20 devices · GMDN 49657
This category includes in vitro diagnostic kits designed to detect immunoglobulin G (IgG) antibodies specific to Epstein-Barr virus (EBV) in patient specimens such as serum or plasma. These kits use an enzyme immunoassay (EIA) format to support the clinical assessment of EBV infection, which is associated with conditions like infectious mononucleosis and glandular fever.
Devices in this category are composed of reagents and associated materials intended for use in laboratory settings to perform qualitative and/or quantitative detection of EBV IgG antibodies. They are regulated as in vitro diagnostic medical devices and are supplied as complete kits for use with appropriate instrumentation and protocols.
This category summary is AI-generated from the GMDN nomenclature and has not been verified by a human reviewer.