CEN/TC 206
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
9497 | EN ISO 10993-5:1999 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) | Atcelts |
9497 | LVS EN ISO 10993-5:1999 | Biological evalution of medical devices - Part 5: Tests for in vitro cytotoxicity | Atcelts |
9498 | EN ISO 10993-8:2000 | Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests (ISO 10993-8:2000) | 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 |
9499 | EN ISO 10993-17:2002 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) | Atcelts |
9499 | LVS EN ISO 10993-17:2003 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | Atcelts |
9500 | EN ISO 10993-18:2005 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) | Atcelts |
9500 | LVS EN ISO 10993-18:2005 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials | Atcelts |
9501 | EN ISO 10993-10:2002 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002) | Atcelts |
9501 | LVS EN ISO 10993-10:2003 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
Displaying 41-50 of 190 results.