CEN/TC 204
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
60763 | EN ISO 13408-1:2015 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013) | Atcelts |
9283 | EN 550:1994 | Sterilization of medical devices - Validation and routine control of ethylene oxide sterilization | Atcelts |
9302 | LVS EN 552:1994/A1:1999 | Sterilization of medical devices - Validation and routine control of sterilization by irradiation | 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 |
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 |
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 |
27134 | CEN ISO/TS 17665-2:2009 | Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO/TS 17665-2:2009) | Atcelts |
41915 | EN ISO 17664:2017 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017) | Atcelts |
35154 | EN ISO 13408-1:2011 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008) | 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 |
Displaying 51-60 of 173 results.