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

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    QUICKVUE ONE-STEP H. PYLORI II TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    FUJIFILM Duodenoscope Model ED-580XT

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

    FLAATZ 500

    FDA 510(k)
    FDA Class 2 ·Radiology

    FUJIFILM DUODENOSCOPE MODEL ED-580T

    FDA Adverse Event
    Injury ·FUJIFILM CORPORATION·Product code FDT·September 5, 2023

    FUJIFILM ENDOSCOPE

    FDA Adverse Event
    Malfunction ·FUJIFILM CORPORATION·Product code FDS·March 18, 2022

    FUJIFILM DUODENOSCOPE ED-580T

    FDA Adverse Event
    Injury ·FUJIFILM CORPORATION·Product code FDT·March 5, 2025

    LINEAGE(R) TRANSCEND(R) SUPERFINISHED FEMORAL HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDL·March 6, 2013

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    KAPPA 700 DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·February 15, 2011