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
9487LVS EN ISO 10993-13:2000Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devicesAtcelts
67095LVS EN ISO 10993-12:2021Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)Standarts spēkā
32766LVS EN ISO 10993-12:2012Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)Atcelts
32008LVS EN ISO 10993-12:2009Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)Atcelts
24852LVS EN ISO 10993-12:2008Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsAtcelts
21140LVS EN ISO 10993-12:2005Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsAtcelts
9486LVS EN ISO 10993-12:1996Biological evalution of medical devices - Part 12: Sample preparation and reference materialsAtcelts
60721LVS EN ISO 10993-1:2021Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-11)Standarts spēkā
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
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