BEUDAMED
    4 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ADVIA 1800

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·May 30, 2014

    FRESENIUS DIALYZER-OGDEN

    FDA Adverse Event
    Injury ·OGDEN MANUFACTURING·Product code KDI·November 14, 2012

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·September 23, 2010

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 22, 2016