BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    SYMPHONY Navigation Ready Instruments, Universal Navigation Adaptor Set

    FDA 510(k)
    FDA Class 2 ·Neurology

    Oticon

    FDA UDI
    Oticon A/S·05707131340405·SIYA 2, KIT 10 85 C001

    BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 30, 2018

    SYNTHETIC, POWDER-FREE NITRILE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    POWERHEART AED G3, MODEL 9390E, POWERHEART AED G3 AUTOMATIC, MODEL 9390A

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    UNKNOWN GEL IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 18, 2018

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·October 9, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 22, 2011