BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    RADIATION EXIT VERIFICATION SYSTEM/BACK POINTER SYSTEM

    FDA 510(k)
    FDA Class 1 ·Radiology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867060036·ARTHREX ECLIPSE HUMERAL HEAD, 45/19

    AGFA DIAGNOSTIC CENTER (ADC)

    FDA 510(k)
    FDA Class 2 ·Radiology

    CALMTONE

    FDA 510(k)
    FDA Class 2 ·Neurology

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 11, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·November 23, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 1, 2014

    GLENOID, PE WITH PEG, MEDIUM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 3, 2019