BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    MUI SCIENTIFIC

    Reg #: 9611668 · FEI: 3002807135 · Expires 2026
    View on FDA
    Products
    5
    Proprietary Names
    30
    Establishment Types
    3
    Classifications
    5

    Registration Details

    Registration Name
    MUI SCIENTIFIC
    Registration Number
    9611668
    FEI Number
    3002807135
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    145 TRADERS BLVD. EAST, # 34
    City
    MISSISSAUGA Ontario
    Country
    CA

    Regulatory Submissions

    510(k) Number
    K823701

    Owner / Operator

    Firm Name
    H & A MUI ENTERPRISES INC.
    Operator Number
    8020404
    Address
    145 TRADERS BLVD. EAST, #34, --
    City
    Mississauga
    State
    Ontario
    Postal Code
    L4Z 3L3
    Country
    CA
    Correspondent
    Fatemeh - Rahimi

    Products

    Device Name Product Code
    System, Gastrointestinal Motility (Electrical) FFX
    Endoscopic Access Overtube, Gastroenterology-Urology FED
    Monitor, Esophageal Motility, Anorectal Motility, And Tube KLA
    Camera, Television, Endoscopic, Without Audio FWF
    Nasopharyngoscope (Flexible Or Rigid) EOB

    Proprietary Names

    Anorectal Balloon Expulsion Catheters Barostat Catheters Anorectal Catheters Small Bowel Catheters Colonic Catheters Esophageal Catheters Manometric Pumps and Catheters PatCom Single-Use Introducer Portable Pressurized Infusion Pump Pressurized Infusion Pump Manometric Pump Water Perfusion Pump Water Perfused Catheter Sleeve Catheters Motility Catheter Manometric Catheter Dentsleeve Catheter Patcom Image Pro USB Camera Henke-Sass Wolf Rapid Barostat Bag Pump SOM Catheter Sphincter of Oddi Manometric Pump SOM Pump Toouli SOM Sleeve Catheter Sphincter of Oddi Manometric System PatCom Distal Chip Endoscope Esophageal Barostat Catheters Rapid Barostat Bags Barostat / Motility Catheters Y-Type Gastric and Rectal Barostat Catheters

    Establishment Types

    Manufacture Medical Device Export Device to the United States But Perform No Other Operation on Device Foreign Private Label Distributor