BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    APTT-ES REAGENT

    FDA 510(k)
    FDA Class 2 ·Hematology

    FOCUS COBALT CHROMIUM TOTAL HIP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BILIARY INDWELLING STENT

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

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·July 16, 2014

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·January 30, 2013

    CONCIERGE GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DQY·November 23, 2010

    MINILINK TRANSMITTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 15, 2014

    REDUCTION FORCEPS W/SERRATED JAW-MEDIUM HANDLE-SOFT RATCHET

    FDA Adverse Event
    Malfunction ·SYNTHES SALZBURG·Product code HTD·August 11, 2016

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 13, 2021

    ECHOTIP ULTRA ULTRASOUND ASPIRATION NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·November 19, 2010

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·July 29, 2014

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·September 17, 2014