BEUDAMED
    4 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DUROM ACETABULAR COMPONENT 48/42 H

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·May 27, 2014

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·November 29, 2010

    FINELINE II

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·January 11, 2013

    VITEK® 2 AST-GP75 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·February 12, 2018