BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    LIA-1 Catheter (542-1)

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517631985·CoRoent Ant TLIF Ti, 15x11x40mm 12°

    Phantom

    FDA UDI
    Innovative Med·00851314007038·Surgical Aspirator:1/3 hp. 0-3.6 scfm / 0-27.5 ...

    ONEPASS NUCLEAR MEDICINE IMAGING SYSTEM

    FDA 510(k)
    FDA Class 1 ·Radiology

    Powersculp laser lipolysis system

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 9, 2025

    MEDTRONIC ANEURX BIFURCATED STENT GRAFT (FLEXIBLE)

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·September 13, 2011

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·November 14, 2014

    JOHNSON & JOHNSON FLOSS, MINT WAXED

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON CONSUMER PRODUCTS·Product code JES·July 29, 2013