Registration number (WIID)Project No.TitleStatus
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
27051EN 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
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
27092EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO/FDIS 10993-1:2009)Atcelts
27092LVS EN ISO 10993-1:2010Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)Atcelts
28616EN ISO 10993-10:2010Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO/DIS 10993-10:2008)Atcelts
28616LVS EN ISO 10993-10:2011Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)Atcelts
30062EN ISO 10993-16:2010Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO/DIS 10993-16:2008)Atcelts
30062LVS EN ISO 10993-16:2010Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)Atcelts
30398EN ISO 10993-3:2014Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO/DIS 10993-3:2011)Standarts spēkā
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