BEUDAMED
    6 results · 19ms · 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 Regulation: Us FDA ×

    ALEXOTEK LINGUAL TUBES

    FDA 510(k)
    FDA Class 1 ·Dental

    SURGITEK NEPHROSTENT KIT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OXYGEN MONITOR OHIO 5100

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·May 6, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 15, 2012

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DSI·September 15, 2010