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

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