BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Intellijoint HIP(tm) System

    FDA 510(k)
    FDA Class 2 ·Neurology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517575371·CoRoent Ant TLIF Ti, 15x11x36mm 4°

    LANX FACET SCREW SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    VPAP ADAPT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 26, 2024

    ECT INTERNAL FRACTURE FIXATION DRILL BIT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTW·May 30, 2013

    KLEENSPEC 590 SERIES DISP. VAGINAL SPECULA

    FDA Adverse Event
    Malfunction ·WELCH ALLYN·Product code HIB·June 8, 2011

    TURBOVAC 90 WITH INTEGRATED CABLE

    FDA Adverse Event
    Injury ·ARTHROCARE CORP.·Product code GEI·September 9, 2008

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·December 13, 2018