Core Viewpoint - The company, Maike Biological (300463.SZ), has received a medical device registration certificate from the National Medical Products Administration for its pneumonia chlamydia IgG antibody test kit, which is used for the qualitative detection of pneumonia chlamydia IgG antibodies in human serum or plasma samples [1]. Group 1 - The product is named "Pneumonia Chlamydia IgG Antibody Test Kit (Direct Chemiluminescence Method)" [1]. - The test kit is designed for in vitro qualitative detection [1]. - The approval indicates a significant advancement in the company's product offerings in the medical diagnostics sector [1].

Core Viewpoint - The company, Mike Biologics (300463.SZ), has received a medical device registration certificate from the National Medical Products Administration for its pneumonia chlamydia IgG antibody test kit, which is used for the qualitative detection of IgG antibodies in human serum or plasma samples [1] Group 1 - The product is named "Pneumonia Chlamydia IgG Antibody Test Kit (Direct Chemiluminescence Method)" [1] - The test kit is designed for in vitro qualitative detection [1] - The approval indicates a significant step for the company in expanding its product offerings in the medical diagnostics field [1]