BEUDAMED
    3,745 results · 39ms · Sources: EU EUDAMED, US FDA

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    ERBE

    FDA Adverse Event
    Malfunction ·ERBE ELEKTROMEDIZIN GMBH·Product code FEQ·December 28, 2022

    ERBE APC 300

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·October 18, 2022

    ERBE VIO 300 S

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 15, 2022

    ERBE VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 16, 2022

    ERBE VIO 300 S

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·October 26, 2022

    ERBE BICLAMP LAPAROSCOPIC FENESTRATED INSERT

    FDA Adverse Event
    Malfunction ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·October 28, 2022

    ERBE APC 2

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 2, 2022

    ERBE

    FDA Adverse Event
    Malfunction ·ERBE ELEKTROMEDIZIN GMBH·Product code FEQ·October 18, 2022

    ERBE VIO 3

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·November 11, 2022

    ERBE VIO 300 D

    FDA Adverse Event
    Other ·ERBE ELECTROMEDIZIN GMBH·Product code GEI·March 24, 2009

    ERBE APC 2

    FDA Adverse Event
    Injury ·ERBE ELECTROMEDIZIN GMBH·Product code GEI·February 9, 2012

    ERVE VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·January 30, 2009

    ERBEFLO CLEVERCAP® HYBRID CO2 TUBING/CAP SETS

    FDA Adverse Event
    Malfunction ·ERBE MEDICAL. LLC·Product code FEQ·April 17, 2026

    FIAPC PROBE 2200 A W/ FILTER

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·May 27, 2026

    ERBE APC 300

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·May 8, 2002

    RELAXOR THERAPY DEEPKNEADING MASSAGE

    FDA Adverse Event
    Malfunction ·J.B. RESEARCH INC.·Product code ISA·January 2, 1998

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    FDA Adverse Event
    Malfunction ·ERBE USA, INC.·Product code GEI·March 18, 2015

    ERBE BICLAMP LAPAROSCOPIC MARYLAND SERRATED INSERT

    FDA Adverse Event
    Malfunction ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·November 8, 2023

    ERBE APC 3

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 13, 2023

    ERBE

    FDA Adverse Event
    Malfunction ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 4, 2023