CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9290 | EN 1174-1:1996 | Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 1: Requirements | Atcelts |
| 37341 | EN ISO 13408-6:2011/A1:2013 | Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005/DAM 1:2012) | Atcelts |
| 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 |
| 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 |
| 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 |
| 9289 | EN 556:1994 | Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile" | Atcelts |
| 9300 | EN 556:1994 + A1:1998 | Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile" | Atcelts |
Displaying 41-50 of 176 results.