Myeloperoxidase Quantitative Test Kit (Colloidal Gold Method) - NMPA Registration 滇械注准20162400088
Access comprehensive regulatory information for Myeloperoxidase Quantitative Test Kit (Colloidal Gold Method) in the China medical device market through Pure Global AI's free database. This Class II medical device is registered under NMPA registration number 滇械注准20162400088 and owned by Yunnan Haoxu Biotechnology Co., Ltd.. The device was approved on September 27, 2021.
This page provides complete registration details including registrant information, province location (Yunnan), intended use, and regulatory compliance data from the official China NMPA medical device database. Pure Global AI offers free access to China's complete medical device registry, helping global MedTech companies navigate NMPA regulations efficiently.
For in vitro quantitative detection of medullary peroxidase in human serum/plasma/whole blood
用于体外定量检测人血清/血浆/全血中髓过氧化酶
"1. Myeloperoxidase detection reagent: MPO monoclonal antibody and sheep anti-mouse IgG are pre-coated with colloidal gold binding pad, sample pad, and absorbent paper, respectively, coated with phase nitrate membrane and colloidal gold labeled; 2. Other components: straw, manual, SD card; "
"1、髓过氧化物酶检测试剂：系由MPO单克隆抗体及羊抗鼠IgG分别包被于相硝酸纤维膜和胶体金标记的MPO单克隆抗体预包被于胶体金结合垫，以及样本垫、和吸水纸组成； 2、其他组成：吸管、说明书、SD卡； "
The kit is stored at 4~30 °C, and the aluminum foil bag is sealed and the validity period is 18 months; After the foil bag is unpacked, it is valid for 1 hour.
试剂盒于4~30℃保存，铝箔袋密封状态下存放，有效期为18个月；铝箔袋拆封后，有效期为1小时。