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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 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
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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
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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
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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
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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
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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
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Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity and developmental toxicity
(Évaluation biologique des dispositifs médicaux — Partie 3: Évaluation de la génotoxicité, de la cancérogénicité, de la toxicité sur la reproduction et de la toxicité sur le développement)
Standard published on 6.8.2026
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Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood
(Évaluation biologique des dispositifs médicaux — Partie 4: Choix des essais pour les interactions avec le sang)
Standard published on 12.4.2017
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Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1
(Évaluation biologique des dispositifs médicaux — Partie 4: Choix des essais pour les interactions avec le sang — Amendement 1)
Change published on 8.1.2025
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Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity
(Évaluation biologique des dispositifs médicaux — Partie 5: Essais concernant la cytotoxicité in vitro)
Standard published on 20.5.2009
Selected format:Latest update: 2026-08-21 (Number of items: 2 298 377)
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