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

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    HALL VEIN STRIPPER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DePuy Synthes Femoral Recon Nail System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 13, 2014

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·December 6, 2012

    SERIES 20000 LEGACY

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·October 14, 2010

    PM3544 QUADRA RELIEVE and PM3562 QUADRA ALLURE MP These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. These devices are used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·October 25, 2017