BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    LUCENT XP ARC

    DI: 00840606167451 · Model: P11303-510 · SPINAL ELEMENTS, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    LUCENT XP ARC
    Primary DI
    00840606167451
    Version / Model
    P11303-510
    Company Name
    SPINAL ELEMENTS, INC.
    Labeler DUNS
    610712213
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-07-27
    Public Version
    2
    Public Version Date
    2022-08-26
    Public Version Status
    Update
    Public Device Record Key
    9d19ef82-c219-4264-ad1a-5f85cee80056

    Device Description

    LUCENT XP ARC™ 13MM x 37MM X 10MM 5° CAGE, PC

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    Yes
    PM Exempt
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    MAX Intervertebral Fusion Device With Bone Graft, Lumbar

    GMDN Terms

    Code Name
    61230 Metal-polymer composite spinal interbody fusion cage

    Identifiers

    Type ID
    Primary 00840606167451