CEN/TC 204
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
21434 | LVS EN 556-2:2004 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices | Atcelts |
9296 | 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 (ISO 14160:1998) | Atcelts |
26001 | LVS EN 15424:2007 | Sterilization of medical devices - Development, validation and routine control of sterilization processes - Low Temperature Steam and Formaldehyde | Atcelts |
9302 | LVS EN 552:1994/A1:1999 | Sterilization of medical devices - Validation and routine control of sterilization by irradiation | Atcelts |
9289 | LVS EN 556:1994 | Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile" | Atcelts |
37321 | LVS EN ISO 13408-1:2011 /A1:2013 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013) | Atcelts |
9283 | EN 550:1994 | Sterilization of medical devices - Validation and routine control of ethylene oxide sterilization | 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 |
24012 | EN ISO 14937:2000/AC:2005 | 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 |
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 41-50 of 173 results.