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    FDA UDI In Commercial Distribution 🇺🇸 United States

    iFlash 9000 CLIA Analyzer

    DI: 06925912718154 · Model: iFlash 9000-A · Shenzhen YHLO Biotech Co., Ltd.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    iFlash 9000 CLIA Analyzer
    Primary DI
    06925912718154
    Version / Model
    iFlash 9000-A
    Catalog Number
    FG0076
    Company Name
    Shenzhen YHLO Biotech Co., Ltd.
    Labeler DUNS
    420735989
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-10-26
    Public Version
    1
    Public Version Date
    2022-11-03
    Public Version Status
    New
    Public Device Record Key
    feb3de0c-3f79-40c1-b19a-f4a01a0ff3cc

    Device Description

    Type A, autoload

    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
    Yes
    Has Serial Number
    Yes
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

    GMDN Terms

    Code Name
    56701 Chemiluminescent immunoassay analyser IVD

    Identifiers

    Type ID
    Primary 06925912718154