Registration number (WIID)Project No.TitleStatus
35979ISO/TS 10993-20:2006Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devicesAtcelts
18963ISO 10993-4:1992Biological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodAtcelts
32086ISO 10993-4:2002Biological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodAtcelts
44789ISO 10993-6:2007Biological evaluation of medical devices — Part 6: Tests for local effects after implantationAtcelts
22694ISO 10993-15:2000Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloysAtcelts
18973ISO 10993-12:1996Biological evaluation of medical devices — Part 12: Sample preparation and reference materialsAtcelts
59992ISO 14155:2011/Cor 1:2011Clinical investigation of medical devices for human subjects — Good clinical practice — Technical Corrigendum 1Atcelts
22695ISO 10993-16:1997Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
69217ISO/TR 15499:2016Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management processAtcelts
71514ISO/TS 21726:2019Biological evaluation of medical devices — Application of the threshold of toxicological concern (TTC) for assessing biocompatibility of medical device constituentsAtcelts
Displaying 61-70 of 146 results.