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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 ISO 11138-2:2009

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EN ISO 10993-4:2009

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Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd...

EN ISO 10993-7:2008/AC:2009

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Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)

EN ISO 10993-12:2012

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Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)

EN ISO 10993-13:2010

Medical devices Directive (93/42/EEC)

Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medic...

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