BEUDAMED
    10 results · 31ms · Sources: EU EUDAMED, US FDA

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    IMMUNOSCAN(TM) DIRECT NEISSERIA MENINGITIDIS KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Arthrex

    FDA UDI
    Provision·B504OMAR18700890·

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867381407·Drill Bit, 1.2 mm, AO, Short

    U-Motion II Acetabular System— Additional sizes

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTERMED LIVE

    FDA 510(k)
    FDA Class 2 ·Radiology

    DRILL BIT, 1.2 MM, AO, SHORT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTW·November 14, 2022

    BB-TAK, SMALL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 14, 2022

    CROSSBOSS CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·June 12, 2014

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES, INC.·Product code LWR·October 7, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·Product code OYC·December 12, 2012