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

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    Filters Regulation: Us FDA ×

    Q Guidance System; Mako Spine System;

    FDA 510(k)
    FDA Class 2 ·Neurology

    INFUSIONCATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZIMMER PLATES AND SCREWS (ZPS)-NON-STERILE PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RAYONE TORIC

    FDA Adverse Event
    Malfunction ·RAYNER INTRAOCULAR LENSES LIMITED·Product code HQL·August 6, 2024

    PEN NEEDLE 31X5 ITALY 100 PACK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 19, 2019

    ELCAM FOUR WAY STANDARD BORE STOPCOCK WITH

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code FMG·November 20, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    INSERT-HANDLE F/A2FN

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code LXH·July 22, 2013