BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LEAD EXTRACTION BYRD POLYPROPYLENE EXTRA LONG DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VANDERGRIFT INC·Product code GCC·January 22, 2021

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·November 19, 2014

    ONE LINK NEEDLE-FREE IV CONNECTOR WITH NEUTRAL FLUID DISPLAC

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FPA·June 3, 2014

    AQVATRACK

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code DQX·November 5, 2010

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·September 29, 2008

    LEAD EXTRACTION BYRD POLYPROPYLENE DILATOR SHEATH SET

    FDA Adverse Event
    Malfunction ·COOK VANDERGRIFT INC·Product code GCC·March 9, 2022