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

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    Filters FDA Adverse Event ×

    MAMMARY PROSTHESIS

    FDA Adverse Event
    MCGHAN MEDICAL CORP.·Product code FTR·May 18, 1994

    PROMUS ELEMENT¿ PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 13, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 28, 2011

    CALAXO SCREW

    FDA Adverse Event
    Injury ·SMITH AND NEPHEW·Product code HWC·February 20, 2008

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 12, 2025

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 22, 2016