CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 23028 | LVS EN ISO 11137-2:2006 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | Atcelts |
| 9311 | LVS EN ISO 11137-3:2006 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects | Atcelts |
| 35748 | LVS EN ISO 25424:2011 | Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009) | Atcelts |
Displaying 101-110 of 179 results.