BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·January 6, 2020

    HEARTMATE GOGEAR SHOWER BAG

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 19, 2019

    HEARTMATE SYSTEM MONITOR

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·January 2, 2020

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 30, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 27, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·September 22, 2020

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 27, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 11, 2019

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·June 10, 2013

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NIK·October 10, 2014

    GORE TIGRIS® VASCULAR STENT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·October 11, 2016

    GORE TIGRIS® VASCULAR STENT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·September 6, 2016