BEUDAMED
    6 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SINOVIAL

    FDA Adverse Event
    Injury ·IBSA FARMACEUTICI ITALIA SRL·Product code MOZ·April 20, 2020

    0001825034-2018-06038

    FDA Adverse Event
    Injury ·August 6, 2018

    SM104 MSERIES W5TH WHL

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

    SENSATION? SHORT THROW

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code FDI·May 20, 2013

    DRIVER RX CORONARY STENT SYSTEM

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

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

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