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About This Item

 

Full Description

Specifies requirements for the safe design and manufacture of high frequency surgical equipment. This Standard modifies and has been reproduced from IEC 60601-2-2:1998 with a ZZ Appendix for additional Australian and New Zealand requirements. A thorough working knowledge of its Parent Standard, AS/NZS 3200.1.0:1998, or a readily available copy, is necessary to deal with some of the technical issues raised.
 

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

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    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


    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