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

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    Filters Status: Malfunction ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 25, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 11, 2012

    CAPSURE SP

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·June 10, 2015