BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    Aerosol Tee

    DI: 00709078008979 · Model: 0219 · WESTMED, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    50

    Let the assistant research this device

    The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Brand Name
    Aerosol Tee
    Primary DI
    00709078008979
    Version / Model
    0219
    Company Name
    WESTMED, INC.
    Labeler DUNS
    092673953
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    50
    Record Status
    Published
    Publish Date
    2020-08-31
    Public Version
    4
    Public Version Date
    2023-05-01
    Public Version Status
    Update
    Public Device Record Key
    58997025-8aea-409c-9e59-bbb88d452d6e
    Distribution End Date
    2023-04-30

    Device Description

    Aerosol Tee

    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
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    BYX Tubing, Pressure And Accessories

    GMDN Terms

    Code Name
    12875 Oxygen administration tubing

    Identifiers

    Type ID
    Unit of Use 10709078008976
    Primary 00709078008979