CEN/TC 204
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
27633 | LVS EN 556-1:2002 /AC:2007 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | Atcelts |
9297 | LVS EN ISO 14937:2002 | 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 | Atcelts |
28190 | LVS EN ISO 11137-2:2007 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | Atcelts |
9299 | LVS EN 13824:2005 | Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements | Atcelts |
9283 | EN 550:1994 | Sterilization of medical devices - Validation and routine control of ethylene oxide sterilization | 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 |
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 |
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 131-140 of 173 results.