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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    G7 DUAL MOBILITY LINER 40MM D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 7, 2025

    ACT ARTIC E1 HIP BRG 28X40MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 7, 2025

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE·Product code KDJ·June 10, 2014

    ARTICUL/EZE BALL 32 +1 GR

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code JDI·October 6, 2010

    RECAP CEMENTED FEMORAL HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KXA·December 10, 2012