BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    INSET

    FDA Adverse Event
    Injury ·UNOMEDICAL UM-D·Product code FPA·February 9, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 22, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 22, 2026

    INSET

    FDA Adverse Event
    Injury ·UNOMEDICAL UM-D·Product code FPA·February 9, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 22, 2026

    INSET

    FDA Adverse Event
    Injury ·UNOMEDICAL UM-D·Product code FPA·February 9, 2026

    ASR ACETABULAR IMPLANT 60

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 20, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·March 10, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 10, 2008

    BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 8, 2022