Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)

Die Norm herausgegeben am 16.2.2022

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

Die Norm herausgegeben am 17.11.2010

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

Die Norm herausgegeben am 9.9.2009

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

Die Norm herausgegeben am 17.1.2024

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

Die Norm herausgegeben am 16.5.2018

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

Die Norm herausgegeben am 22.5.2024

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

Die Norm herausgegeben am 20.1.2021

Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)

Änderung herausgegeben am 22.5.2024

Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)

Die Norm herausgegeben am 12.7.2023

Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021)

Die Norm herausgegeben am 13.10.2021