BEUDAMED
    6 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    FENESTRATED BIPOLAR FORCEPSINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 4, 2013

    INSIGNIA

    FDA Adverse Event
    Malfunction ·GUIDANT CLONMEL IRELAND·Product code NVZ·April 8, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 23, 2011

    XIA LP POLYAXIAL SCREW 5.5 X 45MM

    FDA Adverse Event
    Injury ·STRYKER SPINE BORDEUX·Product code HWC·May 6, 2008

    BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 100 MG/20 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·December 28, 2018

    BD VACUTAINER® BLOOD ALCOHOL DETERMINATIONS SODIUM FLUORIDE: POTASSIUM OXALATE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·June 25, 2019