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

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    Piper GO-IO Intraosseous Infusion System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Oticon

    FDA UDI
    Oticon A/S·05707131340290·SIYA 2, KIT 13 2.4G NFM R C001

    INTERFACE ACETABULAR SYSTEM, ACETABULAR INSERT +4 OFFSET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOMET PHOENIX ANKLE NAIL AND ANKLE ARTHRODESIS NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HISTOACRYL FLEXIBLE PACK 5

    FDA Adverse Event
    Injury ·B.BRAUN SURGICAL SA·Product code MPN·July 23, 2019

    VITEK® 2 AST-ST01 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·October 24, 2017

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 4, 2011