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

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    MYO-ACTUATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209113972·

    MEDIQ VERSION 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    BTL-899TT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    QUADROX-ID ADULT

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY AG·Product code DTZ·November 21, 2012

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 18, 2015