β2-microglobulin test kit (latex immunoturbidimetric method) - NMPA Registration 吉械注准20242400360
Access comprehensive regulatory information for β2-microglobulin test kit (latex immunoturbidimetric 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 吉械注准20242400360 and owned by Jilin Base Egg Biological Technology Co., Ltd.. The device was approved on July 16, 2024.
This page provides complete registration details including registrant information, province location (Jilin), 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.
It is used for in vitro quantitative determination of β2-microglobulin content in human serum, plasma and urine.
用于体外定量测定人血清、血浆和尿液中β2-微球蛋白的含量。
试剂1(R1):氯化铵缓冲液 20mmol/L;聚乙二醇6000 1.5g/L;氯化钠 80mmol/L. 试剂2(R2):兔抗人β2-微球蛋白抗体0.25g/L;胶乳微球 25mL/L;甘氨酸缓冲液50mmol/L. 校准品(可选配):β2-微球蛋白抗原,具体浓度详见标签. 质控品(可选配):β2-微球蛋白抗原,具体浓度详见标签.
试剂1(R1):氯化铵缓冲液 20mmol/L;聚乙二醇6000 1.5g/L;氯化钠 80mmol/L。 试剂2(R2):兔抗人β2-微球蛋白抗体0.25g/L;胶乳微球 25mL/L;甘氨酸缓冲液50mmol/L。 校准品(可选配):β2-微球蛋白抗原,具体浓度详见标签。 质控品(可选配):β2-微球蛋白抗原,具体浓度详见标签。

