CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 9310 | prEN ISO 11137-3 | Sterilization of medical devices - Microbiological methods - Part 3: Guidance on the evaluation and interpretation of bioburden data | Izstrādē |
| 9284 | prEN 551 | Sterilization of medical devices - Method for validation and routine control of ethylene oxide sterilization - Guidance | Izstrādē |
| 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 |
| 62287 | prEN ISO 17665-1 rev | Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices | Izstrādē |
| 31155 | prEN ISO 11137-2 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | Izstrādē |
| 78646 | prEN ISO 14937 | 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 | Izstrādē |
| 76997 | CEN ISO/TS 11137-4:2023 | Sterilization of health care products - Radiation - Part 4: Guidance on process control (ISO/TS 11137-4:2020) | Izstrādē |
| 72399 | prEN ISO 11135 | Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2023) | 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 |
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