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About This Item

 

Full Description

Specifies particular requirements for the safety of laser equipment for medical applications classified as Class 3B or Class 4 laser product. This Standard is to be read in conjunction with AS 3200.1.0-1990, and is technically equivalent to IEC 602-2-22:1993 and incorporates an Appendix ZZ of additional requirements for Australia and New Zealand.
 

Document History

  1. AS IEC 60601.2.22:2014


    Medical electrical equipment, Part 2.22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment

    • Most Recent
  2. AS/NZS 3200.2.22:1997

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    Approval and test specification - Medical electrical equipment, Part 2.22: Particular requirements for safety - Diagnostic and therapeutic laser equipment

    • Historical Version
  3. AS/NZS 3200.2.22:1993


    Approval and test specification - Medical electrical equipment, Part 2.22: Particular requirements for safety - Diagnostic and therapeutic laser equipment

    • Historical Version