BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Pro-Nox

    DI: 00709078006708 · Model: WES-PROSMLKIT · WESTMED, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    20

    Basic Information

    Brand Name
    Pro-Nox
    Primary DI
    00709078006708
    Version / Model
    WES-PROSMLKIT
    Company Name
    WESTMED, INC.
    Labeler DUNS
    092673953
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    20
    Record Status
    Published
    Publish Date
    2019-05-06
    Public Version
    3
    Public Version Date
    2022-10-24
    Public Version Status
    Update
    Public Device Record Key
    54ce1406-b9d6-4546-afca-cbc9e330f549

    Device Description

    Pro-Nox Small Adult Disposable Kit

    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
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    OFP Anesthesia Breathing Circuit Kit (Adult & Pediatric)

    GMDN Terms

    Code Name
    37704 Anaesthesia breathing circuit, single-use

    Identifiers

    Type ID
    Primary 00709078006708
    Unit of Use 10709078006705