BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    MODEL 556 MONITOR

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    ACL CROSSPIN

    FDA UDI
    Biomet Sports Medicine, LLC·00880304421318·

    Lucitone® FRS®

    FDA UDI
    Dentsply International Inc.·D0019058560·

    VEN-O-VAC BLOOD COLLECTION VACUUM TUBES

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CUSTOM WOUND MANAGEMENT KITS AND TRAYS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GEMSTAR PAIN MGE SNG

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 29, 2014

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code NBW·July 10, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013