BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Richmar

    DI: 00850030915375 · Model: 400-851 · Clearlake-Tech Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    Richmar
    Primary DI
    00850030915375
    Version / Model
    400-851
    Company Name
    Clearlake-Tech Inc.
    Labeler DUNS
    137311285
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-08-02
    Public Version
    3
    Public Version Date
    2025-07-09
    Public Version Status
    Update
    Public Device Record Key
    d810a28f-6e87-4c16-a1df-10fec29dbd0f

    Device Description

    MultiStim 3 x 5 Foam

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    GXY Electrode, Cutaneous

    GMDN Terms

    Code Name
    65318 Transcutaneous electrical stimulation electrode, reusable

    Identifiers

    Type ID
    Package 20850030915379
    Primary 00850030915375