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

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    EMG REPORT GENERATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    DAYPAK SYSTEM III CATHETER CARE KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UTERINE MANIPULATOR 4.5MM

    FDA 510(k)

    UHR BIPOLAR 26X48MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWL·June 3, 2014

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·November 12, 2012

    VASOVIEW HEMOPRO EVH SYSTEM

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·September 23, 2010