BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    CARDINAL HEALTH

    DI: 10885380009020 · Model: CF-1001 · Cardinal Health 200, LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    CARDINAL HEALTH
    Primary DI
    10885380009020
    Version / Model
    CF-1001
    Catalog Number
    CF-1001
    Company Name
    Cardinal Health 200, LLC
    Labeler DUNS
    961027315
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-09-08
    Public Version
    7
    Public Version Date
    2023-02-03
    Public Version Status
    Update
    Public Device Record Key
    e337004d-0c16-4dca-a7ee-81f089b78bbe
    Distribution End Date
    2019-11-01

    Device Description

    Anti-Fog Solution W/Foam Pad

    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
    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
    OCT Anti fog solution and accessories, endoscopy

    GMDN Terms

    Code Name
    45220 Multi-modality skin surface treatment system

    Identifiers

    Type ID
    Package 50885380009028
    Primary 10885380009020

    Premarket Submissions

    Submission Number Supplement Number
    K932449 000