GE GEH-ECG 1200 User Manual Download Page 6

Controls and Indicators 

Page 6 

    

2102322-111 REV 1

 

DAMAGE TO DEVICE AND ACCESSORIES 

 Unauthorized personnel do not have the proper training to 

repair the device. Repairs carried out by unauthorized personnel could result in damage to the device 

or accessories. Send the device for inspection to an authorized facility if you find or even suspect a 

malfunction. Please add a detailed description of the observed malfunction. 

DAMAGE TO THE DEVICE 

 Take care to prevent chemicals\liquids from entering the connectors or 

internal part of the device. 

PACEMAKER - It is recommended that a minimum separation of 15 cm (6 inches) be maintained 

between the wireless patient unit 1200W and a pacemaker to avoid potential interference with 

pacemaker. Some studies have shown that wireless devices might interfere with implanted cardiac 

pacemakers if used within eight inches of the pacemaker. Pacemaker users may want to avoid placing 

or using a wireless device this close to their pacemaker. If you have any reason to suspect that 

interference is taking place, turn off the ECG immediately. 

Caution

Use only while patient unit 1200W is worn on patient with its strap. 

Use only with battery compartment of patient unit 1200W is closed. 

NOTE 

The GEH-ECG 1200 complies with Part 15 of the FCC Rules. Operation is subject to the following two 

conditions: 

This device may not cause harmful interference and 

This device must accept any interference received, including interference that may cause 

undesired operation. 

The manufacturer is not responsible for any Radio or TV interference caused by unauthorized 

modifications to this equipment. Such modifications could void the user’s authority to operate the 

equipment. 

NOTE 

NO OPTIMUM WIRELESS PERFOMANCE 

Note that the complete data transfer cannot be guaranteed under all circumstances when using Norav 

proprietary RF technology and that range loss can occur if this technology and other RF Devices (Bluetooth, 

WLAN.) are used near each other. Also, other devices could interfere with the equipment, even if the other 

devices comply with CISPR emission requirements 

In case of interruptions with the Norav proprietary RF technology: 

Remove any objects from the line of sight between patient acquisition unit 1200W and Receiver 

unit 1200WR 

Remove any possible RF interfering devices from the vicinity of 1200W and 1200WR. 

Do not position the devices closer than 50cm to each other or more than 10m from each other. 

Controls and Indicators 

Element 

Description 

Patient unit 1200W – Power ON/OFF Button 

Patient unit 1200W – Low Battery indicator 

Patient unit 1200W – Power ON/OFF indicator. Transmit/Standby indicator 

Patient unit 1200W – Detachable ECG Leadwires 

Patient unit 1200W – Leadwires guides. Strap Holders. 

Patient unit 1200W – 

Battery compartment door 

Receiver unit 1200WR – Detachable RF Antenna 

Receiver unit 1200WR – Power ON/OFF indicator. 

Receiver unit 1200WR – Detachable USB Cable 

10 

Receiver unit 1200WR – Auxiliary BNC output 

Summary of Contents for GEH-ECG 1200

Page 1: ...322 111 REV 1 NOTE The information in this manual only applies to the product GEH ECG 1200 Due to continuing product innovation specifications in this manual are subject to change without notice 2019 General Electric Company All rights reserved ...

Page 2: ...e program other than the original design or intended use thereof is not advised and considered a misuse of the software product Norav Limited Warranty Norav products are warranted to be free from manufacturing and material defects for a period of one 1 year from the date of shipment from Norav or the dealer to the original purchaser Excluded from this warranty are expendable supply items including...

Page 3: ...ols and Indicators 6 Battery Assembly 7 Belt Strap Assembly 8 Electrode Application 8 Patient Leadwires Assembly 9 Maintenance and Cleaning 10 Storage 10 Service 11 Calibration 11 Troubleshooting 11 ECG Cables and Accessories 12 Technical Specifications 12 Electromagnetic Emissions and Immunity Information 13 ...

Page 4: ...e device or signify an important step or procedure that requires special attention Device Labels Symbols Definition Defibrillation proof type CF Applied part Caution Refer to operation manual NOTE On ME EQUIPMENT Follow instructions for use 2797 CE marking Manufacturer Name and Address Device Serial Number Device Reference Number Date of manufacture Contains MIC certified RF module FCC ID Contains...

Page 5: ...hich are part of the system must meet the requirements of the Standard for Information Technology Equipment IEC EN 60950 1 and the Standard for Electrical Medical Devices IEC EN 60601 1 The personal computer should be approved to the appropriate safety standard for non medical electrical equipment IEC EN 60950 1 or its national variants Accessory equipment connected to the analogue and digital int...

Page 6: ...nd This device must accept any interference received including interference that may cause undesired operation The manufacturer is not responsible for any Radio or TV interference caused by unauthorized modifications to this equipment Such modifications could void the user s authority to operate the equipment NOTE NO OPTIMUM WIRELESS PERFOMANCE Note that the complete data transfer cannot be guaran...

Page 7: ...ore than two weeks when the recorder is not in use If you use rechargeable batteries the battery recharger should be kept out ofthe patient environment and hook up area Dispose of used batteries carefully using environmentally friendly methods wherever possible following the state s recycling laws or your facility srecycling policy Use only the recommended battery type as instructed in the technic...

Page 8: ...suitable for use As ECG electrodes from different manufacturers have different electrical properties the choice of ECG electrodes can considerably affect the measurement results and quality Ensure that only high quality electrodes are used Wet gel electrodes are recommended Always refer to the ANSI AAMI EC12 2000 Standard for safety performance and labeling requirements for the disposable electrod...

Page 9: ...eat height or wear and tear chafed patches on the cable Do not use the instrument or the leadwires if you detect cracks melted areas or any other signs of damage to the leadwires or housing Caution Verify that dates on applicable accessories have not expired ECG electrodes can cause skin irritation Examine the skin for signs of irritation or inflammation and avoid placement of the electrode in tho...

Page 10: ... measures as the rejected items Use the recorder after all the items become accepted Unit check shall be performed by each medical institution or by Norav personnel representative agent or an authorized third party For more details do not hesitate to consult your dealer or Norav Medical personnel Details of the check Check Method Criteria Operation manual Check that the operation manual is kept in...

Page 11: ...te before packing unless you suspect they are associated with the problem Wherever possible use the original shipping carton and packing materials Include a packing list and the Norav Return Material Authorization RMA number It is recommended that all returned goods be insured Claims for loss or damage to the product must be initiated by the sender Calibration The device does not need any calibrat...

Page 12: ...500 Lead OFF Detection Yes Communication Digital RF 2400 2483 MHz 0 4mW conform to FCC Part 15 249 Power Battery Size AA x 2 Alkaline or NiMH Operation time Up to 40 hours with Alkaline Batteries Mechanical Size 140 x 95 x 50 mm Weight 350g Environmental Operating Temp Range 10 to 40 C Storage Temp Range 20 to 60 C Relative Humidity 10 to 95 non condensing 1200WR Receiver Auxiliary output ECG Out ...

Page 13: ...N A Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 5 UT 95 dip in UT for 0 5 cycle 40 UT 60 dip in UT for 5 cycles 70 UT 30 dip in UT for 25 cycles 5 UT 95 dip in UT for 5 sec N A Mains power quality should be that of a typical commercial or hospital environment Po...

Page 14: ...ween portable and mobile RF communications equipment and NR recorder This device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled Users of this device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communication equipment transmitters and the device as recommended below according t...

Page 15: ...Electromagnetic Emissions and Immunity Information 2102322 111 REV 1 Page 15 ...

Page 16: ...www gehealthcare com ...

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