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About This Item

 

Full Description

Incorporates general requirements for safety of electromedical equipment (including associated accessories and materials), and is the 'parent' of a series of approval and test specifications to cover individual items of equipment. It specifies the degrees of isolation of patient-circuits from both live parts and earth, sufficient to ensure the safety of the patient from electric shock made under conditions likely to be experienced in service. It provides for three classes of patient-circuit.
 

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


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

    • Historical Version
  5. AS 3200-1986

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    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
 

Amendments, rulings, supplements, and errata

  1. AS 3200-1986 AMDT 1


    Approval and test specification - Electromedical equipment - General requirements