CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9311 | EN ISO 11137-3:2006 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006) | Atcelts |
| 9297 | EN ISO 14937:2000 | 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 |
| 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 |
| 9307 | EN ISO 11737-2:2000 | Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process (ISO 11737-2:1998) | 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 |
| 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 |
| 27794 | EN ISO 14160:2011 | Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO/DIS 14160:2009) | 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 |
| 35154 | EN ISO 13408-1:2011 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008) | Atcelts |
| 35155 | EN ISO 13408-2:2011 | Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003) | Atcelts |
Displaying 101-110 of 179 results.