Reference number
ISO 11135-1:2007
© ISO 2025
ISO 11135-1:2007
Sterilization of health care products — Ethylene oxide — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
Edition 1
2007-05
Withdrawn
Withdrawn (Edition 1, 2007)

Abstract

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.

General information

  • Status
     : Withdrawn
    Publication date
     : 2007-05
    Corrected version (en)
     : 2007-10
    Corrected version (fr)
     : 2007-10
    Stage
    : Withdrawal of International Standard [95.99]
  • Edition
     : 1
    Number of pages
     : 41
  • Technical Committee :
    ISO/TC 198
    ICS :
    11.080.01 
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