Status : Published (To be revised)

This standard was last reviewed and confirmed in 2020. Therefore this version remains current.
This standard will be replaced by ISO/DIS 11135.2
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Abstract

ISO 11135:2014 specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the industrial and health care facility settings, and it acknowledges the similarities and differences between the two applications.

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General information

  • Status
     : Published
    Publication date
     : 2014-07
    Stage
    : International Standard to be revised [90.92]
  • Edition
     : 2
    Number of pages
     : 78
  • Technical Committee :
    ISO/TC 198
    ICS :
    11.080.01 
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Life cycle

Sustainable Development Goals

This standard contributes to the following Sustainable Development Goal

3
Good Health and Well-being

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