Registration number (WIID)Project No.TitleStatus
9472LVS EN 30993-5:1994Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)Atcelts
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
27050EN ISO 10993-9:2009Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO/FDIS 10993-9:2009)Atcelts
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
32006LVS EN ISO 10993-6:2009Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)Atcelts
9488LVS EN ISO 10993-14:2003Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramicsAtcelts
23327LVS EN ISO 10993-4:2003 /A1:2006Biological evaluation of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
21140LVS EN ISO 10993-12:2005Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsAtcelts
9500LVS EN ISO 10993-18:2005Biological evaluation of medical devices - Part 18: Chemical characterization of materialsAtcelts
32007LVS EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
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