Regolamento (UE) 2017/745: quali cambiamenti per la tracciabilità dei dispositivi medici?

La perdita di rintracciabilità dei DM rappresenta un serio rischio per la salute di pazienti e utilizzatori. Il nuovo Regolamento del Parlamento Europeo ha fornito una strategia comune, fondata su principi internazionalmente riconosciuti, attraverso l’istituzione di un sistema di identificazione unica del dispositivo (sistema UDI). 

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Data: 06.2020   Fonte:

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