BEUDAMED
    136 results · 74ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    VNUS MEDICAL TECHNOLOGIES, INC.

    FDA Adverse Event
    Injury ·VNUS·Product code GEI·September 30, 2011

    VNUS ClosureFAST catheters, Model Number: CL7-7-100, VNUS Medical Technologies, Inc., San Jose, CA 95138

    FDA Recall
    Terminated ·VNUS Medical Technologies Inc·Product code GEI·March 6, 2007

    VNUS 7F ClosureFAST Catheter, Order #: CF7-7-60 (60 cm working length), Manufactured by VNUS Medical Technologies, Inc., 5799 Fontanoso Way, San Jose, CA 95138

    FDA Recall
    Terminated ·VNUS Medical Technologies Inc·Product code GEI·August 8, 2007

    VNUS 7F ClosureFAST Catheter, Order # ClF7-7-100 (100 cm working length), Manufactured by VNUS Medical Technologies, Inc., 5799 Fontanoso Way, San Jose, CA 95138

    FDA Recall
    Terminated ·VNUS Medical Technologies Inc·Product code GEI·August 8, 2007

    VNUS CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·February 2, 2009

    VNUS CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·January 26, 2009

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Death ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·January 13, 2010

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·January 14, 2010

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·March 30, 2010

    RADIO FREQUENCY STYLET CATHETER (RFS)

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·March 12, 2010

    CLOSURE CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code DQO·January 16, 2002

    CLOSURE CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code DQO·March 8, 2002

    CLOSURE CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·February 13, 2002

    CLOSURE CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code DQO·March 8, 2002

    CLOSURE CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·March 15, 2002

    VNUS CLOSURE FAST CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·May 17, 2007

    VNUS CLOSURE FAST CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·April 12, 2007

    VNUS CLOSURE FAST CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·June 11, 2007

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·November 19, 2009

    CLOSURE CATHETER

    FDA Adverse Event
    Injury ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·July 21, 2004