Standards STN - Slovak standards - Page 6785

Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2019)

Standard published on 1.1.2022

Biological evaluation of medical devices - Part 10: Tests for skin sensitization (ISO 10993-10:2021)

Standard published on 1.5.2023

Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)

Standard published on 1.11.2018

Biological evaluation of medical devices — Part 12: Sample preparation and reference materials

Standard published on 1.9.2021

Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)

Standard published on 1.11.2010

Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)

Standard published on 1.8.2009

Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2019)

Standard published on 1.8.2023

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)

Standard published on 1.6.2018

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

Standard published on 1.3.2024

Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)

Standard published on 1.9.2020