BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    MEDI

    DI: 00636257205105 · Model: DW1AR02 · MEDI MANUFACTURING, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    MEDI
    Primary DI
    00636257205105
    Version / Model
    DW1AR02
    Company Name
    MEDI MANUFACTURING, INC.
    Labeler DUNS
    960754430
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2025-06-24
    Public Version
    2
    Public Version Date
    2026-02-09
    Public Version Status
    Update
    Public Device Record Key
    a42f7274-b232-4ac9-8a0b-5e3b0d1b11b2

    Device Description

    !DO CARPAL TUNNEL SUPPORT BEIGERIGHT SM

    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
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    IQI ORTHOSIS, LIMB BRACE

    GMDN Terms

    Code Name
    41458 Wrist orthosis

    Identifiers

    Type ID
    Primary 00636257205105

    Customer Contacts

    Phone
    +1(800)633-6334
    Email
    [email protected]