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EVS-EN 60601-2-23:2002

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

General information

Withdrawn from 04.11.2015
Base Documents
IEC 60601-2-23:1999; EN 60601-2-23:2000
Directives or regulations
93/42/EEC Medical devices (MDD)

Although the standard’s status is withdrawn, it still has the presumption of conformity in the meaning of regulation 93/42/EEC and conformance with the regulation ’s requirements can be guaranteed by using the withdrawn version of the standard. The presumption of conformity is valid until a corresponding amendment is published in the Official Journal of the European Union.
 
To view the latest lists of harmonised standards published in the Official Journal of the European Union, visit: 
http://ec.europa.eu/growth/single-market/european-standards/harmonised-standards/

Directive 93/42/EEC (Medical devices) Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.

Standard history

Status
Date
Type
Name
04.11.2015
Main
01.01.2003
Main
Main
EVS-EN 60601-2-23:2001
Specifies the particular requirements for the safety of transcutaneous partial pressure monitoring equipment. Applies to transcutaneous monitors used with adults, children and neonates and includes the use of these
devices in foetal monitoring during birth.

Required fields are indicated with *

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