【Medical Device Registration Certificate No. / Product Technical Requirement No.】: National Instrument Registration Permit 20183401728
【Intended Use】: This kit uses highly specific antibody-antigen reactions and immunochromatographic analysis technology to qualitatively detect the presence of Neisseria gonorrhoeae antigens in clinical reproductive tract specimens. It is suitable for rapid detection of gonorrhea and is especially useful for physical examinations or mass population screening.
Storage and validity: Store at 2-30°C in a cool, dark place; shelf life is 24 months.
Specimen: Secretion
Specification: 20T / Kit
Cat. No.: SNG-502
Format: Cassette
Brief Description:
1. Simple and quick operation, no additional instruments required;
2. Direct and rapid qualitative detection, with results in 10-15 minutes;
3. Clear and straightforward results, accurate and reliable;
4. Stable at room temperature with a long shelf life, facilitating storage and transportation.