BAS EN ISO 10993-3:2016
Biološko ocjenjivanje medicinskih sredstava - Dio 3: Ispitivanja genotoksičnosti, kancerogenosti i reproduktivne toksičnosti
Opće informacije
Status: Važeći
Broj strana: 40
Jezik: Engleski
Izdanje: 3.
Metoda usvajanja: Proglašavanje
Nadnevak objave: 18.05.2016
Tehnički komitet:
Direktiva:
90/385/EEC, Aktivna ugradiva medicinska sredstva
93/42/EEC, Medicinska sredstva;
93/42/EEC, Medicinska sredstva;
...
Apstrakt
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.
Životni ciklus
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Izvorni dokument i stepen usklađenosti
- EN ISO 10993-3:2014, identičan
- ISO 10993-3:2014, identičan