Multiplex Respiratory Rapid Test Kit 6 in 1
One nasopharyngeal swab. Six respiratory pathogen targets. The ECOTEST FLU A/FLU B/RSV/ADV/MP/COVID-19 Combo Test supports rapid, qualitative antigen screening for SARS-CoV-2, Influenza A and B, RSV, Adenovirus, and Mycoplasma pneumoniae—with visual results read in 15 minutes.
ECOTEST reference MI-S46001 · Intended for healthcare professionals; not for self-testing.
Schematic for layout orientation only, not a clinical result or a photograph of the product. Refer to the package insert for result interpretation.
Six Pathogen Targets in One Rapid Combo Test
Overlapping respiratory symptoms can have different infectious causes. This four-strip immunoassay qualitatively screens for five viral targets and one bacterial target from a nasopharyngeal swab to support clinical assessment.
SARS-CoV-2 (COVID-19)
Detects SARS-CoV-2 antigen in a dedicated COVID-19 test strip, with a separate procedural control line.
Influenza A (Flu A)
Detects Influenza A antigen on the combined influenza strip. A and B result regions are read separately.
Influenza B (Flu B)
Detects Influenza B antigen independently of Influenza A. Both influenza target bands may appear together.
Respiratory Syncytial Virus
RSV antigen is read within the shared RSV/ADV strip, with distinct regions for each viral target.
Adenovirus (ADV)
Detects respiratory Adenovirus antigen on the dual RSV/ADV strip without combining the two target readings.
Mycoplasma pneumoniae (MP)
Detects M. pneumoniae antigen on its own strip. This target is bacterial, unlike the five viral targets.
Clinical Performance by Target
Manufacturer IFU · Relative to PCR / RT-PCR| Respiratory Target | Relative Sensitivity | Relative Specificity | Overall Agreement | Study Samples |
|---|---|---|---|---|
| COVID-19 | 97.7% | 98.3% | 98.1% | 309 |
| Influenza A | 96.1% | 99.2% | 98.5% | 344 |
| Influenza B | 95.4% | 98.9% | 98.3% | 344 |
| RSV | 96.2% | 97.7% | 97.4% | 383 |
| Adenovirus (ADV) | 95.2% | 96.8% | 96.3% | 383 |
| Mycoplasma pneumoniae (MP) | 90.9% | 99.5% | 96.6% | 295 |
4-Step Respiratory Rapid Test Procedure
The following summary follows the MI-S46001 manufacturer's instructions. Trained personnel must consult the complete IFU before testing.
Collect the Swab
Obtain a nasopharyngeal specimen using the appropriate synthetic-fibre, plastic-shaft swab. Process as soon as possible after collection.
Extract the Sample
Place the swab in the extraction buffer. Rotate it while squeezing the lower tube 10–15 times. Remove the swab, squeezing out retained liquid, then fit the nozzle.
Load All Four Wells
Place the test device on a clean, flat surface. Add 3 drops of extracted solution into each sample well, as specified in the IFU.
Read at 15 Minutes
Read the COVID-19, Flu A/B, RSV/ADV and MP strips at 15 minutes. Do not interpret test results after 30 minutes.
Understand the Four Result Windows
Every strip has its own control region (C). Target lines must be interpreted within the appropriate COVID-19, Flu A/B, RSV/ADV or MP strip.
Visual Result Guide
Apply these principles separately to each of the four strips.
A visible C band plus a band in a relevant target position (COV, Flu A, Flu B, RSV, ADV or MP). Flu A/B and RSV/ADV may each show two target bands.
The relevant strip shows its C band with no target band. A negative result does not exclude infection.
If a strip's C band does not appear, its result is invalid, even if another band is visible. Follow the IFU's repeat-test instructions.
Interpretation & Clinical Limits
A screening result is not a stand-alone clinical diagnosis.
The Flu A and Flu B regions are interpreted separately; so are RSV and ADV. Each of the four strips has a procedural control line.
Any visible shade of a target band at the specified read time should be treated as positive, as directed by the manufacturer.
Review symptoms, exposure history and other laboratory findings. Negative results may require confirmation by molecular methods.
Do not read or reinterpret the cassette after the manufacturer’s 30-minute limit.
Materials Listed in the Manufacturer's Kit
The supplied IFU identifies these components. Box counts and fixed shelf life are not specified in the document.
Required but not supplied in the IFU: clock/timer/stopwatch and transfer pipette. Confirm exact sales pack configuration with QuRapid before ordering.
Frequently Asked Questions
Need the manufacturer's IFU, evaluation data or a wholesale quotation for a UAE clinic, hospital or laboratory? Contact QuRapid to confirm availability and pack configuration.
Contact Product SupportWhich six pathogens can the Respiratory Rapid Test Kit 6 in 1 detect?
The test detects antigens from SARS-CoV-2 (COVID-19), Influenza A, Influenza B, Respiratory Syncytial Virus (RSV), Adenovirus (ADV), and Mycoplasma pneumoniae (MP). Mycoplasma pneumoniae is a bacterium; the other five targets are viruses.
What sample is required for the 6-in-1 respiratory combo test?
The manufacturer specifies a nasopharyngeal swab specimen. The kit is intended for professional in vitro diagnostic use only.
How long does the six-in-one respiratory antigen test take?
Read the result at 15 minutes and do not interpret it after 30 minutes, as directed in the manufacturer's instructions for use.
How much sample extract is needed?
After swab extraction, dispense three drops of prepared solution into each of the test device's four sample wells, following the manufacturer's instructions for use.
Can a negative rapid test exclude respiratory infection?
No. A negative antigen test does not rule out infection. A clinician should interpret the result alongside symptoms and other findings, with molecular confirmation when indicated.
How should the Respiratory Rapid Test Kit 6 in 1 be stored?
Store unused kits at 2–30°C without freezing. Follow the labelled expiry date; the supplied instructions do not specify a uniform fixed shelf life or number of tests per box.
Equip Your Laboratory with the Respiratory 6-in-1 Combo Test
Request professional supply information for the ECOTEST MI-S46001 respiratory antigen kit from QuRapid UAE. Ask for current quotation, sales pack configuration and product documentation.