DIN EN ISO 11135 E:2011-09
Requirements for the development, validation and routine control of ethylene oxide medical device sterilization processes for sterilization of healthcare products (draft)
- Standard No.
- DIN EN ISO 11135 E:2011-09
- Release Date
- 1970
- Published By
- /
- Status
- Replace By
- DIN EN ISO 11135:2012
- Latest
- DIN EN ISO 11135:2023-05
DIN EN ISO 11135 E:2011-09 history
- 2023 DIN EN ISO 11135:2023-05 Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2023); German and English version prEN ISO 11135:2023 / Note: Date o...
- 2023 DIN EN ISO 11135:2023 Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2023); German and English version prEN ISO 11135:2023
- 2020 DIN EN ISO 11135:2020-04 Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018); German version EN ISO 11135:2014 + A1:2019
- 2020 DIN EN ISO 11135:2020 Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018) (includes Amendment :2019)
- 1970 DIN EN ISO 11135 A1 E:2017-09
- 2014 DIN EN ISO 11135:2014 Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014); German version EN ISO 11135:2014
- 2012 DIN EN ISO 11135:2012 Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2012); German version prEN ISO 11135:2012
- 1970 DIN EN ISO 11135 E:2011-09 Requirements for the development, validation and routine control of ethylene oxide medical device sterilization processes for sterilization of healthcare products (draft)
