BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Y-KNOT

    DI: 10845854033142 · Model: Y-G002 · Conmed Corporation
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Y-KNOT
    Primary DI
    10845854033142
    Version / Model
    Y-G002
    Catalog Number
    Y-G002
    Company Name
    Conmed Corporation
    Labeler DUNS
    071595540
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-04-28
    Public Version
    6
    Public Version Date
    2022-09-22
    Public Version Status
    Update
    Public Device Record Key
    db837d38-229d-4ee8-a0b8-aeb22a84f082

    Device Description

    Y-Knot Flex, Slim Reusable Drill Guide, Crown

    Device Characteristics

    Single Use
    No
    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
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    FZX Guide, surgical, instrument

    GMDN Terms

    Code Name
    12143 Instrument tray, reusable

    Identifiers

    Type ID
    Primary 10845854033142
    Direct Marking 20845854033149

    Customer Contacts

    Phone
    +1(866)426-6633
    Email
    [email protected]

    Storage Conditions

    Type
    Special Storage Condition, Specify
    Special Conditions
    KEEP DRY