BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    RIWOLITH 2135

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

    Tranquil-C™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788226440·Cervical Trial, Thin Shaft, 7x18x14, 6 deg

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172972342·

    ARTIS ZEE/ZEEGO WITH CSX-10 DETECTOR SW VC21

    FDA 510(k)
    FDA Class 2 ·Radiology

    RETRO REPAIR KIT, MODEL PRRK5

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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2014

    HS LONG 5MM CURVED SHEARS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEI·November 27, 2007

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 7, 2012

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018