BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    TRIDENT

    DI: 08053307591087 · Model: 3030 R 20 CS · TECHNIX SPA
    View on AccessGUDID
    Product Codes
    3
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    TRIDENT
    Primary DI
    08053307591087
    Version / Model
    3030 R 20 CS
    Company Name
    TECHNIX SPA
    Labeler DUNS
    437977127
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2024-11-06
    Public Version
    1
    Public Version Date
    2024-11-14
    Public Version Status
    New
    Public Device Record Key
    3e8f7118-e1bf-437e-b231-12942ceeab73

    Device Description

    Mobile equipment for radioscopy and radiography Brand: Dornier MedTech America, Inc

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    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
    No
    PM Exempt
    No
    Has Serial Number
    Yes
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    JAA System, X-Ray, Fluoroscopic, Image-Intensified
    OWB Interventional Fluoroscopic X-Ray System
    OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

    GMDN Terms

    Code Name
    37646 Mobile general-purpose fluoroscopic x-ray system, digital

    Identifiers

    Type ID
    Primary 08053307591087