BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    ULTI-LANCE

    DI: 00743820000095 · Model: 00009 · Boca Med, LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    3
    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
    ULTI-LANCE
    Primary DI
    00743820000095
    Version / Model
    00009
    Company Name
    Boca Med, LLC
    Labeler DUNS
    121164730
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-02-08
    Public Version
    2
    Public Version Date
    2023-02-22
    Public Version Status
    Update
    Public Device Record Key
    19d3a426-63ad-48d1-9279-368efa8c4e16

    Device Description

    Ulti-Lance Fingertip Lancing Device NDC number: 08326-0000-09

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    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
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    QRL Multiple Use Blood Lancet For Single Patient Use Only

    GMDN Terms

    Code Name
    37243 Manual blood lancing device, reusable

    Identifiers

    Type ID
    Primary 00743820000095
    Package 20743820000099
    Package 30743820000096