CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 23724 | LVS EN ISO 10993-10:2003 /A1:2006 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
| 9501 | LVS EN ISO 10993-10:2003 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
| 9477 | LVS EN ISO 10993-10:1995 | Biological evalution of medical devices - Part 10: Tests for irritation and sensitization | Atcelts |
| 9480 | LVS EN 30993-6:1994 | Biological evalution of medical devices - Part 6: Tests for local effects after implantation | Atcelts |
| 9472 | LVS EN 30993-5:1994 | Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992) | Atcelts |
| 9479 | LVS EN 30993-4:1993 | Biological evalution of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 9475 | LVS EN 30993-3:1993 | Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 9471 | LVS EN 30993-1:1994 | Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992) | Atcelts |
| 77182 | FprEN ISO 14155 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/FDIS 14155:2025) | Izstrādē |
| 75885 | FprEN ISO 10993-7 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/FDIS 10993-7:2025) | Izstrādē |
Displaying 91-100 of 192 results.