BEUDAMED
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    ELC-THERMO-SYSTEM

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    TWINTRODE ELC 134 ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ELC 35-UP MODEL NUMBER 116015 AND ELC 54-UP MODEL NUMBER 115606

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ELC

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code GDO·November 12, 2007

    ELC

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code GDO·November 12, 2007

    ELC

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code GDO·July 16, 2007

    ELC

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code GDO·July 16, 2007

    Adapt AO, Akreos Advanced Optics Aspheric Lens. Bausch & Lomb Incorporated, Rochester, NY. Manufactured by Bausch & Lomb Incorporated, Clearwater, FL.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQL·December 8, 2008

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·CONMED·Product code GDO·April 20, 2012

    REFLEX ELC

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code HBT·February 8, 2002

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code HBT·March 14, 2002

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·CONMED CORP.·Product code HBT·August 12, 2003

    "REFLEX" ELC

    FDA Adverse Event
    Injury ·RICHARD - ALLAN MEDICAL INDUSTRIAL·Product code GDO·May 15, 2000

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·IMAGYN SURGICAL·Product code GDO·August 14, 1998

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·IMAGYN SURGICAL·Product code GDO·September 17, 1998

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·CONMED ENDOSURGERY·Product code GDO·February 9, 2011

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·CONMED COMPANY·Product code HBT·November 9, 2001

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·CONMED CORP.·Product code HBT·December 5, 2001

    REFLEX ELC

    FDA Adverse Event
    Injury ·CONMED CORP.·Product code HBT·October 29, 2004

    REFLEX ELC

    FDA Adverse Event
    Malfunction ·CONMED CORP.·Product code HBT·September 28, 2001