CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 27305 | LVS EN ISO 11737-1:2006 /AC:2009 | Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006/Cor 1:2007) | Atcelts |
| 9290 | LVS EN 1174-1:1996 | Sterilization of medical devices - Estimation of the population of microorganisms on product - Part 1: Requirements | Atcelts |
| 27913 | LVS EN ISO 11737-2:2010 | Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009) | Atcelts |
| 9294 | LVS EN 1174-3:1996 | Sterilization of medical devices - Estimation of the population of microorganisms on product - Part 3: Guide to the methods for validation of microbiological techniques | Atcelts |
| 27134 | LVS CEN ISO/TS 17665-2:2009 | Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO 17665-2:2009) | Atcelts |
| 23112 | LVS EN ISO 14937:2002 /AC:2004 | 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 |
| 37754 | LVS EN ISO 11137-1:2006 /A1:2013 | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/Amd 1:2013) | Atcelts |
| 35154 | LVS EN ISO 13408-1:2011 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008) | 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 |
Displaying 51-60 of 173 results.