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GE Healthcare

GEH-ECG 1200

User Guide

2102322-111 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

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Содержание GEH-ECG 1200

Страница 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 ...

Страница 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...

Страница 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 ...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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 ...

Страница 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...

Страница 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...

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

Страница 16: ...www gehealthcare com ...

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