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

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    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·December 12, 2017

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014

    KAPPA 900 DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code DXY·October 15, 2012