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

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    PROVIDENT HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704263015·

    ACCU-TEC SYSTEM FOR TISSUE EXPANDER INJECTION PORT

    FDA 510(k)
    FDA Unclassified ·Unknown

    URETHRALPRESSURE PROFILE CATHETER

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

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·January 30, 2013

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FPA·December 15, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014

    ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020