BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    XRT-7.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    SONO-VU US(TM)

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    CARDIAC PERFORMANCE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    AHTO IRRIGATION PUMP

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCX·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·July 29, 2014