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

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    StimRouter Neuromodulation System

    FDA 510(k)
    FDA Class 2 ·Neurology

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994235893·PLATE 6190047 ANTERIOR CERVICAL 47.5MM

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00763000868130·PLATE 6190047 ANTERIOR CERVICAL 47.5MM

    Oticon

    FDA UDI
    Oticon A/S·05707131340818·OPN 2 FW 6.0

    Pre-Finisher

    FDA UDI
    TP ORTHODONTICS INC·00192029041499·Non-Extraction

    SYNTHES (USA) 1.5MM MINI FRAGMENT LCP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUREFIT DUAL DISPERSIVE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    OPMI PENTERO

    FDA Adverse Event
    Injury ·CARL ZEISS SURGICAL, GMBH·Product code EPT·October 6, 2008

    SJM MASTERS SERIES MECHANICAL HEART VALVE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL PUERTO RICO, INC·Product code LWQ·June 21, 2013

    OLYMPUS EVIS EXERA BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP·Product code EOQ·June 29, 2011