BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Polyhesive Patient Return Electrode

    Reg #: 1219930 · FEI: 1219930 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Covidien
    Registration Number
    1219930
    FEI Number
    1219930
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    60 Middletown Ave
    City
    North Haven
    State
    CT
    ZIP
    06473
    Country
    US

    Regulatory Submissions

    510(k) Number
    K822572

    Owner / Operator

    Firm Name
    Covidien llc
    Operator Number
    1282497
    Address
    15 HAMPSHIRE STREET, --
    City
    Mansfield
    State
    MA
    Postal Code
    02048
    Country
    US

    Products

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

    Proprietary Names

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

    Establishment Types

    Repack or Relabel Medical Device