CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9310 | prEN ISO 11137-3 | Sterilization of medical devices - Microbiological methods - Part 3: Guidance on the evaluation and interpretation of bioburden data | Izstrādē |
| 9305 | 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 (ISO 17665-1:2006) | Atcelts |
| 23028 | EN ISO 11137-2:2006 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006) | Atcelts |
| 35154 | EN ISO 13408-1:2011 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008) | Atcelts |
| 9294 | EN 1174-3:1996 | Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 3: Guide to the methods for validation of microbiological techniques | Atcelts |
| 41106 | LVS CEN ISO/TS 13004:2014 | Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO/TS 13004:2013) | Atcelts |
| 21434 | EN 556-2:2003 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices | Atcelts |
| 41106 | CEN ISO/TS 13004:2014 | Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO/TS 13004:2013) | Atcelts |
| 41915 | LVS EN ISO 17664:2018 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017) | Atcelts |
| 9308 | LVS EN ISO 11137-1:2006 | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices | Atcelts |
Displaying 21-30 of 173 results.