CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 27913 | EN ISO 11737-2:2009 | Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO/FDIS 11737-2:2009) | Atcelts |
| 28190 | EN ISO 11137-2:2007 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006, corrected version 2006-08-01) | Atcelts |
| 37321 | EN ISO 13408-1:2011/A1:2013 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2011/DAM 1:2011) | Atcelts |
| 27305 | EN ISO 11737-1:2006/AC:2009 | Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006/Cor 1:2007) | Atcelts |
| 32632 | EN ISO 11137-2:2007/AC:2009 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006/Cor 1:2009) | Atcelts |
| 60763 | EN ISO 13408-1:2015 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013) | Atcelts |
| 39251 | EN 556-2:2015 | Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE'' - Part 2: Requirements for aseptically processed medical devices | Atcelts |
| 27633 | EN 556-1:2001/AC:2006 | Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices | Atcelts |
| 41915 | EN ISO 17664:2017 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO/DIS 17664:2016) | 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 |
Displaying 71-80 of 179 results.