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

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    FUJI I

    FDA 510(k)
    FDA Class 2 ·Dental

    MOBILE I.V. SYSTEMS 10,20,60

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FBC 921 (ALIF)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEPUY PINNACLE ACETABULAR CUP, 52-MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·February 7, 2011

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code IKX·August 5, 2014