BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CRITICAL CARE ASSESSMENT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INSIGHT GENESIS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Intervertebral Fusion Device With Bone Graft, Cervical

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

    Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

    FDA classification
    FDA Class 2 ·Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

    Device, Biofeedback

    FDA classification
    FDA Class 2 ·Device, Biofeedback