AS/NZS 3200.2.23:1994
Approval and test specification - Medical electrical equipment - Particular requirements for safety - Transcutaneous partial pressure monitoring equipment
This document has been re-assessed by the committee, and judged to still be up to date.
Specifies the particular requirements for the electrical safety of transcutaneous partial pressure monitoring equipment and applies to equipment used with adults, children and neonates. It does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body. It is supplementary to AS 3200.1-1990/NZS 6150:1990 Approval and test specification - Medical electrical equipment, Part 1: General requirements for safety. This standard is identical to and reproduced from IEC 60601-2-23:1993.
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Publishing information
Status: SUPERSEDED
Published: No published date found.
Pages: 22
Committee: HE/03
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Approval and test specification - Medical electrical equipment - Particular requirements for safety - Transcutaneous partial pressure monitoring equipment
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