Dehydroepiandrosterone (DHEA) IVD, kit, enzyme immunoassay (EIA)

This category includes in vitro diagnostic (IVD) kits designed to measure the concentration of dehydroepiandrosterone (DHEA) in clinical specimens such as serum or plasma. These kits use an enzyme immunoassay (EIA) method to provide quantitative results that assist in evaluating adrenal function, hormonal imbalances, or conditions related to androgen production.

Devices in this category are composed of reagents and associated materials calibrated for DHEA detection via EIA and are intended for use in laboratory settings. They are regulated as IVD medical devices and must meet performance and safety requirements for analytical accuracy, precision, and reliability in clinical testing environments.