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

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    VENTILATION TUBE TEFLON SHEPARD TYPE

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

    G.E. TELEMETRY MONITORING

    FDA 510(k)
    FDA Class 2 ·Neurology

    DDU-2300 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    132 SIZE 8 SECUR-FIT ADVANCED STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LWJ·April 30, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·October 10, 2012

    COSYCOT INFANT WARMER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code FMT·July 27, 2010

    L.C. 5000/CE 2-CHANNEL PUMP (50/CASE)

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·August 22, 2013

    11MM/130 DEG TI CANN TFNA 360MM/RIGHT - STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·August 16, 2019