BEUDAMED
    3 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DRY·December 23, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN·Product code FWM·March 21, 2014