BEUDAMED
    3 results · 15ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·Product code JKA·December 2, 2020

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

    BD¿ SYRINGE WITH NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 22, 2018