BEUDAMED
    4 results · 53ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    STRETTA 8800 CATHETER AND ACCESSORIES KIT

    FDA Adverse Event
    Death ·MEDERI THERAPEUTICS / MEDERI RF LLC·Product code GEI·August 5, 2019

    SECCA

    FDA Adverse Event
    Injury ·MEDERI THERAPEUTICS INC.·Product code GEI·October 28, 2011

    SECCA

    FDA Adverse Event
    Injury ·MEDERI THERAPEUTICS INC.·Product code GEI·October 20, 2011

    MEDERI STRETTA CATHETER

    FDA Adverse Event
    Malfunction ·MEDERI THERAPEUTICS INC·Product code GEI·April 4, 2017