CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 28616 | LVS EN ISO 10993-10:2011 | Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) | Atcelts |
| 9471 | LVS 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 |
| 9489 | EN ISO 10993-15:2000 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) | Atcelts |
| 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 |
| 9501 | LVS EN ISO 10993-10:2003 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
| 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 |
| 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 151-160 of 194 results.