BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Revital-Ox Rigid Container System (2D93Q0) (SL-CFE, SLDC-RR)

    Reg #: 1933443 · FEI: 1000510740 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    STERIS CORPORATION
    Registration Number
    1933443
    FEI Number
    1000510740
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    8525 Page Ave
    City
    Breckenridge Hills
    State
    MO
    ZIP
    63114
    Country
    US

    Owner / Operator

    Firm Name
    STERIS Corporation
    Operator Number
    10078069
    Address
    5960 Heisley Road
    City
    Mentor
    State
    OH
    Postal Code
    44060
    Country
    US

    Products

    Device Name Product Code
    Basin For Endoscope Reprocessing PHT

    Proprietary Names

    Revital-Ox Rigid Container System (2D93Q0) (SL-CFE, SLDC-RR) Revital-Ox Flexible Container - Round (2D94Q0) (SL-CFE, SLDC-RR)

    Establishment Types

    Repack or Relabel Medical Device