BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    mo-vis

    DI: 05407008321109 · Model: P011-62 Head Control Omni Switched · mo-Vis
    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
    mo-vis
    Primary DI
    05407008321109
    Version / Model
    P011-62 Head Control Omni Switched
    Company Name
    mo-Vis
    Labeler DUNS
    370456732
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2024-09-02
    Public Version
    2
    Public Version Date
    2025-03-24
    Public Version Status
    Update
    Public Device Record Key
    3c24f5c3-0c54-4113-a568-f9d67a6d6530

    Device Description

    Switched Head Control

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    Yes
    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
    Yes
    Has Serial Number
    Yes
    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
    KNN Components, Wheelchair

    GMDN Terms

    Code Name
    30018 Wheelchair steering/control unit

    Identifiers

    Type ID
    Primary 05407008321109