BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Drug Relief v1

    DI: 08908006064083 · Model: Drug 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
    Drug Relief v1
    Primary DI
    08908006064083
    Version / Model
    Drug 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
    e2798090-5f16-4caa-9f70-ef08911d54df

    Device Description

    Drug 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
    PZR Percutaneous Nerve Stimulator For Opioid Withdrawal

    GMDN Terms

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

    Identifiers

    Type ID
    Primary 08908006064083