Registration number (WIID)Project No.TitleStatus
31999LVS EN ISO 10993-13:2009Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998)Atcelts
9496LVS EN ISO 10993-4:2003Biological evaluation of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
9488LVS EN ISO 10993-14:2003Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramicsAtcelts
9480LVS EN 30993-6:1994Biological evalution of medical devices - Part 6: Tests for local effects after implantationAtcelts
31982LVS EN ISO 10993-10:2009Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002, including Amd 1:2006)Atcelts
9472LVS EN 30993-5:1994Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)Atcelts
30062LVS EN ISO 10993-16:2010Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)Atcelts
31978LVS EN ISO 10993-3:2009Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003)Atcelts
31981LVS EN ISO 10993-9:2009Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999)Atcelts
31979LVS EN ISO 10993-4:2009Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)Atcelts
Displaying 31-40 of 198 results.