BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    SYSTEM 3000 XENON VIDEOLAP LIGHT

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

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613154677108·BARRY ELEVATOR, LEFT

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111048·INSTRUMENT CASE SMALL ALUMINUM

    ClotTriever XL Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SEEDLINKS, MODELS 70301, 70302, 70303

    FDA 510(k)
    FDA Class 2 ·Radiology

    CODMAN EXTERNAL DRAINAGE SYSTEM III

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC·Product code JXG·January 18, 2013

    ZIMMER TM REVERSE SHOULDER HUMERAL STEM

    FDA Adverse Event
    Malfunction ·ZIMMER INC.·Product code HSD·November 9, 2010

    QUICKFLEX XL LV LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 9, 2014