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

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    GORE® EXCLUDER® CONFORMABLE AAA ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·August 4, 2021

    NON ROHS ANSPACH CONSOLE - 200030

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code HBE·April 21, 2020

    NON ROHS ANSPACH CONSOLE - 200030

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code HBE·April 24, 2020

    NON ROHS ANSPACH CONSOLE - 200030

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code HBE·April 24, 2020

    NON ROHS ANSPACH CONSOLE - 200030

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code HBE·April 24, 2020

    NON ROHS ANSPACH CONSOLE - 200030

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code HBE·April 23, 2020

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·October 24, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 10, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 1, 2013