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

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    SALIVARY BYPASS TUBE

    FDA 510(k)

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377020963·RELINE-C Ti Rod, 3.5x350mm Straight

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704400182·

    Clarify DL

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYNTHES (USA) CHRONOS

    FDA 510(k)
    FDA Class 2 ·Neurology

    12MM/130 DEG TI CANN TFNA 170MM - STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HSB·November 1, 2016

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·May 30, 2014

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code LZH·October 23, 2012

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·September 22, 2010

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code FGE·September 14, 2018