Registration number (WIID)Project No.TitleStatus
9494LVS EN ISO 10993-16:1997Biological evalution of medical devices - Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
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
32003LVS EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)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
32008LVS EN ISO 10993-12:2009Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)Atcelts
9486LVS EN ISO 10993-12:1996Biological evalution of medical devices - Part 12: Sample preparation and reference materialsAtcelts
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
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
23724LVS EN ISO 10993-10:2003 /A1:2006Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivityAtcelts
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