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

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    Filters FDA Adverse Event ×

    TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC (AF-MINNETONKA)·Product code DRC·May 16, 2014

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 29, 2012

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Malfunction ·COOK INC.·Product code MIH·September 21, 2010