BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    System 4 Pro

    DI: 00718175004005 · Model: 850-000 · BIODEX MEDICAL SYSTEMS, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    System 4 Pro
    Primary DI
    00718175004005
    Version / Model
    850-000
    Catalog Number
    850-000
    Company Name
    BIODEX MEDICAL SYSTEMS, INC.
    Labeler DUNS
    043833813
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2017-12-18
    Public Version
    3
    Public Version Date
    2023-08-04
    Public Version Status
    Update
    Public Device Record Key
    6ca23395-eeba-4c46-823a-b0d00b56930a

    Device Description

    Biodex System 4 Pro

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    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
    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
    IKK System, Isokinetic Testing And Evaluation

    GMDN Terms

    Code Name
    63457 Biomechanical function analysis system, force-testing, stationary

    Identifiers

    Type ID
    Primary 00718175004005