BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    BONE PAD REMOVER

    FDA 510(k)
    FDA Class 1 ·Neurology

    Folding Readers

    FDA UDI
    Diversified Products, Inc.·00842894113363·

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756349246·AV FISTULA PACK

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450216125·

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K1102250·Tray, Base, 2.25", Universal

    DOSIMETRY CHECK

    FDA 510(k)
    FDA Class 2 ·Radiology

    ANGIODYNAMICS, INC. VENACURE 1470 LASER

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

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    FDA Adverse Event
    Injury ·MEDTRONIC, INC·Product code NEK·January 8, 2013

    COBAS INTEGRA 400

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 30, 2010

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 2, 2014