Registration number (WIID)Project No.TitleStatus
9499LVS EN ISO 10993-17:2003Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substancesAtcelts
9500EN ISO 10993-18:2005Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
9501LVS EN ISO 10993-10:2003Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivityAtcelts
9471EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
32001EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
9487LVS EN ISO 10993-13:2000Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devicesAtcelts
9489EN ISO 10993-15:2000Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
9471LVS EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
9486EN ISO 10993-12:1996Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:1996)Atcelts
28616LVS EN ISO 10993-10:2011Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)Atcelts
Displaying 61-70 of 200 results.