DIN EN ISO 11135/A1 - DRAFT Historical [ Withdrawn ]

1992059

Draft Document - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014/DAM 1:2017); German and English version EN ISO 11135:2014/prA1:2017

standard by DIN-adopted European-adopted ISO Standard , 09/01/2017

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Document History

  1. DIN EN ISO 11135


    Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018) (includes Amendment :2019)

    • Most Recent

  2. DIN EN ISO 11135/A1 - DRAFT

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    Draft Document - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014/DAM 1:2017); German and English version EN ISO 11135:2014/prA1:2017

    • Historical Version

  3. DIN EN ISO 11135


    Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014)

    • Historical Version

  4. DIN EN ISO 11135 - DRAFT


    Draft Document - Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2012); German version prEN ISO 11135:2012

    • Historical Version

  5. DIN EN ISO 11135 - DRAFT


    Draft Document - Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2011); German version prEN ISO 11135:2011

    • Historical Version

  6. DIN EN ISO 11135-1


    Sterilization of health care products - Ethylene oxide - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)

    • Historical Version

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Product Details

Published:

09/01/2017

Number of Pages:

15

File Size:

1 file

Product Code(s):

2690727, 2690727

Note:

This product is restricted and cannot be purchased in the following countries Ukraine, Russia, Belarus