BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Frontier Medical Devices Posterior Cable Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GC ORAL MOISTURIZING GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    RESOLUTIONMD MOBILE MODEL RMB-MOB-2X

    FDA 510(k)
    FDA Class 2 ·Radiology

    EVITA INFINITY

    FDA Adverse Event
    Malfunction ·DRAGER MEDICAL, INC.·Product code CBK·June 3, 2013

    UNKNOWN DEPUY ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KXA·June 30, 2011

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORP.·Product code LGW·September 4, 2008

    C-QUR MOSAIC

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code FTL·October 9, 2015