BEUDAMED
    2,869 results · 24ms · 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 Regulation: Us FDA ×

    CA_MISC_064_SIS_V1.png

    FDA UDI
    ZimVie US Corp LLC·00889024012493·

    CA_MISC_064_SIS_V1.png

    FDA UDI
    ZimVie US Corp LLC·00889024012028·

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780026532·NeuraGen® Nerve Guide 7mm (ID) X 3cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780071839·NeuraGen® Nerve Guide 2mm (ID) X 2cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780071822·NeuraGen® Nerve Guide 1.5mm (ID) X 3cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780026471·NeuraGen® Nerve Guide 3mm (ID) X 2cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780026501·NeuraGen® Nerve Guide 5mm (ID) X 2cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780026518·NeuraGen® Nerve Guide 5mm (ID) X 3cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780071860·NeuraGen® Nerve Guide 7mm (ID) X 2cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780026495·NeuraGen® Nerve Guide 4mm (ID) X 3cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780026488·NeuraGen® Nerve Guide 3mm (ID) X 3cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780026525·NeuraGen® Nerve Guide 6mm (ID) X 3cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780026464·NeuraGen® Nerve Guide 2mm (ID) X 3cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780071853·NeuraGen® Nerve Guide 6mm (ID) X 2cm (Length)

    NeuraGen®

    FDA UDI
    Integra Lifesciences Corporation·10381780071846·NeuraGen® Nerve Guide 4mm (ID) X 2cm (Length)

    TITANIUM IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, KIT, 8F

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code LJT·June 3, 2022

    BD ULTRASAFE¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·October 31, 2025

    BD ULTRASAFE¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code FMI·August 21, 2025

    BD ULTRASAFE¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code FMI·September 11, 2025

    BD ULTRASAFE¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code FMI·August 25, 2025