This COVID-19 Antigen Test Kit (FDA EUA Approved) is a rapid, accurate, and reliable test for the detection of SARS-CoV-2, the virus that causes COVID-19. This test is designed to detect the presence of the virus in the upper respiratory tract and is intended for use in individuals who are suspected of having an active COVID-19 infection.
The test is easy to use and provides results in as little as 15 minutes. The test kit includes a nasal swab, a sample collection tube, and a test cassette. The nasal swab is used to collect a sample from the upper respiratory tract, which is then placed into the sample collection tube. The sample is then added to the test cassette, which contains a reagent that reacts with the virus if it is present. The results are then read from the test cassette, with a positive result indicating the presence of the virus.

The COVID-19 Antigen Test Kit (FDA EUA Approved) is highly accurate, with a sensitivity of 97.2% and a specificity of 99.6%. It is also easy to use, with minimal training required. The test is also cost-effective, making it an ideal choice for screening large numbers of people. Overall, the COVID-19 Antigen Test Kit (FDA EUA Approved) is an accurate, reliable, and cost-effective way to detect the presence of SARS-CoV-2 in individuals who are suspected of having an active COVID-19 infection.

     FDA EUA Approved (No. EUA240006)

Stay ahead of the curve and ensure your health with our latest Tyfast Flu A/B & COVID-19 Multiplex Rapid Home Test Kit (OTC options). This state-of-the-art rapid test empowers you to quickly check for both flu (A & B) and COVID-19 infection from the comfort of your home in just 10 minutes. Perfect for anyone experiencing symptoms of respiratory diseases, our kit offers peace of mind with swift and accurate results.

• Enjoy Fast Results: Get clear answers fast, enabling you to take the next steps sooner.
• Multi Target: Taking control of your health has never been easier or more convenient. Get fast, accurate, and reliable results, and stay one step ahead of flu and COVID-19.
• Rely on Precision: Trust in the clinical accuracy that accurately detects flu and COVID-19 antigens, giving you the certainty you need.
• User-Friendly: Our simple, straightforward design makes at-home testing a breeze, no matter where you are.
• Nasal Swab

INTENDED USE
Monkeypox Virus Antigen Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of monkeypox virus antigen in human rash exudates and blood samples.

MATERIALS PROVIDED
•    Monkeypox Virus Ag Test
•    Instructions Sheet
•    Pipette
•    Swab
•    Treatment tube containing sample treatment solution
•    Buffer solution

INTENDED USE
Monkeypox Virus IgM/IgG Ab Test is a lateral flow chromatographic immunoassay used for the qualitative detection of monkeypox virus IgM and IgG antibodies in human whole blood/serum/plasma samples.

MATERIALS PROVIDED
•    Monkeypox Virus IgM/IgG Test
•    Instructions Sheet
•    Buffer solution
•    Pipette
•    Alcohol cotton
•    Sterilized lancet

INTENDED USE
Monkeypox Virus IgM/IgG Ab Test is a lateral flow chromatographic immunoassay used for the qualitative detection of monkeypox virus IgM and IgG antibodies in human whole blood/serum/plasma samples.

MATERIALS PROVIDED
•    Monkeypox Virus IgM/IgG Test
•    Instructions Sheet
•    Buffer solution
•    Pipette
•    Alcohol cotton
•    Sterilized lancet

INTENDED USE:
The saliva collection system is designed for self-contained saliva sample collection which provides critical sample consistency while amplifying, preserving, and protecting transcripts at the point of collection for highly sensitive and highly specific analysis. Sample self-collection using a saliva collection kit provides 100% in-device live viral neutralization in 10 seconds at room temperature, mitigating any risk of exposure for downstream processes. The saliva kits have no special storage or transport temperature-control requirements for collected saliva samples and eliminate the need for UN3373 biohazard shipping designation with clearance from USPS, FedEx, & UPS.

FEATURES:

• First FDA Authorized COVID-19 saliva testing solution
• First FDA Authorized at-home saliva collection device for COVID-19 testing.
• Identify infections at their earliest stage before the onset of symptoms.
• In-device 100% inactivation of the live virus within the device at ambient temps
• Maintains critical bio-sample consistency.
• 99.998% testing accuracy & more sensitive
• No temperature-controlled storage or sample transport
• Post-collection stability with no degradation in sample efficacy
• Process multiple tests from a single collected sample
• Eliminate the need for UN3373 shipping designation.
• Supported system and validated testing process.
• At-home and direct-to-patient fulfillment
• simplicity and effectiveness of saliva collection devices have delivered a new standard of care for patients and laboratories.