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EVS-EN 60601-2-40:2019

Medical electrical equipment - Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment

General information

Valid from 16.01.2019
Base Documents
IEC 60601-2-40:2016; EN 60601-2-40:2019
ICS Groups
11.040.20 Transfusion, infusion and injection equipment 11.040.55 Diagnostic equipment 11.040.99 Other medical equipment
Directives or regulations
None

Standard history

Status
Date
Type
Name
Main
prEN IEC 60601-2-40:2023
16.01.2019
Main
EVS-EN 60601-2-40:2019
01.05.2001
Main
EVS-EN 60601-2-40:2001
Establishes particular requirements for the safety of electromyographs and evoked response equipment as defined in clause 2 of this standard.

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English (PDF 557 KB)

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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