BEUDAMED
    FDA Registration Active 🇧🇪 Belgium

    ME-FD1000 Fixation Device Hip Set

    Reg #: 3012396476 · FEI: 3012396476 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    MEDENVISION
    Registration Number
    3012396476
    FEI Number
    3012396476
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Boskant 16
    City
    Westerlo Antwerpen
    Country
    BE

    Owner / Operator

    Firm Name
    Medenvision
    Operator Number
    10051140
    Address
    Boskant 16
    City
    Westerlo
    State
    Antwerpen
    Postal Code
    2260
    Country
    BE
    Correspondent
    Pieter Deboeck

    US Agent

    Business Name
    Qserve Group US Inc.
    Contact Name
    Mindy McCann
    Address
    350 S Main Street, Suite 309
    City
    Doylestown
    State
    PA
    ZIP
    18901
    Country
    US
    Email
    [email protected]
    Phone
    424 2718169

    Products

    Device Name Product Code
    Retractor GAD

    Proprietary Names

    ME-FD1000 Fixation Device Hip Set Gripper ME-GR1000 ME-FD3000 ME-FD4000 Fixation Device Knee Set ME-FD5000 Fixation Device Shoulder Set

    Establishment Types

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