Skip to main content
Back

Sorry - this product is no longer available

EVS-EN 60601-2-33:2010

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 06.12.2010
Base Documents
IEC 60601-2-33:2010; EN 60601-2-33:2010
Directives or regulations
None

Standard history

Status
Date
Type
Name
Main
prEVS-EN IEC 60601-2-33
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
03.04.2009
Corrigendum
EVS-EN 60601-2-33:2002/A2:2008/AC:2008
Main
EVS-EN 60601-2-33:2002
Amendment
EVS-EN 60601-2-33:2002/A1:2005
Amendment
EVS-EN 60601-2-33:2002/A2:2008
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  ESSENTIAL PERFORMANCE requirements related to INTERVENTIONAL MR EXAMINATIONS.

Required fields are indicated with *

*
*
*
PDF
39.68 € incl tax
Paper
39.68 € incl tax
Browse standard from 2.48 € incl tax
Standard monitoring

Customers who bought this item also bought

Main

EVS-EN 60601-2-37:2008

Medical electrical equipment -- Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment
Withdrawn from 16.12.2024
Main

EVS-EN ISO 14971:2012

Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
Withdrawn from 02.01.2020
Main

EVS-EN ISO 11608-4:2007

Pen-injectors for medical use - Part 4: Requirements and test methods for electronic and electromechanical pen-injectors
Withdrawn from 17.05.2022
Main + corrigendum

EVS-EN ISO 13485:2012

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)
Withdrawn from 02.03.2016