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EN ISO 10993-7:2008 Standard

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  Keywords:

#corrigendum #devices #residuals #sterilization #oxide

This standard can be totally or partially supervised by:
  •   EN ISO 10993-7:2008/AC:2009
  •   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

      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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