CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9487 | EN ISO 10993-13:1998 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998) | Atcelts |
| 9484 | EN ISO 10993-2:1998 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:1992) | Atcelts |
| 9479 | EN 30993-4:1993 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:1992) | Atcelts |
| 9478 | EN ISO 10993-11:1995 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:1993) | Atcelts |
| 21140 | EN ISO 10993-12:2004 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2002) | Atcelts |
| 40815 | EN ISO 10993-4:2017 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017) | Atcelts |
| 24852 | LVS EN ISO 10993-12:2008 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
| 30062 | EN ISO 10993-16:2010 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO/DIS 10993-16:2008) | Atcelts |
| 31982 | 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 |
| 32008 | EN ISO 10993-12:2009 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007) | Atcelts |
Displaying 121-130 of 190 results.