BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    BONEBAC T-PLIF INTERVERTEBRAL BODY FUSION DEVICE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, WATCHBP OFFICE TARGET (BP3MD1-4).

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MMODIFICATION TO LAMINARIA

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Dilator, Cervical, Hygroscopic-Laminaria

    FDA classification
    FDA Class 2 ·Dilator, Cervical, Hygroscopic-Laminaria

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    System, Measurement, Blood-Pressure, Non-Invasive

    FDA classification
    FDA Class 2 ·System, Measurement, Blood-Pressure, Non-Invasive