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

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    IMMULTE 2000 RUBELLA QUANTITATIVE IGG CALIBRATION VERIFICATION MATERIAL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Bernafon

    FDA UDI
    Bernafon AG·05711584053089·JU7 ITEPD, WL L BE JUNA 7

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973868·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973783·

    TSRH(R) SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DATEX-OHMEDA PRESTN.01 MODULE (MODEL FAMILY M-PRESTN.01) AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® PLUS PLASTIC SST TUBE. GOLD BD HEMOGARD¿ CLOSURE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 6, 2017

    CANTATA 2.9 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·September 14, 2017

    PARADIGM QUICKSERTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    FREESTYLE FREEDOM

    FDA Adverse Event
    Injury ·Product code NBW·June 27, 2011