BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    Nelaton-Robinson catheter, cylindrical; Nelaton-Robinson catheter, Tiemann pattern;

    Reg #: 3014656749 · FEI: 3014656749 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    RHENUS SE & CO. KG
    Registration Number
    3014656749
    FEI Number
    3014656749
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Rhenus Platz 1
    City
    Holzwickede North Rhine-Westphalia
    Country
    DE

    Owner / Operator

    Firm Name
    Rhenus SE & Co. KG
    Operator Number
    10057982
    Address
    Elisabeth-Selbert-Strasse 3
    City
    Rodgau
    State
    Hesse
    Postal Code
    63110
    Country
    DE
    Correspondent
    Christopher Hans Essig

    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

    Nelaton-Robinson catheter, cylindrical; Nelaton-Robinson catheter, Tiemann pattern; Rusch all purpose Robinson / Nelation; Rusch Silicone Coated Foley, and pediatric; Rusch all purpose red rubber; ERU Catheter PVC Tiemann Pattern; Female catheter; Nelaton catheter rubber, cylindrical / Robinson pattern / whistle tip / coaxial / Tiemann pattern;

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device