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Full Description

Specifies essential safety requirements for high frequency surgical equipment (other than medical diathermy equipment) which is required to have patient-circuits isolated from earth (at d.c. and mains supply frequencies) and either isolated at operating frequencies or fitted with devices to monitor the integrity of the dispersive electrode connection. Requirements for separate supply isolation transformers and power reduction ratios are deleted from this edition.
 

Document History

  1. AS/NZS IEC 60601.2.2:2016


    Medical electrical equipment, Part 2.2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories

    • Most Recent
  2. AS/NZS 3200.2.2:1999


    Medical electrical equipment, Part 2.2: Particular requirements for safety - High frequency surgical equipment

    • Historical Version
  3. AS 3200-1986 AMDT 1


    Approval and test specification - Electromedical equipment - General requirements

    • Historical Version
  4. AS 3200.2.2-1992


    Approval and test specification - Medical electrical equipment, Part 2.2: Particular requirements for safety - High frequency surgical equipment

    • Historical Version
  5. AS 3202-1989

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    Approval and test specification - Electrosurgical equipment

    • Historical Version
  6. AS 3200-1986


    Approval and test specification - Electromedical equipment - General requirements

    • Historical Version
  7. AS 3200-1980


    Approval and test specification - Electromedical equipment - General requirements

    • Historical Version
  8. AS 3202-1979


    Approval and test specification for electrosurgical equipment

    • Historical Version
  9. AS 3200-1978


    Approval and test specification for electromedical equipment - General requirements

    • Historical Version
  10. AS C200-1970


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

    • Historical Version