BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    First Relief v1

    DI: 08908006064243 · Model: First Relief v1 · DYANSYS INDIA PRIVATE LIMITED
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    First Relief v1
    Primary DI
    08908006064243
    Version / Model
    First Relief v1
    Company Name
    DYANSYS INDIA PRIVATE LIMITED
    Labeler DUNS
    916731981
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2026-03-16
    Public Version
    1
    Public Version Date
    2026-03-24
    Public Version Status
    New
    Public Device Record Key
    fd651348-50a9-4f69-ac84-c9a21c6a8b86

    Device Description

    First Relief v1

    Device Characteristics

    Single Use
    Yes
    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
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    QHH Non-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs)

    GMDN Terms

    Code Name
    63321 Opioid withdrawal/irritable bowel symptom-relief periauricular nerve percutaneous electrical stimulator

    Identifiers

    Type ID
    Primary 08908006064243