中文
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.
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.
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 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 |
| 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 |
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.
This kit is only used for qualitative detection and can not be used for the determination content.
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.
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.
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.
The positive samples obtained by rapid test should be confirmed by other methods.
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.
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.
Waste samples and test should be treated as potential infectious agents.
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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