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SRPS EN 60601-2-23:2009

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

Dec 29, 2009
Dec 29, 2009
95.99   Withdrawal of Standard   Dec 17, 2018

General information

95.99     Dec 17, 2018

ISS

N062

European Norm

11.040.55  

Serbian  

Buying

Withdrawn

Language in which you want to receive the document.

Scope

Specifies requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment, whether this equipment is stand alone or part of a system. Applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Harmonized

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS IEC 60601-2-23:1999

NOW

WITHDRAWN
SRPS EN 60601-2-23:2009
95.99 Withdrawal of Standard
Dec 17, 2018

REVISED BY

PUBLISHED
SRPS EN 60601-2-23:2017

Related project

Adopted from EN 60601-2-23:2000