The Measles Virus IgG ELISA is intended for the qualitative determination of IgG class antibodies against Measles Virus in human serum or plasma (citrate, heparin).


Product Overview

The Measles Virus IgG ELISA is intended for the qualitative determination of IgG class antibodies against Measles Virus in human serum or plasma (citrate, heparin).
Measles Virus IgG ELISA - EIA-3844


Device Description

A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin A (IgA), immunoglobulin G (IgG) and immunoglobulin M (IgM) antibodies to Measles virus in a clinical specimen, using an enzyme immunoassay (EIA) method.


Environmental Conditions

No Data Available


Device Sizes

  • Total Volume: 2 Milliliter
  • Substrate TMB
  • Cut Off
  • Total Volume: 50 Milliliter
  • Total Volume: 3 Milliliter
  • Conjugate
  • Controls +/-
  • Total Volume: 20 Milliliter
  • Total Volume: 15 Milliliter
  • Diluent G
  • Stop Solution
  • Wash Buffer
  • Total Volume: 100 Milliliter
    • Total Volume: 2 Milliliter
    • Substrate TMB
    • Cut Off
    • Total Volume: 50 Milliliter
    • Total Volume: 3 Milliliter
    • Conjugate
    • Controls +/-
    • Total Volume: 20 Milliliter
    • Total Volume: 15 Milliliter
    • Diluent G
    • Stop Solution
    • Wash Buffer
    • Total Volume: 100 Milliliter


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: LJB

    Device Name: Enzyme Linked Immunoabsorbent Assay, Rubeola Igg

    Device Class: 1

    Physical State: IVD reagent kit

    Definition: The qualitative detection of measles specific IgG antibodies in serum or plasma.

    Submission Type ID: 4

    Review Panel: MI

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: antigens and antisera used for the detection of measles antibodies

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: Not applicable in vitro use

    Regulation Number: 866.3520

    Third Party Flag: N

    Medical Specialty: MI


    Device Identifiers

    Device Id: 00840239038449

    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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