N末端B型利钠肽前体（NT-proBNP）检测试剂盒（荧光免疫层析法） - NMPA Registration 鄂械注准20252405406
Access comprehensive regulatory information for N末端B型利钠肽前体（NT-proBNP）检测试剂盒（荧光免疫层析法） in the China medical device market through Pure Global AI's free database. This Class II medical device is registered under NMPA registration number 鄂械注准20252405406 and owned by Wuhan Easy Diagnosis Biomedicine Co., Ltd.. The device was approved on January 26, 2025.
This page provides complete registration details including registrant information, province location (Hubei), 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.
本检测试剂适用于体外定量检测人血清、血浆、全血中的NT-proBNP的含量。
试剂盒由测试卡、弹夹（AF2型号适配）、干燥剂和定标卡组成。其中，测试卡由测试卡外壳、硝酸纤维素膜、鼠抗人NT-proBNP抗体、羊抗鼠IgG抗体、结合垫、荧光标记的鼠抗人NT-proBNP抗体、样本垫、吸水纸、PVC板组成；定标卡包含试剂的标准曲线、批次、项目名称、生产日期信息。（具体内容详见说明书）
试剂盒应在2℃～30℃干燥环境下避光保存，有效期为18个月。