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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Withdrawn from 04.11.2015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
ICS Groups
11.040.55 Diagnostic equipment
Directives or regulations
None

Standard history

Status
Date
Type
Name
04.11.2015
Main
EVS-EN 60601-2-23:2015
01.01.2003
Main
EVS-EN 60601-2-23:2002
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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Standards designation

EVS Estonian standard
EN European standard (published by an CEN or CENELEC)
EN ISO International standard adopted as an European standard
ISO International Organization for Standardization’s standard
IEC International Electrotechnical Commission’s standard
HD CENELEC’s harmonisation document
   
EVS-EN European standard implemented in Estonia
EVS-EN ISO International standard adopted in Europe and implemented in Estonia
EVS-EN ISO/IEC International standard/International electrotechnical standard adopted in Europe and implemented in Estonia
EVS-IEC International electrotechnical standard implemented in Estonia
EVS-ISO International standard implemented in Estonia
   
A, AMD amedment
+A a full standard plus the amendment
/A only amendment
COR, AC corrigendum
+COR a full standard plus the corrigendum
NA national annex
+NA a full standard plus the national annex
/NA only national annex
TS technical specification
TR technical report
CWA agreement, developed by a CEN or CENELEC
prEVS-EN (etc) draft standard
   
et the standard is in Estonian only
en the standard is in English only
et-en the standard is in Parallel text Estonian-English