V-CHEK Antigen Lollipop rapid test, 1 ST

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Lollipop rapid test - The new "one-step method" is easy to use, completely painless and can be carried out independently. The test kit consists of only two parts. No buffer solution required. Sensitivity 95.65 % & specificity 98.44 %.

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Quantity	Unit price
To 19	€1.69* €6.99* (75.82% saved)
From 20	€1.39* €6.99* (80.11% saved)

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Product number: RA8073085

Stück: 1

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Product information "V-CHEK Antigen Lollipop rapid test"

Beipackzettel ansehen

The V-Chek 2019-nCoV Ag Saliva Rapid Test enables rapid (<15 minutes) and simple detection of SARS-CoV-2 virus infections. The lollipop test is individually packaged and easy to use - the sample spatula must be sucked for 90 seconds. According to the manufacturer, the test has a specificity of 98.44% and a sensitivity of 95.65% and works for all known virus mutations. According to the BASG list, this test is suitable for use by laypersons.

The test card is a lateral flow immunoassay for the qualitative detection of the nucleocapsid protein antigen of 2019-nCoV in saliva samples collected directly from individuals suspected of COVID-19 by their healthcare provider within the first 7 days of symptom onset. The results relate to the identification of the 2019nCoV nucleocapsid protein antigen. Positive results indicate the presence of viral antigens, but clinical correlation with medical history and other diagnostic information is necessary to determine infection status. Positive results do not rule out a bacterial infection or co-infection with other viruses. The pathogen detected may not be the definite cause of the disease. Negative results should be treated as presumptive and do not rule out 2019-nCoV infection 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, medical history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay for patient management when appropriate. The test card is intended for use by trained clinical laboratory personnel specifically instructed and trained in vitro diagnostic procedures.

Characteristics

Sensitivity: 95.65 %
Specificity: 98.44 %
Effective even with known mutations**
Indicator control
Result after exactly 10 minutes
Location-independent
CE certified
BfArM listed (AT015/21)
BASG listed
Expiry - 12/2023

How to use

Carefully follow the steps in the instructions for use.

For private use:

For personal detection of Covid-19 disease only. When used correctly, the result is 95.65% correct and indicates a negative or positive Covid-19 disease.
The V-CHEK Antigen Lollipop rapid test is on the list of the Federal Office for Safety in Health Care (BASG). The BASG has classified this antigen rapid test as suitable for self-testing by private individuals.

Contents (depending on order quantity)

Test cassette
Lollipop sponge
Package leaflet (German)

Important notes:

There is an obligation to report positive test results according to the Epidemic Law as well as negative results according to the Laboratory Reporting Ordinance. (Tel. 1450 - Austria)
The result of a rapid antigen test is only a current snapshot. The test result is for your information only and is not suitable for submission to the authorities or your employer.

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Warnhinweise - V-CHEK Antigen Lollipop rapid test

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V-CHEK Antigen Lollipop rapid test, 1 ST

How to use

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