BEUDAMED
    6 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.

    MODIFIED CARDIOTOMY RESERVOIR 5M1470

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TELEMETRY PACEMAKER MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENTREX DATA REDUCTION & QUAL. CONTR. SY

    FDA 510(k)
    FDA Class 2 ·Hematology

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 22, 2014

    EXPRESS VASCULAR LD PREMOUNTED STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·October 8, 2010

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·December 10, 2012