Publish Time: 2026-02-09 Origin: Bioteke
The SARS-CoV-2/Flu A/Flu B/RSV/ADV/HMPV antigen rapid test kit from BIOTEKE is a 6-in-1 point-of-care solution designed to detect six common respiratory viruses from a single swab. Delivering reliable, easy-to-read results in 10–20 minutes, this multiplex antigen rapid test is built for clinics, pharmacies, hospitals and distributors who need faster triage, simpler inventory, and clear regulatory documentation.
What it detects: Simultaneous viral antigen detection for SARS-CoV-2, Influenza A, Influenza B, Respiratory Syncytial Virus (RSV), Adenovirus (ADV), and Human Metapneumovirus (HMPV).
Time to result: Typically 10–20 minutes at point of care.
Sample types: Nasal swab, opharyngeal swab depending on manufacturer instructions.
Typical users: Primary care clinics, emergency departments, occupational health services, pharmacies, and medical device distributors.
Faster patient triage: Immediate results let clinicians isolate, treat, or refer without waiting for lab PCR.
Operational efficiency: One swab, one cassette, one workflow — less training and fewer handling errors.
Inventory simplicity: One product covers multiple diagnostic needs, lowering warehousing and procurement effort.
Regulatory readiness: CE-marked and manufactured under ISO quality systems; documentation available for tenders and registrations.
OEM & private-label options: Flexible packaging, MOQ, and branding for distributors.
Primary care & urgent care: Rapid triage and immediate patient counseling.
Hospitals & emergency departments: Fast decision support for isolation and bed allocation.
Pharmacy clinics & occupational health: On-site screening for symptomatic employees or customers.
Wholesale & distribution: One-stop solution for resellers serving clinics and care homes.
Public health & outbreak response: Efficient screening during localized respiratory outbreaks where multiplex detection is advantageous.
| Target | SARS-CoV-2 | Influenza A | Influenza B | Respiratory Syncytial Virus | Adenovirus | Human Metapneumovirus |
| Sensitivity | 96.47% | 95.89% | 97.56% | 95.45% | 96.15% | 96.92% |
| Specificity | 100% | 100% | 100% | 100% | 100% | 100% |
| Total coincidence rate | 99.46% | 99.46% | 99.64% | 99.46% | 99.46% | 99.64% |
*All the positive references are positive for the corresponding pathogens, which is consistent with the known results of the reference. All the negative references are negative for the corresponding pathogen.
* The width of the membrane strip of the kit is not less than 2.5mm, and the liquid migration speed is not less than 10 mm/min.
*For detailed clinical study datasheet, please refer to the user instructions.
| Attribute | Specification (example) |
|---|---|
| Method | Immunochromatographic Assay |
| Time to result | 10–20 minutes |
| Sample type | Nasal & opharyngeal swab |
| Pathogens | SARS-CoV-2, Flu A, Flu B, RSV, ADV, HMPV |
| Storage Condition | 2-30℃ |
| Shelf life | 24 months |
| Packaging | 1 / 20 tests per box (configurable) |
| Certifications | IVD-CE; ISO-manufactured |
| OEM | Private-label/OEM options available |
This multiplex antigen rapid test kit is designed to simultaneously detect six common respiratory viruses: SARS-CoV-2 (COVID-19), Influenza A, Influenza B, RSV, Adenovirus (ADV), and Human Metapneumovirus (HMPV) from a single patient sample.
Results are typically available within 10–20 minutes, making the test ideal for point-of-care use in clinics, pharmacies, emergency departments, and screening settings.
Most SARS-CoV-2/Flu A/Flu B/RSV/ADV/HMPV antigen rapid test kits support nasal swabs or nasopharyngeal swabs. Always follow the manufacturer’s instructions for approved sample types and collection methods.
Yes. The test is designed for professional use, offering fast results, simple operation, and minimal equipment requirements. It is widely used in clinics, urgent care centers, pharmacies, and occupational health services.
High-quality kits are typically IVD CE-marked and manufactured under ISO-certified quality systems. Buyers should always confirm regulatory status and local registration requirements before purchasing or distributing the product.
Download the IFU & spec sheet (PDF)
Contact BIOTEKE Sales for registration support and MOQ details.