BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    CDR SYSTEMS, INC.

    FDA registration
    CDR SYSTEMS, INC.·1 product·🇨🇦 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

    Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr

    FDA Enforcement
    Class II ·Terminated·Pdg Product Design Group Inc·October 1, 2014

    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