BEUDAMED
    10 results · 32ms · 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 ×

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 29, 2013

    EGIA ULTRA UNIVERSAL XL STAPLER

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·December 10, 2010

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code KDJ·July 14, 2014

    PS TIBIAL INSERTS SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 14, 2023

    CC FEMORAL SZ 3

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 10, 2024

    CEMENTED FINNED TIB. TRA SZ 3F/3T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 19, 2024

    OPTETRAK KNEE SYSTEM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 23, 2024

    OPTETRAK KNEE COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 29, 2024

    PS TIBIAL INSERTS SZ 2, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 13, 2025

    CC TIBIAL INSERT SZ 4, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 4, 2024