BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    INSET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 9, 2025

    INSET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 9, 2025

    SYNCHROMED II 8637-40

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LKK·February 22, 2011

    OASYS BRAND CONTACT LENSES WITH HYDRACLEAR

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·February 26, 2008

    ARTICULAR SURFACE FIXED BEARING CRUCIATE RETAINING (CR)

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·March 9, 2023

    UNKNOWN OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·August 4, 2020

    UNKNOWN OXFORD BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·August 4, 2020

    UNK OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·August 24, 2021

    UNK OXFORD FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·August 24, 2021

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 29, 2023