CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9498 | LVS EN ISO 10993-8:2001 | Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests | Atcelts |
| 62983 | EN ISO 14155:2020 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020) | Atcelts |
| 9486 | EN ISO 10993-12:1996 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:1996) | Atcelts |
| 9488 | LVS EN ISO 10993-14:2003 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics | Atcelts |
| 9496 | LVS EN ISO 10993-4:2003 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 21801 | LVS EN ISO 10993-6:2007 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | Atcelts |
| 31982 | LVS EN ISO 10993-10:2009 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002, including Amd 1:2006) | 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 |
| 21797 | LVS EN ISO 10993-11:2006 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity | Atcelts |
| 24852 | LVS EN ISO 10993-12:2008 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
Displaying 81-90 of 198 results.