BEUDAMED
    4 results · 22ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    ARDIS INTERBODY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LATERAL ANGIOGRAPHIC C-ARM SUPPORT MH-400

    FDA 510(k)
    FDA Class 2 ·Radiology

    System, X-Ray, Angiographic

    FDA classification
    FDA Class 2 ·System, X-Ray, Angiographic

    Intervertebral Fusion Device With Bone Graft, Lumbar

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