BEUDAMED
    FDA Registration Active 🇺🇸 United States

    DITEK CONSULTING LLC

    Reg #: 3017059592 · FEI: 3017059592 · Expires 2026
    View on FDA
    Products
    5
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    5

    Registration Details

    Registration Name
    DITEK CONSULTING LLC
    Registration Number
    3017059592
    FEI Number
    3017059592
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    99 Commerce St
    City
    Glastonbury
    State
    CT
    ZIP
    06033
    Country
    US

    Owner / Operator

    Firm Name
    Ditek Consulting LLC
    Operator Number
    10075817
    Address
    160 OAK ST STE 210
    City
    Glastonbury
    State
    CT
    Postal Code
    06033
    Country
    US
    Correspondent
    Daniel DelMastro

    Products

    Device Name Product Code
    Blood And Urine Collection Kit (Excludes Hiv Testing) OIB
    Container, Specimen Mailer And Storage, Non-Sterile NNK
    Urine Collection Kit (Excludes Hiv Testing) OIE
    Container, Specimen, Non-Sterile NNI
    Container, Specimen Mailer And Storage, Sterile KDT

    Proprietary Names

    Ditek Collection Kit Colofit Kit Direk Urine Collection Ditek Specimen Container Non-Sterile Demorea Tube

    Establishment Types

    Repack or Relabel Medical Device