BEUDAMED
    201 results · 89ms · Sources: EU EUDAMED, US FDA

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    ACS (ADVANCED CARDIOVASCULAR SYSTEMS INC)

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS INC·Product code MAF·November 5, 1998

    VENTAK MINI AICD

    FDA Adverse Event
    ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LWS·July 19, 1996

    ACS TX 2000 CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS INC·Product code LOX·September 30, 1996

    CORONARY DILATION CATHETER

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LOX·July 24, 1996

    ACS EXTRA S'PORT .014 300CM LONG

    FDA Adverse Event
    Malfunction ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·July 3, 1996

    ACS S'PORT GUIDE WIRE SYSTEM

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·September 30, 1996

    ACS OTW LIFESTREAM CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LOX·September 24, 1996

    PRISM BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LOX·July 18, 1996

    HI-TORQUE FLOPPY EXTRA SUPPORT GUIDEWIRE

    FDA Adverse Event
    Death ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·September 5, 1996

    ACS CONCORDE CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LOX·September 30, 1996

    ACS TOURGUIDE CORONARY GUIDING CATHETER/GUIDING CATHETER

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DYB·September 6, 1996

    ACS HI-TORQUE EXTRA SUPPORT GUIDE WIRE

    FDA Adverse Event
    Death ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·September 26, 1996

    HI-TORQUE FLOPPY OO

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·September 6, 1996

    ACS CORO WIRE

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·July 1, 1996

    HI-TORQUE GUIDE WIRE

    FDA Adverse Event
    Malfunction ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·September 20, 1996

    HI-TORQUE FLOPPY II GUIDE WIRE

    FDA Adverse Event
    Death ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·June 4, 1996

    GUIDE WIRE

    FDA Adverse Event
    ADVANCED CARDIOVASCULAR SYSTEMS,INC.·Product code DQX·April 8, 1996

    ANGIOPLASTY WIRE

    FDA Adverse Event
    Malfunction ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·May 7, 1996

    EXTRA S'PORT WIRE

    FDA Adverse Event
    Death ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code DQX·June 11, 1996

    ELIPSE ANGIOPLASTY BALLOON CATHETER, 3.0

    FDA Adverse Event
    Malfunction ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LOX·February 15, 1994