CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 38868 | LVS EN ISO 11137-2:2013 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013) | Atcelts |
| 37321 | LVS EN ISO 13408-1:2011 /A1:2013 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013) | Atcelts |
| 35154 | LVS EN ISO 13408-1:2011 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008) | Atcelts |
| 78154 | prCEN ISO/TS 17664-3 | Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 3: Guidance on the designation of a reusable medical device to a quantitative cleaning classification | Izstrādē |
| 82878 | prEN ISO 11737-3 | Sterilization of health care products - Microbiological methods - Part 3: Bacterial endotoxin testing (ISO 11737-3:2023) | Izstrādē |
| 9284 | prEN 551 | Sterilization of medical devices - Method for validation and routine control of ethylene oxide sterilization - Guidance | Izstrādē |
| 82923 | EN ISO 14937:2009/prA1 | 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 — Amendment 1 | Izstrādē |
| 82958 | EN ISO 17665:2024/prA1 | Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices — Amendment 1 | Izstrādē |
| 9291 | - | Method(s) of bioburden determination - Methods for validating bioburden techniques | Izstrādē |
Displaying 151-160 of 176 results.