IEC 60601-2-23:2011 ED3

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 ED3

Publication date:   Feb 25, 2011

General information

60.60 Standard published   Feb 25, 2011

IEC

TC 62/SC 62D

International Standard

11.040.55   Diagnostic equipment

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Published

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Scope

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.

Life cycle

PREVIOUSLY

WITHDRAWN
IEC 60601-2-23:1999 ED2

NOW

PUBLISHED
IEC 60601-2-23:2011 ED3
60.60 Standard published
Feb 25, 2011

REVISED BY

ABANDON
IEC 60601-2-23 ED4

IN_DEVELOPMENT
IEC 80601-2-23 ED1