Ecotest Flu A/B + COVID Rapid Antigen Test Pen

Point of care viral Flu RAT testing made easy
Reliable results in only 15 minutes

The Ecotest Influenza A/B + COVID-19 Rapid Antigen Nasal Test is developed for point of care use. Negative results do not exclude the possibility of COVID-19 or Influenza A/B infection, and government health advice should be followed as well as taking protective measures including social distancing and wearing face masks when administering tests.

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Ready for Point of Care use

Easy to use

The only Flu/Covid two-step RAT  test on the Australian market makes Flu and COVID testing as simple a quick nasal swab, followed by popping the test pen into the buffer cap. No more messing around with solutions or cassettes. It’s fast, simple and safe.

Up to date with strains

Developed to test for the most current Influenza A/B strains in the Southern hemisphere as well as COVID-19, it’s a simple rapid test that offers a lot of information.

Accurate and reliable

With an impressive 99% accuracy, this fully self-contained testing mechanism is easy to store and administer to even sensitive or young patients, while minimising risk of cross-contamination.

A 3-in-1 test designed for convenience 

Ecotest Flu A+B & Covid-19 Tests feature a patented design and are convenient to store, stack or display, as well as easy to use and dispose of. Our flu RAT tests are ideal for government, corporate or private applications, and are available for delivery in custom order quantities of 5 and 20 packs, to suit your distribution needs.

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Convenient 3-in-1 Influenza & Covid testing

Designed to be non-invasive and easy to self-administer, the Ecotest Flu A+B & Covid-19 RAT Test Pen’s patented two-step design streamlines the process of testing for common seasonal viruses (SARS-CoV-2, Influenza A, and Influenza B). Test by swabbing your nose, then placing the pen into its buffer cap, and reading results in 15 minutes. No need for extra components, or mixing reagents: it’s as easy as that.

Each 20PK Point of Care test kit includes the following:

- 20 Individually packaged Flu + Covid Rapid Antigen tests in foil wrappers with desiccant
- 1 packaged insert for the Rapid Antigen Test
- 1 positive external control swab
- 1 negative external control swab
- 2 single buffer pouches for external control
- 1 package insert for external control

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Two-step procedure

STEP 1. Remove the Flu test protector and insert the nasal collector into a nostril. Rotate the collector 5 times against the nasal wall. Repeat in other nostril.

STEP 2. Place the Flu A/B test device vertically into the tube with the extraction buffer. Ensure the top of the base aligns to the middle of the supporting line.

NOTE: Wait 15 minutes, then check your results flu RAT results. Do not read results after 30 minutes, as they will be invalid.

Results interpretation (COVID) 

COVID Positive

Two coloured bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).

COVID Negative

Body: Only one coloured band appears in the control region (C). No apparent coloured band appears in the test region (T).

Invalid

Control band fails to appear. Results from any test which has not produced a control band at the specified read time must be discarded. 

Results interpretation (Influenza A+B)

Influenza A
Positive

One coloured band appears in the control region (C), and another coloured band in region (A).

Influenza B
Positive

One coloured band appears in the control region (C), and another coloured band in region (B).

Influenza A+B
Positive

One coloured band appears in the control region (C), and two other coloured bands appear in both region (A) and region (B).

Influenza A+B Negative

 Only one coloured band appears in the control region (C), and band appears neither in region (A) nor region (B). 

Invalid

 No coloured band appears in the control region (C), whether a test band(s) is present or not. Repeat invalid tests with a new sample, new test device and reagent.

COVID, Influenza A+B  test specifications

Assay formatLateral flow
TypePen
Testing time15 minutes to results; maximum 30 minutes
AntigenNucleocapsid protein (N)
Sample materialNasopharyngeal swab
ReagentsTBC

Clinical evaluation

COVID sensitivity96.0% (92.3%~98.0%)
COVID specificity96.0% (92.3%~98.0%)
Influenza A sensitivity96.1% (90.4%~98.5%)
Influenza A specificity99.5 % (98.5%~99.8%)
Influenza B sensitivity94.0 % (86.8%~97.4%)
Influenza B specificity99.7 % (98.8%~99.9%)

About Biolink

Global Clientele

International supplier of rapid antigen tests to government and multi-industry clients

End-to-end

Access to global supply networks and technologies to support your brand

Rapid & Reliable

Rapid and reliable shipping and logistics to support your network and supply chain

Versatile

Experts in at-home and point-of-care rapid testing across Europe, Australia, and North America

Easy

Straightforward ordering and distribution processes, with 24-hour global support channels

Safe

We work with specialists in user-friendly rapid antigen pens and cassettes for various diseases

Downloads

Instructions for use

Download the comprehensive instructions guide to using the Ecotest Influenza A/B + COVID-19 Antigen Nasal Test.

Download instructions →

Result reference sheet

Download a detailed description of how to read Ecotest Influenza A/B + COVID-19 Antigen Nasal Test results.

Download reference sheet →

Product brochure

Download our product brochure, which includes details and features of the Ecotest Influenza A/B + COVID-19 Antigen Nasal Test.

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FAQ

More details

Made for convenience

Our pens are designed to be used in scenarios that don't allow for the easy mixing of reagents or buffer solutions. This makes it ideal for use in locations like schools, workplaces, day-cares, or hospitals, where it may be hard or inconvenient to perform a cassette style test. Just as quick and accurate as other RATs; but an easier, more comfortable user experience.

Summary of use

The Influenza A/B + COVID-19 Antigen Nasal Test Kit is an in-vitro immunoassay intended for the qualitative detection of antigens in nasal swab specimens from patients with COVID-19, and/or Influenza A/B (within first 4 days of symptom onset). This test doesn't discriminate between SARS-coronavirus and SARS-CoV-2 (COVID-19).

Precautions for use

The test is intended for point-of-care use; and not intended for home testing (or self-testing). It obtains a preliminary result only, to aid diagnosis of COVID-19, and Influenza A/B. Please note that negative results do not preclude viral infections—test results should not be the sole basis for treatment or other management decisions.