CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 65050 | LVS EN ISO 13408-6:2021 | Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2021) | Standarts spēkā |
| 58414 | EN ISO 13408-2:2018 | Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018) | Standarts spēkā |
| 62264 | EN ISO 25424:2019 | 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 |
| 65050 | EN ISO 13408-6:2021 | Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2021) | Standarts spēkā |
| 76989 | LVS EN ISO 17664-2:2024 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021) | Standarts spēkā |
| 58413 | LVS EN ISO 11737-1:2018 | Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2018) | Standarts spēkā |
| 9307 | EN ISO 11737-2:2000 | Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process (ISO 11737-2:1998) | Atcelts |
| 35153 | LVS EN ISO 13408-6:2011 | Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005) | Atcelts |
| 9297 | EN ISO 14937:2000 | Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2000) | Atcelts |
| 9311 | EN ISO 11137-3:2006 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006) | Atcelts |
Displaying 51-60 of 173 results.