BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Valleylab™ REM Polyhesive™ Adult Patient Return Electrode, E7507DB

    Reg #: 3009380063 · FEI: 3009380063 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Medtronic Distribution Center
    Registration Number
    3009380063
    FEI Number
    3009380063
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5300 Airways Blvd
    City
    Memphis
    State
    TN
    ZIP
    38116
    Country
    US

    Regulatory Submissions

    510(k) Number
    K822572

    Owner / Operator

    Firm Name
    Medtronic, Inc.
    Operator Number
    2112641
    Address
    710 Medtronic Parkway
    City
    Minneapolis
    State
    MN
    Postal Code
    55432
    Country
    US

    Products

    Device Name Product Code
    Electrosurgical, Cutting & Coagulation & Accessories GEI

    Proprietary Names

    Valleylab™ REM Polyhesive™ Adult Patient Return Electrode, E7507DB Valleylab™ REM Polyhesive™ Adult Patient Return Electrode, E7507 Polyhesive Patient Return Electrode Valleylab™ REM Polyhesive™ Adult Cordless Patient Return Electrode, E7508 Valleylab™ Non-REM Polyhesive™ Patient Return Electrode, E7506

    Establishment Types

    Repack or Relabel Medical Device