CEN/TC 204
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
9305 | EN ISO 17665-1:2006 | Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) | Atcelts |
23028 | EN ISO 11137-2:2006 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006) | 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 |
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 |
9289 | EN 556:1994 | Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile" | Atcelts |
35153 | LVS EN ISO 13408-6:2011 | Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005) | 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 |
41106 | LVS CEN ISO/TS 13004:2014 | Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO/TS 13004:2013) | Atcelts |
37341 | LVS 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 |
Displaying 51-60 of 173 results.