CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 35153 | LVS EN ISO 13408-6:2011 | Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005) | Atcelts |
| 60763 | LVS EN ISO 13408-1:2015 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013) | Atcelts |
| 9308 | LVS 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 | Atcelts |
| 9303 | LVS EN ISO 11135-1:2007 | Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 9293 | LVS EN 1174-2:1996 | Sterilization of medical devices - Estimation of the population of microorganisms on product - Part 2: Guidance | Atcelts |
| 27133 | LVS 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 |
| 32635 | LVS 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 |
| 9303 | EN ISO 11135-1:2007 | Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007) | Atcelts |
| 9296 | LVS EN ISO 14160:1998 | Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilants | Atcelts |
| 9301 | LVS EN 556-1:2002 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | Atcelts |
Displaying 131-140 of 179 results.