Progesterone IVD, kit, chemiluminescent immunoassay

35 devices · GMDN 54322

Progesterone IVD kits using chemiluminescent immunoassay detect hormone levels in clinical specimens like serum or plasma. Clinically, these devices help monitor reproductive health, diagnose fertility issues, and assess conditions such as polycystic ovary syndrome (PCOS) or menopausal status by quantifying progesterone concentrations.

These kits are typically regulated as in vitro diagnostics (IVDs) and may require compliance with standards like ISO 13485 or FDA 21 CFR Part 820. They are usually supplied as reagent cartridges or test systems, designed for laboratory use and often require specialized equipment for chemiluminescent detection.

This category summary is AI-generated from the GMDN nomenclature and has not been verified by a human reviewer.

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