BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    TUBE-TITLE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    VIATRONIX V3D VASCULAR, REVISION 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    Sunny Cup and Applicator

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BD VACUTAINER GLASS SERUM TUBE

    FDA Adverse Event
    Injury ·BD·Product code JKA·May 14, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·November 15, 2012

    COOK MEDICAL

    FDA Adverse Event
    Malfunction ·COOK MEDICAL INC.·Product code GCA·September 8, 2010