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About This Item

 

Full Description

Specifies the particular requirements for the safety, including essential performances, of automatic cycling non-invasive blood pressure monitoring equipment, which may be attended or unattended. It does not apply to blood pressure measuring equipment which uses finger transducers or to semi-automatic blood pressure measuring equipment, typically in which each determination needs to be initiated manually. This Standard is to be read in conjunction with AS/NZS 3200.1.0:1998. It modifies and has been reproduced from IEC 60601-2-30:1999 with variations for Australia and New Zealand included in Appendix ZZ.
 

Document History

  1. AS 80601.2.30:2018


    Medical electrical equipment, Part 2.30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers (IEC 80601-2-30:2018, MOD)

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  2. AS/NZS 3200.2.30:2001

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    Medical electrical equipment, Part 2.30: Particular requirements for safety - Automatic cycling non-invasive blood pressure monitoring equipment (IEC 60601-2-30:1999, MOD)

    • Historical Version
  3. AS/NZS 3200.2.30:1996


    Approval and test specification - Medical electrical equipment, Part 2.30: Particular requirements for safety - Automatic cycling indirect blood pressure monitoring equipment

    • Historical Version