BEUDAMED
    7 results · 36ms · Sources: EU EUDAMED, US FDA

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    CDI OneView Monitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO X-PORT DUO PORT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ROSA ONE Brain application

    FDA 510(k)
    FDA Class 2 ·Neurology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 22, 2025

    SMART NITINOL STENT ENDOSCOPIC BILIARY SYSTEM

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code FGE·November 4, 2008

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·August 29, 2011

    JOSTENT GRAFTMASTER

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·July 18, 2013