Guangzhou Decheng Biotechnology Co., LTD.

Guangzhou Decheng Biotechnology Co., LTD.

Guangdong,China

Guangzhou Decheng Biotechnology Co., LTD.

Guangdong,China

Guangzhou Decheng Biotechnology Co., LTD.
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Guangzhou Decheng Biotechnology Co., LTD.

Guangdong,China

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2019-nCoV Ag Saliva Rapid Test Card (Immunochromatography) with CE approved

FOB Price : Get a Price/Quote

Min.Order : 50000 Piece(s)

Certification : CE,TGA,TGA,Other

Brand Name : V-CHEK

Payment Terms : T/T,EXW

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product information

  • brand name : V-CHEK

  • certification : CE,TGA,TGA,Other

  • min.order : 50000 Piece(s)

  • warranty : 2years

  • payment terms : T/T,EXW

  • Packaging : carton packing

  • Specification : 1test/box,5test/box,20test/box

  • place of origin : Guangdong

product description

2019 nCoV Ag Saliva Rapid Test Card

User-friendly lollipop type saliva test card for detecting COVID-19 antibodies in a fast, painless and comfortable way. Taking the test is pleasant and doesn’t require using a buffer solution or a nasal swab – just place the saliva swab in your mouth for around 90 seconds, then insert it into the test card holder and wait for the answer.

 

 

Saliva Rapid Test Card is a non-invasive diagnostical health instrument based on the principle of SARS-CoV-2 antigens detection in human saliva of persons suspected with COVID-19 infection.

 

The tested person gathers saliva in their mouth for 30 seconds (approx. 0,5 ml), the sample is extracted, mixed in the tube, and evaluated in 10 minutes using a special testing card.

 

Saliva Rapid Test Card also contains an internal control element in the testing card which shows whether the sample flow was sufficient, thus implying the test is relevant or not.

 

This secures the test relevancy and ensures high testing efficiency and success.

The Test Card is a lateral flow immunoassay intended for the in vitro qualitative detection of
N-protein antigen from 2019-nCoV in human saliva specimens. The Test Card can be used for
individuals with or without symptoms or other epidemiological reasons to suspect COVID-19
infection.
A positive result indicates 2019-nCoV infection, Please quarantine yourself and contact a doctor.
Additional testing is necessary. Positive results do not rule out bacterial infection or co-infection with
other viruses.
A negative result should be treated as presumptive. It do not rule out 2019-nCoV infection. 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. Contact a doctor and Confirm
with a PCR test, if necessary.
For in vitro use only. Suitable for self-testing use.
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.
This Test Card uses double-antibody sandwich to legally detect the antigen of novel coronavirus
(2019-nCoV) in saliva samples. During detection, the gold labeled anti-2019-nCoV monoclonal
antibody in the labeling pad binds to the 2019-nCoV antigen in the sample to form a complex, and
the reaction complex moves forward along the nitrocellulose membrane under the action of
chromatography, it is captured by the anti-2019-nCoV monoclonal antibody pre-coated by the Test
area (T) on the nitrocellulose membrane, and finally a red color reaction line is formed in the Test
area (T). If the sample does not contain 2019-nCoV antigen, a red color reaction line cannot be
formed in the Test area (T). Regardless of whether the sample to be tested contains 2019-nCoV
antigen, a red reaction

 

 

 

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Guangzhou Decheng Biotechnology Co., LTD.

Ordinary verified

Business Type Manufacturer

Country / Region Guangdong,China

Main Products In vitro Diagnosis Consumables, In vitro Diagnosis Reagents, Blood Diagnosis Reagents, Immune Diagnostic Reagents, POCT Diagnostic Reagents, Tumor Marker Diagnostic Reagents

Main Markets

2019-nCoV Ag Saliva Rapid Test Card (Immunochromatography) with CE approved
share :

product information

product description

2019 nCoV Ag Saliva Rapid Test Card

User-friendly lollipop type saliva test card for detecting COVID-19 antibodies in a fast, painless and comfortable way. Taking the test is pleasant and doesn’t require using a buffer solution or a nasal swab – just place the saliva swab in your mouth for around 90 seconds, then insert it into the test card holder and wait for the answer.

 

 

Saliva Rapid Test Card is a non-invasive diagnostical health instrument based on the principle of SARS-CoV-2 antigens detection in human saliva of persons suspected with COVID-19 infection.

 

The tested person gathers saliva in their mouth for 30 seconds (approx. 0,5 ml), the sample is extracted, mixed in the tube, and evaluated in 10 minutes using a special testing card.

 

Saliva Rapid Test Card also contains an internal control element in the testing card which shows whether the sample flow was sufficient, thus implying the test is relevant or not.

 

This secures the test relevancy and ensures high testing efficiency and success.

The Test Card is a lateral flow immunoassay intended for the in vitro qualitative detection of
N-protein antigen from 2019-nCoV in human saliva specimens. The Test Card can be used for
individuals with or without symptoms or other epidemiological reasons to suspect COVID-19
infection.
A positive result indicates 2019-nCoV infection, Please quarantine yourself and contact a doctor.
Additional testing is necessary. Positive results do not rule out bacterial infection or co-infection with
other viruses.
A negative result should be treated as presumptive. It do not rule out 2019-nCoV infection. 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. Contact a doctor and Confirm
with a PCR test, if necessary.
For in vitro use only. Suitable for self-testing use.
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.
This Test Card uses double-antibody sandwich to legally detect the antigen of novel coronavirus
(2019-nCoV) in saliva samples. During detection, the gold labeled anti-2019-nCoV monoclonal
antibody in the labeling pad binds to the 2019-nCoV antigen in the sample to form a complex, and
the reaction complex moves forward along the nitrocellulose membrane under the action of
chromatography, it is captured by the anti-2019-nCoV monoclonal antibody pre-coated by the Test
area (T) on the nitrocellulose membrane, and finally a red color reaction line is formed in the Test
area (T). If the sample does not contain 2019-nCoV antigen, a red color reaction line cannot be
formed in the Test area (T). Regardless of whether the sample to be tested contains 2019-nCoV
antigen, a red reaction

 

 

 

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