• I.S. EN ISO 80601-2-13:2012/A2:2019

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation - Amendment 2 (ISO 80601-2- 13:2011/Amd 2:2018)

    Available format(s):  Hardcopy, PDF

    Superseded date:  19-12-2019

    Language(s):  English

    Published date:  18-12-2019

    Publisher:  National Standards Authority of Ireland

    For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
    Only cited Standards give presumption of conformance to New Approach Directives/Regulations.

    Dates of withdrawal of national standards are available from NSAI.

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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 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
    201.101 Additional requirements for ANAESTHETIC GAS DELIVERY SYSTEMS
    201.102 Additional requirements for an ANAESTHETIC BREATHING SYSTEM
    201.103 Additional requirements for an ANAESTHETIC GAS SCAVENGING SYSTEM
    201.104 Additional requirements for an ANAESTHETIC VAPOUR DELIVERY SYSTEM
    201.105 Additional requirements for an ANAESTHETIC VENTILATOR
    201.106 Display loops
    201.107 Clinical evaluation
    202 Electromagnetic compatibility — Requirements and tests
    203 General requirements for radiation protection in diagnostic X-ray equipment
    206 Usability
    208 General requirements, tests and guidance for ALARM SYSTEMS in MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS
    209 Requirements for environmentally conscious design
    210 PROCESS requirements for the development of physiologic closed-loop controllers
    211 Requirements for MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS used in
    Annex C (informative) Guide to marking and labelling requirements for ME EQUIPMENT and ME SYSTEMS or their parts
    Annex D (informative) Symbols on marking
    Annex AA (informative) Particular guidance and rationale
    Annex BB (normative) Test for flammability of anaesthetic agent
    Annex DD (informative) Reference to the essential principles
    Bibliography

    Abstract - (Show below) - (Hide below)

    This International Standard is applicable to the BASIC SAFETY and ESSENTIAL PERFORMANCE of an ANAESTHETIC WORKSTATION for administering inhalational anaesthesia whilst continuously attended by a professional OPERATOR.

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

    Committee TC 121
    Document Type Standard
    Product Note The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document.
    Publisher National Standards Authority of Ireland
    Status Superseded
    Superseded By
    Supersedes
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