BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    NeutrArt

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IQ FLEX M

    FDA Adverse Event
    Malfunction ·FIRST SOURCE INC.·Product code IZL·May 29, 2024

    INFINI RADIOFREQUENCY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BRESAGEN CATHETER, MODEL CS-3000

    FDA 510(k)
    FDA Class 2 ·Neurology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 3, 2014

    BUTTONSWITCH PENCIL

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·August 17, 2011

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·July 2, 2013