BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    Natus

    DI: 00382830049405 · Model: 9033B0721 · NATUS MANUFACTURING LIMITED
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    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
    Natus
    Primary DI
    00382830049405
    Version / Model
    9033B0721
    Company Name
    NATUS MANUFACTURING LIMITED
    Labeler DUNS
    896421240
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2024-04-19
    Public Version
    2
    Public Version Date
    2026-04-22
    Public Version Status
    Update
    Public Device Record Key
    29164081-be94-420a-b9f0-9143f43dc5f5
    Distribution End Date
    2026-04-21

    Device Description

    CART FOR FOCUS DESKTOP SYSTEM OEM KNRR

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    GWF Stimulator, Electrical, Evoked Response

    GMDN Terms

    Code Name
    11474 Electromyograph

    Identifiers

    Type ID
    Primary 00382830049405