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

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    ARGUS HYSTEROSCOPY INSTRUMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690122791·Modular Stem 25mm x 150mm

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690199519·Modular Knee Straight Reamer - 25mm

    ARTHORALIX 8500, MODELS 110-0199G1, 110-0199G2, 110-0199G3, 110-0199G4

    FDA 510(k)
    FDA Class 2 ·Dental

    xvision Spine system

    FDA 510(k)
    FDA Class 2 ·Neurology

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 27, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·December 13, 2010

    GYNECARE GYNEMESH* PS

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTO·February 8, 2013