BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Duet DRF

    DI: 03701440100035 · Model: 63111976 · THALES AVS FRANCE SAS
    View on AccessGUDID
    Product Codes
    2
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Duet DRF
    Primary DI
    03701440100035
    Version / Model
    63111976
    Company Name
    THALES AVS FRANCE SAS
    Labeler DUNS
    276065299
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-10-23
    Public Version
    1
    Public Version Date
    2020-11-02
    Public Version Status
    New
    Public Device Record Key
    165a9f30-b11c-486f-9510-836907099628

    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
    No
    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
    MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

    GMDN Terms

    Code Name
    37679 Stationary general-purpose fluoroscopic x-ray system, digital

    Identifiers

    Type ID
    Primary 03701440100035