BEUDAMED
    FDA Registration Active 🇺🇸 United States

    BAYONETED WOODSON PROBE 45DEG

    Reg #: 2132732 · FEI: 1000306694 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    4
    Classifications
    1

    Registration Details

    Registration Name
    TECOMET, INC.
    Registration Number
    2132732
    FEI Number
    1000306694
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5307 95th Ave
    City
    KENOSHA
    State
    WI
    ZIP
    53144
    Country
    US

    Owner / Operator

    Firm Name
    Tecomet
    Operator Number
    10031318
    Address
    5307 95th Avenue
    City
    Kenosha
    State
    WI
    Postal Code
    53144
    Country
    US
    Correspondent
    Julie Davis

    Products

    Device Name Product Code
    Instrument, Surgical, Non-Powered HAO

    Proprietary Names

    BAYONETED WOODSON PROBE 45DEG BAYONETED BALL PROBE 110DEGSHT BAYONETED WOODSON PROBE 90DEG ROD ROTATION FORCEPS BAYONETED BALL PROBE 110DEGLNG

    Establishment Types

    Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer)