CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 35155 | LVS EN ISO 13408-2:2011 | Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003) | 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 |
| 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 |
| 9307 | LVS EN ISO 11737-2:2001 | Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process | Atcelts |
| 27633 | LVS EN 556-1:2002 /AC:2007 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | 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 |
| 28190 | LVS EN ISO 11137-2:2007 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | Atcelts |
| 9298 | LVS EN ISO 17664:2004 | Sterilization of medical devices - Information to be provided by the manufacturer for the reprocessing of resterilizable devices | Atcelts |
| 9299 | LVS EN 13824:2005 | Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements | Atcelts |
| 20669 | LVS EN ISO 11737-1:2006 | Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products | Atcelts |
Displaying 111-120 of 176 results.