BEUDAMED
    85 results · 52ms · Sources: EU EUDAMED, US FDA

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    MEDI-TECH INC MAGIC TORQUE

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code DQX·June 8, 1994

    MEDITECH ULTRATHIN 5F ANGIOPLASTY CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code LIT·July 25, 1996

    MEDI-TECH GUIDEWIRE AND INTRODUCER SET

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code DQX·July 16, 1996

    GUIDE WIRE AND INTRODUCER SET

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code DQX·May 22, 1996

    GUIDE WIRE AND INTRODUCER SET

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code DQX·May 20, 1996

    GREENFIELD FILTER

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·February 4, 1994

    APD CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code KPM·February 25, 1994

    RADIFOCUS GUIDE WIRE M

    FDA Adverse Event
    Injury ·MEDI TECH, INC.·Product code DQX·January 28, 1994

    PERCUFLEX

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code FAD·June 16, 2000

    VTC BILIARY FIRM SYSTEM W/LOCKING PIGTAIL

    FDA Adverse Event
    Malfunction ·MEDI-TECH, INC.·Product code GCA·April 8, 1992

    TITANIUM GREENFIELD VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·MEDI-TECH, INC.·Product code DTK·March 17, 1995

    BALLOON DILATATION CATHETER

    FDA Adverse Event
    Death ·MEDI-TECH, INC.·Product code LIT·March 10, 1995

    ASAP

    FDA Adverse Event
    Malfunction ·MEDI-TECH, INC·Product code KNW·January 4, 1995

    RADIFOCUS GUIDE WIRE M

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code DQX·November 22, 1994

    MEDI-TECH 8MM-2CM ULTRATHIN BALLOON CATHETER

    FDA Adverse Event
    Death ·MEDI-TECH, INC.·Product code LIT·October 13, 1994

    MEDI-TECH

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code LIT·October 1, 1996

    UV FLASH AUTO

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code KDJ·August 20, 2002

    MEDITECH

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code LIT·November 9, 1993

    MEDI-TECH

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code LJT·January 3, 1997

    MEDI-TECH 6 MM ANGIOPLASTY BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·MEDI-TECH, INC.·Product code LIT·July 11, 1994