BEUDAMED
    586 results · 39ms · Sources: EU EUDAMED, US FDA

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    GUIDANT CORP

    FDA Adverse Event
    Injury ·GUIDANT CORP.·Product code DXY·December 15, 2000

    GUIDANT CORP

    FDA Adverse Event
    Injury ·GUIDANT CORP·Product code LWS·November 16, 2006

    GUIDANT CORP

    FDA Adverse Event
    Injury ·CARDIAC RHYTHM MANAGEMENT GROUP·Product code LWS·January 24, 2005

    GUIDANT CORP

    FDA Adverse Event
    Injury ·CARDIAC RHYTHM MANAGEMENT GROUP·Product code LWS·January 24, 2005

    GUIDANT CORP

    FDA Adverse Event
    Injury ·CARDIAC RHYTHM MANAGEMENT GROUP ST·Product code LWS·January 24, 2005

    GUIDANT CORP

    FDA Adverse Event
    Injury ·GUIDANT CORP., CARDIAC RHYTHM MFG GROUP·Product code LWS·December 9, 2002

    GUIDANT CORP

    FDA Adverse Event
    Injury ·*·Product code DXY·December 10, 2002

    ACTROS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DXY·January 6, 2006

    CPI BY GUIDANT CORP

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC.·Product code DXY·October 21, 1998

    BELOS VR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code LWS·January 6, 2006

    PROTOS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DXY·January 6, 2006

    PROTOS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO·Product code DXY·January 6, 2006

    PROTOS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO·Product code DXY·January 6, 2006

    ACTROS SLR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DXY·January 6, 2006

    BA03 DDDR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DXY·January 6, 2006

    PIKOS 01

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DXY·January 6, 2006

    MYOCARDIAL SUTURELESS PERMANENT PACING LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIV., INC.·Product code DTB·March 22, 2002

    MYOCARDIAL SUTURELESS PERMANENT PACING LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIV., INC.·Product code DTB·March 22, 2002

    20/20 PRIORITY PACK W/CO-PILOT

    FDA Adverse Event
    Malfunction ·GUIDANT VASCULAR INTERVENTION·Product code DQX·March 9, 2006

    ACS HI-TORQUE GUIDE WIRE

    FDA Adverse Event
    Injury ·GUIDANT, ADVANCED CARDIOVASCULAR SYSTEMS·Product code DQX·February 13, 2002