BEUDAMED
    FDA Registration Active 🇺🇸 United States

    THERAKOS® CELLEX® Photopheresis System Procedural Kit

    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

    PMA Number
    P860003

    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
    System, Photopheresis, Extracorporeal LNR

    Proprietary Names

    THERAKOS® CELLEX® Photopheresis System Procedural Kit THERAKOS® UVAR XTS® Photopheresis System procedural Kit THERAKOS CELLEX Photopheresis Procedural Kit/CLXUSA THERAKOS UVAR XTS Photopheresis Procedural Kit/XT001 Therakos Cellex Photopherisis Procedural Kit - CLXUSA/CLXECP/CLXSP-I/CLXCC-I

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer)