BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Lancing Device

    DI: 06949517001978 · Model: LF-LD-E · Shandong Lianfa Medical Plastic Products CO.,LTD
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    40

    Basic Information

    Brand Name
    Lancing Device
    Primary DI
    06949517001978
    Version / Model
    LF-LD-E
    Company Name
    Shandong Lianfa Medical Plastic Products CO.,LTD
    Labeler DUNS
    421330121
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    40
    Record Status
    Published
    Publish Date
    2019-04-30
    Public Version
    1
    Public Version Date
    2019-05-08
    Public Version Status
    New
    Public Device Record Key
    56281db4-332c-47d8-8119-1605250a04ab

    Device Description

    Lancing Device with Ejector (MINI) (Box of 40 devices)

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    Yes
    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
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    FMK Lancet, Blood

    GMDN Terms

    Code Name
    37243 Manual blood lancing device, reusable

    Identifiers

    Type ID
    Primary 06949517001978
    Unit of Use 56949517065128