• BS EN 60601-2-3:2015

    Withdrawn A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

    Medical electrical equipment Particular requirements for the basic safety and essential performance of short-wave therapy equipment

    Available format(s):  Hardcopy, PDF

    Withdrawn date:  29-01-2020

    Language(s):  English

    Published date:  30-06-2015

    Publisher:  British Standards Institution

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    Table of Contents - (Show below) - (Hide below)

    FOREWORD
    INTRODUCTION
    201.1 Scope, object and related standards
    201.2 Normative references
    201.3 Terms and definitions
    201.4 General requirements
    201.5 General requirements for testing of ME
           EQUIPMENT
    201.6 Classification of ME EQUIPMENT and
           ME SYSTEMS
    201.7 ME EQUIPMENT identification, marking
           and documents
    201.8 Protection against electrical HAZARDS from
           ME EQUIPMENT
    201.9 Protection against MECHANICAL HAZARDS
           of ME EQUIPMENT and ME SYSTEMS
    201.10 Protection against unwanted and excessive
           radiation HAZARDS
    201.11 Protection against excessive temperatures and
           other HAZARDS
    201.12 Accuracy of controls and instruments and
           protection against hazardous outputs
    201.13 HAZARDOUS SITUATIONS and fault conditions for ME EQUIPMENT
    201.14 PROGRAMMABLE ELECTRICAL MEDICAL
           SYSTEMS (PEMS)
    201.15 Construction of ME EQUIPMENT
    201.16 ME SYSTEMS
    201.17 Electromagnetic compatibility of ME EQUIPMENT
           and ME SYSTEMS
    Annexes
    ANNEX C (informative) - Guide to marking and labelling
             requirements for ME EQUIPMENT and ME SYSTEMS
    Annex AA (informative) - Particular guidance and rationale
    Index of defined terms used in this particular standard
    Annex ZZ (informative) - Coverage of Essential
             Requirements of EU Directives

    Abstract - (Show below) - (Hide below)

    Describes the requirements for the safety of SHORT-WAVE THERAPY EQUIPMENT, hereafter referred to as ME EQUIPMENT, as defined in subclause 201.3.206.

    Scope - (Show below) - (Hide below)

    IEC 60601-2-3:2012 specifies the requirements for the basic safety and essential performance of short-wave therapy equipment. Short-wave therapy equipment are defined as medical equipment for the therapeutic treatment of a patient by exposure to electric or magnetic fields produced in the frequency range of more than 13 MHz but not exceeding 45 MHz. Equipment having a rated output power not exceeding 10 W are exempted from certain requirements of this standard. This third edition cancels and replaces the second edition of IEC 60601-2-3 published in 1991 and its amendment 1 published in 1998. This edition constitutes a technical revision and has been aligned with IEC 60601-1:2005.

    General Product Information - (Show below) - (Hide below)

    Committee CH/62/4
    Development Note Renumbers and supersedes BS 5724-2.3(1992). Supersedes 97/560804 DC, 88/51885 DC & BS 5724-2-3(1983). 1993 version incorporates amendment 7879 to BS 5724-2.3(1992) (11/2005) 1993 Edition along with its amendment remains active & will be Withdrawn on 14/04/2018. Supersedes 10/30210934 DC. (06/2015) Supersedes 15/30322777 DC. 2015 Edition remains active & will be withdrawn on 30/09/2019. 2015 Edition Re-Issued in October 2016 & incorporates AMD 1 2016. (10/2016)
    Document Type Standard
    Publisher British Standards Institution
    Status Withdrawn
    Supersedes
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