BEUDAMED
    9 results · 40ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    IV TUBING, 100 ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW CORP.·Product code FPA·January 13, 1994

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/12 MM L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·February 22, 2023

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 12, 2013

    OLYMPUS LIGHT SOURCE

    FDA Adverse Event
    Other ·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code GCT·February 9, 2011

    SIG MOD TIB TRAY CEM COCR 2.5

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 19, 2008

    FREESTYLE AORTIC ROOT BIOPROSTHESIS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·June 30, 2021

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 30, 2021

    GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 26, 2022

    EVIS EXERA III BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·August 23, 2024