Abstract / scope
ISO 10993-11:2006 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
ISO 10993-11:2006Withdrawn
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
Évaluation biologique des dispositifs médicaux — Partie 11: Essais de toxicité systémique
This edition has been replaced by ISO 10993-11:2017.