CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9299 | EN 13824:2004 | Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements | Atcelts |
| 9301 | EN 556-1:2001 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | Atcelts |
| 9311 | EN ISO 11137-3:2006 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006) | 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 |
| 35154 | LVS EN ISO 13408-1:2011 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008) | Atcelts |
| 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 |
| 9305 | LVS EN ISO 17665-1:2006 | Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 9284 | prEN 551 | Sterilization of medical devices - Method for validation and routine control of ethylene oxide sterilization - Guidance | Izstrādē |
| 76997 | CEN ISO/TS 11137-4:2023 | Sterilization of health care products - Radiation - Part 4: Guidance on process control (ISO/TS 11137-4:2020) | Izstrādē |
| 9310 | prEN ISO 11137-3 | Sterilization of medical devices - Microbiological methods - Part 3: Guidance on the evaluation and interpretation of bioburden data | Izstrādē |
Displaying 151-160 of 178 results.