We need your consent to use the individual data so that you can see information about your interests, among other things. Click "OK" to give your consent.
ISO (International Organization for Standardization) is the world’s largest producer of optional international standards. International standards determine current specifications of products, services and certified methods, helping to streamline the industry. As they are created on the basis of international agreement, they assist in overcoming barriers in international trade.
Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process
(Évaluation biologique des dispositifs médicaux — Partie 18: Caractérisation chimique des matériaux des dispositifs médicaux au sein d´un processus de gestion du risque)
Standard published on 13.1.2020
Selected format:
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
(Évaluation biologique des dispositifs médicaux — Partie 18: Caractérisation chimique des matériaux des dispositifs médicaux au sein d´un processus de gestion du risque — Amendement 1: Détermination du coefficient d´incertitude)
Change published on 11.5.2022
Selected format:
Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials
(Évaluation biologique des dispositifs médicaux — Partie 19: Caractérisations physicochimique, morphologique et topographique des matériaux)
Standard published on 12.3.2020
Selected format:
Biological evaluation of medical devices — Part 2: Animal welfare requirements
(Évaluation biologique des dispositifs médicaux — Partie 2: Exigences relatives a la protection des animaux)
Standard published on 3.11.2022
Selected format:
Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devices
(Évaluation biologique des dispositifs médicaux — Partie 20: Principes et méthodes relatifs aux essais d´immunotoxicologie des dispositifs médicaux)
Standard published on 3.8.2006
Selected format:
Biological evaluation of medical devices — Part 22: Guidance on nanomaterials
(Évaluation biologique des dispositifs médicaux — Partie 22: Lignes directrices sur les nanomatériaux)
Standard published on 14.7.2017
Selected format:
Biological evaluation of medical devices — Part 23: Tests for irritation
(Évaluation biologique des dispositifs médicaux — Partie 23: Essais d´irritation)
Standard published on 20.1.2021
Selected format:
Biological evaluation of medical devices — Part 23: Tests for irritation — Amendment 1: Additional in vitro reconstructed human epidermis models
(Évaluation biologique des dispositifs médicaux — Partie 23: Essais d´irritation — Amendement 1: Modeles supplémentaires d´épiderme humain reconstruit in vitro)
Change published on 1.5.2025
Selected format:
Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
(Évaluation biologique des dispositifs médicaux — Partie 3: Essais concernant la génotoxicité, la cancérogénicité et la toxicité sur la reproduction)
Standard published on 24.9.2014
Selected format:
Biological evaluation of medical devices — Part 33: Guidance on tests to evaluate genotoxicity — Supplement to ISO 10993-3
(Évaluation biologique des dispositifs médicaux — Partie 33: Directives sur les essais pour évaluer la génotoxicité — Supplément a l´ISO 10993-3)
Standard published on 6.3.2015
Selected format:Latest update: 2026-01-02 (Number of items: 2 253 797)
© Copyright 2026 NORMSERVIS s.r.o.