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

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    Filters FDA Adverse Event ×

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 2, 2023

    ACCLAIM ENCORE 2.25

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 7, 2014

    MINI MAGNA-FX CANNULATED SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HWC·November 2, 2012

    GIA UNIVERSAL

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·August 30, 2010