BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Trinity Sterile, Inc.

    DI: 10841767103545 · Model: 5088 · Trinity Sterile, Inc.
    View on AccessGUDID
    Product Codes
    0
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Trinity Sterile, Inc.
    Primary DI
    10841767103545
    Version / Model
    5088
    Company Name
    Trinity Sterile, Inc.
    Labeler DUNS
    154424043
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-08-30
    Public Version
    1
    Public Version Date
    2023-09-07
    Public Version Status
    New
    Public Device Record Key
    c160e36c-3099-420e-a39a-64ecd483617a

    Device Description

    HARTMANN FCP CVD 3 1/2 STRL

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    Yes
    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
    Yes
    PM Exempt
    Yes
    Has Serial Number
    Yes
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Ethylene Oxide

    GMDN Terms

    Code Name
    62479 Surgical soft-tissue manipulation forceps, tweezers-like, single-use

    Identifiers

    Type ID
    Package 00841767103548
    Primary 10841767103545