Standards STN - Slovak standards - Page 6853

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 17: Toxicological risk assessment of medical device constituents (ISO 10993-17: 2023/Amd 1: 2025)

Change published on 1.4.2026

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

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

Change published on 1.10.2023

Biological evaluation of medical devices — Part 23: Tests for irritation

Standard published on 1.9.2021

Biological evaluation of medical devices - Part 23: Tests for irritation - Amendment 1: Additional in vitro reconstructed human epidermis models (ISO 10993-23: 2021/Amd 1: 2025)

Change published on 1.11.2025

Biological evaluation of medical devices. Part 1: Evaluation and testing

WITHDRAWN published on 1.11.1999