BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ACIST CVi® BT2000 Manifold Kit, ACIST CVi® AngioTouch® Kit AT P65 , ACIST CVi® AngioTouch® Kit AT P54, ACIST CVi® Contra

    Reg #: 2022435 · FEI: 2022435 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Sterigenics U.S., LLC
    Registration Number
    2022435
    FEI Number
    2022435
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1401 Morgan Cir
    City
    Tustin
    State
    CA
    ZIP
    92780
    Country
    US

    Regulatory Submissions

    510(k) Number
    K171646

    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
    Injector And Syringe, Angiographic DXT

    Proprietary Names

    ACIST CVi® BT2000 Manifold Kit, ACIST CVi® AngioTouch® Kit AT P65 , ACIST CVi® AngioTouch® Kit AT P54, ACIST CVi® Contra

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer)