BEUDAMED
    14 results · 45ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ELLMAN SURGITRON 4.0 DUAL RF S5

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·May 21, 2010

    DENTO-SURGE

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL INC.·Product code EKZ·March 26, 2004

    DENTO-SURG 90 FFP

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL INC.·Product code EKZ·July 17, 2000

    ELLMAN SURGITRON EMC

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL INC.·Product code GEI·September 28, 2000

    SURGITRON 120 IEC/SURGITRON 4.0 DUAL

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·December 11, 2008

    SURGITRON RADIOLASE

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·October 24, 2008

    SURGITRON

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·April 14, 2006

    SURGITRON

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·April 13, 2006

    SURGITRON FFPF EMC

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·September 29, 2009

    ELLMAN SURGITRON FFPF OPHTHALMOLOGY

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code BWA·July 2, 2007

    BIPOLAR TRIGGER-FLEX PROBE

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code KNS·May 27, 2008

    ELLMAN SURGITRON

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·November 25, 1997

    ELLMAN SURGITRON EMC

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·March 10, 1999

    SCALPEL ELECTRODE

    FDA Adverse Event
    Injury ·ELLMAN INTERNATIONAL, INC.·Product code GEI·September 9, 2010