BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    LATIS SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEUROTECH BAXOLVE TYPE 294

    FDA 510(k)
    FDA Class 2 ·Neurology

    REPROCESSED ULTRASOUND INTRACARDIAC ECHO CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Reprocessed Intravascular Ultrasound Catheter

    FDA classification
    FDA Class 2 ·Reprocessed Intravascular Ultrasound Catheter

    Stimulator, Nerve, Transcutaneous, For Pain Relief

    FDA classification
    FDA Class 2 ·Stimulator, Nerve, Transcutaneous, For Pain Relief