BEUDAMED
    7 results · 15ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Death ×

    GUIDANT

    FDA Adverse Event
    Death ·GUIDANT CORP·Product code DTB·March 17, 2008

    VENTAK PRIZM 2 DR

    FDA Adverse Event
    Death ·Product code LWS·March 24, 2006

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Death ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·November 23, 2005

    PULSAR MAX DR

    FDA Adverse Event
    Death ·CLONMEL·Product code DXY·April 20, 2007

    PULSAR MAX DR

    FDA Adverse Event
    Death ·*·Product code DXY·April 6, 2007

    NUCLUES 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Death ·COCHLEAR LTD.·Product code MCM·October 17, 2005

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Death ·CORDIS LLC (PR)·Product code NIQ·November 2, 2005