CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 27305 | 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 |
| 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 |
| 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 |
| 27133 | LVS 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 |
| 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 |
| 26001 | LVS EN 15424:2007 | Sterilization of medical devices - Development, validation and routine control of sterilization processes - Low Temperature Steam and Formaldehyde | Atcelts |
| 26001 | EN 15424:2007 | Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 24012 | LVS EN ISO 14937:2002 /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 | 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 | 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 |
Displaying 111-120 of 176 results.