China Rapid Antigen Test Kit manufacturer
Shenzhen Kisshealth Biotechnology Co., Ltd
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SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection

SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection

Brand Name KISSH
Model Number K903-1
Certification CE
Place of Origin CHINA
Minimum Order Quantity 1000 tests
Price Negotiable
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
Detailed Product Description

SARS-CoV-2 Antigen Detection Kit(Immunofluorescence)

 

 

Product Information

Product nameSARS-CoV-2 Antigen Detection Kit(Immunofluorescence)
Main CompositionTest Cassette individually foil pouched with a desiccant, Sample Tube, with cap and antigen extraction buffer,Sampling swab, Instruction for use
Package1 Test/Kit
Keep temperature2-30℃
Shelf-life12 months
Place of OriginShenzhen 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.

 

 

 

Product Tags: SARS-CoV-2 Antigen Detection Kit   Rtk Saliva Accuracy Delta Variant Detection   SARS-CoV-2 Rtk Saliva Accuracy  
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