BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    ULTRA FLOW

    DI: 00380658170011 · Model: 00380658170011 · Alcon Laboratories, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    ULTRA FLOW
    Primary DI
    00380658170011
    Version / Model
    00380658170011
    Company Name
    Alcon Laboratories, Inc.
    Labeler DUNS
    008018525
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2017-06-07
    Public Version
    3
    Public Version Date
    2021-06-18
    Public Version Status
    Update
    Public Device Record Key
    a42ffb9e-23c4-438c-85e9-d9ade85382dd

    Device Description

    ULTRAFLOW S/P STRAIGHT TIP, .3MM

    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
    No
    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
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    NKK NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED

    GMDN Terms

    Code Name
    63231 Ophthalmic surgical irrigation/infusion/aspiration handle, reusable

    Identifiers

    Type ID
    Primary 00380658170011