BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    NEW COBE CARDIOPLEGIA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113164·PS Insert, Size 3 x 12mm

    Polyfusion IV Administration Sets

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTIMA SNORING MIKE, MODEL 0540

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 16, 2015

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·December 10, 2010

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·December 17, 2012

    Upper Extremity Pack, part number AMS4670 Upper Extremity Pack, part number AMS4670(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017