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Project

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis (IEC 62B/1247/CDV:2021); German and English version prEN IEC 60601-2-33:2021

Abstract

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.

Begin

2021-06-24

Planned document number

DIN EN IEC 60601-2-33

Project number

02230361

Responsible national committee

DKE/GK 813 - Elektrische und mechanische Sicherheit in der radiologischen Technik  

draft standard

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis (IEC 62B/1247/CDV:2021); German and English version prEN IEC 60601-2-33:2021
2022-09
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previous edition(s)

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 + COR1:2012 + A1:2013 + A2:2015 + COR2:2016); German version EN 60601-2-33:2010 + Cor.:2010 + A11:2011 + A1:2015 + A2:2015 + AC:2016 + A12:2016
2017-11

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Contact

Dr.

Renate Förch

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63069 Offenbach am Main

Tel.: +49 69 6308-344

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