BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TUFF TT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 6, 2025

    TUFF TT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 6, 2025

    CEMENTED GLENOID SMALL

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWT·September 21, 2020

    EASYPUMP

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·September 10, 2007

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 13, 2013

    UNKNOWN ZIMMER MIS TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 18, 2011

    JUVEDERM ULTRA

    FDA Adverse Event
    Injury ·CORNEAL·Product code LMH·February 20, 2008