BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    MyLift

    DI: 07290016586794 · Model: Model VXU-302 · POLLOGEN LTD
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    MyLift
    Primary DI
    07290016586794
    Version / Model
    Model VXU-302
    Catalog Number
    34693000BM-ML
    Company Name
    POLLOGEN LTD
    Labeler DUNS
    514905681
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2026-02-22
    Public Version
    2
    Public Version Date
    2026-03-31
    Public Version Status
    Update
    Public Device Record Key
    bc470127-9151-4f5f-b0d0-831e65b1b71b

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    Yes
    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
    PAY Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction

    GMDN Terms

    Code Name
    44832 Multi-modality skin/body contouring system

    Identifiers

    Type ID
    Primary 07290016586794