BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Kitpack

    DI: 05056100712614 · Model: 2-469 · NETWORK MEDICAL PRODUCTS LIMITED
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    50

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    Basic Information

    Brand Name
    Kitpack
    Primary DI
    05056100712614
    Version / Model
    2-469
    Company Name
    NETWORK MEDICAL PRODUCTS LIMITED
    Labeler DUNS
    458670304
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    50
    Record Status
    Published
    Publish Date
    2022-03-22
    Public Version
    1
    Public Version Date
    2022-03-30
    Public Version Status
    New
    Public Device Record Key
    a27491ea-236a-4f37-a7c3-247fe20b0dec

    Device Description

    Wick and Wipe3"x3"x1mm Sterile

    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
    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
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    HOZ Sponge, Ophthalmic

    GMDN Terms

    Code Name
    13704 Ophthalmic sponge

    Identifiers

    Type ID
    Unit of Use 05056100712621
    Primary 05056100712614

    Premarket Submissions

    Submission Number Supplement Number
    K130117 000