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

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    VARELISA COMBINED DNA ANTIBODIES EIA

    FDA 510(k)
    FDA Class 2 ·Immunology

    PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VIVALITH II 301 PULSE GENERATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 5, 2013

    THROUGH THE -PEG (TTP) JEJUNAL FEEDING TUBE KIT, MODEL M00566320,M00566330, M005

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·January 3, 2011

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    UNKNOWN·Product code INM·July 18, 2014

    TM-ECOCHGTRODE

    FDA Adverse Event
    Other ·NATUS MEDICAL INC·Product code GXY·January 9, 2009