BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Tampax

    DI: 00073010013476 · Model: Tampax Pearl · PROCTER & GAMBLE MANUFACTURING COMPANY, THE
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    4
    Pkg Device Count
    36

    Basic Information

    Brand Name
    Tampax
    Primary DI
    00073010013476
    Version / Model
    Tampax Pearl
    Company Name
    PROCTER & GAMBLE MANUFACTURING COMPANY, THE
    Labeler DUNS
    004238200
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    36
    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
    1a075062-1470-4fc8-93cf-358a23378ef9

    Device Description

    TAMPAX PEARL DUOPACK REGULAR-SUPER 36CT

    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 40073010013474
    Package 10073010013473
    Primary 00073010013476
    Unit of Use 50073010013471