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

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    DURAFLOR

    FDA 510(k)
    FDA Class 2 ·Dental

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471149854·K-WIRE - DOUBLE TROCAR FULLY THREADED 1.8mm DIA...

    Neuromonitoring Kit

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    INTEGRA RADIONICS XKNIFE RT 4

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 14, 2013

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·DOLOMITE AB·Product code ITJ·July 28, 2014

    RENAL-DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 14, 2011

    LIGHT CABLE, 3.5MM X 300CM. LGTH 9.8 FT

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code FCW·November 27, 2023