BEUDAMED
    11 results · 35ms · Sources: EU EUDAMED, US FDA

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    MODEL 8800 ASPIRATOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00673978963341·INST 963-775 CANNULA, 2.5 MM DIAMETER

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000055424·CANNULA 963-775, 2.5 MM DIAMETER

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000337292·CANNULA 963-775 2.5 MM DIAMETER

    ELIA GLIADIN IGA, IGG AND CELIAC CONTROL

    FDA 510(k)
    FDA Class 2 ·Immunology

    RK VACUUM FIXATION RING SYSTEM

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·August 1, 2024

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·May 20, 2014

    GLADIATOR¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·February 15, 2013

    INFORCE REINFORCEMENT MESH 6.5CM X 9CM

    FDA Adverse Event
    Injury ·ORGANGENESIS INC.·Product code FTM·January 11, 2011

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·July 7, 2022