CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 9498 | LVS EN ISO 10993-8:2001 | Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests | Atcelts |
| 32007 | LVS EN ISO 10993-11:2009 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | Atcelts |
| 27050 | EN ISO 10993-9:2009 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO/FDIS 10993-9:2009) | Atcelts |
| 9478 | LVS EN ISO 10993-11:1995 | Biological evalution of medical devices - Part 11: Tests for systemic toxicity | Atcelts |
| 9497 | LVS EN ISO 10993-5:1999 | Biological evalution of medical devices - Part 5: Tests for in vitro cytotoxicity | Atcelts |
| 9481 | LVS EN ISO 10993-7:2000 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | 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 |
| 9494 | LVS EN ISO 10993-16:1997 | Biological evalution of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
Displaying 61-70 of 195 results.