BEUDAMED
    8 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VIZIGO SHEATH

    FDA Adverse Event
    Injury ·CARDIOFOCUS, INC.·Product code DYB·August 12, 2023

    UNK_SMART TOUCH BIDIRECTIONAL SF

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·July 7, 2023

    HEARTLIGHT ENDOSCOPIC ABLATION SYSTEM

    FDA Adverse Event
    Injury ·CARDIOFOCUS, INC.·Product code OAE·September 5, 2023

    HEATLIGHT LASER BALLOON

    FDA Adverse Event
    Injury ·CARDIOFOCUS, INC.·Product code OAE·August 9, 2023

    HEARTLIGHT

    FDA Adverse Event
    Malfunction ·CARDIOFOCUS, INC·Product code OAE·January 5, 2023

    LIGHTSTIC 360 DIFFUSER

    FDA Adverse Event
    Malfunction ·RARE EARTH MEDICAL INC·Product code LQJ·August 26, 2002

    THERMOCOOL SMARTTOUCH

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·January 9, 2025

    THERMOCOOL SMARTTOUCH

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·March 17, 2026