BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    HELENA THROMBOPLASTIN REAGENT, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Hematology

    Lucitone® FRS®

    FDA UDI
    Dentsply International Inc.·D0019058570·

    NON STERILE PARENTERAL SUPPLY KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GADOLINIUM-153 BONE DENSITOMETER (GDC.10413)

    FDA 510(k)
    FDA Class 2 ·Radiology

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 10, 2013

    PEG, S.P. PULL, 20CH - EURO

    FDA Adverse Event
    Other ·COVIDIEN·Product code KNT·November 12, 2010

    2520274-2013-11167

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 2, 2013