Registration number (WIID)Project No.TitleStatus
9499EN ISO 10993-17:2002Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
9494EN ISO 10993-16:1997Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)Atcelts
9496EN ISO 10993-4:2002Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)Atcelts
32004LVS EN ISO 10993-18:2009Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
60213EN ISO 22442-1:2015Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015)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
9500EN ISO 10993-18:2005Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
32001EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
9471EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
9501LVS EN ISO 10993-10:2003Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivityAtcelts
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