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
9482LVS EN ISO 10993-9:2000Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation productsAtcelts
9481LVS EN ISO 10993-7:2000Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residualsAtcelts
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
9484LVS EN ISO 10993-2:2000Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
9487LVS EN ISO 10993-13:2000Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devicesAtcelts
9492LVS EN ISO 10993-1:2000Biological evaluation of medical devices - Part 1: Evalution and testingAtcelts
9498LVS EN ISO 10993-8:2001Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological testsAtcelts
9471EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
9496LVS EN ISO 10993-4:2003Biological evaluation of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
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