RSV Rapid Test

The rsv screening test initially diagnoses diseases by detecting respiratory viruses and bacterial pathogens such as SARS-COV-2, influenza A/B, respiratory syncytial virus, group A streptococci, Mycobacterium tuberculosis and other viral bacteria. It is a means for early diagnosis of respiratory tract-related infections, identification of pathogenic bacteria and selection of reasonable diagnosis and treatment plans.

Features of Respiratory Pathogens Test Devices
Quick results: Results are available in just 5-20 minutes（Depends on the product）, making them ideal for use in various settings.
Shelf life: 12-24 month long shelf life and can be stored easily. （Depends on the product）.
simple and convenient: micro sample detection.
Transport Easy: the kits are stored at room temperature and do not require refrigeration or cold chain transport.
Complete qualifications: CE, ISO13485 and NMPA（Depends on the product）.

Product Details
Product name Respiratory Pathogens Test Devices
Format/Shape Cassette
Strip size The regular strip is 3~4 mm
Specimen secretion/serum/plasma/whole blood
Time to result within 15-20 minutes
Service OEM available
Shelf life/validity 12/24 months
Certifications CE, ISO13485
Storage between 4-30®C
Packing aluminum foil pouch
Manufacture Beijing Zhongjian Antai Diagnostic Technology Co., Ltd

Why Choose Our COVID-19 Test Solutions?
Provide a complete set of COVID-19 rapid test solutions, including antigens, antibodies and neutralizing antibodies test.

Test Items
ITEMS SPECIMEN TEST/KIT REGISTRATION
COVID-19 IgM/IgG WB/S/P 1, 10, 25, 40 CE
SARS-COV-2 Antigen Secretion 1, 10, 25, 40 CE
COVID-19 Neutralization Antibody WB/S/P 1, 10, 25, 40 CE
Infuenza A/B Antigen Secretion 1, 10, 25, 40 CE
Respiratory syncytial Virus Antigen Secretion 1, 10, 25, 40 CE
Group A Streptococcus Antigen Secretion 1, 10, 25, 40 CE
M.tuberculosis Antibody WB/S/P 1, 10, 25, 40 CE
M.tuberculosis IgG/IgM WB/S/P 1, 10, 25, 40 CE
M.pneumoniae IgM WB/S/P 1, 10, 25, 40 CE
C.pneumoniae IgM WB/S/P 1, 10, 25, 40 CE
Respiratory virus Antigen
Combined-Test 3 in 1 Secretion 1, 20, 40 CE
Respiratory virus Antigen
Combined-Test 4 in 1 Secretion 1, 20, 40 CE

FAQs of Respiratory Pathogens Test Devices
Q.What kind of samples can be added?
A.This product can only be used for the sample types specified in the instructions and cannot be used for sample types not specified in the instructions.
Q.Can reagents be used for quantitative testing?
A.This kit is only used for qualitative detection and can not be used for the determination content.
Q.Can the reagent be used to confirm the diagnosis?
A.The test results of this product are only for clinical reference and should not be used as the only basis for clinical diagnosis and treatment. The clinical management of patients should be considered comprehensively with the information of symptoms/signs, medical history, other laboratory examinations, treatment response and epidemiology.
Q.What can affect the accuracy of the results?
A.The results of sample testing are related to factors such as sample collection, testing, transportation and storage. Any error will affect the accuracy of the results.
Q.In what environment can be used?
A.If the state of the kit and sample is not restored to 18~30 ℃, the operation should not be carried out, otherwise the accuracy of the results will be affected.
Q.Can the reagent be used to confirm the diagnosis?
A.The positive samples obtained by rapid test should be confirmed by other methods.
Q.In what environment can be saved and used?
A.The test reagent should be sealed and stored in a dry place. The test kit should be tested as soon as possible after it is removed from the package, so as not to stay in the air for too long and cause moisture.
Q.Is there a relationship between color shade and concentration?
A.The color of the test line is not necessarily related to the titer of the antigen in the sample, and the interpretation result is invalid after 15minutes.
Q.What to do after use?
A.Waste samples and test should be treated as potential infectious agents.
Q.Questions about interpretation time?
A.The time of occurrence of the quality control line should not be used as the basis for judging the time of the test line results. The color results should be observed and judged within the time specified in the instructions.

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