BioPlex 2200 Lyme Total Assay Protocol File CD SW4.3_v1.0


Product Overview

BioPlex 2200 Lyme Total Assay Protocol File CD SW4.3_v1.0
BioPlex 2200 - 4.3_v1.0


Device Description

A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin G (IgG) and immunoglobulin M (IgM) antibodies to Borrelia burgdorferi in a clinical specimen, using a chemiluminescent immunoassay method. The assay is designed to detect infection with Borrelia burgdorferi, the bacteria associated with Lyme disease.


Environmental Conditions

No Data Available


Device Sizes

  • 1 Each
    • 1 Each


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: LSR

    Device Name: Reagent, Borrelia Serological Reagent

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: MI

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 866.3830

    Third Party Flag: N

    Medical Specialty: MI


    Device Identifiers

    Device Id: 03610520506462

    Device Type: Primary

    DeviceId Issuing Agency: GS1

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


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