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

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    RADIFOCUS Torque Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    priti®multidisc ZrO2

    FDA UDI
    Pritidenta GmbH·04251366905133·

    Tizian Blank 5.0

    FDA UDI
    Pritidenta GmbH·04251366906178·

    DR. JAPAN FACIL POINT SPINAL NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PROTEXIS LATEX BASIC STERILE LATEX POWDER-FREE SURGICAL GLOVE WITH PROTEIN CONTENT LABEL CLAIM OF 50 UG/DM OR LESS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    QT SCANNER 2000 MODEL A

    FDA Adverse Event
    Injury ·QT IMAGING HOLDINGS, INC.·Product code IYO·October 30, 2025

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·November 3, 2014

    FREESTYLE NAVIGATOR

    FDA Adverse Event
    Malfunction ·Product code LFR·August 23, 2011

    URETEX SUPPORT PP TRANSOBTUR2 KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·July 3, 2013