BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·June 10, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 2, 2012

    UNKNOWN NEXGEN LPS-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER INC.·Product code HSA·September 21, 2010