BEUDAMED
    5 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PLUM A+ DRIVER REFU

    FDA Adverse Event
    Malfunction ·HOSPIRACOSTA RICA LTD.·Product code FRN·February 10, 2014

    MINI TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·November 14, 2012

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·September 3, 2010

    XVWEB

    FDA Adverse Event
    Injury ·PLANET DDS·Product code LLZ·March 13, 2025

    SECOND OPINION

    FDA Adverse Event
    Injury ·PEARL INC.·Product code MYN·March 13, 2025