BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    NON REBREATHING MASK

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613023577·Stevens Scissors, Straight, Blunt/Blunt, Overal...

    SURSHIELD SAFETY WINGED BLOOD COLLECTION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DISCOVERY TMAX MANUAL WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DRILL F.RADIOLUCENT TARGETING DEVICE SIDEWINDER Ø3,2 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·September 16, 2013

    MINIMAL ACCESS ATTACHMENT

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·January 8, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Death ·Product code KDJ·December 2, 2010

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code INM·July 3, 2014

    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