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About This Item

 

Full Description

Specifies safety requirements for the safety of endoscopic equipment and integrated instrumentation used for medical diagnosis and for treatment in body cavities. It enables testing and certification of individual component parts of endoscopic equipment. This Standard is technically identical to IEC 601-2-18:1990, with the addition of an Appendix which lists Australian requirements. It is supplementary to AS 3200.1-1990, Approval and test specification - Medical electrical equipment, Part 1: General requirements for safety.
 

Document History

  1. AS/NZS IEC 60601.2.18:2015


    Medical electrical equipment, Part 2.18: Particular requirements for basic safety and essential performance of endoscopic equipment

    • Most Recent
  2. AS 3200-1986 AMDT 1


    Approval and test specification - Electromedical equipment - General requirements

    • Historical Version
  3. AS/NZS 3200.2.18:1997


    Approval and test specification - Medical electrical equipment, Part 2.18: Particular requirements for safety - Endoscopic equipment

    • Historical Version
  4. AS 3200.2.18-1992

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    Approval and test specification - Medical electrical equipment, Part 2.18: Particular requirements for safety - Endoscopic equipment

    • Historical Version
  5. AS 3200-1986


    Approval and test specification - Electromedical equipment - General requirements

    • Historical Version
  6. AS 3200-1980


    Approval and test specification - Electromedical equipment - General requirements

    • Historical Version
  7. AS 3200-1978


    Approval and test specification for electromedical equipment - General requirements

    • Historical Version
  8. AS C200-1970


    Approval and test specification for definitions and general requirementsfor electro-medical equipment

    • Historical Version