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

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    VAC (OSCILLATING VITRECTOR)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517311603·Archon Screw, 4.5x20mm S.T. Fixed

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799006141·

    Avance® Solo

    FDA UDI
    Mölnlycke Health Care AB·07323190236015·Avance Solo Border Dressing 15x20 cm

    Snowden-Pencer

    FDA UDI
    CAREFUSION 2200, INC·10885403151941·Snowden-Pencer HOOKS MILLARD THIMBLE DOUBLE HOO...

    Sirona Dental CAD/CAM System

    FDA 510(k)
    FDA Class 2 ·Dental

    SENSITITRE VIZION

    FDA 510(k)
    FDA Class 2 ·Microbiology

    OMNIPOD INUSLIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·May 28, 2014

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP·Product code LZG·October 19, 2010

    SUMMIT DUOFIX TAP SZ5 STD OFF

    FDA Adverse Event
    Malfunction ·DEPUY WARSAW·Product code LPH·December 20, 2012

    Medtronic Sofamor Danek USA, CD Horizon Spinal System Agile Dynamic Stabilization Device, REF 7881520, 15mm, 5.5mm dia x 120mm, size: 15mm x 120mm, 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