Recently, Xingtong Medical Technology (Suzhou) Co., Ltd., an enterprise located in Suzhou Nano Park, announced that its self-developed clinical immunodiagnostic instrument products have obtained the products of two immunoassay instruments issued by China Food and Drug Administration. The registration certificate, meanwhile, the instrument is also officially introduced to the market. The introduction of this instrument will help hospitals improve medical quality and shorten patient visit time. According to reports, the detection accuracy and convenience of this instrument have reached the international advanced level.

Xingtong Medical Technology (Suzhou) Co., Ltd., which developed this immunoassay instrument, was established in 2012. Its products include immunoassay systems and supporting reagents. The testing programs cover cardiovascular diseases, inflammation, prenatal and postnatal diseases, and tumors. The company's core technologies include new immunoassay methodology, micro-biosensors, instrument design, nanomaterials, reagents, automation, and analysis software. At present, he has obtained more than a dozen invention patents in the United States, China and other countries.

The two instruments that Starchild has obtained the product registration certificate are Matrix Core and Pylon Core products, which are based on the loop enhanced fluorescence detection technology developed by Starchild. The instrument does not require a liquid path system and is easy to install and use. The single-package reagents used with the instrument can perform both POCT and fully automated batch analysis. The instrument can be duplexed with the laboratory information system to automate information.

Starchild Medical said that Starchild was aiming at China's in vitro diagnostic high-end market at the beginning of its establishment, and strived to upgrade domestically produced immunoassay technology to the world's leading level. The two instrument products of Starchild have obtained the product registration certificate of China Food and Drug Administration, which indicates that Xingtong's efforts have gradually achieved results.

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