BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    MODIFIED REFLUX REDUCER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CATHETER HOLDER

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

    UNIVERSAL ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    LONG NAIL KIT R2.0, TI, RIGHT GAMMA3 11X360MM X 1

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code JDS·October 11, 2012

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 19, 2014

    J-VAC RESERVOIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code KOG·October 22, 2010

    LUMAX 340 DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code MRM·November 16, 2012