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EVS-EN IEC 60601-2-33:2024

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

General information

Valid from 15.10.2024
Base Documents
IEC 60601-2-33:2022; EN IEC 60601-2-33:2024
Directives or regulations
None

Standard history

Status
Date
Type
Name
06.12.2016
Amendment
EVS-EN 60601-2-33:2010/A12:2016
04.04.2016
Corrigendum
EVS-EN 60601-2-33:2010/AC:2016
06.10.2015
Amendment
EVS-EN 60601-2-33:2010/A2:2015
08.06.2015
Amendment
EVS-EN 60601-2-33:2010/A1:2015
02.11.2011
Amendment
EVS-EN 60601-2-33:2010/A11:2011
06.12.2010
Main
EVS-EN 60601-2-33:2010
06.12.2010
Corrigendum
EVS-EN 60601-2-33:2010/AC:2010

IEC 60601-2-33 applies to the basic safety and essential performance of magnetic resonance (MR) equipment and magnetic resonance (MR) systems. It does not cover the application of MR equipment beyond the intended use.

If a clause or subclause is specifically intended to apply to MR equipment or 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 MR systems, as relevant. IEC 60601-2-33 does not formulate additional requirements for MR equipment, or MR systems used in interventional MR examinations.

IEC 60601-2-33:2022 text has been approved in Europe as EN IEC 60601-2-33:2024 without any changes.

Required fields are indicated with *

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