BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    DermaSci1232 (WT) - sterile saline

    Reg #: 9680143 · FEI: 3002807308 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    STERIS Applied Sterilization Technologies ULC
    Registration Number
    9680143
    FEI Number
    3002807308
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    184 CROWN CT.
    City
    WHITBY Ontario
    Country
    CA

    Regulatory Submissions

    510(k) Number
    K992732

    Owner / Operator

    Firm Name
    STERIS Corporation
    Operator Number
    1527821
    Address
    5960 Heisley Rd, --
    City
    Mentor
    State
    OH
    Postal Code
    44060
    Country
    US

    US Agent

    Business Name
    STERIS Corporation
    Contact Name
    Becky Aldhizer
    Address
    5960 Heisley Rd
    City
    Mentor
    State
    OH
    ZIP
    44060
    Country
    US
    Email
    [email protected]
    Phone
    440 3927490

    Products

    Device Name Product Code
    Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days FOZ

    Proprietary Names

    DermaSci1232 (WT) - sterile saline DermaSci1232 (WT) - sterile water

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer)