Registration number (WIID)Project No.TitleStatus
9478LVS EN ISO 10993-11:1995Biological evalution of medical devices - Part 11: Tests for systemic toxicityAtcelts
9484LVS EN ISO 10993-2:2000Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
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
32003LVS EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
9496LVS EN ISO 10993-4:2003Biological evaluation of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
9486LVS EN ISO 10993-12:1996Biological evalution of medical devices - Part 12: Sample preparation and reference materialsAtcelts
9482LVS EN ISO 10993-9:2000Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation productsAtcelts
32766LVS EN ISO 10993-12:2012Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)Atcelts
9472LVS EN 30993-5:1994Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)Atcelts
32006LVS EN ISO 10993-6:2009Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)Atcelts
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