BEUDAMED
    7 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    WALLFLEX DUODENAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MUM·January 22, 2025

    FR MARSEILLE

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·December 22, 2010

    THERAPY COOL FLEX, 1304-CF-7-0.5(2)2-L-TE4BE1EB

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (AF-IRVINE)·Product code OAD·March 22, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·March 17, 2011

    MAXI LD LARGE DIAMETER DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·March 27, 2008

    UNK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·July 22, 2011

    FR VILLEURBANNE

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·December 22, 2010