CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9290 | LVS EN 1174-1:1996 | Sterilization of medical devices - Estimation of the population of microorganisms on product - Part 1: Requirements | Atcelts |
| 28190 | LVS EN ISO 11137-2:2007 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | Atcelts |
| 35154 | LVS EN ISO 13408-1:2011 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008) | Atcelts |
| 41915 | LVS EN ISO 17664:2018 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017) | 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 |
| 27305 | LVS 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 |
| 21434 | LVS EN 556-2:2004 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices | Atcelts |
| 27794 | LVS 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 14160:2011) | Atcelts |
| 9308 | LVS EN ISO 11137-1:2006 | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 37754 | LVS EN ISO 11137-1:2006 /A1:2013 | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/Amd 1:2013) | Atcelts |
Displaying 71-80 of 179 results.