Pumen Technology: Obtained the medical device registration certificate for folic acid testing reagent kit.

Pumen Technology announced that the company recently received the "Medical Device Registration Certificate of the People's Republic of China" issued by the Guangdong Provincial Food and Drug Administration. The product name is Folic Acid Determination Reagent Kit, registered as Class II. The registration certificate number is Yue Medical 20252401644, valid until December 18, 2030. This product is used for the quantitative determination of folic acid content in human serum or plasma samples, clinically used for the auxiliary diagnosis of megaloblastic anemia. The folic acid determination reagent kit obtained this time is the company's new generation product, using sandwich chemiluminescence immunoassay, which improves the sensitivity and precision of the reagent, helping to enhance the company's market competitiveness in the field of anemia detection. As of the disclosure date of the announcement, the company and its subsidiaries have obtained 106 electrochemiluminescence supporting reagent registration certificates, further enriching and improving the company's electrochemiluminescence reagent project testing menu, enhancing the company's market competitiveness in the field of immunodiagnosis. However, the actual sales of the product after it is launched will depend on the promotion effect of the future market, and it is currently impossible to predict the specific impact on the company's future performance.