UNI EN ISO 11135:2020
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Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
Published date
09-01-2020
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ISO 11135:2014 specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices.
| Committee |
TC 44
|
| DocumentType |
Standard
|
| ProductNote |
This standard also refers to ISO 11138-2:2009.
|
| PublisherName |
Ente Nazionale Italiano di Unificazione (UNI)
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| ISO 11135:2014 | Identical |
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