BEUDAMED
    11 results · 30ms · Sources: EU EUDAMED, US FDA

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    LAPIDUS PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDION 6000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MODIFICATION TO CD SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD MICRO-FINE¿ PRO PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 17, 2023

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 13, 2025

    BD MICRO-FINE¿+ PRO PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·December 29, 2022

    PURACOL PLUS COLLAGEN WOUND DRESSING

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, LP·Product code KGN·April 16, 2026

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 25, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 4, 2014

    CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code KRH·June 13, 2008

    BD MICRO-FINE¿ PRO PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 17, 2023