BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    VISTA OPHTHALMOSCOPE (BATTERY AND AC-POWERED)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    QUANTITATIVE ELECTROCARDIOGRAPHIC DETECTOR (QED 1000)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Luna XD Ti Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BZE·December 22, 2009

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 25, 2014

    RECAP MAGNUM SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 29, 2010

    ENTERRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·January 2, 2013