Glycylproline dipeptidyl peptidase detection reagent kit (rate method)
- Device class
- Class II
- Approval department
- Hebei Food and Drug Administration河北省食品药品监督管理局
- Registration number
- 冀械注准20142400365
- Approval date
- November 07, 2019
- Expiry date
- November 06, 2024
- Name
- Langfang Hengyi Biotechnology Co., Ltd.廊坊恒益生物技术有限公司
- Province/Region
- Hebei河北
- Address
- No. 1, Yilan Road, Yongqing Taiwan New Industrial City, Langfang City, Hebei Province河北省廊坊市永清台湾工业新城宜兰道1号
- Production address
- 河北省廊坊市永清台湾工业新城宜兰道1号
For in vitro quantitative determination of glycylproline dipeptide aminopeptidase activity in serum or urine.
用于体外定量测定血清或尿液中甘氨酰脯氨酸二肽氨基肽酶的活性。
Reagent 1: Diglycinopeptide, 8.32 g/L; Trihydroxyaminomethane (Tris), 8.5g/L; Reagent 2: sodium azide, 1 g/L; Glycylproline p-nitroaniline, 1.62 g/L.
试剂1：双甘肽，8.32g/L ； 三羟基氨基甲烷（Tris）， 8.5g/L；试剂2：叠氮钠，1g/L ； 甘氨酰脯氨酸对硝基苯胺，1.62g/L。
Access comprehensive regulatory information for Glycylproline dipeptidyl peptidase detection reagent kit (rate 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 冀械注准20142400365 and owned by Langfang Hengyi Biotechnology Co., Ltd.. The device was approved on November 07, 2019.
This page provides complete registration details including registrant information, province location (Hebei), 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.