BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    ORTHO ARCH

    DI: D90922692018 · Model: .019 X .025 UPPER · Ortho Arch Company Inc
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    ORTHO ARCH
    Primary DI
    D90922692018
    Version / Model
    .019 X .025 UPPER
    Catalog Number
    226-920
    Company Name
    Ortho Arch Company Inc
    Labeler DUNS
    020956330
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-10-31
    Public Version
    1
    Public Version Date
    2022-11-08
    Public Version Status
    New
    Public Device Record Key
    215af157-cc12-4c03-8be5-a7f3b5428f98

    Device Description

    .019 X .025 UPPER NITINOL MULTI-MODULUS WITH DIMPLE**WHILE SUPPLIES LAST. DISCONTINUED ITEM. NON-REFUNDABLE**

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    Yes
    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
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    DZC Wire, Orthodontic

    GMDN Terms

    Code Name
    41397 Orthodontic archwire

    Identifiers

    Type ID
    Primary D90922692018