19 devices · GMDN 52475
This category includes in vitro diagnostic kits designed to detect the genetic material of Trichomonas vaginalis, a parasite that causes a common sexually transmitted infection. These kits use nucleic acid amplification techniques to identify the presence of the organism in clinical samples such as vaginal swabs or urine, aiding in diagnosis and guiding treatment decisions.
Devices in this category are supplied as complete reagent kits containing all necessary components for sample processing and detection. They are regulated as in vitro diagnostic medical devices and are intended for use by trained laboratory personnel in clinical settings following the manufacturer’s instructions for use.
This category summary is AI-generated from the GMDN nomenclature and has not been verified by a human reviewer.