CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9500 | EN ISO 10993-18:2005 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) | Atcelts |
| 32001 | EN ISO 10993-15:2009 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) | Atcelts |
| 9471 | EN 30993-1:1994 | Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992) | Atcelts |
| 21140 | LVS EN ISO 10993-12:2005 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
| 9500 | LVS EN ISO 10993-18:2005 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials | Atcelts |
| 32007 | LVS EN ISO 10993-11:2009 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | Atcelts |
| 21797 | LVS EN ISO 10993-11:2006 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity | Atcelts |
| 21801 | LVS EN ISO 10993-6:2007 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | Atcelts |
| 24852 | LVS EN ISO 10993-12:2008 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
| 32003 | LVS EN ISO 10993-17:2009 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) | Atcelts |
Displaying 131-140 of 194 results.