BEUDAMED
    FDA Registration Active 🇮🇪 Ireland

    ARROTEK MEDICAL LTD

    Reg #: 3005255160 · FEI: 3005255160 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    4

    Registration Details

    Registration Name
    ARROTEK MEDICAL LTD
    Registration Number
    3005255160
    FEI Number
    3005255160
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    Finisklin Business Park
    City
    Co. Sligo Connaught
    Country
    IE

    Owner / Operator

    Firm Name
    Arrotek Medical Ltd
    Operator Number
    10033099
    Address
    Finisklin Business Park
    City
    Co. Sligo
    State
    Connaught
    Postal Code
    F91 RR99
    Country
    IE

    US Agent

    Business Name
    Registrar Corp
    Contact Name
    David Lennarz
    Address
    144 Research Drive
    City
    Hampton
    State
    VA
    ZIP
    23666
    Country
    US
    Email
    [email protected]
    Phone
    757 2240177

    Products

    Device Name Product Code
    Tube, Tympanostomy ETD
    Catheter, Percutaneous DQY
    Catheter, Intravascular Occluding, Temporary MJN
    Catheter, Intravascular, Diagnostic DQO

    Proprietary Names

    TUBE, TYMPANOSTOMY LiquID 051 6F LP Guide Catheter Extension Neuescue Device Liquid 061 Guide Catheter extension, Liquid 071 catheter Extension

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)