Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/DIS 10993-3:2025)
prEN ISO 10993-3
Αντικείμενο
ISO 10993-3:2014 specifies strategies for risk estimation and selection of hazard identification tests, 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.
Η δημόσια κρίση έχει λήξει.
Πληροφορίες
Τεχνικές Επιτροπές
TE-T 14
CEN/TC 206
Τομέας Τυποποίησης
Επιστήμες Υγείας
Ημερομηνία Δημοσίευσης
2025-04-03
Ημερομηνία Λήξης
2025-05-27