CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 27791 | LVS EN ISO 14937:2010 | 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 14937:2009) | Standarts spēkā |
| 76162 | LVS EN 556-2:2024 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices | 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 |
| 76163 | EN 556-1:2024 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | Standarts spēkā |
| 72687 | LVS EN ISO 11137-2:2015/A1:2023 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose - Amendment 1 (ISO 11137-2:2013/Amd 1:2022) | Standarts spēkā |
| 80411 | prEN ISO 11135 | Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2025) | Aptauja slēgta |
| 80417 | EN ISO 13408-2:2018/prA1:2025 | Aseptic processing of health care products - Part 2: Sterilizing filtration - Amendment 1 (ISO 13408-2:2018/DAmd1:2025) | Aptauja |
| 9298 | LVS EN ISO 17664:2004 | Sterilization of medical devices - Information to be provided by the manufacturer for the reprocessing of resterilizable devices | Atcelts |
| 24012 | LVS EN ISO 14937:2002 /AC:2005 | 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 | Atcelts |
| 21434 | LVS EN 556-2:2004 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices | Atcelts |
Displaying 51-60 of 176 results.