BEUDAMED
    3 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN FORMERLY REGISTERED AS UNITED STATES·Product code GDW·February 26, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 21, 2012

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·September 22, 2010