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FprEN IEC 60601-2-33:2022 Edition 11/2022
Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
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Abstract

This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MAGNETIC RESONANCE (MR) EQUIPMENT and MAGNETIC RESONANCE (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.

Status

Final draft - Active

Origin

Technical Committee :
CLC/TC 62 : Electrical equipment in medical practice

Implementation

start of the vote on the project    16/07/2021   date of ratification (dor)    08/09/2022
end of the vote on the project    08/10/2021   date of anouncement (doa)    08/02/2023
start of the vote on the final project    15/04/2022   date of publication (dop)    09/05/2023
end of the vote on the final project    27/05/2022   date of withdrawal (dow)    09/05/2023


Publication Official Journal
of the Grand-Duchy of Luxembourg
Reference

Relations

Relations to older standards
ILNAS-EN 60601-2-33:2010/AC:2016-03
ILNAS-EN 60601-2-33:2010/A12:2016

Relations to international standards
IEC 60601-2-33 ED4 
IEC 60601-2-33:2022 
IEC 60601-2-33 Ed.4.0 

International Classification for Standards (ICS codes) :

11.040.55 : Diagnostic equipment

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