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.

    NASAL INTERFACE MODEL 7910

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LABELLING MODIFICATION TO MAXX PLUS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    UNIVERSAL TIBIAL NAIL AND UNREAMED TIBIAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SCREWDRIVER HEX BALL END 3.5MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HXX·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014