BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    TALOS®-A

    DI: 07640375237903 · Model: 3-21512-12 · SpineArt SA
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    TALOS®-A
    Primary DI
    07640375237903
    Version / Model
    3-21512-12
    Catalog Number
    3-21512-12
    Company Name
    SpineArt SA
    Labeler DUNS
    483016148
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2025-11-19
    Public Version
    1
    Public Version Date
    2025-11-27
    Public Version Status
    New
    Public Device Record Key
    0c44409d-3ba5-48af-9b8b-b39bdfa4b6e7

    Device Description

    TALOS®-A (HA) PEEK PLANAR, SYMMETRIC IBFD D28 W39 H12 12°

    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
    MR Conditional
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    MAX Intervertebral Fusion Device With Bone Graft, Lumbar

    GMDN Terms

    Code Name
    60762 Polymeric spinal interbody fusion cage

    Identifiers

    Type ID
    Primary 07640375237903