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About This Item

 

Full Description

Specifies the particular requirements for the safety, including essential performances, of transcutaneaous partial pressure monitoring equipment, and applies to equipment used with adults, children and neonates, including their use in foetal monitoring during birth. It does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin. This Standartd is to be read in conjunction with AS/NZS 3200.1.0:1998. It is identical with, and reproduced from, IEC 60601-2-23:1999.
 

Document History

  1. AS 60601.2.23:2018


    Medical electrical equipment, Part 2.23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment (IEC 60601-2-23:2011 (ED. 3.0), MOD)

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  2. AS/NZS 3200.2.23:2001

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    Medical electrical equipment, Part 2.23: Particular requirements for safety - Transcutaneous partial pressure monitoring equipment

    • Historical Version
  3. AS/NZS 3200.2.23:1994


    Approval and test specification - Medical electrical equipment, Part 2.23: Particular requirements for safety - Transcutaneous partial pressure monitoring equipment

    • Historical Version