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

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    COMBINATION 6X-MAGNIFIER AND TWEEZERS

    FDA 510(k)
    FDA Not Classified ·Unknown

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867241312·5.0mm Threaded Drill Sleeve, Short

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ARGENCO 40 TYPE III DENTAL GOLD ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    IDENTITY ADX DR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·November 10, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·January 16, 2014

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 20, 2012