Ecer asks for your consent to use your personal data to:
Personalised advertising and content, advertising and content measurement, audience research and services development
Store and/or access information on a device
Your personal data will be processed and information from your device (cookies, unique identifiers, and other device data) may be stored by, accessed by and shared with 135 TCF vendor(s) and 65 ad partner(s), or used specifically by this site or app.
Some vendors may process your personal data on the basis of legitimate interest, which you can object to by do not consent. Contact our platform customer service, you can also withdraw your consent.
Your message must
be between 20-3,000 characters!
Submit Requirement
Thank You！
Your requirement has been sent. we will contact you quickly!
{"title":"15 min SARS-CoV-2 Influenza AB Test Kit RSV Rapid Test Nasopharyngeal Swab","imgUrl":"https:\/\/img.silkroadsl.com\/nimg\/4e\/2d\/a5cfbc227e26f36e59a8b00a5c5b-200x200-1\/15_min_sars_cov_2_influenza_ab_test_kit_rsv_rapid_test_nasopharyngeal_swab.jpg","attrs":{"Brand Name":"Citest","Model Number":"ISIR-535","Certification":"CE","Place of Origin":"-"}}
{"title":"99.6% Specificity COVID 19 Antigen Rapid Test Kit CE1434 OTC Covid 19 Self Test","imgUrl":"https:\/\/img.silkroadsl.com\/nimg\/66\/54\/38e505c8e53d6c8169004c886a2d-200x200-1\/99_6_25_specificity_covid_19_antigen_rapid_test_kit_ce1434_otc_covid_19_self_test_kit.jpg","attrs":{"Brand Name":"Citest","Model Number":"ICOV-502S","Certification":"CE1434","Place of Origin":"-"}}
{"title":"Citest COVID 19 Antigen Rapid Test Kit Qualitative Detection Of SARS-CoV-2","imgUrl":"https:\/\/img.silkroadsl.com\/nimg\/fb\/7b\/63567a78c9162df8c591959ddde5-200x200-1\/citest_covid_19_antigen_rapid_test_kit_qualitative_detection_of_sars_cov_2.jpg","attrs":{"Brand Name":"Citest","Model Number":"ICOV-502","Certification":"CE","Place of Origin":"-"}}
{"title":"CE COVID19 Infectious Disease Test Kit Oral Fluid Test Kit Rapid Qualitative","imgUrl":"https:\/\/img.silkroadsl.com\/nimg\/c9\/81\/b79691a7a07cbe8392bdd3271879-200x200-1\/ce_covid19_infectious_disease_test_kit_oral_fluid_test_kit_rapid_qualitative_detection.jpg","attrs":{"Brand Name":"Citest","Model Number":"INCP-802","Certification":"CE","Place of Origin":"-"}}
{"title":"25T COVID 19 Antigen Rapid Test Kit SARS-CoV-2 Nucleocapsid Protein Antigen Test","imgUrl":"https:\/\/img.silkroadsl.com\/nimg\/ba\/12\/5989fadd90dff670b774a926cf46-200x200-1\/25t_covid_19_antigen_rapid_test_kit_sars_cov_2_nucleocapsid_protein_antigen_test.jpg","attrs":{"Brand Name":"Citest","Model Number":"INCP-502","Certification":"CE","Place of Origin":"-"}}
{"title":"SARS-COV-2 Antigen Rapid Test Kit Nasal Swab COVID 19 Antigen Rapid Test","imgUrl":"https:\/\/img.silkroadsl.com\/nimg\/c5\/05\/32ca0831bccfe10b0862e2032953-200x200-1\/sars_cov_2_antigen_rapid_test_kit_nasal_swab_covid_19_antigen_rapid_test_cassette.jpg","attrs":{"Brand Name":"Citest","Model Number":"INCP-502-N","Certification":"CE","Place of Origin":"-"}}
{"title":"20T M Pneumoniae RSV Adenovirus Rapid Test Cassette Chromatographic Immunoassay","imgUrl":"https:\/\/img.silkroadsl.com\/nimg\/d2\/c2\/9a23f74b69cc45848031480c89a6-200x200-1\/20t_m_pneumoniae_rsv_adenovirus_rapid_test_cassette_chromatographic_immunoassay.jpg","attrs":{"Brand Name":"Citest","Model Number":"IRT-555","Certification":"CE","Minimum Order Quantity":"N\/A"}}
SARS-CoV-2/Influenza A+B/RSV Antigen Combo Rapid Test (Nasopharyngeal Swab)
Principle
Chromatographic Immunoassay
Format
Cassette
Specimen
Nasopharyngeal Swab
Certificate
CE
Reading Time
15 minutes
Pack
20 T
Storage Temperature
2-30°C
Shelf Life
2 Years
Application
SARS-CoV-2/Influenza A+B/RSV Antigen Combo Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 Nucleocapsid protein, Influenza A, Influenza B and Respiratory Syncytial Virus(RSV) antigens present in human nasopharynx.
