BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    DUMEX PAK-ITS COTTON GAUZE PACKING IMPREGNATED WITH HYDROGEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    REFSTAR WITH QWIKPATCH

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·October 26, 2007

    INRATIO PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·June 23, 2016

    Vinyl Examination Glove (Clear, Non-Colored)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MICRUS ASCENT OCCLUSION BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STERLING¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·February 27, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·February 7, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014