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.
    Filters Regulation: Us FDA ×

    COULTER CLONE T1 MONOCLONAL ANTIBODY

    FDA 510(k)
    FDA Class 2 ·Hematology

    GENESIS B-HCG

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SMART-LOGIC AUTO DIGITAL UPPERARM BLOOD PRESSURE MONITOR, MODEL KP-7500, FULLY FUZZY AUTO DIGITAL UPPER ARM BLOOD PRESSU

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADVANTA VXT GRAFTS < 6MM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code DYF·June 10, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 21, 2012

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 9, 2008