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EN 60601-2-33:2010 Standard

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  Keywords:

#equipment #amendment #essential #performance #safety

This standard is superseded by:
  •   EN 60601-2-33:2010/A1:2015 from: 2018-07-23
  •   EN 60601-2-33:2010/A2:2015
  • This standard can be totally or partially supervised by:
  •   EN 60601-2-33:2010/A1:2015
  •   EN 60601-2-33:2010/A2:2015
  •   EN 60601-2-33:2010/AC:2016-03
  •   EN 60601-2-33:2010/A12:2016
  •   Directive

    Medical devices Directive (93/42/EEC)

      Last Official Journal reference

    Wednesday 14th of April 2021

      Description:

    Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosisIEC 60601IEC 60601-2-33:2010

      Purpose

    Amendment for EN 60601-2-33:2010

      Publication

    Friday 17th of November 2017

      Related Standards

    EN 60601-2-10:2000/A1:2001

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    Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulatorsIEC 60601-2-10:198...

    EN ISO 25539-1:2009

    Medical devices Directive (93/42/EEC)

    Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)

    EN 60601-1-2:2015

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    Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: El...

    EN 60601-1-1:2001

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical el...

    EN 60601-1:2006/A1:2013

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Part 1: General requirements for basic safety and essential performanceIEC 60601-1:2005

    EN 60601-1:2006/AC:2010

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Part 1: General requirements for basic safety and essential performanceIEC 60601-1:2005

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