocardiograph with a RS232 cable.

2. If the PC has no RS232 socket, connect the USB socket of the PC to the RS232 socket of the electrocardiograph by using the RS232-USB assembly. For details about the RS232-USB assembly, please refer to section 6.3.1, Transmitting ECG Data Through the Serial Port.


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1) Press the Up or Down arrow to select the Prev or Next button, and then press the Left or Right arrow to select the GENERAL tab to open the general setting interface.

2) Press the Up or Down arrow to select the AUTO TRANSFER item, and then press the Left or Right arrow to set the AUTO TRANSFER item to UART AUTO.

For SE-3 Narrow screen, press the Up or Down arrow to select the AUTO TRANSFER item, and then press the Left or Right arrow to set the AUTO TRANSFER item to UART AUTO.


4. Press the RECALL key to open the recall window (a).

Figure 7-1 Recall Window (a)

5. Press the Up and Down arrow (for SE-3 Wide screen) or Left and Right arrow (for SE-3 Narrow screen) to select the TRANS ALL button, and then press the PRINT/STOP or MENU key to transmit all the records to the PC.

If the AUTO TRANSFER item is set to OFF before the transmission, WARNING (a) will pop up.

WARNING (a)

6. For SE-3 Wide screen, if you want to transmit a record, press the Up, Down, Left or Right

arrow to select the record in the recall window. Then press the PRINT/STOP or MENU key, and the recall window (b) appears. Press the Up or Down arrow to select the TRANSMIT

Please Select Auto Transfer Option first!

Press PRINT/STOP return

ERROR

YES

0610051702

0610051718

0610051725

TRANS ALL DEL ALL

0710051230

ALL to USB USB to ECG


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button, and then press the PRINT/STOP or MENU key to transmit the record to the PC. After the transmission, press the Up or Down arrow to select the BACK button, and then press the PRINT/STOP or MENU key to return to the recall window (a).

For SE-3 Narrow screen, if you want to transmit a record, press the Up or Down arrow to select the record, and then press the Left or Right arrow to select the TRANSMIT button, and then press the PRINT/STOP or MENU key to transmit the record to the PC.

Figure 7-2 Recall Window (b)

Note: The transmission process is long, and you should be patient to wait.

7. Press the RECALL key to return to the main interface.

7.1.2 Transmitting ECG Records Through the Net Port (Optional,

Only for Net Type)

1. Connect the PC to the electrocardiograph with an Ethernet cable recommended by the manufacturer. If the wireless AP transmission is used, connect the PC to one wireless AP, and connect the electrocardiograph to the other wireless AP. Only the wireless AP recommended by the manufacturer can be used.

Note:

1) For details on configuring the wireless AP, please refer to the user manual delivered with the wireless AP.

2) There should be no shield in or around the room where the wireless AP is used, or else the wireless transmission may fail.

0610051702

0610051725

DELETE

0710051230

TRANSMIT RECORD BACKTo USB


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2. Press the MENU key to open the system setup interface, and set the AUTO TRANSFER, REMOTE IP and LOCAL IP items. Then press the MENU key again to return to the main interface. For details on setting the AUTO TRANSFER, REMOTE

MANUAL Cardiografo EDAN-3

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