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

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    VSP HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111253348·CUSCO VAG SPEC SM 3 X 1.25"

    ARCHITECT HE4, ARCHITECT HE4 CALIBRATORS AND ARCHITECT HE4 CONTROLS, MODELS 2, 2P54, 2P54-01, 2P54-10 SP54-01,

    FDA 510(k)
    FDA Class 2 ·Immunology

    DIACLEAR ULTRAFILTER

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

    ARCHITECT HE4 REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code OIU·February 6, 2026

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 9, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 20, 2010

    TOTAL ASR FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 1, 2014