Registration number (WIID)Project No.TitleStatus
9488LVS EN ISO 10993-14:2003Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramicsAtcelts
9484LVS EN ISO 10993-2:2000Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
9496LVS EN ISO 10993-4:2003Biological evaluation of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
40815LVS EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Atcelts
23327LVS EN ISO 10993-4:2003 /A1:2006Biological evaluation of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
32003LVS EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
35184LVS EN ISO 10993-1:2010 /AC:2010Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process - Technical Corrigendum 1 (ISO 10993-1:2009/Cor 1:2010)Atcelts
22598LVS EN ISO 10993-1:2003Biological evaluation of medical devices - Part 1: Evaluation and testingAtcelts
9482LVS EN ISO 10993-9:2000Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation productsAtcelts
9495LVS EN ISO 10993-3:2003Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
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