BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Sterilance Press Pressure Activated Safety Lancet

    DI: 16945630108829 · Model: 05-052618 · SteriLance Medical (Suzhou) Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    3
    Pkg Device Count
    25

    Basic Information

    Brand Name
    Sterilance Press Pressure Activated Safety Lancet
    Primary DI
    16945630108829
    Version / Model
    05-052618
    Company Name
    SteriLance Medical (Suzhou) Inc.
    Labeler DUNS
    421141183
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    25
    Record Status
    Published
    Publish Date
    2020-11-17
    Public Version
    1
    Public Version Date
    2020-11-25
    Public Version Status
    New
    Public Device Record Key
    a7464f08-f509-4fa7-b0ad-a5cc199948f0

    Device Description

    Sterilance Press Pressure Activated Safety Lancet,26G 1.8mm,25Lancets/box

    Device Characteristics

    Single Use
    Yes
    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
    No
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    FMK Lancet, Blood

    GMDN Terms

    Code Name
    61578 Manual blood lancing device, single-use

    Identifiers

    Type ID
    Package 36945630108823
    Primary 16945630108829
    Unit of Use 06945630108822