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Influenza A/B+RSV/ADV+COVID-19/MP Combo Ag Test
Influenza A/B+RSV/ADV+COVID-19/MP Combo Ag Test
Influenza A/B+RSV/ADV+COVID-19/MP Combo Ag Test is the chromatographic assay used for qualitative detection of the Influenza virus type A and B, respiratory syncytial virus (RSV), adenovirus (ADV) ,COVID-19,mycoplasma pneumoniae(MP) antigens in human pharyngeal swab specimen and nasal swab specemen.
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SPECIMEN PREPARATION

1.Remove the foil from the sample collection tube.

2.Pharyngeal swab preparation

2.1.Remove a Pharyngeal swab from the pouch.

2.2. Hold the Pharyngeal swab across the base of the tongue and wipe up and down the posterior pharyeal wall at least 3 times.

3. Nasal swab preparation

3.1. Remove a nasal swab from the pouch.

3.2. Using the sterile swab provided in the kit, carefully insert the swab into one nostril of the patient. The swab tip should be inserted up to 2-4 cm until resistance is met.

3.3. Roll the swab 5 times in a circular motion around the inside wall ensure that both mucus and cells are collected. Using the same swab, repeat this process for the other nostril to ensure that an adequate sample is collected from both nasal cavities.

3.4. Withdraw the swab from the nasal cavity.

4. Both Pharyngeal swab and Nasal swab processed separately in the same collection tube as follows

4.1 Insert the swab in collection tube to the bottom, rotate and squeeze the swab 10 times, while holding the swab head against the bottom and side of the collection tube.

4.2. Rotate and Squeeze the tube several times with fingers from

outside of the tube to immerse the swab. Remove the swab.

5. Attach the dropper tip firmly onto the tube. Mix thoroughly by swirling or flicking the bottom of the tube.


TEST PROCEDURE

Read the instruction first prior to testing.Bring the pouched test to room temperature prior to testing.Do not open the pouch until ready to begin testing.

1.Remove the test from the sealed pouch.Lay it on a flat,clean and dry surface.

2.Place the test cassette on a flat and clean surface. Add 3 drops of test sample by squeezing the collection solution tube into each of the sample well.

3.Read results within 10-15 minutes.

INTERPRETATION OF RESULTS

1.For Influenza A/B Ag Test

 POSITIVE:

Influenza A Positive:Control line (C) and test line T1 appear in the show window.

Influenza B Positive:Control line (C) and test line T2 appear in the show window.

Influenza A+B Positive:Control line (C) and test lines T1, T2 appear in the show window.

NEGATIVE:Only one line appears in control area (C), no line appears in T1 and T2 areas.

INVALID:If no line appears in the control area (C),the test results are invalid regardless of the presence or absence of line in the test area.The direction may not been followed correctly or the test may be deteriorated.It is recommended that repeat the test using a new device.If the problem persist,please stop using the product and contact local distributor.

2.For RSV/ADV Ag Test

POSITIVE:

RSV Positive:Control line (C) and test line T1 appear in the show window.

ADV Positive:Control line (C) and test line T2 appear in the show window.

RSV+ADV Positive:Control line (C) and test lines T1, T2 appear in the show window.

NEGATIVE:Only one line appears in control area (C), no line appears in T1 and T2 areas.

INVALID:If no line appears in the control area (C),the test results are invalid regardless of the presence or absence of line in the test area.The direction may not been followed correctly or the test may be deteriorated.It is recommended that repeat the test using a new device.If the problem persist,please stop using the product and contact local distributor.

 3.For COVID-19/MP Ag Test

POSITIVE:

COVID-19 Positive:Control line (C) and test line T1 appear in the show window.

MP Positive:Control line (C) and test line T2 appear in the show window.

COVID-19+MP Positive:Control line (C) and test lines T1, T2 appear in the show window.

NEGATIVE:Only one line appears in control area (C), no line appears in T1 and T2 areas.

INVALID:If no line appears in the control area (C),the test results are invalid regardless of the presence or absence of line in the test area.The direction may not been followed correctly or the test may be deteriorated.It is recommended that repeat the test using a new device.If the problem persist,please stop using the product and contact local distributor.

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