Payment Terms | T/T |
Supply Ability | 1,000,000 tests per day |
Delivery Time | Within 7 days |
Packaging Details | 1 Test/Kit, 5 Tests/Kit, 10 Tests/Kit, 20 Tests/Kit |
Product namee | SARS-CoV-2 Antigen Detection Kit(Immunofluorescence) |
Usage | Qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP), nasal swab and saliva specimens |
Sample Type | Nasopharyngeal (NP) and Nasal swab,Saliva,Oropharyngeal (OP) swab |
Pattern | KISSH |
Methodology | Immunofluorescence |
Function | Delta Variant Detection |
Brand Name | KISSH |
Model Number | K903-1 |
Certification | CE |
Place of Origin | CHINA |
View Detail Information
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Product Specification
Payment Terms | T/T | Supply Ability | 1,000,000 tests per day |
Delivery Time | Within 7 days | Packaging Details | 1 Test/Kit, 5 Tests/Kit, 10 Tests/Kit, 20 Tests/Kit |
Product namee | SARS-CoV-2 Antigen Detection Kit(Immunofluorescence) | Usage | Qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP), nasal swab and saliva specimens |
Sample Type | Nasopharyngeal (NP) and Nasal swab,Saliva,Oropharyngeal (OP) swab | Pattern | KISSH |
Methodology | Immunofluorescence | Function | Delta Variant Detection |
Brand Name | KISSH | Model Number | K903-1 |
Certification | CE | Place of Origin | CHINA |
High Light | SARS-CoV-2 Antigen Detection Kit ,Rtk Saliva Accuracy Delta Variant Detection ,SARS-CoV-2 Rtk Saliva Accuracy |
SARS-CoV-2 Antigen Detection Kit(Immunofluorescence)
Product Information
Product name | SARS-CoV-2 Antigen Detection Kit(Immunofluorescence) |
Main Composition | Test Cassette individually foil pouched with a desiccant, Sample Tube, with cap and antigen extraction buffer,Sampling swab, Instruction for use |
Package | 1 Test/Kit |
Keep temperature | 2-30℃ |
Shelf-life | 12 months |
Place of Origin | Shenzhen China |
Basis Information
The SARS-CoV-2 Antigen Detection Kit is a fluorescence immunoassay that is intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP) and nasal swab, saliva specimens and superficial nasal swab directly from individuals who are suspected of COVID- 19 by their healthcare provider.
Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen. 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 bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease.
Negative results should be treated as presumptive and confirmed with a molecular assay, if necessary for patient management. Negative results do not rule out COVID- 19 and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. 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 COVID- 19.The SARS-CoV-2 Antigen Test is intended for use by trained clinical laboratory personnel and individuals trained in point of care settings.
Company Details
Business Type:
Manufacturer
Year Established:
2018
Total Annual:
10,000,000-30,000,000
Employee Number:
50~150
Ecer Certification:
Active Member
Shenzhen Kisshealh Biotechnology Co., Ltd., located in the Pingshan District, Shenzhen, P.R. China. is a diagnostics company focused on the development and manufacture of IVD tests at the Point-of-Care with highly innovative proprietary technology. We focused on the emerging markets of ... Shenzhen Kisshealh Biotechnology Co., Ltd., located in the Pingshan District, Shenzhen, P.R. China. is a diagnostics company focused on the development and manufacture of IVD tests at the Point-of-Care with highly innovative proprietary technology. We focused on the emerging markets of ...
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