Registration number (WIID)Project No.TitleStatus
32003LVS EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)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
32006LVS EN ISO 10993-6:2009Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)Atcelts
24852LVS EN ISO 10993-12:2008Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsAtcelts
21801LVS EN ISO 10993-6:2007Biological evaluation of medical devices - Part 6: Tests for local effects after implantationAtcelts
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
60214EN ISO 22442-2:2015Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO/FDIS 22442-2:2015)Atcelts
21797LVS EN ISO 10993-11:2006Biological evaluation of medical devices - Part 11: Tests for systemic toxicityAtcelts
32007LVS EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)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
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