BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    turbodent touch

    FDA 510(k)
    FDA Class 2 ·Dental

    Disposable Intraoperative Probe (DIOP8)

    FDA 510(k)
    FDA Class 2 ·Radiology

    NEXUS DETACHABLE COIL SYSTEM, HELIX SUPER SOFT CSR

    FDA 510(k)
    FDA Class 2 ·Neurology

    VITROS CHEMISTRY PRODUCTS VANC REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LEH·July 3, 2013

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN·Product code OUT·November 14, 2014

    MAXPLUS CLEAR NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FPA·August 10, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013