CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 17664:2017) | Atcelts |
| 9311 | EN ISO 11137-3:2006 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006) | Atcelts |
| 27133 | CEN ISO/TS 11135-2:2008 | Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008) | Atcelts |
| 9306 | EN 552:1994/A2:2000 | Sterilization of medical devices - Validation and routine control of sterilization by irradiation | Atcelts |
| 9298 | EN ISO 17664:2004 | Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004) | Atcelts |
| 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/Amd 1:2013) | Atcelts |
| 39251 | LVS EN 556-2:2016 | Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices | Atcelts |
| 9289 | EN 556:1994 | Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile" | Atcelts |
| 23112 | EN ISO 14937:2000/AC:2003 | 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 |
Displaying 71-80 of 173 results.