BEUDAMED
    209 results · 54ms · Sources: EU EUDAMED, US FDA

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    BOVIE MEDICAL CORPORATION

    FDA Adverse Event
    Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·March 5, 2014

    BOVIE MEDICAL CORPORATION

    FDA Adverse Event
    Injury ·BOVIE MEDICAL·Product code GEI·April 10, 2008

    BOVIE MEDICAL CORPORATION

    FDA Adverse Event
    Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·August 25, 2016

    R SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 28, 2025

    HF COAG. SUCTION TUBE

    FDA Adverse Event
    Malfunction ·RICHARD WOLF GMBH·Product code GCJ·February 25, 2019

    BOVIE BLADE ELECTRODE 6" (15.24CM)

    FDA Adverse Event
    Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·May 18, 2018

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 19, 2022

    ESUREFIT DISPERSIVE ELECTRODE

    FDA Adverse Event
    Other ·CONMED CORP·Product code GEI·October 18, 2012

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 24, 2022

    HF CONNECTION CABLE MONO L 3M

    FDA Adverse Event
    Malfunction ·RICHARD WOLF GMBH·Product code GEI·September 27, 2023

    CAUTERY HIGH TEMP FINE TIP

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code HQP·December 9, 2016

    J-PLASMA HANDPIECE

    FDA Adverse Event
    Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·December 22, 2016

    BOVIE PAD

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·August 20, 2015

    ARTHREX, INC.

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·November 18, 2014

    BOVIE MEDICAL

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·May 18, 2012

    BOVIE MEDICAL

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·June 6, 2012

    BOVIE MEDICAL

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code HRX·January 23, 2012

    J-PLASMA

    FDA Adverse Event
    Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·November 9, 2017

    J-PLASMA

    FDA Adverse Event
    Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·October 19, 2017

    ES04

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·October 5, 2017