BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Vortex Surgical Inc

    DI: 00810123481354 · Model: VS0520 · Vortex Surgical, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    10

    Basic Information

    Brand Name
    Vortex Surgical Inc
    Primary DI
    00810123481354
    Version / Model
    VS0520
    Company Name
    Vortex Surgical, Inc.
    Labeler DUNS
    080375891
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    10
    Record Status
    Published
    Publish Date
    2023-02-02
    Public Version
    1
    Public Version Date
    2023-02-10
    Public Version Status
    New
    Public Device Record Key
    faf5613b-9bc7-4f60-9a4e-cbbe3140c245

    Device Description

    Injection Pack - Basic plus Drape Box of 10

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    Yes
    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
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    KDD Kit, Surgical Instrument, Disposable

    GMDN Terms

    Code Name
    45150 Ophthalmic surgical procedure kit, non-medicated, single-use

    Identifiers

    Type ID
    Unit of Use 00810123480944
    Primary 00810123481354