Registration number (WIID)Project No.TitleStatus
32004LVS EN ISO 10993-18:2009Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
9494LVS EN ISO 10993-16:1997Biological evalution of medical devices - Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
9488LVS EN ISO 10993-14:2003Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramicsAtcelts
32766LVS EN ISO 10993-12:2012Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)Atcelts
9480LVS EN 30993-6:1994Biological evalution of medical devices - Part 6: Tests for local effects after implantationAtcelts
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
27050LVS EN ISO 10993-9:2010Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)Atcelts
9479LVS EN 30993-4:1993Biological evalution of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
22132LVS EN ISO 10993-2:2006Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
79539EN ISO 14155:2020/A11:2024Clinical investigation of medical devices for human subjects - Good clinical practiceAtcelts
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