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

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    Filters FDA Adverse Event ×

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·September 27, 2023

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011

    T5 SURGICAL HELMET

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code FXZ·July 18, 2013

    GNS II NON-POR TIB SZ 7 RIGHT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 18, 2019

    GEN II RESURF PATELLA 38MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 19, 2019

    LEGION CR NP FEM SZ 8 RT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 18, 2019