AS/NZS 3200.2.23:2001
Approval and test specification - Medical electrical equipment - Particular requirements for safety - Transcutaneous partial pressure monitoring equipment
Specifies the particular requirements for the safety, including essential performances, of transcutaneous 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 Standard 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.
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