CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 68466 | EN ISO 13408-1:2024 | Aseptic processing of health care products - Part 1: General requirements (ISO/DIS 13408-1:2021) | Standarts spēkā |
| 60761 | LVS EN ISO 11137-1:2015 | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013) | Standarts spēkā |
| 35152 | LVS EN ISO 13408-5:2011 | Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006) | Standarts spēkā |
| 35151 | LVS EN ISO 13408-3:2011 | Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006) | Standarts spēkā |
| 62251 | EN ISO 11737-2:2020 | Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO/DIS 11737-2:2018) | Standarts spēkā |
| 62251 | LVS EN ISO 11737-2:2020 | Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019) | Standarts spēkā |
| 72112 | EN ISO 25424:2019/A1:2022 | Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 1 (ISO 25424:2018/DAM 1:2021) | Standarts spēkā |
| 62262 | EN ISO 11135:2014/A1:2019 | Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/DAM 1:2017) | Standarts spēkā |
| 58413 | EN ISO 11737-1:2018 | Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on product (ISO/DIS 11737-1:2016) | Standarts spēkā |
| 62264 | LVS EN ISO 25424:2020 | Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2018) | Standarts spēkā |
Displaying 141-150 of 176 results.