BEUDAMED
    6 results · 26ms · 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.

    Patch-TEA (Model TRI-21)

    FDA 510(k)
    FDA Class 2 ·Neurology

    PaxWire Occlusion Balloon System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Q-SWITCHED ND:YAG OPHTALMIC LASER (WITH SLIT LAMP), MODEL OPTIMIS II

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·November 11, 2014

    GEM PREMIER 4000

    FDA Adverse Event
    Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code CEM·July 27, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 23, 2013