BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    Cure Catheter Insertion Kit (K2)

    Reg #: 3008806809 · FEI: 3008806809 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    13
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ConvaTec Limited, GDC Building
    Registration Number
    3008806809
    FEI Number
    3008806809
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    First Avenue, Deeside Industrial Park
    City
    Deeside Flintshire
    Country
    GB

    Regulatory Submissions

    510(k) Number
    K250891

    Owner / Operator

    Firm Name
    ConvaTec
    Operator Number
    2241599
    Address
    7815 National Service Road, Suite 600
    City
    Greensboro
    State
    NC
    Postal Code
    27409
    Country
    US
    Correspondent
    Courtney Smith

    US Agent

    Business Name
    ConvaTec
    Contact Name
    Courtney Smith
    Address
    20 Maguire
    City
    Lexington
    State
    MA
    ZIP
    02421
    Country
    US
    Email
    [email protected]
    Phone
    239 7762947

    Products

    Device Name Product Code
    Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) FCM

    Proprietary Names

    Cure Catheter Insertion Kit (K2) Cure Catheter Closed System Kit (CS10) Cure Catheter Closed System Kit (CS14C) Cure Catheter Closed System Kit (CS8) Cure Catheter Insertion Kit (K1) Cure Pocket Catheter Kit (M14UK) Cure Catheter Insertion Kit (K3) Cure Catheter Closed System Kit (CS12) Cure Hydrophilic Catheter Kit (HM14UK) Cure Hydrophilic Catheter Kit (HM12UK) Cure Catheter Closed System Kit (CS14) Cure Hydrophilic Catheter Kit (HM16UK) Cure Catheter Insertion Kit (K2-90)

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility