BEUDAMED
    5 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 24, 2018

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 24, 2018

    HS III PROXIMAL SEAL SYSTEM 3.8 MM

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC.·Product code DXC·October 10, 2014

    UNIVERSAL STABLILZER ARM HERCULES

    FDA Adverse Event
    Malfunction ·ENDOSCOPIC TECHNOLOGIES·Product code DWS·June 5, 2013

    ACCU-CHEK TENDERLINK

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FPA·June 17, 2011