BEUDAMED
    13 results · 115ms · Sources: EU EUDAMED, US FDA

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    NONE

    FDA Adverse Event
    Other ·THE ELECTRODE STORE, INC.·Product code DRX·April 25, 2005

    CLEARTRAC ADULT ECG ELECTRODE

    FDA Adverse Event
    CONMED CORPORATION·Product code DRX·July 21, 2011

    EMBLEM S-ICD

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·January 20, 2026

    ERBE VIO 3

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 8, 2025

    SYNCHRON LX20 PRO CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·December 19, 2008

    COULTER® LH 780 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·February 7, 2011

    ERBE VIO 3

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·July 11, 2025

    ERBE VIO 3

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 12, 2025

    ERBE VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·February 19, 2026

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 24, 2026

    ERBE VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·November 23, 2022

    PULSE GEN MODEL 1000

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·December 29, 2022

    Advena Limited

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