Dal 26 maggio 2021 è pienamente applicabile il Regolamento (UE) 2017/745 relativo al sistema UDI. UDI (Unique Device Identification) serve per identificare e marcare i dispositivi medici lungo la supply chain sanitaria, per: -Garantire la sicurezza dei pazienti a livello globale. -Assicurare la tracciabilità e la rintracciabilità dei dispositivi medici. -Ottimizzare i processi di cura con l’uso di standard globali. VAI...Read More
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