Our See Now rapid tests are for in vitro diagnostic of: pregnancy (hCG), fertility (LH), HIV, tumor markers (AFP, PSA), cardiac markers (Troponin), hepatitis,DOA, Syphilis, Gonorrhea and Malaria.
The See Now strips are 50 pieces in a plastic box.
The See Now cassettes are 30 pieces in a plastic box.
Our products are rapid tests for in vitro diagnostics of infectious diseases, tumor markers, cardiac markers, sexually transmited diseases, drugs of abuse, pregnancy.
Our products are delivered in plastic boxes, 30 cassettes or 50 strips in a box.
See now human immunodeficiency virus type 1 and 2 (hiv-1/2) antibody test is a rapid and convenient immunochromatographic in vitro assay. It is used for detection of antibodies to hiv-1/2 in human serum, plasma or whole blood.
Intended Use
Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture.
Contents of Kit
Flu A + B Test Card 20 ea
Sample Extraction Buffer 1 ea
Extraction Tube 20 ea
Nozzle With Filter 21 ea
Sterilized Swab 20 ea
Tube Stand 1 ea
Instructions For Use 1 ea
Storage And Stability
Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial.
Pre Cautions
1. For in vitro diagnostic use only.
2. Do not use after the expiration date.
3. The test device should remain in the sealed pouch until use.
4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test.
5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers.
6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation.
7. Visibly bloody samples should not be used for the testing.
For in vitro qualitative detect of Covid-19 antigen in nasal(NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days of the onset of the symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, and not for at home testing.
1.Easy to collect samples simple operation without professional equipment.
2.The test results are available in 15 minutes, and the test results are clearly visible. 3.Convenient transportation and low price, higher accuracy.
4.Suitable for large-scale rapid screening.
Shelf life: 24 Months
Test Result time: 10 Mins
Packing: 25 Pieces per Box
The novel Antigen Rapid Test swab is an in vitro diagnostic test for the qualitative detection of novel coronavirus antigens in Nasopharyngeal swab and Oropharyngeal swab using the rapid method with a reading result in 10-15 minutes.
COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of
