• CSA C22.2 No. 60601.2.34 : 2012

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    MEDICAL ELECTRICAL EQUIPMENT - PART 2-34: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT

    Available format(s):  Hardcopy, PDF

    Superseded date:  20-01-2020

    Language(s):  English

    Published date:  01-01-2012

    Publisher:  Canadian Standards Association

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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
     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
    208 General requirements, tests and guidance for alarm
        systems in medical electrical equipment and medical
        electrical systems
    Annexes
    Annex AA (informative) - Particular guidance and rationale
    Annex BB (informative) - Alarm diagrams 208/IEC 60601-1-8:2006
    Bibliography
    Index of defined terms used in this particular standard

    Abstract - (Show below) - (Hide below)

    Pertains to BASIC SAFETY and ESSENTIAL PERFORMANCE of INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT, hereinafter referred to as ME EQUIPMENT.

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

    Development Note To be read in conjunction with CSA C22.2.60601.1. (07/2013)
    Document Type Standard
    Publisher Canadian Standards Association
    Status Superseded
    Superseded By
    Supersedes

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

    IEC 80601-2-30:2009+AMD1:2013 CSV Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers
    ISO 15223-1:2016 Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements
    CSA C22.2 No. 60601.1.2 : 2016 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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