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Product Details:
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| Product Name: | PocRoc® SARS-CoV-2 / Influenza A+B/RSV Antigen Combo Rapid Test Kit (Colloidal Gold) | Function Antigen From SARS-CoV-2, Influenza A Virus And/or Influenza B Virus，and Respiratory Syncyti: | Detect And Differentiate Nucleocapsid Antigen From SARS-CoV-2, Influenza A/B Virus，and Respiratory Syncytial Virus (RSV) |
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| Application: | In Vitro Diagnose Test In Hospital Clinic Laboratory | Method: | Colloidal Gold |
| Format: | Rapid Test Cassette | Specimen: | Nasal Swab |
| Storage Temp: | 4℃-30℃ | Sensitivity: | 93.33 |
| Test Time: | 15 Minutes | ||
| Highlight: | RSV Antigen Combo Rapid Test Kit,Covid 19 Combo Rapid Test Kit,Colloidal Gold Combo Rapid Test Kit |
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RSV Antigen Combo Rapid Test Kit Detect Covid 19, Flu A Flu B, RSV Antigen By Colloidal Gold Method
PocRoc® SARS-CoV-2 / Influenza A+B / RSV Antigen Combo Rapid Test Kit (Colloidal Gold)
Respiratory virus infection refers to a group of very common respiratory diseases caused by viruses, accounting for 70-80% of acute respiratory infectious diseases.
Pneumonia caused by novel coronavirus (SARS CoV-2) infection is the largest public health event in the world at present. Its transmission routes include droplet transmission, aerosol transmission, and object surface contact transmission.
Influenza is the most common in autumn and winter, and its virus has four types: A, B, C, and D. Type A influenza is the most common, followed by type B influenza. Both are highly infectious, with similar symptoms, such as fatigue, nasal congestion, cough, headache, sore throat, body pain, cold, fever, vomiting, or diarrhea.
Human respiratory syncytial virus (HRSV) is the main pathogen of lower respiratory tract infection in infants and frail adults. It is also the main reason for infants and young children suffer from bronchiolitis and pneumonia. It is usually spread among infants and children in winter and early spring. After infection, there will be a runny nose, fever, cough, wheezing, and other clinical symptoms. In severe cases, severe dyspnea and temporary respiratory arrest will occur.
| Product Name | PocRoc® SARS-CoV-2 / Influenza A+B/RSV Antigen Combo Rapid Test Kit(Colloidal Gold) |
| Method | Colloidal Gold |
| Specimen | Nasal Swab |
| Detention Time | 15 mins |
| Storage Temperature | 4℃-30℃ |
| Shelf Life | 24 months |
| Package | 1 test/box, 5 tests/box, 10 tests/box, 25 tests/box |
| Carton Dimension (cm) | 70cm * 45cm * 53cm |
| G.W/N.W(kg) | 19.5 / 17.5 |
| Cat.No | Package | Test Cassette | Nasal Swab | Extraction Reagent | Tube Holder | IFU |
| 1 | 1 Test/ Box | 1 | 1 | 1 | - | 1 |
| 2 | 5 Tests/ Box | 5 | 5 | 5 | 1 | 1 |
| 3 | 10 Tests/ Box | 10 | 10 | 10 | 1 | 1 |
| 4 | 25 Tests/ Box | 25 | 25 | 25 | 1 | 1 |
| 5 | 50 Tests/ Box | 50 | 50 | 50 | 1 | 1 |
Materials Not Supplied With the PocRoc® SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold): Timer, Hand soap or hand sanitizer for cleaning
Positive Results: The control line (C) and at least one test line show red or pink color in the result window, the results are positive.
Negative Results: Only the quality control line (C) shows color, the test lines are colorless, the test results are negative.
Invalid Result: When the quality control line (C) of a specific result window is colorless after performing the test, the test of that window is considered invalid.
The positive result indicates that SARS-CoV-2/Flu A/Flu B/RSV antigen is detected in the sample, and it is suspected with SARS-CoV-2/Flu A/Flu B/RSV infection. The negative result indicates that no SARS-CoV-2/Flu A/Flu B/RSV antigen is detected in the sample, but the negative result cannot completely rule out the possibility of SARS-CoV-2/Flu A /Flu B/RSV infection. If necessary, it is recommended for further examination. The invalid result means that the test is invalid, and the test should be repeated with a new test cassette and sample.
PocRoc® Helicobacter Pylori Antigen Rapid Test Kit (Colloidal Gold)
Helicobacter pylori Antigen Rapid Test Kit (Colloidal Gold) is a rapid lateral flow immunoassay for the qualitative detection of Helicobacter pylori specific antigen in a single test cassette. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms.
Contact Person: Bonnie
Tel: 86-13814877381
