STB PDF

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021). Original standard BS EN ISO 10993-12-2021 in PDF full version. Additional info + preview on request

Document status: Active

Biological evaluation of medical devices. Identification and quantification of degradation products from polymeric medical devices. Original standard BS EN ISO 10993-13-2010 in PDF full version. Additional info + preview on request

Document status: Active

Biological evaluation of medical devices. Identification and quantification of degradation products from ceramics. Original standard BS EN ISO 10993-14-2009 in PDF full version. Additional info + preview on request

Document status: Active

Biological evaluation of medical devices - Identification and quantification of degradation products from metals and alloys. Original standard BS EN ISO 10993-15-2023 in PDF full version. Additional info + preview on request

Document status: Active

Biological evaluation of medical devices. Toxicokinetic study design for degradation products and leachables. Original standard BS EN ISO 10993-16-2017 (2020) in PDF full version. Additional info + preview on request

Document status: Active

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023). Original standard BS EN ISO 10993-17-2023 in PDF full version. Additional info + preview on request

Document status: Active