Antigen Single Test (Nasal or Saliva Swab) - CAS-Envision (5 Tests Minimum Order for €8) SALE
Testing is a vital part in fighting this unprecedented global healthcare emergency. The reliable SARS-CoV-2 Rapid Antigen Nasal/Throat Test provides fast answers wherever you need them.
- Test kit is approved by the EU Health Security Committee (page 41) and CE certified.
Why use SARS-CoV-2 Rapid Antigen Nasal/Throat Test?
- Inexpensive and simple to use
- Test should be operated at the room temperature
- High accuracy, specificity and sensitivity
- No instrument required
- Obtain a quick result within 20 minutes
- No need for a follow-up appointment to discuss result
- Easy handling which does not require specific training
- The kit is used for the qualitative detection of SARS-CoV-2 in vitro diagnostic medical devices for self-testing.
The nasal swabs clinical performance
| Clinical Sensitivity | 97.50 % |
| Clinical Specificity | 99.20 % |
| Total Coincidence Rate | 98.50 % |
The oral and saliva swabs clinical performance
| Clinical Sensitivity | 95.80 % |
| Clinical Specificity | 98.40 % |
| Total Coincidence Rate | 97.10 % |
- Single-used. Single patient only.
- The test should be operated at room temperature（4-30℃).
- EC Certificate, ISO13485
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This item is non-returnable.
Kit Components
- SARS-CoV-2 Antigen Test Device
- Nasal swab
- Collection bag (with 1ml extraction solution)
- Disposable dropper (antigen extraction tube)
- Instructions for Use Kit components
- Test Card should be used right after opening the pouch.
Contact us directly at info@marathonsafetysolutions.ie for bulk pricing
Free, tracked DPD delivery for orders of €35 and more.
Minimum delivery charge, €9.
DELIVERY TIME
Ireland - 24/48 hrs (DPD)
UK - 48/72 hrs via courier
Secure Payment
Refund and Return Policy
Contact Us – Marathon Safety Solutions
Marathon Safety Solutions - Irish owned, Dublin based.
NOTE: Results are for the identification of SARS-CoV-2 nucleocapsid antigen. The positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. The positive results do not rule out bacterial infection or co-infection with other viruses.
The negative results do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions.