BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Fecobionics Anorectal System

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

    PANEL PHOENIX NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·December 13, 2022

    Scrambler Therapy MC-5 A Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    LUTH-ALL SUB-Q NEEDLE SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD VACUTAINER® ECLIPSE¿ SIGNAL¿ BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FMI·December 9, 2024

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSH·November 20, 2008

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 19, 2013