CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 75885 | FprEN ISO 10993-7 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/FDIS 10993-7:2025) | Izstrādē |
| 75596 | EN ISO 10993-1:2025 | Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO/FDIS 10993-1:2025) | Izstrādē |
| 9483 | - | Biological evaluation of medical devices - Methods of testing for degradation products | Izstrādē |
| 77335 | prEN ISO 18969 | Clinical evaluation of medical devices | Izstrādē |
| 77182 | FprEN ISO 14155 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/FDIS 14155:2025) | Izstrādē |
| 76054 | prEN ISO 8250 | Cleanliness of medical devices -- Process design and test methods | Izstrādē |
| 40661 | prEN ISO 10993-7 rev | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Izstrādē |
| 31980 | prEN ISO 10993-5 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) | Izstrādē |
| 9485 | - | Biological evaluation of medical devices - Glutaraldehyde and formaldehyde residuals | Izstrādē |
| 40814 | prEN ISO 10993-5 rev | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) | Izstrādē |
Displaying 171-180 of 192 results.