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

    Device, Anti-Snoring

    FDA classification
    FDA Class 2 ·Device, Anti-Snoring

    Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

    FDA classification
    FDA Class 2 ·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

    Spinal Vertebral Body Replacement Device

    FDA classification
    FDA Class 2 ·Spinal Vertebral Body Replacement Device