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EVS-EN 60601-2-23:2015

Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment

General information

Valid from 04.11.2015
Base Documents
EN 60601-2-23:2015; IEC 60601-2-23:2011
Directives or regulations
None

Standard history

Status
Date
Type
Name
Main
prEN IEC 80601-2-23:2024
04.11.2015
Main
01.01.2003
Main
IEC 60601-2-23:2011 applies to the basic safety and essential performance of transcutaneous partial pressure monitoring equipment. It applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth. IEC 60601-2-23:2011 does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa). This third edition cancels and replaces the second edition published in 1999 and constitutes a technical revision. This edition of IEC 60601-2-23 was revised to align structurally with the 2005 edition of IEC 60601-1.

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