BEUDAMED
    104 results · 68ms · Sources: EU EUDAMED, US FDA

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    HEART TECHNO CORO WIRE

    FDA Adverse Event
    Injury ·HEART TECHNOLOGY, INC.·Product code DQX·July 1, 1996

    ROTABLATOR

    FDA Adverse Event
    Malfunction ·HEART TECHNOLOGY, INC.·Product code DQX·July 3, 1996

    ROTABLATOR GUIDE WIRE WITH WIRECLIP TORQUER

    FDA Adverse Event
    Malfunction ·HEART TECHNOLOGY, INC.·Product code DQX·July 31, 1996

    ROTABLATOR

    FDA Adverse Event
    Death ·HEART TECHNOLOGY, INC.·Product code MCX·April 25, 1996

    ROTABLATOR GUIDE WIRE

    FDA Adverse Event
    Injury ·HEART TECHNOLOGY, INC.·Product code MCW·January 26, 1994

    HEART TECHNOLOGY ROTABLATOR

    FDA Adverse Event
    Death ·HEART TECHNOLOGY, INC.·Product code MCX·January 31, 1995

    ROTOBLATER

    FDA Adverse Event
    HEART TECHNOLOGY, INC.·Product code MCX·December 7, 1994

    CARDIAC CATHETER

    FDA Adverse Event
    Injury ·HEART TECHNOLOGY, INC.·Product code LOX·November 14, 1994

    ROTABLATOR GUIDE WIRE

    FDA Adverse Event
    Malfunction ·HEART TECHNOLOGY, INC.·Product code DQX·June 24, 1997

    HEART ROTO BLADE

    FDA Adverse Event
    Injury ·HEART TECHNOLOGY, INC.·Product code MCX·April 10, 1997

    ROTOLBLATOR/ROTABLATOR/FLOPPY WIRE

    FDA Adverse Event
    Malfunction ·HEART TECHNOLOGY, INC.·Product code DQX·January 3, 1997

    ROTABLATOR

    FDA Adverse Event
    Injury ·HEART TECHNOLOGY, INC·Product code MCX·January 10, 1997

    ROTABLATOR

    FDA Adverse Event
    Injury ·HEART TECHNOLOGY, INC.·Product code MCX·July 8, 1994

    ROTOBLATOR

    FDA Adverse Event
    Injury ·HEART TECHNOLOGY INC.·July 29, 1994

    C TYPE GUIDE WIRE

    FDA Adverse Event
    Death ·HEART TECHNOLOGY,INC.·Product code DQX·September 16, 1994

    ROTABLATOR

    FDA Adverse Event
    HEART TECHNOLOGY, INC.·Product code MKI·April 29, 1994

    ROTOBLATOR GUIDE WIRE

    FDA Adverse Event
    Malfunction ·HEART TECHNOLOGY, INC.·Product code MCX·May 20, 1994

    ROTABLATOR TYPE C GUIDE WIRE .009

    FDA Adverse Event
    HEART TECHNOLOGY, INC.·Product code DQX·July 1, 1995

    ROTOBLATOR GUIDE WIRE (BURR SIZE - 3.0 GUIDE WIRE TYPE - C)

    FDA Adverse Event
    HEART TECHNOLOGY, INC.·Product code DQX·July 2, 1992

    ROTABLATOR

    FDA Adverse Event
    Death ·HEART TECHNOLOGY INC·Product code DQX·April 12, 2001