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

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    HEEL GARD

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Fundus Camera

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ATLAS WOUND MATRIX

    FDA 510(k)
    FDA Unclassified ·Unknown

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 5, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 15, 2012

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH LTD / HUNTINGTON·Product code HQL·August 4, 2010