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EN ISO 10993-1:2009/AC:2010 Standard

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  Keywords:

#corrigendum #process #management #risk #testing

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)

  Purpose

Corrigendum to EN ISO 10993-1:2009.

  Publication

Friday 17th of November 2017

  Correction

This standard is a correction for "EN ISO 10993-1:2009"

  Related Standards

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EN 60601-2-54:2009

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Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipmen...

EN 61217:2012

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Radiotherapy equipment - Coordinates, movements and scalesIEC 61217:2011

EN 62304:2006

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Medical device software - Software life-cycle processesIEC 62304:2006

EN 62304:2006/AC:2008

Medical devices Directive (93/42/EEC)

Medical device software - Software life-cycle processesIEC 62304:2006

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