Published
ISO 10993-3:2014 specifies strategies for risk estimation, selection of hazard identification tests and risk management, with respect to the possibility of the following potentially irreversible biological effects arising as a result of exposure to medical devices:
genotoxicity;
carcinogenicity;
reproductive and developmental toxicity.
ISO 10993-3:2014 is applicable when the need to evaluate a medical device for potential genotoxicity, carcinogenicity, or reproductive toxicity has been established.
Revises
ISO 10993-3:2003
PUBLISHED
ISO 10993-3:2014
90.92
Standard to be revised
Dec 16, 2019
IN_DEVELOPMENT
ISO/CD 10993-3
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