CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 76054 | prEN ISO 8250 | Cleanliness of medical devices -- Process design and test methods | Izstrādē |
| 75885 | FprEN ISO 10993-7 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/FDIS 10993-7:2025) | Izstrādē |
| 31980 | prEN ISO 10993-5 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) | Izstrādē |
| 40661 | prEN ISO 10993-7 rev | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Izstrādē |
| 73021 | prEN ISO 10993-3 rev | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive and developmental toxicity | Izstrādē |
| 9483 | - | Biological evaluation of medical devices - Methods of testing for degradation products | Izstrādē |
| 40814 | prEN ISO 10993-5 rev | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) | Izstrādē |
| 9485 | - | Biological evaluation of medical devices - Glutaraldehyde and formaldehyde residuals | Izstrādē |
| 77182 | FprEN ISO 14155 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/FDIS 14155:2025) | Izstrādē |
| 77391 | FprEN ISO 10993-6 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO/FDIS 10993-6:2025) | Izstrādē |
Displaying 1-10 of 194 results.