BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    CORDIS INFLATOR DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SEAFORIA SPERM SEPARATION ASSISTANCE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    REPROCESSED TROCARS AND CANNULAS

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

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 13, 2014

    ON-Q PAIN PUMP

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code MEB·January 8, 2013

    AORTIC AP

    FDA Adverse Event
    Injury ·MEDTRONIC ARS, INC.·Product code LWQ·November 24, 2010