Roche Rapid Antigen Test. Box of 25


Sensitivity of 96.52% – Specificity of 99.68%
Each test contains:
  • Test device  (individual in foil pouch with desiccant)
  • Extraction buffer tube
  • Nozzle cap
  • Sterile Swab
  • Film (can be attached to the test device when performing outdoor testing)

The COVID-19 Rapid Antigen Test is intended for professional use only.

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8 in stock (can be backordered)

SKU: HS09327592190 Category: Tags: , , ,

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Roche Rapid Antigen Test. Box of 25 (COVID-19 rapid test)

This test is intended to detect antigen from the SARS‑CoV‑2 virus in individuals suspected of COVID‑19.  The test provides results in 15-30 minutes.

Each Roche antigen test contains:
  • Test device  (individual in foil pouch with desiccant)
  • Extraction buffer tube
  • Nozzle cap
  • Sterile Swab
  • Film (can be attached to the test device when performing outdoor testing)
  • Instructions for use and quick reference guide


This pack comes with additional items to support administering  the test:

  • 25 Biohazard waste yellow bags. (BS EN 61340-5-1:2007)


This product is strictly intended for professional use in laboratory and point of care environments.

Coronaviruses can cause a variety of acute and chronic diseases. Common signs of a person infected with coronavirus include respiratory symptoms, fever, cough, shortness of breath, and dyspnea. In more severe cases, infection can cause pneumonia, severe acute respiratory syndrome, kidney failure and even death. The 2019 new coronavirus, or SARS‑CoV‑2, was discovered in 2019 after viral pneumonia cases in Wuhan and a pandemic was declared by the World Health Organisation on March 11, 2020. WHO confirmed that COVID‑19 can cause colds and more serious diseases such as severe acute respiratory syndrome (SARS).

The COVID-19 antigen test is intended for professional use only.

Additional information:

Clinical Performance of the SARS-CoV-2 Rapid test.

The test was found to have a high accuracy, firstly, a sensitivity of 96.52% and secondly a specificity of 99.68%. This was determined from a sample cohort of 426 samples from two independent study centres.

SARS-CoV-2 Rapid test Data sheet

Reading and interpreting results

A coloured line appears in the top section of the results window to show that the test is working properly. This line is the control line (C). Even if the control line is faint or not uniform, the test should be considered to have been performed properly. If no control line is visible the test result should be considered as invalid.

In the case of a positive result, a coloured line appears in the lower section of the result window. This line is the test line of the SARS‑CoV‑2 antigen (T).

Even if the test line is very faint or not uniform the test result should be interpreted as a positive result.

Lateral Flow self-swab video tutorial for healthcare staff

Furthermore, Asymptomatic COVID-19 testing is being made available to all patient-facing healthcare staff.

This short training video provides step-by-step instructions on self-administering a Lateral Flow COVID-19 test. It covers the use of test packs, instructions for individual tests and each step of the evaluation process.

The test itself is quick and relatively easy to use, but please watch the video all the way through before commencing the self-swab process. This will help to ensure the tests are carried out correctly, and the results are as accurate and reliable as possible.




Additional information

Test Type


Sample type

Nasopharyngeal swap

Target antigen

Nucleocapsid (N)

Time to result

15 minutes (Readout window 15 – 30 minutes)

Storage temperature

2 – 30 °C / 36 – 86 °F

Stability (test, opened pouch)

1 hour once the test has been opened


Positive and negative controls are optional components and can be ordered separately

Bio Hazard Waste Bag

• Highly visible printed bag for disposal of medical and
clinical waste
• Compact self-seal bags are an ideal supplement to first aid
• Size: 28x19cm

Where applicable it provides assurance that electrostatic discharge sensitive devices have been handled and packed under conditions that meet the administrative and technical requirements of the ANSI/ESD S20.20:2014 and BS EN 61340-5-1:2007 Electrostatic Control Standards.



Commodity information

HS 38 22 00 00 00


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Roche SARS-CoV-2-Rapid-Antigen-Test-1000x680
Roche Rapid Antigen Test. Box of 25