BEUDAMED
    3 results · 18ms · 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·July 5, 2015

    ATLAS PLUS DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014

    FOX PLUS PTA CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code LIT·October 22, 2010