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C-Reactive Protein/Serum Amyloid A (CRP/SAA) Dual Test Kit (Quantum Dot Fluorescence Immunoassay) - NMPA Registration 粤械注准20232400713

Access comprehensive regulatory information for C-Reactive Protein/Serum Amyloid A (CRP/SAA) Dual Test Kit (Quantum Dot 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 粤械注准20232400713 and owned by Labnovation Technologies,inc.. The device was approved on April 25, 2023.

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20232400713
C-Reactive Protein/Serum Amyloid A (CRP/SAA) Dual Test Kit (Quantum Dot Fluorescence Immunoassay)
C反应蛋白/血清淀粉样蛋白A(CRP/SAA)二合一测定试剂盒(量子点荧光免疫法)
NMPA Registration Number: 粤械注准20232400713
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Intended Use
English

It is suitable for the quantitative detection of C-reactive protein (CRP) and serum amyloid A (SAA) in human serum in vitro clinically, mainly as a non-specific inflammatory index.

中文

适用于临床体外定量检测人血清中的C反应蛋白(CRP)和血清淀粉样蛋白A(SAA)的含量,主要作为一种非特异性炎症指标。

Device Classification
Device Class
Class II
Model Specifications
20 servings/box, 50 servings/box
20人份/盒、50人份/盒
Approval Department
Guangdong Provincial Drug Administration
广东省药品监督管理局
Registration Information
Registration Number
粤械注准20232400713
Approval Date
April 25, 2023
Expiry Date
April 24, 2028
Registrant
Name
Labnovation Technologies,inc.
深圳市雷诺华科技实业有限公司
Province/Region
Guangdong
广东
Address
102, 602, 702, 802, 802, Shenghui Red Star Innovation Plaza, Tianliao Community, Yutang Street, Guangming District, Shenzhen
深圳市光明区玉塘街道田寮社区同仁路盛荟红星创智广场102、602、702、802
Production Facility
Production Address
广东省深圳市光明区玉塘街道田寮社区同仁路盛荟红星创智广场602、702、802
Structure and Composition
English

The kit is mainly composed of a test card, sample diluent, and IC card (optional). Thereinto: 1. The test card is composed of test strips and plastic card shells. The main components on the test strip are: marking pad, nitrocellulose membrane, absorbent paper, PVC board. Nitrocellulose membrane coated with murine anti-human CRP monoclonal antibody, mouse anti-human SAA monoclonal antibody and sheep anti-rabbit IgG; The labeling pad mainly contains fluorescently labeled murine anti-human CRP monoclonal antibody, murine anti-human SAA monoclonal antibody and rabbit IgG. 2. The main components of the sample diluent are Tris buffer and surfactant. 3. IC card mainly provides the calibration curve of each batch of reagents.

中文

试剂盒主要由检测卡、样本稀释液、IC卡(选配)组成。其中: 1.检测卡由试纸条、塑料卡壳组成。试纸条上的主要成分有:标记垫、硝酸纤维素膜、吸水纸、PVC板。硝酸纤维素膜包被有鼠抗人CRP单克隆抗体、鼠抗人SAA单克隆抗体和羊抗兔IgG;标记垫上主要有荧光标记的鼠抗人CRP单克隆抗体、鼠抗人SAA单克隆抗体和兔IgG。 2.样本稀释液主要成分为Tris缓冲液及表面活性剂。 3.IC卡主要提供每批试剂的校准曲线。

Storage Conditions and Expiration
English

The kit is stored at 2~30 °C in the dark, moisture-proof and avoided heavy pressure, and the validity period is 18 months; After the detection card foil bag is opened, it should be used as soon as possible within 1 hour under the condition of 18-28 ° C and 40-60% humidity.

中文

试剂盒于2~30℃避光、防潮保存并避免重压,有效期为18个月; 检测卡铝箔袋开封后,在18-28℃,40-60%湿度条件下,应在1小时内尽快使用。

Additional Information
Remark
本文件与“粤械注准20232400713”注册证共同使用。
Changes
2023-06-16: 1、注册人住所由“深圳市光明区凤凰街道塘家社区光明高新区十八号路68号1栋101及5楼”变更为“深圳市光明区玉塘街道田寮社区同仁路盛荟红星创智广场102、602、702、802”。 2、生产地址由“深圳市光明区凤凰街道塘家社区光明高新区十八号路68号1栋5楼”变更为“广东省深圳市光明区玉塘街道田寮社区同仁路盛荟红星创智广场602、702、802”。
Appendix
产品技术要求、说明书