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

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    AXSYM RUBELLA IGG ANTIBODY ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Armada

    FDA UDI
    Nuvasive, Inc.·00887517391476·ARM15S Screw, 4x45mm Fixed

    CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEMBRANE OXYGENATING SYS ADULT BMOS-7 & BMOS-3 PED

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·July 1, 2011

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 16, 2010

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 23, 2014

    ICY CATHETER

    FDA Adverse Event
    Injury ·ALSIUS CORP.·Product code NCX·November 26, 2007