BEUDAMED
    9 results · 25ms · 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 Country: Canada ×

    AORTIC OCCLUSION SYSTEMS

    Device
    EU MDR · Eu Md Class 3 ·Front Line Medical Technologies Inc.·On the market·12 countries

    COBRA-OS Device

    Basic UDI-DI
    EU MDR · Eu Md Class 3 ·Front Line Medical Technologies Inc.·1 device

    Front Line Medical Technologies Inc.

    Manufacturer
    🇨🇦 Canada·2 Basic UDI-DIs·2 Devices·2 Importers·Intertek Medical Notified Body AB and Intertek Medical Notified Body AB

    Limbus AI Inc.

    Manufacturer
    🇨🇦 Canada·Kiwa Dare B.V.

    SmileSonica Inc.

    Manufacturer
    🇨🇦 Canada·Intertek Medical Notified Body AB

    21M00123CRT01

    Certificate
    MDR QMS·Limbus AI Inc.·Kiwa Dare B.V.

    28620156455

    Certificate
    MDR QMS·SmileSonica Inc.·Intertek Medical Notified Body AB

    28620163227

    Certificate
    MDR Technical Documentation·Front Line Medical Technologies Inc.·Intertek Medical Notified Body AB

    28620163227

    Certificate
    MDR Technical Documentation·Front Line Medical Technologies Inc.·Intertek Medical Notified Body AB·1 Basic UDI-DI