BEUDAMED
    7 results · 28ms · Sources: EU EUDAMED, US FDA

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    cNeuro cDAT

    FDA 510(k)
    FDA Class 2 ·Radiology

    Vu a-POD™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981041915·39x30mm Trial Rasp 8mm 8 deg

    N HIGH SENSITIVITY CRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    SKR 3000

    FDA 510(k)
    FDA Class 2 ·Radiology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 7, 2014

    ASR ACETABULAR IMPLANT 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 6, 2011

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·November 13, 2008