BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    URETEROSCOPE, 8,6/9,8 FR. X 430 MM, 7°, 6,4 FR. CHANNEL, WITH A0396

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FGB·December 16, 2016

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·May 17, 2016

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 9, 2013

    FINELINE II

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·January 6, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014

    ECHOTIP PROCORE HD ENDORONCHIAL BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·April 30, 2014