Registration number (WIID)Project No.TitleStatus
9475LVS EN 30993-3:1993Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
32008LVS EN ISO 10993-12:2009Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)Atcelts
32002LVS EN ISO 10993-16:2009Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)Atcelts
9492LVS EN ISO 10993-1:2000Biological evaluation of medical devices - Part 1: Evalution and testingAtcelts
9486LVS EN ISO 10993-12:1996Biological evalution of medical devices - Part 12: Sample preparation and reference materialsAtcelts
32003LVS EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
9497EN ISO 10993-5:1999Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999)Atcelts
9480EN 30993-6:1994Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:1994)Atcelts
9487LVS EN ISO 10993-13:2000Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devicesAtcelts
32006LVS EN ISO 10993-6:2009Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)Atcelts
Displaying 61-70 of 198 results.