BEUDAMED
    FDA Registration Active 🇲🇽 Mexico

    Rusch Ureteral Catheter-Braasch Bulb

    Reg #: 3004365956 · FEI: 3004365956 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Teleflex Medical de Mexico, S. de R.L. de C.V.
    Registration Number
    3004365956
    FEI Number
    3004365956
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Ave. Industrias No 5954, Parque Industrial Finsa,
    City
    NUEVO LAREDO Tamaulipas
    Country
    MX

    Regulatory Submissions

    510(k) Number
    K850335

    Owner / Operator

    Firm Name
    Teleflex
    Operator Number
    9062981
    Address
    3015 Carrington Mill Blvd.
    City
    Morrisville
    State
    NC
    Postal Code
    27560
    Country
    US
    Correspondent
    Divya Raman

    US Agent

    Business Name
    Teleflex, Inc.
    Contact Name
    Divya Raman
    Address
    3015 Carrington Mill Boulevard
    City
    Morrisville
    State
    NC
    ZIP
    27560
    Country
    US
    Email
    [email protected]
    Phone
    612 4231738

    Products

    Device Name Product Code
    Catheter, Urological KOD

    Proprietary Names

    Rusch Ureteral Catheter-Braasch Bulb Rusch Ureteral Catheter-Round Tip Rusch Ureteral Catheter-Olive Tip Rusch Ureteral Catheter-Cone Tip Rusch Ureteral Catheter-Whistle Tip Rusch Ureteral Catheter-Blassucci Spiral

    Establishment Types

    Manufacture Medical Device