ISO-11135-1 › Historical Revision Information
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices

ISO-11135-1 - 1ST EDITION REPRINT - SUPERSEDED -- See the following: ISO-11135
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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.

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11.080.01 (Sterilization and disinfection in general Including sterilization methods, air quality of surgery rooms, etc.)

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Document Number

ISO 11135-1:2007

Revision Level

1ST EDITION REPRINT

Status

Superseded

Publication Date

Nov. 1, 2007

Committee Number

ISO/TC 198