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EVS-EN 60601-2-33:2010+A11+A1+A2+A12:2016

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2010+ IEC 60601-2-33:2010/A1:2013 + IEC 60601-2-33:2010/A2:2015)

General information

Valid from 01.04.2019
Base Documents
EN 60601-2-33:2010; IEC 60601-2-33:2010; EN 60601-2-33:2010/A1:2015; IEC 60601-2-33:2010/A1:2013; EN 60601-2-33:2010/A11:2011; EN 60601-2-33:2010/A12:2016; EN 60601-2-33:2010/A2:2015; IEC 60601-2-33:2010/A2:2015; EN 60601-2-33:2010/Corr:2010; EN 60601-2-33:2010/AC:2016-03; IEC 60601-2-33:2010/COR2:2016
Directives or regulations
None

Standard history

Status
Date
Type
Name
Main
prEN IEC 60601-2-33:2021
01.04.2019
Main + amendment
06.12.2016
Amendment
04.04.2016
Corrigendum
06.10.2015
Amendment
08.06.2015
Amendment
02.11.2011
Amendment
06.12.2010
Corrigendum
06.12.2010
Main
Clause 1 of the general standard applies, except as follows:
201.1.1  Scope
Replacement:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MR EQUIPMENT and MR SYSTEMS, hereafter referred to also as ME EQUIPMENT.
This standard does not cover the application of MR EQUIPMENT beyond the INTENDED USE.
If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.
The standard does not formulate specific requirements for MR EQUIPMENT or MR SYSTEMS used
in INTERVENTIONAL MR EXAMINATIONS.

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