Xiamen Baysen Medica l Technology Co., Ltd. is a high-tech logical enterprise that dedicates itself to the field of rapid diagnostic reagent and integrates research and development, production and sales into a whole. Our factory dedicates itself to developing new rapid diagnostic reagents and instruments to meet the market demand, continuous innovation and enterprising and continuous improvement to detect diseases, the level of prevention and treatment, to protect the life and health of all people. Our company strictly follows with I S O 1 3 4 8 5 and I S O 9 0 0 1 quality management system operation with research, production, quality control, international sales, etc. And has a number of advanced research staff and marketing managers in the company, not only in quality management but also in service . We won a good reputation from both overseas and domestic clients. Companies adhere to the "people-oriented" employment concept, respect and care for the value of employees, and strive to build a good working environment, win-win values and management concepts to create a more innovative, cohesive and competitive human resources system, and the expectations of companies and employees develop together. Abbott is our sole agent for some reagents in China, we are the first manufacturer to register CFDA for Calprotectin rapid test kit in China, and the quality in China is also on the top. Our mission is to be an integrated solution provider of point-of-care testing products for a better living for the whole world. Get MHRA approval for 46 types of rapid test kits including A101 portable immunoassay analyzer. Get CE approval for 78 types of rapid test kits including A101 portable immunoassay analyzer Self-test products for covid-19 antigen were launched on the market and obtained Bfarm list, CE certificates and approved by French, Swiss, Austrian and others. Obtained CE certificate for Covid-19 rapid antigen test and the overseas market spread rapidly. Gained five product registration numbers WIZ-A101 portable immunoassay analyzer obtained Fujian CFDA certificate. Second-class in vitro diagnostic reagents approved by Fujian Food and Drug Administration. "WIZ-A202 continuous immunoassay analyzer" won the Fujian Medical Device Registration Certificate. The enterprises Listed in the National Equities Exchange and Quotations System for small and medium-sized enterprises (The new board). Obtained by SGS ISO13485, ISO9001 quality system certification Obtain the "High-tech enterprise certificate". Obtain the Food and Drug Administration "medical equipment manufacturing enterprises allow".