CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 9477 | LVS EN ISO 10993-10:1995 | Biological evalution of medical devices - Part 10: Tests for irritation and sensitization | Atcelts |
| 9499 | LVS EN ISO 10993-17:2003 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 32766 | LVS EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) | Atcelts |
| 27050 | LVS EN ISO 10993-9:2010 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009) | Atcelts |
| 24852 | LVS EN ISO 10993-12:2008 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
| 9488 | LVS EN ISO 10993-14:2003 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics | 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 |
| 21801 | LVS EN ISO 10993-6:2007 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | Atcelts |
| 9479 | LVS EN 30993-4:1993 | Biological evalution of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
Displaying 51-60 of 192 results.