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

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    EXACTECH ALL POLY ACETABULAR CUP

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    SeaSpine Spacer System - Hollywood™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981031220·10mm Hollywood Trial, Lordotic

    ORTHO MUNE OKT3,4, AND 8 MONOCLONAL ANTIBODY

    FDA 510(k)
    FDA Class 2 ·Hematology

    PBC IV SET NON-VENTED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·June 27, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC0·Product code JAA·January 7, 2013

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·November 23, 2010