Pure Global AI
China NMPA legacy archive 吉械注准20252400066

Carcinoembryonic Antigen Determination Reagent Kit (Chemiluminescent Immunoassay Method)

癌胚抗原测定试剂盒(化学发光免疫分析法)
Dirui Industrial Co., Ltd.Class IINMPAApproved January 24, 2025
Static archiveNMPA · legacy registration snapshot
Device classification
Device class
Class II
Model specifications
1×50 test/box; 1×50 test/box (excluding calibrators and quality controls); 2×50 tests/box; 2×50 test/box (excluding calibrators and quality controls); 1×100 tests/box; 1×100 tests/box (excluding calibrators and quality controls); 2×100 tests/box; 2×100 tests/box (excluding calibrators and quality controls); 4×100 tests/box; 4×100 tests/box (excluding calibrators and quality controls); 1×200 tests/box; 1×200 tests/box (excluding calibrators and quality controls); 2×200 tests/box; 2×200 tests/box (excluding calibrators and quality controls).
1×50测试/盒;1×50测试/盒(不含校准品、质控品); 2×50测试/盒;2×50测试/盒(不含校准品、质控品); 1×100测试/盒;1×100测试/盒(不含校准品、质控品); 2×100测试/盒;2×100测试/盒(不含校准品、质控品); 4×100测试/盒;4×100测试/盒(不含校准品、质控品); 1×200测试/盒;1×200测试/盒(不含校准品、质控品); 2×200测试/盒;2×200测试/盒(不含校准品、质控品)。
Approval department
Jilin Provincial Drug Administration
吉林省药品监督管理局
Registration information
Registration number
吉械注准20252400066
Approval date
January 24, 2025
Expiry date
February 03, 2030
Registrant
Name
Dirui Industrial Co., Ltd.
迪瑞医疗科技股份有限公司
Province/Region
Jilin
吉林
Address
No. 95, Yunhe Street, Changchun High-tech Industrial Development Zone
长春市高新技术产业开发区云河街95号
Production facility
Production address
长春市高新技术产业开发区云河街95号
Intended use
English

用于体外定量检测人血清或血浆中癌胚抗原(CEA)的含量。主要用于对恶性肿瘤患者进行动态监测以辅助判断疾病进程或治疗效果,不能作为恶性肿瘤早期诊断或确诊依据,不用于普通人群的肿瘤筛查。

Structure and composition
English

Reagent 1, Reagent 2, Reagent 3, Calibrator (high value, low value), Quality control (level 1, level 2). (Please refer to the manual for details)

中文

试剂1、试剂2、试剂3、校准品(高值、低值)、质控品(水平1、水平2)。(具体内容详见说明书)

Additional information
Appendix
产品技术要求
About this record

This static archive preserves historical registration fields and translations for Carcinoembryonic Antigen Determination Reagent Kit (Chemiluminescent Immunoassay Method), registration 吉械注准20252400066. It does not establish current authorization or complete current product details.

The default China search uses the separately verified domestic-registration listing, checked daily. Its published listing fields and scope differ from this older snapshot.