BEUDAMED
    3 results · 21ms · Sources: EU EUDAMED, US FDA

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    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    5.0MM ALLTHREAD TI III ANCHOR

    FDA Adverse Event
    Malfunction ·BIOMET·Product code MBI·November 22, 2010

    LARGE NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 1, 2014