BEUDAMED
    3 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 31, 2014

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - GUANGZHOU·Product code KDI·November 21, 2012

    VENTRICULAR CATHETER, STANDARD, BIOGLIDE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·September 21, 2010