BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    FLXFIT INTERVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE

    FDA 510(k)
    FDA Class 2 ·Neurology

    SOPRO 281

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Led Light Source

    FDA classification
    FDA Class 2 ·Led Light Source

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Device, Neurovascular Embolization

    FDA classification
    FDA Class 2 ·Device, Neurovascular Embolization