ISO Certified 15mins Rapid Covid 19 Test Kits Antigen Saliva Test Kit High Sensitivity

Product description:ISO 15mins Covid-19 Antigen Saliva Test Kit High Sensitivity

Antigen Rapid Test Kit is faster and less intrusive than a Polymerase Chain Reaction(PCR)test.This makess it easy for the public to use to test themselves if needed.In general,Antigen Rapid Test Kid has a sensitivity(ability of a test to identify patients with the disease)of about 95% for cases with higher viral loads and a specificity(ability of a test to identify patients without the disease)range of 99.1%.As the sensitivity and specificity of Antigen Rapid Test Kit are lower as compared to PCR tests,if you test Antigen Rapid test Kit positive or invalid twice,you will need to follow up with a confirmatory PCR test.You should not repeat the Antigen Rapid Test Kit.Even if you do test negative in the repeated test,it may be a false negative result and hence you need to go for a confirmatory PCR test.Poweray Antigen Rapid Test Kits has good performance and with high sensitivity to detect the antigen at the early stage of infection.High performance rapid test enable immediate treatment or isolation measures to minimize transmission

Product usage:

This kit is used for vitro qualitative detection of coronavirus(Covid-19) in human pharyngeal or nasal secretions,sailva samples.

Used as a supplementary test indicator for suspected cases of new coronavirus nucleic acid test negative or used in conjunction with nucleic acid testing in the diagnosis of suspected cases

Product features:
• Non-invasive
• Simple to use
• Convenient, no devices required
• Rapid, get the result in 20 minutes
• Stable, with high accuracy
• Economical

Storage Conditions and Validity:
Keep it at 2℃~30℃, and the validity period is tentatively set at 24 months.
Aluminum foil bag is svalid for 4 hour
Production lot number:see details label
For more information:see label

Test procedure:

• Remove the foil from the top of the extraction buffer tube
• Open the swab package at the stick end
• Gently insert the swab into the nostril and the tip of the swab should be inserted 1/2-3/4 inch away from the edge of the nostril
• Roll the swab along the mucous membrane inside the nostril 5 times,taking about 15 seconds to collect the speciman
• Insert the sampling swab into the sample buffer
• Swirl the tube for 30 seconds
• Rotate the swab 5 times while squeezing the tube
• Remove the swab while squeezing the tube
• Cover the emitter
• Add 2 drops to extract the treated sample to the loading well of the test card and then start the timer
• Leave at room temperature for 15 minutes before reading the results.The result will be invalid after 20 minutes

Detailed explanation of test results:

Limitation of test method:
1. This product is used for qualitative testing and only for in vitro assisted diagnosis.
2.This product applies for nose samples. Other sample type results may be inaccurate or invalid.
3. appropriately adds samples for testing. Too large or too small sample size may lead to inaccurate results.
4.It should not be the sole basis for clinical trials and treatment. The final diagnosis can be made after a comprehensive evaluation of all clinical and experimental results.

Precautions:
1. This product is used for in vitro diagnosis only.
2. This product is disposable and cannot be recycled.
3. Read the instructions carefully before 3. operation and strictly follow the reagent instructions.
4. Avoid severe environmental conditions including disinfectant 84, sodium hypochlorite, acid and alkali or acetaldehyde, other high concentrations of corrosive gases and dust, etc., the laboratory shall disinfed
5. All samples and reagents used shall be considered as potentially infectious materials and shall be treated in accordance with local legislation.
6. Use reagents within the validity period indicated in the outer package. Use the test card as soon as possible after removal from the aluminum foil bag.