BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    UREA BROTH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376254272·Rod Template, 60mm

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756600675·Electrode, Lletz

    Cios Alpha

    FDA 510(k)
    FDA Class 2 ·Radiology

    VASCUTEK CANNULA GRAFT, MODEL CGS2008S

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·April 9, 2014

    G2X FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 20, 2010

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·December 17, 2012

    Medtronic Sofamor Danek USA, CD Horizon Spinal System Agile Dynamic Stabilization Device, REF 7881560, 15mm, 5.5mm dia x 60mm, size: 15mm x 60mm, not for distribution in the U.S.A. or its territories, for spinal fixation.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code NQP·November 12, 2007