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  • BS EN 60601-3-1:1997

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    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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    Medical electrical equipment. Particular requirements for performance Specification for transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment

    Available format(s):  Hardcopy, PDF

    Superseded date:  15-06-2000

    Language(s):  English

    Published date:  15-04-1997

    Publisher:  British Standards Institution

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

    INTRODUCTION
    1 Scope and object
    2 Normative references
    3 Definitions
    4 Test conditions
    5 Accompanying documents
    6 Accuracy
    7 Response time
    8 Recorder
    9 Warning signals
    10 Internal electrical power source
    11 Transducers and cables
    Figures
    1 Suggested test fixture for transducer test, if the
        manufacturer does not recommend another test
        chamber
    2 Test cycle for linearity test - Example of typical
        results
    Annex A (informative) Guidance and rationale
    Annex ZA (normative) Normative references to international
    publications with their corresponding European
    publications

    Abstract - (Show below) - (Hide below)

    Defines essential requirements for performance of transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment. Applicable to transcutaneous monitors for foetal monitoring during birth. ALSO NUMBERED AS BS EN 5724 SECTION 3.101 1997

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

    Committee CH/62/4
    Development Note DRAFT FOR COMMENT 93/503826 DC
    Document Type Standard
    Publisher British Standards Institution
    Status Superseded
    Superseded By
    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 60601-2-23:2011 Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment
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