BEUDAMED
    FDA Registration Active 🇺🇸 United States

    PROPAK Injection Kit

    Reg #: 1226074 · FEI: 3002616700 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    4
    Classifications
    1

    Registration Details

    Registration Name
    Microspecialties LLC
    Registration Number
    1226074
    FEI Number
    3002616700
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    430 Smith St
    City
    Middletown
    State
    CT
    ZIP
    06457
    Country
    US

    Owner / Operator

    Firm Name
    MICROSPECIALTIES LLC
    Operator Number
    10053719
    Address
    430 Smith Street
    City
    Middletown
    State
    CT
    Postal Code
    06457
    Country
    US
    Correspondent
    Steve Levesque

    Products

    Device Name Product Code
    Kit, Surgical Instrument, Disposable KDD

    Proprietary Names

    PROPAK Injection Kit

    Establishment Types

    Manufacture Medical Device Repack or Relabel Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) Complaint File Establishment per 21 CFR 820.198