BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    POLY-LITE MODEL 1000

    FDA 510(k)
    FDA Class 2 ·Dental

    Curiteva Porous PEEK Cervical Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 30, 2015

    TOTAL ASR FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·February 11, 2013

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011