BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    Philips PulseRelief

    DI: 00007502005175 · Model: PR3841 · Philips Consumer Lifestyle B.V.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    Philips PulseRelief
    Primary DI
    00007502005175
    Version / Model
    PR3841
    Company Name
    Philips Consumer Lifestyle B.V.
    Labeler DUNS
    489122720
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-08-24
    Public Version
    9
    Public Version Date
    2023-06-02
    Public Version Status
    Update
    Public Device Record Key
    0714cca4-8a38-466f-b35a-53af5ab60fb0
    Distribution End Date
    2017-12-01

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    NUH STIMULATOR, NERVE, TRANSCUTANEOUS, OVER-THE-COUNTER

    GMDN Terms

    Code Name
    46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

    Identifiers

    Type ID
    Package 20075020050858
    Primary 00007502005175