STD Rapid Test Kits | HIV, Syphilis, HPV 16/18, Chlamydia Detection
Advanced Rapid Diagnostic Solutions for Sexually Transmitted Diseases (STDs)
Accurate and timely diagnosis of sexually Transmitted Diseases (STDs) is a critical component of public health screening and effective patient management. Our STD Rapid Test Series offers a comprehensive range of professional-grade diagnostic tools designed for the qualitative detection of key bacterial, viral, and fungal pathogens. From highly specific antigen detection (such as HPV E7/L1 and Chlamydia Ag) to sensitive antibody screening (including HIV Ag/Ab P24 and Syphilis TPHA), these assays provide actionable results within minutes.
STD (Sexually Transmitted Disease) Rapid Test Series Specifications
| Category | Product Name / Target Marker | Specimen Type |
| Vaginitis Panel | Candida Albicans Ag | Vaginal Secretion |
| Vaginitis Panel | Gardnerella Ag | Vaginal Secretion |
| Vaginitis Panel | Trichomonas Vaginalis Ag | Vaginal Secretion |
| Vaginitis Combo | 3-in-1 (Candida / Trichomonas / Gardnerella) | Vaginal Secretion |
| Bacterial STIs | NG (Neisseria Gonorrhoeae) Ag | Cervical / Urethral Swab |
| Bacterial STIs | Chlamydia Trachomatis Ag | Cervical / Urethral Swab |
| Syphilis | TPHA (Syphilis Ab) | Serum (S) / Plasma (P) |
| HPV Screening | HPV 16/18 Ag | Cervical Swab / Urine |
| HPV Advanced | Combo HPV 16/18 / L1 Ag | Cervical Swab |
| HPV Oncology | Combo HPV E7 / L1 Ag | Cervical Swab |
| HIV Screening | HIV Ab (HIV 1/2) | S / P / Whole Blood (WB) |
| HIV Advanced | 4th Gen HIV Ag/Ab (P24 + HIV 1/2) | S / P |
| Multi-Panel | 4-in-1 (HBsAg / HCV / HIV / Syphilis) | S / P |
Key Clinical Applications
Comprehensive Screening: Ideal for initial screening in clinical settings, community health centers, and diagnostic laboratories.
Point-of-Care Testing (POCT): Enables rapid decision-making in acute situations or resource-limited environments.
Outbreak Management: Essential for managing outbreaks of infections like Gonorrhea and Chlamydia through efficient contact tracing.
Vertical Transmission Prevention: Crucial for prenatal screening to prevent parent-to-child transmission of HIV, Syphilis, and Hepatitis B.
Integrated Combo & Panel Solutions
To streamline clinical workflows and optimize diagnostic efficiency, we offer specialized combination tests:
HBsAg/HCV/HIV/Syphilis Combo: A powerful 4-in-1 panel for concurrent screening of major blood-borne pathogens.
Vaginal Secretion 3-in-1: Simultaneously detects Candida albicans, Trichomonas vaginalis, and Gardnerella Ag for comprehensive vaginitis screening.
HPV E7/L1 Ag Combo: Utilizes advanced biomarker detection to assess the risk of progression from HPV infection to cervical precancer.
Technical Performance & Quality Assurance
High Sensitivity & Specificity: Formulated to achieve minimal cross-reactivity and maximal correlation with established molecular diagnostics (e.g., PCR).
Multiple Specimen Compatibility: Tests are validated for a diverse range of samples, including Whole Blood (WB), Serum (S), Plasma (P), Urine, and Swabs.
Visual Interpretation: Clear, easily interpretable results that require no instrumentation, suitable for various settings.
Professional Compliance: Manufactured under ISO 13485 quality management systems and are CE approved for international distribution for professional IVD use.
STD Rapid Diagnostic Solutions - FAQ
1. What types of sexually transmitted infections (STIs) can these rapid kits detect?
Our range covers bacterial (Chlamydia, Gonorrhea, Syphilis), viral (HIV 1/2, HPV 16/18), and fungal (Candida albicans) pathogens, as well as parasitic infections like Trichomonas vaginalis.
2. How does the Vaginal Secretion 3-in-1 combo test benefit clinical diagnosis?
The 3-in-1 combo kit allows for the simultaneous detection and differentiation of Candida albicans, Trichomonas vaginalis, and Gardnerella from a single vaginal secretion specimen, streamlining vaginitis screening.
3. What is the clinical advantage of the HIV Ag/Ab (P24+HIV 1/2) combo test?
This 4th Generation HIV test detects both the P24 antigen (appearing early in acute infection) and antibodies to HIV 1/2, significantly shortening the diagnostic window compared to antibody-only tests.
4. Can the HPV 16/18 Ag rapid test be performed using urine samples?
Yes, our HPV 16/18 Ag kit is validated for both cervical swabs and urine specimens, providing a non-invasive option for high-risk HPV screening.
5. What is the difference between the HPV 16/18/L1 Ag and HPV E7/L1 Ag combo tests?
The HPV 16/18/L1 Ag focuses on viral presence and replication, while the HPV E7/L1 Ag combo assesses the oncoprotein E7, which is a key biomarker for the risk of progression to cervical precancer.
6. Which specimens are required for Chlamydia and Gonorrhea (NG) antigen tests?
These tests are optimized for female cervical swabs and male urethral swabs to ensure high sensitivity in detecting active bacterial infections.
7. Is the TPHA (Syphilis Ab) test compatible with whole blood?
The TPHA (Syphilis Ab) rapid test is specifically designed for use with human Serum (S) or Plasma (P) to provide highly specific qualitative antibody detection.
8. How accurate are these rapid STD tests compared to laboratory PCR methods?
While PCR is the gold standard, our lateral flow assays are engineered for high correlation with molecular methods, offering a rapid, cost-effective primary screening solution with reliable sensitivity.
9. Does the HIV Ab (1/2) test differentiate between HIV Type 1 and Type 2?
The kit qualitatively detects antibodies to both types; however, it provides a combined "HIV 1/2 Positive" result and does not differentiate between the two specific strains.
10. What is included in the HBsAg/HCV/HIV/Syphilis 4-in-1 combo panel?
This multi-pathogen panel allows for the concurrent screening of HIV and Syphilis along with major blood-borne viral markers, using a single serum or plasma specimen.
11. Are specialized instruments needed to interpret the results of these STD tests?
No, these are manual, visual immunoassay tests. Results appear as distinct colored lines within 15–20 minutes and require no additional laboratory equipment.
12. Are these STD diagnostic kits intended for home or over-the-counter use?
No, these products are designed for professional laboratory and clinical use only, ensuring they are administered by trained healthcare providers.
13. What are the storage requirements for these rapid diagnostic cassettes?
The kits should be stored at temperatures between 2°C and 30°C in their original sealed foil packaging to maintain stability and accuracy.
14. Do you provide OEM or private labeling services for STD test kits?
Yes, we offer comprehensive OEM and customized packaging solutions for global distributors and large-scale public health screening programs.
15. Are these STD diagnostic products CE certified?
Yes, all our STD rapid test kits are CE approved and manufactured under ISO 13485 international quality management standards for medical devices.
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