For professional in vitro diagnostic use only
INTENDED USE
The SARS-CoV-2/Influenza A+B/RSV Antigen Combo Rapid Test (Nasopharyngeal Swab) is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 Nucleocapsid protein, Influenza A, Influenza B and Respiratory Syncytial Virus(RSV) antigens in nasopharyngeal swab specimens from individuals with suspected SARS-CoV-2/Influenza/RSV infection in conjunction with clinical presentation and the results of other laboratory tests.
Results are for the detection of SARS-CoV-2 Nucleocapsid protein, Influenza A+B and RSV Antigens. An antigen is generally detectable in upper respiratory specimens during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out other bacterial/viral infection. The agent detected may not be the definite cause of disease.
Negative results do not preclude SARS-CoV-2/Influenza A+B/RSV infection and should not be used as the sole basis for treatment or patient management decisions. Negative results should be treated as presumptive and confirmed with a molecular assay, if necessary for patient management. Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with SARS-CoV-2, Influenza A+B and RSV.
PRECAUTIONS
1. This package insert must be read completely before performing the test. Failure to follow directions in package insert may yield inaccurate test results.
2. For professional in vitro diagnostic use only. Do not use after expiration date.
3. Do not eat, drink or smoke in the area where the specimens or kits are handled.
4. Do not use test if pouch is damaged.
5. Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout in the collection, handling, storage, and disposal of patient samples and used kit contents.
6. Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are assayed.
7. Viral Transport Media (VTM) may affect the test result, do not store specimens in viral transport media; extracted specimens for PCR tests cannot be used for the test.
8. Wash hands thoroughly after handling.
9. Please ensure that an appropriate amount of samples are used for testing. Too much or too little sample size may lead to deviation of results.
10.The used test should be discarded according to local regulations.
11.Humidity and temperature can adversely affect results.
Specimen Collection
1. Insert a sterile swab into the nostril of the patient, reaching the surface of the posterior nasopharynx.
2. Swab over the surface of the posterior nasopharynx.
3. Withdraw the sterile swab from the nasal cavity
DIRECTIONS FOR USE
Allow the test, extracted specimen and/or controls to equilibrate to room temperature (15-30°C) prior to testing.
1. Remove the test from the sealed foil pouch and use it within one hour. Best results will be obtained if the test is performed immediately after opening the foil pouch.
2. Invert the specimen collection tube and add 3 drops of extracted specimen to each of the specimen well(S) respectively and then start the timer.
3. Wait for the colored line(s) to appear. Read the result at 15 minutes. Do not interpret the result after 20 minutes.
SUMMARY
The novel coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection; asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough.
Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases. Influenza (commonly known as ‘flu’) is a highly contagious, acute viral infection of the respiratory tract. It is a communicable disease easily transmitted through the coughing and sneezing of aerosolized droplets containing live virus. Laboratory identification of human influenza virus infections is commonly performed using direct antigen detection, virus isolation in cell culture, or detection of influenza-specific RNA by reverse transcriptase-polymerase chain reaction (RT-PCR). Rapid tests for influenza A and B virus infections, which can provide results within 30 minutes.
Respiratory Syncytial Virus (RSV), which causes infection of the lungs and breathing passages, is a major cause of respiratory illness in young children. In adults, it may only produce symptoms of a common cold, such as a stuffy or runny nose, sore throat, mild headache, cough, fever, and a general feeling of being ill.Most children with RSV infection, both those who were hospitalized and those who were treated as outpatients, had no coexisting medical conditions or characteristics that significantly identified them as being at greater risk for severe RSV disease, except for being under 2 years of age.
Company Details
Bronze Gleitlager
,
Bronze Sleeve Bushings
and
Graphite Plugged Bushings
from Quality China Factory
Business Type:
Manufacturer,Exporter,Trading Company
Total Annual:
80000000-100000000
Employee Number:
500~10000
Ecer Certification：
Verified Supplier
CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies.
... CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies.
...
