BEUDAMED
    FDA Registration Active 🇺🇸 United States

    MYO/WIRE TEMPORARY CARDIAC PACING WIRE

    Reg #: 1319639 · FEI: 1000138054 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Sterigenics U.S., LLC
    Registration Number
    1319639
    FEI Number
    1000138054
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    84 Park Rd
    City
    Queensbury
    State
    NY
    ZIP
    12804
    Country
    US

    Regulatory Submissions

    510(k) Number
    K803086

    Owner / Operator

    Firm Name
    Sotera Health LLC
    Operator Number
    10029425
    Address
    2015 Spring Road, Suite 650
    City
    Oak Brook
    State
    IL
    Postal Code
    60523
    Country
    US
    Correspondent
    Karen Whaley-Krumins

    Products

    Device Name Product Code
    Electrode, Pacemaker, Temporary LDF

    Proprietary Names

    MYO/WIRE TEMPORARY CARDIAC PACING WIRE Balloon Flow-Assisted Bipolar Electrode Catheter & Balloon Flow-Assisted Bipolar Electrode Catheter w/Right Heart Curve Heparin Bonded Balloon Flow-Assisted Bipolar Electrode Catheter & Heparin Bonded Balloon Flow-Assisted Bipolar Electrode NBIH, NBIH Soft Tip, Goetz, Geotz Soft Tip, Semi-Floating, Zucker Lumen, Myler Lumen, CVP & Gorlin Lumen Electrode Cathe MYO/Wire® Ultra-Flex Temporary Pacing Wires

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer)