BEUDAMED
    7 results · 28ms · Sources: EU EUDAMED, US FDA

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    MONITOR, FETAL HEART, MODEL 1980

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    6770292

    FDA Adverse Event
    Malfunction ·August 7, 2017

    DUROM HIP RESURFACING SYSTEM, FEMORAL COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Tri-Ex Extraction Balloon With Multiple Sizing

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OPTISEAL VALVED PTFE PEELABLE INTRODUCER

    FDA Adverse Event
    Malfunction ·GREATBACH MEDICAL .·Product code DYB·February 18, 2014

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·September 28, 2012

    FEMORAL PLATE 6 HOLE RIGHT

    FDA Adverse Event
    Injury ·DEPUY ACE S.A.'R.L.·Product code HRS·July 21, 2010