BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Katena

    DI: 00841668144381 · Model: K5-6220 · KATENA PRODUCTS, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Let the assistant research this device

    The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Brand Name
    Katena
    Primary DI
    00841668144381
    Version / Model
    K5-6220
    Catalog Number
    K5-6220
    Company Name
    KATENA PRODUCTS, INC.
    Labeler DUNS
    085668598
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2026-03-31
    Public Version
    1
    Public Version Date
    2026-04-08
    Public Version Status
    New
    Public Device Record Key
    e1fce655-5551-4686-9314-1647fbb99617

    Device Description

    HERSH-GREENSTEIN-GELLES CTAK INLAY FCPS

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    Yes
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    HNR Forceps, ophthalmic

    GMDN Terms

    Code Name
    42500 Dressing/utility forceps, tweezers-like, reusable

    Identifiers

    Type ID
    Primary 00841668144381