CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9306 | LVS EN 552:1994/A2:2000 | Sterilization of medical devices - Validation and routine control of sterilization by irradiation | Atcelts |
| 35155 | LVS EN ISO 13408-2:2011 | Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003) | Atcelts |
| 9296 | EN ISO 14160:1998 | Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilants (ISO 14160:1998) | Atcelts |
| 9284 | prEN 551 | Sterilization of medical devices - Method for validation and routine control of ethylene oxide sterilization - Guidance | Izstrādē |
| 9310 | prEN ISO 11137-3 | Sterilization of medical devices - Microbiological methods - Part 3: Guidance on the evaluation and interpretation of bioburden data | Izstrādē |
| 9288 | prEN 555 | Sterilization of medical devices - Method for validation and routine control of steam sterilization - Guidance | Izstrādē |
| 78154 | prCEN ISO/TS 17664-3 | Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 3: Guidance on the designation of a reusable medical device to a quantitative cleaning classification | Izstrādē |
| 79283 | prEN ISO 11737-1 rev | Sterilization of health care products — Microbiological methods — Part 1: Determination of a population of microorganisms on products | Izstrādē |
| 21959 | CEN/TC 204 N 470 | Sterilization of medical devices - Development, validation and routine control of sterilization processes - Low Temperature Steam and Formaldehyde | Izstrādē |
| 72399 | 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 11135:2024) | Izstrādē |
Displaying 151-160 of 173 results.