BEUDAMED
    3 results · 27ms · 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·June 14, 2014

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·October 14, 2010

    PULSE GEN MODEL 102R

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·December 14, 2012