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

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    Filters Status: Malfunction ×

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DRY·January 3, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 1, 2014

    BD EMERALD SYRINGE WITH LUER-SLIP TIP AND PRE-ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·November 6, 2019

    SYRINGE 10ML LS 21X1-1/2 AN EMERALD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 27, 2019