BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    NORDENT MANUFACTURING INC

    DI: 00840018645035 · Model: FE51X · NORDENT MANUFACTURING INC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    NORDENT MANUFACTURING INC
    Primary DI
    00840018645035
    Version / Model
    FE51X
    Company Name
    NORDENT MANUFACTURING INC
    Labeler DUNS
    053187985
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-07-10
    Public Version
    1
    Public Version Date
    2020-07-20
    Public Version Status
    New
    Public Device Record Key
    29a823f7-444e-4e58-9e84-241ee80ab25f

    Device Description

    FORCEPS, ENGLISH #51, UPPER ROOT

    Device Characteristics

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    ["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

    Product Codes

    Code Name
    HTD Forceps

    GMDN Terms

    Code Name
    35552 Tooth extraction forceps

    Identifiers

    Type ID
    Primary 00840018645035