Real-time PCR diagnostic kit for simultaneous detection of Trichomonas vaginalis, Mycoplasma hominis, and Ureaplasma parvum/urealyticum in clinical specimens. CE IVDR-marked and ISO 13485-certified for in vitro diagnostic use in urogenital infection screening and confirmation.
Manufactured by
Esch-Sur-Alzette, Luxembourg
We are known for the quality of our in-house developed and validated state-of-the-art molecular diagnostic kits. Benefit from our experience and get in touch with our highly trained staff to realize your project.
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