BEUDAMED
    4 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    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