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

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    MITEK ANCHOR DRILL

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    BORA UP 2080, BORA UP 2080 OP AND BORA UP 2080 MOUNTING

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

    RS85 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    SOLITAIRE REVASCULARIZATION DEVICE

    FDA Adverse Event
    Death ·COVIDIEN (IRVINE)·Product code NRY·July 6, 2015

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 2, 2010

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 28, 2012

    ENDURANT II STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·December 9, 2024