• BS EN 60601-2-10:2015

    Withdrawn A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.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

    Available format(s):  Hardcopy, PDF

    Withdrawn date:  07-02-2020

    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
    202 Electromagnetic compatibility - Requirements and tests
    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 ZA (normative) - Normative references to
             international publications with their
             corresponding European publications
    Annex ZZ (informative) - Coverage of Essential
             Requirements of EU Directives

    Abstract - (Show below) - (Hide below)

    Describes the requirements for the safety of nerve and Muscle STIMULATORS, defined in subclause 201.3.204, for use in the practice of physical medicine, hereinafter referred to as ME EQUIPMENT.

    Scope - (Show below) - (Hide below)

    IEC 60601-2-10:2012 specifies the requirements for the safety and essential performance of nerve and muscle stimulators, for use in the practice of physical medicine. This includes transcutaneous electrical nerve stimulators (TENS) and electrical muscle stimulators (EMS). This second edition cancels and replaces the first edition, published in 1987 and its Amendment 1 (2001). This edition constitutes a technical revision and is aligned with IEC 60601-1:2005+A1:2012.

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

    Committee CH/62/4
    Development Note Supersedes and renumbers BS 5724-2.10(1988) (06/2001) Supersedes 84/52255 DC and 99/565079 DC. (04/2003) 2001 version incorporates amendment 13086 to BS 5724-2.10(1988). (04/2003) 2001 Edition along with its amendment remains active & will be withdrawn on 22/05/2018. Supersedes 10/30210946 DC & 15/30322732 DC. (06/2015) 2015 Edition remains active & will be withdrawn on 16/12/2019. 2015 Edition Re-issued in January 2017 & incorporates AMD 1 2016. (02/2017)
    Document Type Standard
    Publisher British Standards Institution
    Status Withdrawn
    Supersedes

    Standards Referencing This Book - (Show below) - (Hide below)

    IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
    IEC 60601-1-2:2014 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
    EN 60601-1-2:2015 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
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