BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    XEROFORM DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837173814·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837173210·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837190750·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837189280·

    EVTOOL MODEL # V. 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    Fully Automatic Electronic Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INRATIOR PT/INR TEST STRIP

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·March 26, 2014

    MAXIMO VR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code LWS·October 31, 2012

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 2, 2015