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EN ISO 17664:2004 Standard

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  Keywords:

#devices #medical #sterilizable #iso #resterilizable

This standard is superseded by:
  •   EN ISO 17664:2017
  •   Directive

    Medical devices Directive (93/42/EEC)

      Last Official Journal reference

    Wednesday 14th of April 2021

      Description:

    Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004)

      Purpose

    This standard specifies the information to be provided by the medical device manufacturer on the processing of medical devices claimed to be re-sterilizable and medical devices intended to be sterilized by the processor.

      Publication

    Friday 17th of November 2017

      Cessation

    This standard has been withdrawn on 2021-09-30

      Related Standards

    EN 13544-2:2002+A1:2009

    Medical devices Directive (93/42/EEC)

    Respiratory therapy equipment - Part 2: Tubing and connectors

    EN ISO 10651-4:2009

    Medical devices Directive (93/42/EEC)

    Lung ventilators - Part 4: Particular requirements for operator-powered resuscitators (ISO 10651-4:2002)

    EN ISO 10993-9:2009

    Medical devices Directive (93/42/EEC)

    Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation produc...

    EN ISO 10993-7:2008/AC:2009

    Medical devices Directive (93/42/EEC)

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

    EN ISO 10993-7:2008

    Medical devices Directive (93/42/EEC)

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

    EN ISO 10993-6:2009

    Medical devices Directive (93/42/EEC)

    Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)

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