BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Unclassified ×

    EARPOPPER, MODEL EP-2000, EP-2100, EP-3000

    FDA 510(k)
    FDA Unclassified ·Unknown

    Ear Pressure Relief Device(Model:ER813B)

    FDA 510(k)
    FDA Unclassified ·Unknown

    OTOVENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    EARCLEAR

    FDA 510(k)
    FDA Unclassified ·Unknown

    Eustachi Ear Pressure Relief Device

    FDA 510(k)
    FDA Unclassified ·Unknown

    Device, Inflation, Middle Ear

    FDA classification
    FDA Unclassified ·Device, Inflation, Middle Ear