BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    MOOR INSTRUMENTS LTD.

    Reg #: 8043564 · FEI: 1000279065 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    10
    Establishment Types
    2
    Classifications
    4

    Registration Details

    Registration Name
    MOOR INSTRUMENTS LTD.
    Registration Number
    8043564
    FEI Number
    1000279065
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    MILLWEY
    City
    AXMINSTER Devon
    Country
    GB

    Regulatory Submissions

    510(k) Number
    K063586

    Owner / Operator

    Firm Name
    MOOR INSTRUMENTS LTD.
    Operator Number
    9002394
    Address
    MILLWEY INDUSTRIAL ESTATE, --
    City
    AXMINSTER, DEVON
    State
    GB-NOTA
    Postal Code
    EX135HU
    Country
    GB

    US Agent

    Business Name
    MOOR INSTRUMENTS INC.
    Contact Name
    LINDA WADE
    Address
    501 SILVERSIDE ROAD, SUITE 66
    City
    Wilmington
    State
    DE
    ZIP
    19809
    Country
    US
    Email
    [email protected]
    Phone
    302 7987470

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument GEX
    Probe, Blood-Flow, Extravascular DPT
    Oximeter, Tissue Saturation MUD
    Flowmeter, Blood, Cardiovascular DPW

    Proprietary Names

    moorFLPI moorLDI2 moorLDI2-BI moorLDLS-BI moorVMS-OXY moorVMS-LDF1 moorVMS-LDF2 moorFLPI2 moorLDLS moorVMS-PRES

    Establishment Types

    Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198