BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·May 2, 2014

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·May 2, 2014

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 13, 2010

    FMP HIP

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code LPH·January 22, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 14, 2014

    DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DWF·December 15, 2016