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ISO 11135-1:2007 [ Withdrawn ]

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

standard by International Organization for Standardization , 05/01/2007

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Identical versions for sale:
Outside United States: BS EN ISO 11135-1:2007
German: DIN EN ISO 11135-1:2007
Spanish: UNE EN ISO 11135-1:2007

ISO 11135-1:2007 specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices.

Sterilization processes validated and controlled in accordance with the requirements of ISO 11135-1:2007 are not assumed to be effective in inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeld Jacob disease. Specific recommendations have been produced in particular countries for the processing of materials potentially contaminated with these agents.

 

Product Details

Published:
05/01/2007
File Size:
1 file , 310 KB
Same As:
BS EN ISO 11135-1:2007, BS EN ISO 11135-1:2007
Note:
This product is unavailable in Ukraine, Russia, Belarus
 

Document History

  1. ISO 11135:2014


    Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices

    • Most Recent

  2. ISO/TS 11135-2:2008


    Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1

    • Historical Version

  3. ISO 11135-1:2007

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

    • Historical Version

  4. ISO 11135:1994


    Medical devices -- Validation and routine control of ethylene oxide sterilization

    • Historical Version