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ISO/FDIS 11135:2026
Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices
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Summary
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.
Notes
30.99 : CD approuvé pour enregistrement comme DIS
Technical characteristics
| Publisher | International Organization for Standardization (ISO) |
| Publication Date | 05/12/2026 |
| Edition | 3 |
| Page Count | 110 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
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07/07/2014
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07/07/2014
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