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 ×

    URIC ACID PAP

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    THERMOSTAT 900 ADMINISTRATION SET, MODEL ASH 100, 200 AND 300

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Cycler Drain Bag Set

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

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·June 13, 2014

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 19, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 13, 2012