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
78993LVS EN ISO 10993-23:2021/A1:2025Biological evaluation of medical devices - Part 23: Tests for irritation - Amendment 1: Additional in vitro reconstructed human epidermis models (ISO 10993-23:2021/Amd 1:2025)Standarts spēkā
77933prEN ISO 10993-11Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2025)Aptauja slēgta
78991prEN ISO 10993-16Biological evaluation of medical devices - Part 16: Toxicokinetic evaluation for degradation products and leachables (ISO/DIS 10993-16:2025)Aptauja slēgta
78812prEN ISO 21762Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025)Aptauja slēgta
77335prEN ISO 18969Clinical evaluation of medical devices (ISO/DIS 18969:2025)Aptauja slēgta
22132LVS EN ISO 10993-2:2006Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
21797LVS EN ISO 10993-11:2006Biological evaluation of medical devices - Part 11: Tests for systemic toxicityAtcelts
9481LVS EN ISO 10993-7:2000Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residualsAtcelts
32007LVS EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
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