Registration number (WIID)Project No.TitleStatus
9494LVS EN ISO 10993-16:1997Biological evalution of medical devices - Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
60723LVS EN ISO 10993-15:2023Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2019)Standarts spēkā
32001LVS EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
9489LVS EN ISO 10993-15:2003Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloysAtcelts
32000LVS EN ISO 10993-14:2009Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)Standarts spēkā
9488LVS EN ISO 10993-14:2003Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramicsAtcelts
27051LVS EN ISO 10993-13:2010Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)Standarts spēkā
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
78989LVS EN ISO 10993-12:2021/A1:2025Biological evaluation of medical devices - Part 12: Sample preparation and reference materials - Amendment 1 (ISO 10993 12:2021/Amd 1:2025) 
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