Fructosamine assay kit (tetrazolium blue method) - NMPA Registration 京械注准20212400530
Access comprehensive regulatory information for Fructosamine assay kit (tetrazolium blue 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 京械注准20212400530 and owned by Beijing Beijian Xinchuangyuan Biotechnology Co., Ltd.. The device was approved on October 18, 2021.
This page provides complete registration details including registrant information, province location (Beijing), 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.
This product is used for the quantitative determination of fructosamine content in human serum in vitro.
本产品用于体外定量测定人血清中果糖胺的含量。
Reagent 1: Buffer ge; 40mmol/L Reagent 2: Buffer ge; 10mmol/L Nitrotetrazolium blue ge; 0.5mmol/L Calibrator (optional) Bovine serum albumin 50g/L fructosamine (200~400)mu; mol/L Quality control (optional) Bovine serum albumin 50g/L fructosamine (200~400)mu; mol/L There are batch-to-batch differences between calibrators and quality control products, and the specific concentrations are shown in the target value table.
试剂1： 缓冲液 ge;40mmol/L 试剂2： 缓冲液 ge;10mmol/L 硝基四氮唑蓝 ge;0.5mmol/L 校准品（选配） 牛血清白蛋白 50g/L 果糖胺 (200～400)mu;mol/L 质控品（选配） 牛血清白蛋白 50g/L 果糖胺 (200～400)mu;mol/L 校准品、质控品有批间差异，具体浓度见靶值表。
2 °C ~ 8 °C protected sealed storage, valid for 12 months.
2℃～8℃避光密封储存，有效期12个月。