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EN ISO 10993-7:2008/AC:2009 Standard

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  Keywords:

#corrigendum #devices #residuals #sterilization #oxide

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

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

  Purpose

Corrigendum to EN ISO 10993-7:2008.

  Publication

Friday 17th of November 2017

  Correction

This standard is a correction for "EN ISO 10993-7:2008"

  Related Standards

EN 60601-2-13:2006

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systemsI...

EN ISO 10993-12:2012

Medical devices Directive (93/42/EEC)

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

EN ISO 11137-1:2015

Medical devices Directive (93/42/EEC)

Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a ster...

EN ISO 11135-1:2007

Medical devices Directive (93/42/EEC)

Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a...

EN ISO 10993-17:2009

Medical devices Directive (93/42/EEC)

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

EN 60601-2-13:2006/A1:2007

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systemsI...

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