BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Remex Spine Surgery Navigation Instrument

    FDA 510(k)
    FDA Class 2 ·Neurology

    CygneX I System

    FDA 510(k)
    FDA Class 2 ·Radiology

    PERIARTICULAR LOCKING PLATES AND SCREWS, SERIES 2358 AND 2359

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·September 12, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 11, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 23, 2013