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prEN IEC 60601-2-33:2021

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

General information
Draft
Base Documents
IEC 60601-2-33 Ed.4.0; prEN IEC 60601-2-33:2021
Directives or regulations
None
Standard history
Status
Date
Type
Name
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
Main
06.12.2010
Corrigendum
This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MR EQUIPMENT and MR SYSTEMS. NOTE Where ME EQUIPMENT and ME SYSTEMS are used in the clause headings, this is to be understood to indicate MR EQUIPMENT and MR SYSTEMS. This document does not cover the application of MR EQUIPMENT beyond the INTENDED USE. If a clause or subclause is specifically intended to be applicable to MR EQUIPMENT only, or to MR 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 MR EQUIPMENT and to MR SYSTEMS, as relevant. This document does not formulate additional specific requirements for MR EQUIPMENT or MR SYSTEMS used in INTERVENTIONAL MR EXAMINATIONS.
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Standard monitoring