Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices
Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)
53,361 distincte referentiestringen geïndexeerd van officiële bronmomentopnames geraadpleegd op 19 oktober 2026. Omvat eerdere edities. De index en uitgevercollecties hebben verschillende dekking. Zie bronnen en dekking.