BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    SARACAP RESPIRATORY MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209124299·

    BIOFOAM Bone Wedge

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 5, 2014

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MNI·November 30, 2012

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 28, 2010

    7FR COAX HEMOSTATIC PROBE

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC·Product code KNS·July 18, 2019