Registration number (WIID)Project No.TitleStatus
60724LVS EN ISO 10993-16:2018Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)Standarts spēkā
9499LVS EN ISO 10993-17:2003Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substancesAtcelts
32003LVS EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
67767LVS EN ISO 10993-17:2023Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)Standarts spēkā
9500LVS EN ISO 10993-18:2005Biological evaluation of medical devices - Part 18: Chemical characterization of materialsAtcelts
32004LVS EN ISO 10993-18:2009Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
60725LVS EN ISO 10993-18:2020Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)Standarts spēkā
74131LVS EN ISO 10993-18:2020/A1:2023Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)Standarts spēkā
9484LVS EN ISO 10993-2:2000Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
22132LVS EN ISO 10993-2:2006Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
Displaying 131-140 of 190 results.