BEUDAMED
    3 results · 14ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    HETTICH CENTRIFUGE

    FDA Adverse Event
    Malfunction ·ANDREAS HETTICH GMBH & CO. KG·Product code GKG·May 13, 2014

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·February 9, 2013

    MEDFUSION 3010A SYRINGE INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD·Product code FRN·January 3, 2011