BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    BI-ARTICULAR II HIP DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228720191·GC Initial™ PC Pellets Bleached BO, 5pcs. X 2

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556709099·GC Initial™ PC Pellets Bleached BO, 5pcs. X 2

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376680675·Proximity Drill, 19mm

    AKITA2 APIXNEB

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Brisbane ALIF Device, Gladstone ALIF Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·June 13, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 14, 2010

    HUT EXT DR FINAL ASSY-REVERSE

    FDA Adverse Event
    Malfunction ·MALLINCKRODT INC., LIEBEL-FLARSHEIM BUSINESS·Product code IXR·December 11, 2012