ToRC IgG Reagent Pack
BioPlex 2200 - 6651650
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) antibodies to the parasitic protozoan Toxoplasma gondii in a clinical specimen, using a fluorescent immunoassay method.
Environmental Conditions
- 8.00
- 2.00
Device Sizes
- 100 Number of Tests
Device Sterilization
Device Sterile: False
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: OMI
Device Name: Multiplex Flow Immunoassay, T. Gondii, Rubella And Cmv
Device Class: 2
Physical State: The device is a fully automated instrument.
Definition: The kit is a multiplex immunoassay intended for the quantitative detection of IgG antibodies to Toxoplasma gondii (T. gondii) and Rubella, and qualitative detection of Cytomegalovirus (CMV) IgG in human serum and/ or plasma. Indicated as an aid in the determination of serological status to T. gondii, Rubella and CMV. This kit is not intended for use in screening blood or plasma donors.
Submission Type ID: 1
Review Panel: MI
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: The device utilizes multiplex immunofluorescence technology to assess the presence of IgG antibodies for each of the analytes in the panel in a single sample by binding to antigen-coated fluoromagnetic beads with unique fluorescent signatures.
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: Assay
Regulation Number: 866.3510
Third Party Flag: N
Medical Specialty: MI
Device IdentifiersDevice Id: 00847865000444
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