CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9499 | LVS EN ISO 10993-17:2003 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | 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 |
| 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 |
| 31999 | LVS EN ISO 10993-13:2009 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998) | Atcelts |
| 32006 | LVS EN ISO 10993-6:2009 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) | Atcelts |
| 23327 | LVS EN ISO 10993-4:2003 /A1:2006 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 9497 | LVS EN ISO 10993-5:1999 | Biological evalution of medical devices - Part 5: Tests for in vitro cytotoxicity | Atcelts |
| 9478 | LVS EN ISO 10993-11:1995 | Biological evalution of medical devices - Part 11: Tests for systemic toxicity | Atcelts |
| 9486 | LVS EN ISO 10993-12:1996 | Biological evalution of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
| 9494 | LVS EN ISO 10993-16:1997 | Biological evalution of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
Displaying 91-100 of 192 results.