CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9296 | LVS 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 | 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 |
| 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 |
| 9298 | EN ISO 17664:2004 | Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004) | 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 |
| 9299 | EN 13824:2004 | Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements | Atcelts |
| 9300 | EN 556:1994 + A1:1998 | Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile" | Atcelts |
| 9300 | LVS EN 556:1994 +A1:1998 | Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile" | Atcelts |
| 9301 | EN 556-1:2001 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | Atcelts |
Displaying 21-30 of 173 results.