BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ADVANTA V12,COVERED STENT SYS,9X59X80

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·April 7, 2026

    ADVANTA V12 COVERED STENT SYSTEM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code NIO·August 13, 2025

    ADVANTA V12 COVERED STENT

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·September 10, 2025

    ADVANTA V12,COVERED STENTSYS, 9X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026

    ADVANTAV12,COVERED STENTSYS, 6X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026

    LEAD MODEL UNKNOWN

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·May 20, 2013

    SM104 MSERIES W5TH WHL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·May 26, 2011

    ENDEAVOR ZOTAROLIMUS-ELUTING CORONARY STENT OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·August 14, 2008

    S.M.A.R.T. NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·January 28, 2016