BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    3M MAXI-DRIVER II DBATTERY POWERED SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CAP BONE SUBSTITUTE MATERIAL

    FDA 510(k)
    FDA Class 2 ·Neurology

    VIDA LED SURGICAL LIGHTING SYSTEM

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

    VERSAPORT V2 5MM TROCAR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GCJ·April 4, 2014

    HT70 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENT·Product code CBK·January 24, 2013

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·December 17, 2010