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

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    FORCEPS, SURGICAL GYNECOLOGICAL

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

    QUALICHECK 4+, LEVEL 3

    FDA UDI
    Radiometer Medical ApS·05700699440556·S7450 QUALICHECK4+, level 3 BLUE box of 30 ampo...

    ESOPHAGEAL STETHO SCOPE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PINCH SENSOR, MODEL PF001

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 29, 2010

    TAXUS® LIBERTÉ® LONG

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·February 5, 2013

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·July 18, 2014

    STERRAD® NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·February 20, 2018