BEUDAMED
    3 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Fda510k ×

    BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19, BeneVision N22, BeneVision N1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPINAL EPIDURAL NEEDLES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MIC

    FDA 510(k)
    FDA Class 2 ·Neurology