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

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    Filters FDA Adverse Event ×

    POLYFLUX 210H

    FDA Adverse Event
    Injury ·GAMBRO DIALYSATOREN GMBH·Product code KDI·June 25, 2014

    THORACIC SCREW BONE AWL, SS

    FDA Adverse Event
    Malfunction ·ALPHATEC SPINE INC·Product code KWP·November 9, 2010

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC., SLEEP & HOME RESPIRATORY GROUP·Product code CBK·December 27, 2012