BEUDAMED
    4 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    ProLift Lateral HELO Fixated

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIMENSION CLINICAL CHEMISTRY SYSTEM, MODEL XPAND

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Electrode, Ion Specific, Potassium

    FDA classification
    FDA Class 2 ·Electrode, Ion Specific, Potassium