BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Tritanium X

    DI: 07613327366426 · Model: 680220105 · Stryker Corporation
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Tritanium X
    Primary DI
    07613327366426
    Version / Model
    680220105
    Catalog Number
    680220105
    Company Name
    Stryker Corporation
    Labeler DUNS
    149183167
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-03-23
    Public Version
    1
    Public Version Date
    2020-03-31
    Public Version Status
    New
    Public Device Record Key
    1d84b15d-7ea4-4183-b643-644a16114b49

    Device Description

    Small O-Ring

    Device Characteristics

    Single Use
    No
    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
    12696 Orthopaedic implant inserter/extractor, reusable

    Identifiers

    Type ID
    Package 37613327366427
    Primary 07613327366426