BEUDAMED
    FDA Registration Active 🇨🇳 China

    PREGMATE® Digital Ovulation Reader

    Reg #: 3017904598 · FEI: 3017904598 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    15
    Establishment Types
    3
    Classifications
    1

    Registration Details

    Registration Name
    Guangzhou Decheng Biotechnology Co., Ltd.
    Registration Number
    3017904598
    FEI Number
    3017904598
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Floor 3/4/5/7, Building A1, No.12, Nanyun 1st Road, Science City, Huangpu District
    City
    Guangzhou Guangdong
    Country
    CN

    Owner / Operator

    Firm Name
    Guangzhou Decheng biotechnology co., Ltd.
    Operator Number
    10079520
    Address
    Floor 3/4/5/7, Building A1, No.12, Nanyun 1st Road, Science City, Huangpu District
    City
    Guangzhou
    State
    Guangdong
    Postal Code
    510663
    Country
    CN
    Correspondent
    haisheng Hu

    US Agent

    Business Name
    LSI International Inc
    Contact Name
    Joe Xia
    Address
    504E Diamond Ave.
    City
    Gaithersburg
    State
    MD
    ZIP
    20877
    Country
    US
    Email
    [email protected]
    Phone
    240 5057880

    Products

    Device Name Product Code
    Test, Luteinizing Hormone (Lh), Over The Counter NGE

    Proprietary Names

    PREGMATE® Digital Ovulation Reader Pregmate Ovulation Test MGC HEALTH™ OVULATION RAPID TEST PREGMATE® OVULATION TEST STRIP MissLan® One Step LH Urine Test Strip Amazewell™ Semi-quantitative Ovulation Rapid Test Strip exchange select™ Ovulation Rapid Test Amazewell™ Ovulation Rapid Test Midstream PREGMATE® Digital Ovulation Test MissLan® One Step LH Urine Test Midstream Amazewell™ Digital Ovulation Test Kit MissLan® Digital Ovulation Rapid Test Amazewell™ Ovulation Rapid Test Strip SAVVONA Color Scale Ovulation Predictor Test kozekoze Ovulation Test

    Establishment Types

    Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) Complaint File Establishment per 21 CFR 820.198