BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    Lumify Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583027289·CR40 P, VC PS BE CHEER 40

    THE ASCENSION MOVEMENT GREAT TOE SYSTEM TOTAL ARTHROPLASTY

    FDA 510(k)
    FDA Unclassified ·Unknown

    XLTEK STIMULATOR PROBES, MODELS 105233, 105234, 105235, 105236, 105237 AND 105238

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 14, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 11, 2013