BEUDAMED
    FDA Registration Active 🇲🇽 Mexico

    Valleylab™ REM Polyhesive™ Infant Patient Return Electrode, E7510-25

    Reg #: 9610849 · FEI: 3002807391 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Covidien
    Registration Number
    9610849
    FEI Number
    3002807391
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Boulevard Insurgentes 19030 Libramiento
    City
    TIJUANA, B.C. Mexico
    Country
    MX

    Regulatory Submissions

    510(k) Number
    K160290

    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

    Valleylab™ REM Polyhesive™ Infant Patient Return Electrode, E7510-25 Valleylab™ REM Polyhesive™ Infant Patient Return Electrode, E7510-25DB

    Establishment Types

    Manufacture Medical Device