BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    CurPro Dermal Curettes, 7 mm

    DI: 00840117338548 · Model: 4159 · Dynarex Corporation
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    3
    Pkg Device Count
    50

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    Basic Information

    Brand Name
    CurPro Dermal Curettes, 7 mm
    Primary DI
    00840117338548
    Version / Model
    4159
    Company Name
    Dynarex Corporation
    Labeler DUNS
    008124539
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    50
    Record Status
    Published
    Publish Date
    2024-12-16
    Public Version
    1
    Public Version Date
    2024-12-24
    Public Version Status
    New
    Public Device Record Key
    ecd84eda-4743-462e-99d2-f185d5544406

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    Yes
    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
    FZS Curette, Surgical, General Use

    GMDN Terms

    Code Name
    63259 Dermal curette, single-use

    Identifiers

    Type ID
    Unit of Use 00810180840750
    Primary 00840117338548
    Package 00840117338531