BEUDAMED
    308 results · 57ms · Sources: EU EUDAMED, US FDA

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    COBE CARDIOVASCULAR INC.

    FDA Adverse Event
    Injury ·COBE CARDIOVASCULAR, INC.·Product code DTZ·January 7, 2000

    DIDECO ELECTA AUTOTRANSFUSION KIT

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code CAC·September 6, 2006

    DIDECO ELECTA AUTOTRANSFUSION KIT

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code CAC·September 6, 2006

    DIDECO ELECTA PREASSEMBLED SURGICAL WASH SET

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code CAC·September 6, 2006

    DIDECO ELECTA AUTOTRANSFUSION KIT

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L·Product code CAC·September 6, 2006

    COBE PRECISION BLOOD PUMP

    FDA Adverse Event
    Other ·COBE CARDIOVASCULAR, INC (NOW SORIN GROUP USA)·Product code DWA·January 25, 2011

    ELECTA WASH SET 225 ML BOWL

    FDA Adverse Event
    Malfunction ·SORIN GRP ITALIA S.R.I, A SORIN GRP CO., DISTRIBUTED BY COBE CARDIOVASCULAR, INC·Product code CAC·August 30, 2006

    ELECTA WASH SET 225 ML BOWL

    FDA Adverse Event
    Malfunction ·SORIN GRP ITALIA S.R.I., A SORIN GRP CO., DISTRIBUTED BY COBE CARDIOVASCULAR INC·Product code CAC·August 30, 2006

    DIDECO COMPACT AUTOTRANSFUSION KIT

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code CAC·September 6, 2006

    ELECTA WASH SET 225 ML BOWL

    FDA Adverse Event
    Malfunction ·SORIN GRP ITALIA S.R.I., A SORIN GRP CO, DISTRIBUTED BY COBE CARDIOVASCULAR, INC·Product code CAC·August 30, 2006

    DIDECO ELECTA AUTOTRANSFUSION KIT

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code CAC·September 6, 2006

    DIDECO ELECTRA AUTOTRANSFUSION KIT

    FDA Adverse Event
    Malfunction ·SORINE GROUP ITALIA S.R.L.·Product code CAC·September 6, 2006

    TBG, PVC, W/SMA, 3/8 X 3/32

    FDA Adverse Event
    Malfunction ·COBE CARDIOVASCULAR, INC.·Product code DWE·October 25, 2006

    TBG, PVC W/SMA, 3/8 X 3/32

    FDA Adverse Event
    Malfunction ·COBE CARDIOVASCULAR, INC.·Product code DWE·October 12, 2006

    COBE CARDIOVASCULAR

    FDA Adverse Event
    Death ·COBE CARDIOVASCULAR, INC·Product code CAC·January 22, 2004

    ULTIMATE PACK FAIRFIELD MEDICAL CENTER, LANCASTER OH

    FDA Adverse Event
    Malfunction ·COBE CARDIOVASCULAR, INC·Product code DWE·March 31, 2004

    COBE 4.1 BLOOD; CRYSTALLOID CARDIOPLEGIA DELIVERY SET

    FDA Adverse Event
    Malfunction ·COBE CARDIOVASCULAR, INC.·Product code DWF·August 15, 1996

    COBE BRAT

    FDA Adverse Event
    Malfunction ·COBE CARDIOVASCULAR, INC.·Product code CAC·July 11, 1996

    PERFUSION PACK, BLUE RIBBON W/UTUBE EMORY UNIVERSITY

    FDA Adverse Event
    Malfunction ·COBE CARDIOVASCULAR, INC.·Product code DWE·March 23, 2004

    DIDECO D 903 AVANT 2

    FDA Adverse Event
    Other ·COBE CARDIOVASCULAR, INC.·Product code DTZ·January 28, 2004