BEUDAMED
    FDA Registration Active 🇨🇳 China

    XL-B 21G, XL-B 28G, XL-B 30G, XL-C 21G, XL-C 28G, XL-C 30G, XL-E 21G, XL-E 28G, XL-E 30G

    Reg #: 3014498762 · FEI: 3014498762 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    HEBEI XINLE SCI&TECH CO.,LTD
    Registration Number
    3014498762
    FEI Number
    3014498762
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    No. 2, Xingye Street, Xinle City
    City
    Shijiazhuang City Hebei
    Country
    CN

    Regulatory Submissions

    510(k) Number
    K221839

    Owner / Operator

    Firm Name
    Hebei Xinle Sci&Tech Co.,Ltd
    Operator Number
    10057534
    Address
    No. 2, Xingye Street, Xinle City
    City
    Shijiazhuang City
    State
    Hebei
    Postal Code
    050700
    Country
    CN
    Correspondent
    Ming Li

    US Agent

    Business Name
    MID-LINK INTERNATIONAL CO., LTD
    Contact Name
    Marco Mu
    Address
    2219 Rimlang Drive, Suite 301
    City
    Bellingham
    State
    WA
    ZIP
    98226
    Country
    US
    Email
    [email protected]
    Phone
    702 2095185

    Products

    Device Name Product Code
    Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature FMK

    Proprietary Names

    XL-B 21G, XL-B 28G, XL-B 30G, XL-C 21G, XL-C 28G, XL-C 30G, XL-E 21G, XL-E 28G, XL-E 30G Lancet

    Establishment Types

    Manufacture Medical Device