BEUDAMED
    9 results · 30ms · Sources: EU EUDAMED, US FDA

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    AGILTRAC .035 PERIPHERAL DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code LIT·May 2, 2006

    OMNILINK .035 STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code FGE·May 8, 2009

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 18, 2013

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·March 2, 2011

    RENAL - DISPOSABLE

    FDA Adverse Event
    Death ·Product code KDJ·January 15, 2011

    AGILTRAC .035 PERIPHERAL DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code LIT·February 2, 2009

    SYRINGE 50ML CT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 23, 2021

    CURAPLEX

    FDA Adverse Event
    Malfunction ·BOUND TREE MEDICAL, LLC·Product code BTM·December 21, 2023