BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    CAPIOX HEMOCONCENTRATOR

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

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    NuBorne Infant Warmer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·February 22, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·January 19, 2011

    DLT TS CER HD 12/14 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code LZO·August 1, 2014