BEUDAMED
    38 results · 19ms · Sources: EU EUDAMED, US FDA

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    AU2 SYSTEM

    FDA Adverse Event
    Other ·BIOSOUND ESAOTE, INC.·Product code ITX·August 6, 1997

    BOLERO

    FDA Adverse Event
    Other ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·November 11, 2009

    FLEXIBLE URETEROSCOPE

    FDA Adverse Event
    Other ·GYRUS ACMI, INC.·Product code FGB·January 31, 2012

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code FGB·January 6, 2012

    FILSHIE CLIP

    FDA Adverse Event
    Other ·COOPER SURGICAL, INC.·Product code HGB·May 19, 2010

    *

    FDA Adverse Event
    Other ·*·Product code FGB·November 25, 2003

    FILSHIE CLIP APPLIER

    FDA Adverse Event
    Other ·AVALON MEDICAL CORP·Product code HGB·May 29, 2007

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ ENDOVISION·Product code FGB·June 8, 2007

    OLYMPUS OES URETERO-RENOFIBERSCOPE

    FDA Adverse Event
    Other ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FGB·December 4, 2009

    WOLF

    FDA Adverse Event
    Other ·MEDICAL INSTRUMENT CORP·Product code HGB·June 7, 1999

    RICHARD WOLF

    FDA Adverse Event
    Other ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HGB·October 6, 1994

    FLEXIBLE URETEROPYELOSCOPE KIT

    FDA Adverse Event
    Other ·GYRUS ACMI, INC.·Product code FGB·July 1, 2011

    FLEXIBLE URETEROPYELOSCOPE KIT

    FDA Adverse Event
    Other ·GYRUS ACMI, INC.·Product code FGB·February 4, 2011

    AUTOCLAVABLE URETEROSCOPE

    FDA Adverse Event
    Other ·GYRUS ACMI, INC.·Product code FGB·January 13, 2011

    1221826-2006-00062

    FDA Adverse Event
    Other ·Product code FGB·October 17, 2006

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ ENDOVISION·Product code FGB·October 17, 2006

    FILSHIE CLIP APPLICATOR

    FDA Adverse Event
    Other ·AVALON MEDICAL CORP·Product code HGB·July 31, 2002

    MR-6LA

    FDA Adverse Event
    Other ·GYRUS ACMI, INC. - NORWALK·Product code FGB·December 19, 2007

    MR-6A

    FDA Adverse Event
    Other ·GYRUS ACMI, INC. - NORWALK·Product code FGB·December 19, 2007

    1221826-2003-00008

    FDA Adverse Event
    Other ·Product code FGB·May 9, 2003