CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 20669 | EN ISO 11737-1:2006 | Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006) | Atcelts |
| 9293 | EN 1174-2:1996 | Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 2: Guidance | Atcelts |
| 9309 | EN ISO 11137-2:2012 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2012) | Atcelts |
| 9299 | EN 13824:2004 | Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements | Atcelts |
| 9301 | EN 556-1:2001 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | Atcelts |
| 9311 | EN ISO 11137-3:2006 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006) | Atcelts |
| 32635 | CEN ISO/TS 11135-2:2008/AC:2009 | Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008/Cor 1:2009) | Atcelts |
| 37754 | EN ISO 11137-1:2006/A1:2013 | 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/Amd 1:2013) | Atcelts |
| 35748 | EN ISO 25424:2011 | Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009) | Atcelts |
| 9302 | EN 552:1994/A1:1999 | Sterilization of medical devices - Validation and routine control of sterilization by irradiation | Atcelts |
Displaying 131-140 of 173 results.