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

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    HEDROCEL ACETABULAR RESTRICTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799003799·

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799004369·

    SPECTRUM M2 MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ClearCheck

    FDA 510(k)
    FDA Class 2 ·Radiology

    X-STOP INTERSPINOUS SPACER SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code NQO·February 14, 2013

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·January 7, 2011

    INRATIO PT/INR TEST STRIPS

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code GJS·July 11, 2014