CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 38868 | EN ISO 11137-2:2013 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013) | Atcelts |
| 35154 | EN ISO 13408-1:2011 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008) | Atcelts |
| 9287 | EN 554:1994 | Sterilization of medical devices - Validation and routine control of sterilization by moist heat | Atcelts |
| 26001 | EN 15424:2007 | Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 9285 | EN 552:1994 | Sterilization of medical devices - Validation and routine control of sterilization by irradiation | Atcelts |
| 9308 | 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 (ISO 11137-1:2006) | Atcelts |
| 9300 | EN 556:1994 + A1:1998 | Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile" | Atcelts |
| 9289 | EN 556:1994 | Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile" | 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 17664:2017) | Atcelts |
| 27794 | EN ISO 14160:2011 | Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO/DIS 14160:2009) | Atcelts |
Displaying 71-80 of 173 results.