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  1. Home
  2. CAN/CSA C22.2 NO. 60601-2-4:12 (R2021) + A1:19 (R2021) CONSOLIDATED

CAN/CSA C22.2 NO. 60601-2-4:12 (R2021) + A1:19 (R2021) CONSOLIDATED ✓ Most Recent

2089294  Preview

Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators (Adopted IEC 60601-2-4:2010, third edition, 2010-12, consolidated with amendment 1:2018, with Canadian deviations)

standard by Canadian Standards Association / National Standard of Canada , 10/01/2019

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Full Description

Scope:

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of CARDIAC DEFIBRILLATORS, hereafter referred to as ME EQUIPMENT.

If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.

NOTE See also 4.2 of the general standard.

This particular standard does not apply to implantable DEFIBRILLATORS, remote control DEFIBRILLATORS, or separate stand-alone cardiac monitors (which are standardized by IEC 60601-2-27:2011 [2]2). Cardiac monitors which use separate ECG monitoring electrodes are not within the scope of this standard unless they are used as the sole basis for AED rhythm recognition detection or beat detection for synchronized cardioversion. DEFIBRILLATOR electrodes as described in 201.108 can also be used for ECG monitoring; however, due to the larger electrode area, the requirements of IEC 60601-2-27 are not applicable for DEFIBRILLATOR ELECTRODES.

Defibrillation waveform technology is evolving rapidly. Published studies indicate that the effectiveness of waveforms varies. The choice of a particular waveform including waveshape, delivered energy, efficacy, and safety has been specifically excluded from the scope of this standard.

However, due to the critical importance of the therapeutic waveform, comments have been added to the rationale which addresses considerations in waveform selection.

The object of this particular standard is to establish particular BASIC SAFETY and ESSENTIAL PERFORMANCE requirements for cardiac defibrillators as defined in 201.3.202. See more

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Document History

  1. CAN/CSA C22.2 NO. 60601-2-4:12 (R2021) + A1:19 (R2021) CONSOLIDATED

    You are currently viewing this product 👀 currently
    viewing

    October 2019
    Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators (Adopted IEC 60601-2-4:2010, third edition, 2010-12, consolidated with amendment 1:2018, with Canadian deviations)

    • Most Recent  Most Recent
  2. CAN/CSA C22.2 NO. 60601-2-4:12 (R2021)

    March 2012
    Medical Electrical Equipment - Part 2-4: Particular Requirements for the Safety of Cardiac Defibrillators

    • Historical Version
  3. CAN/CSA C22.2 NO. 60601-2-4-04

    April 2004
    Medical Electrical Equipment - Part 2-4: Particular Requirements for the Safety of Cardiac Defibrillators

    • Historical Version

Browse related products from Canadian Standards Association / National Standard of Canada

  • CSA Group > Health Care and Medical Devices > Applications of Electricity in Health Care

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Price: $675.00
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Product Details

Published:

10/01/2019

ISBN(s):

9781488326547

Number of Pages:

354

File Size:

2 files

Product Code(s):

2427705, 2427705

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This product is restricted and cannot be purchased in the following countries Russia, Ukraine, Belarus
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