BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    Up & Up

    DI: 00492450308629 · Model: Digital Ovulation Test · TARGET CORPORATION
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    3
    Pkg Device Count
    10

    Basic Information

    Brand Name
    Up & Up
    Primary DI
    00492450308629
    Version / Model
    Digital Ovulation Test
    Company Name
    TARGET CORPORATION
    Labeler DUNS
    006961700
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    10
    Record Status
    Published
    Publish Date
    2018-02-12
    Public Version
    5
    Public Version Date
    2020-07-20
    Public Version Status
    Update
    Public Device Record Key
    d45f458c-5c03-4bdb-a46f-1fcab57fe856
    Distribution End Date
    2020-07-17

    Device Description

    up&up 10ct Digital Ovulation Test

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    NGE Test, Luteinizing Hormone (Lh), Over The Counter

    GMDN Terms

    Code Name
    60862 Natural conception assistance kit

    Identifiers

    Type ID
    Package 10492450308626
    Primary 00492450308629
    Unit of Use 00633472000102

    Customer Contacts

    Phone
    1-800-910-6874
    Email
    [email protected]

    Storage Conditions

    Type
    Storage Environment Temperature
    Temperature Range
    2 – 30 Degrees Celsius