BEUDAMED
    FDA Registration Active 🇺🇸 United States

    HiArc

    Reg #: 1219738 · FEI: 1219738 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    3

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    Registration Details

    Registration Name
    HiArc
    Registration Number
    1219738
    FEI Number
    1219738
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    220 DANIEL WEBSTER HWY.
    City
    Merrimack
    State
    NH
    ZIP
    03054
    Country
    US

    Owner / Operator

    Firm Name
    KMC Systems
    Operator Number
    9024188
    Address
    220 DANIEL WEBSTER HWY., --
    City
    Merrimack
    State
    NH
    Postal Code
    03054
    Country
    US
    Correspondent
    Andrew Sageman

    Products

    Device Name Product Code
    Plasma, Coagulation Control GGN
    Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control DAP
    System, Multipurpose For In Vitro Coagulation Studies JPA

    Proprietary Names

    ACUSTAR

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)