Placenta Growth Factor (PlGF) Assay Kit (Fluorescence Immunoassay)
- Device class
- Class II
- Model specifications
- 20 servings/box, 25 servings/box, 40 servings/box, 50 servings/box, 80 servings/box, 100 servings/box.20人份/盒、25人份/盒、40人份/盒、50人份/盒、80人份/盒、100人份/盒。
- Approval department
- Beijing Municipal Drug Administration北京市药品监督管理局
- Registration number
- 京械注准20232400296
- Approval date
- May 06, 2023
- Expiry date
- May 05, 2028
- Name
- Beijing Tigsun Diagnostics Co., Ltd.北京泰格科信生物科技有限公司
- Province/Region
- Beijing北京
- Address
- Building 1, No. 16, District 1, Guba Road, Chengguan Street, Fangshan District, Beijing北京市房山区城关街道顾八路一区16号1幢
- Production address
- 北京市房山区城关街道顾八路一区16号1幢
This kit is used for the quantitative determination of placental growth factor content in human serum and plasma in vitro.
本试剂盒用于体外定量测定人血清、血浆中胎盘生长因子的含量。
Note: 1. This product is traced to the enterprise work calibration product; 2. The components in different batch kits cannot be interchanged, and calibration information cards and reagents of different batch numbers cannot be mixed.
注：1、本产品溯源至企业工作校准品； 2、不同批号试剂盒中各组分不能互换，不同批号的校准信息卡和试剂不能混用。
The kit is stored at 2 °C ~ 30 °C and is effective
试剂盒2℃～30℃储存，有效
- Appendix
- 产品技术要求、说明书
Access comprehensive regulatory information for Placenta Growth Factor (PlGF) Assay Kit (Fluorescence Immunoassay) 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20232400296 and owned by Beijing Tigsun Diagnostics Co., Ltd.. The device was approved on May 06, 2023.
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.