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EN 60601-2-33:2010/A12:2016 Standard

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  Keywords:

#equipment #amendment #essential #performance #safety

  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

  Amendment

This standard is an amendment for "EN 60601-2-33:2010"

  Reference

This standard supersedes the "EN 60601-2-33:2010/AC:2016 (-03)"

Anyway is still possible use the "EN 60601-2-33:2010/AC:2016 (-03)" until November 1st, 2019

  Related Standards

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EN ISO 7197:2009

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Neurosurgical implants - Sterile, single-use hydrocephalus shunts and components (ISO 7197:2006, including Cor 1:2007)

EN ISO 7376:2009

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EN ISO 7396-1:2007

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Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2007)

EN ISO 7396-1:2007/A1:2010

Medical devices Directive (93/42/EEC)

Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2007)

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