BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    TIDIShield

    DI: 01618125142155 · Model: 5408 · TIDI PRODUCTS, LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    TIDIShield
    Primary DI
    01618125142155
    Version / Model
    5408
    Company Name
    TIDI PRODUCTS, LLC
    Labeler DUNS
    063519193
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-10-11
    Public Version
    3
    Public Version Date
    2023-03-06
    Public Version Status
    Update
    Public Device Record Key
    059b6b69-69a3-4dc7-b58c-eeca40b14d94
    Distribution End Date
    2023-03-03

    Device Description

    TIDIShield C-arm Equipment Covers Clear Kit Sterile Fits OEC 9600 and 9800 C-Arm with 9IN Image Intens 20 per Case

    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
    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
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    KKX Drape, surgical

    GMDN Terms

    Code Name
    12535 Medical equipment drape, single-use

    Identifiers

    Type ID
    Package 00618125142156
    Primary 01618125142155