BEUDAMED
    4 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 9, 2023

    SUREFIRE SCORPION

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code GAB·November 19, 2008

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWA·August 25, 2011

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·July 23, 2013