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  • 12/30269739 DC : 0

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    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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    IEC 61010-2-101 ED 2 - SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL AND LABORATORY USE - PART 2-101: PARTICULAR REQUIREMENTS FOR LABORATORY EQUIPMENT FOR IN VITRO DIAGNOSTIC (IVD) MEDICAL EQUIPMENT

    Available format(s):  Hardcopy, PDF

    Superseded date:  31-03-2017

    Language(s):  English

    Published date: 

    Publisher:  British Standards Institution

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

    1 Scope and object
    2 Normative references
    3 Terms and definitions
    4 Tests
    5 MARKING and documentation
    6 Protection against electric shock
    7 Protection against mechanical HAZARDS
    8 Resistance to mechanical stresses
    9 Protection against the spread of fire
    10 Equipment temperature limits and resistance to heat
    11 Protection against HAZARDS from fluids
    12 Protection against radiation, including laser
       sources, and against sonic
       and ultrasonic pressure
    13 Protection against liberated gases and substances,
       explosion and implosion
    14 Components and subassemblies
    15 Protection by interlocks
    16 HAZARDS resulting from application
    17 RISK assessment
    Annexes
    Annex L (informative) - Index of defined terms
    Annex BB (informative) - Instructions for use for self-test
             IVD medical equipment
    Bibliography

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

    Comment Closes On
    Committee EPL/66
    Document Type Draft
    Publisher British Standards Institution
    Status Superseded
    Superseded By

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

    ASTM D 4169 : 2016 : REDLINE Standard Practice for Performance Testing of Shipping Containers and Systems
    ISO/IEC Guide 51:2014 Safety aspects Guidelines for their inclusion in standards
    ISO 14971:2007 Medical devices Application of risk management to medical devices
    EN 980:2008 Symbols for use in the labelling of medical devices
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