BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    VES-TEC

    DI: 08033891320577 · Model: 10201/A · DIESSE DIAGNOSTICA SENESE SPA
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    VES-TEC
    Primary DI
    08033891320577
    Version / Model
    10201/A
    Catalog Number
    10201/A
    Company Name
    DIESSE DIAGNOSTICA SENESE SPA
    Labeler DUNS
    435036669
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-11-25
    Public Version
    1
    Public Version Date
    2022-12-05
    Public Version Status
    New
    Public Device Record Key
    78b70647-d087-474c-8ec9-3222513e181b

    Device Characteristics

    Single Use
    Yes
    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
    Yes
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    GHC Tube, Sedimentation Rate

    GMDN Terms

    Code Name
    55974 Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD

    Identifiers

    Type ID
    Primary 08033891320577