BEUDAMED
    111 results · 21ms · Sources: EU EUDAMED, US FDA

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    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED) X System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·FRED X System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·FRED

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED) and FRED X System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System, FREDX System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED) and FRED X System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED) System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·FRED X System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED) System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517426505·X-CORE 2 Ti Core, Ø18x21-27mm

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·14026704795304·

    FINN KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304005402·

    Fixation Screw

    FDA UDI
    I.T.S. GmbH·09120047297117·Fixation Screw, Proximal Lateral Tibia Plate

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009375·PedFuse, Adjustable Cross Connector, Angled, 55mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009344·PedFuse, Adjustable Cross Connector, Angled, 30mm