BEUDAMED
    3 results · 41ms · Sources: EU EUDAMED, US FDA
    Filters FDA Classification ×

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Varnish, Cavity

    FDA classification
    FDA Class 2 ·Varnish, Cavity

    Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

    FDA classification
    FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)