BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    MODIFIED HAND INSTRUMENT DEVICES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ES-Series

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO XIA 4.5 SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·December 16, 2010

    2520274-2013-10181

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 11, 2013

    DLT TS CER HD 12/14 36MM +5.0

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code KWA·July 28, 2014