BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Tampax

    DI: 00073010021440 · Model: Tampax Radiant · PROCTER & GAMBLE MANUFACTURING COMPANY, THE
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    6
    Pkg Device Count
    32

    Basic Information

    Brand Name
    Tampax
    Primary DI
    00073010021440
    Version / Model
    Tampax Radiant
    Company Name
    PROCTER & GAMBLE MANUFACTURING COMPANY, THE
    Labeler DUNS
    004238200
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    32
    Record Status
    Published
    Publish Date
    2016-09-15
    Public Version
    3
    Public Version Date
    2022-06-10
    Public Version Status
    Update
    Public Device Record Key
    53cd447e-4baa-4069-8a66-a5eddb7fb773

    Device Description

    TAMPAX RADIANT SUPER 32 CT

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    Yes
    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
    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
    No

    Product Codes

    Code Name
    HEB TAMPON, MENSTRUAL, UNSCENTED

    GMDN Terms

    Code Name
    35694 Menstrual tampon, unscented

    Identifiers

    Type ID
    Package 40073010021448
    Package 10073010021447
    Primary 00073010021440
    Package 40073010021912
    Package 00073010021914
    Unit of Use 50073010021445