Mike Bio: New product obtained product registration certificate.

Mike Biotech announced that the company recently received the "Medical Device Registration Certificate" issued by the National Medical Products Administration. The product name is pneumonia chlamydia IgG antibody test kit, registration certificate number is National Standard 20253402233, registration category is Class III, and the registration certificate is valid from November 4, 2025 to November 3, 2030. This product is used for in vitro qualitative detection of pneumonia chlamydia IgG antibodies in human serum or plasma samples, mainly for the auxiliary diagnosis of pneumonia chlamydia infection. It is compatible with the company's fully automated chemiluminescence immune analysis instruments i6000, i3000 series, i1000 series, and i800 series.