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Gastrin-releasing peptide precursor (proGRP) assay kit (chemiluminescence immunoassay with magnetic microspheres) - NMPA Registration 粤械注准20242401373

Access comprehensive regulatory information for Gastrin-releasing peptide precursor (proGRP) assay kit (chemiluminescence immunoassay with magnetic microspheres) in the China medical device market through Pure Global AI's free database. This Class II medical device is registered under NMPA registration number 粤械注准20242401373 and owned by Shenzhen AmTech Bioengineering Ltd,Inc. The device was approved on October 16, 2024.

This page provides complete registration details including registrant information, province location (Guangdong), 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.

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Class II
粤械注准20242401373
Gastrin-releasing peptide precursor (proGRP) assay kit (chemiluminescence immunoassay with magnetic microspheres)
胃泌素释放肽前体(proGRP)测定试剂盒(磁微粒化学发光法)
NMPA Registration Number: 粤械注准20242401373
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Pricing
Intended Use
English

用于体外定量测定人血清中胃泌素释放肽前体(proGRP)的含量,临床上用于小细胞肺癌(SCLC)的治疗监测.不能作为恶性肿瘤早期诊断或确诊的依据,不宜用于普通人群的肿瘤筛查.

中文

用于体外定量测定人血清中胃泌素释放肽前体(proGRP)的含量,临床上用于小细胞肺癌(SCLC)的治疗监测。不能作为恶性肿瘤早期诊断或确诊的依据,不宜用于普通人群的肿瘤筛查。

Device Classification
Device Class
Class II
Model Specifications
50人份/盒、100人份/盒、2×100人份/盒、5×100人份/盒、校准品:2×1 mL(2个水平,选配)、质控品:2×1 mL(2个水平,选配).
50人份/盒、100人份/盒、2×100人份/盒、5×100人份/盒、校准品:2×1 mL(2个水平,选配)、质控品:2×1 mL(2个水平,选配)。
Approval Department
Guangdong Provincial Drug Administration
广东省药品监督管理局
Registration Information
Registration Number
粤械注准20242401373
Approval Date
October 16, 2024
Expiry Date
October 15, 2029
Registrant
Name
Shenzhen AmTech Bioengineering Ltd,Inc
深圳上泰生物工程有限公司
Province/Region
Guangdong
广东
Address
901, Building A1A2, Building A1, Building A1, Guangming Science and Technology Park, Phoenix Community Tourist Road, Guangming District, Shenzhen
深圳市光明区凤凰街道凤凰社区观光路招商局光明科技园A1A2栋A1栋901
Production Facility
Production Address
深圳市光明区凤凰街道凤凰社区观光路招商局光明科技园A1A2栋A1栋901、1001、1101
Structure and Composition
English

试剂盒由试剂盒由链霉亲和素磁珠试剂、吖啶标记物试剂、生物素化胃泌素释放肽前体试剂、校准品(选配)、质控品(选配)组成,主要成分如下: 1.链霉亲和素磁珠试剂:Tris, BSA,链霉亲和素包被的磁珠. 2.吖啶标记物试剂:PBS,BSA,吖啶标记的胃泌素释放肽前体单克隆抗体(鼠源). 3.生物素化胃泌素释放肽前体试剂:PBS, BSA,生物素化胃泌素释放肽前体单克隆抗体(鼠源). 4.校准品(2个水平,选配)、质控品(2个水平,选配):PBS, BSA,胃泌素释放肽前体抗原(大肠杆菌重组表达).

中文

试剂盒由试剂盒由链霉亲和素磁珠试剂、吖啶标记物试剂、生物素化胃泌素释放肽前体试剂、校准品(选配)、质控品(选配)组成,主要成分如下: 1.链霉亲和素磁珠试剂:Tris, BSA,链霉亲和素包被的磁珠。 2.吖啶标记物试剂:PBS,BSA,吖啶标记的胃泌素释放肽前体单克隆抗体(鼠源)。 3.生物素化胃泌素释放肽前体试剂:PBS, BSA,生物素化胃泌素释放肽前体单克隆抗体(鼠源)。 4.校准品(2个水平,选配)、质控品(2个水平,选配):PBS, BSA,胃泌素释放肽前体抗原(大肠杆菌重组表达)。

Storage Conditions and Expiration
English

本试剂盒在2~8℃避光贮存,禁止冷冻,有效期为12个月.试剂开封后在机2~15℃可稳定28天.校准品和质控品在2~8℃避光贮存,有效期为12个月.校准品、质控品开瓶后20~25℃可稳定4小时;2~8℃可稳定28天.

中文

本试剂盒在2~8℃避光贮存,禁止冷冻,有效期为12个月。试剂开封后在机2~15℃可稳定28天。校准品和质控品在2~8℃避光贮存,有效期为12个月。校准品、质控品开瓶后20~25℃可稳定4小时;2~8℃可稳定28天。

Additional Information
Appendix
产品技术要求、说明书