BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    E-Fit

    DI: 05999887598012 · Model: EF-1280 · Fit-Pro Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    E-Fit
    Primary DI
    05999887598012
    Version / Model
    EF-1280
    Company Name
    Fit-Pro Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag
    Labeler DUNS
    366811421
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2017-02-16
    Public Version
    7
    Public Version Date
    2023-06-02
    Public Version Status
    Update
    Public Device Record Key
    6c974796-7698-4487-89af-4d426de36f7b

    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
    No
    Has Serial Number
    Yes
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    NGX Stimulator, Muscle, Powered, For Muscle Conditioning

    GMDN Terms

    Code Name
    46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

    Identifiers

    Type ID
    Primary 05999887598012