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

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    NEEDLE SET, A-V FISTULA

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

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515200159·Mini Open Kolbel Retr, hinged and third arm, fr...

    AVANTE Z; PELLET, PRESSABLE STAIN, ADD-ON PORCELAIN, PORCELAIN

    FDA 510(k)
    FDA Class 2 ·Dental

    MULTI-TEST

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MNS UNKNOWN VALVE/SHUNT

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·April 24, 2014

    MUSTANG¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·October 3, 2012

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·July 27, 2010

    Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature.

    FDA Enforcement
    Class II ·Terminated·Abbott Vascular·October 3, 2012