COVID-19 Antigen Rapid Test – GREEN SPRING

Ossenberg GmbH

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ShopHomeNew productsCOVID-19 Antigen Rapid Test – GREEN SPRING® 25-pack – TOP 10 best tests

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COVID-19 Antigen Rapid Test – GREEN SPRING® 25-pack – TOP 10 best tests

25 Piece

 

SKU: 4335-25

EAN: 4250415678417

suitable for detection of Omicron and other mutations

 

4 sampling methods

● Saliva (lolly test) – especially suitable for children!

● Anterio-nasal swab (nose in front)

● Nasopharyngeal swab (nose and throat)

● Oropharyngeal swab (mouth-throat)

sensitivity 96,77% und specificity 100,00%

 

fast and reliable test results in only 15 minutes

 

● BfArM listet (BfArM-Test-ID: AT1188/21)

● Paul-Ehrlich-Institut proof

● HSC common list (Device-ID: 2109)

● PZN: 17394138

Advantages

• BfArM Zulassung

• easy to handle

• fast and reliable test results in only 15 minutes

• 4 sampling methods

• Room temperature storage

• no cross-reactivity with different Coronaviren wie MERS, 229E, NL63, KHU1 oder Influenza A, B

Sensitivity 96,77%

describes how well a test actually detects infected persons and how many infected persons pass through its meshes. In statistics, this is referred to as false-negative results. The closer the value is to 100 percent, the more reliably the test detects all infected persons.

specificity 100,00%

describes how rarely a test falsely classifies people as infected. This is about the statistically false-positive results. Again, the closer the value is to 100 per cent, the better.

Ossenberg GmbH

MENU

0

 

ShopHomeNew productsCOVID-19 Antigen Rapid Test – GREEN SPRING® 25-pack – TOP 10 best tests

🔍

4335-25-Pack_mit_Anl_Green-frei-Web2.jpg4335-25-Pack_mit_Anl_Green-frei-Web2.jpg4335-25-Packung_einz_1Green-frei-tiff.jpg4335-25-werkzeug-Green-frei-tiff-web.jpg

4335-25-Pack_mit_Anl_Green-frei-Web2.jpg4335-25-Packung_einz_1Green-frei-tiff.jpg4335-25-werkzeug-Green-frei-tiff-web.jpg

Previous

Next

COVID-19 Antigen Rapid Test – GREEN SPRING® 25-pack – TOP 10 best tests

25 Piece

 

SKU: 4335-25

EAN: 4250415678417

suitable for detection of Omicron and other mutations

 

4 sampling methods

● Saliva (lolly test) – especially suitable for children!

● Anterio-nasal swab (nose in front)

● Nasopharyngeal swab (nose and throat)

● Oropharyngeal swab (mouth-throat)

sensitivity 96,77% und specificity 100,00%

 

fast and reliable test results in only 15 minutes

 

● BfArM listet (BfArM-Test-ID: AT1188/21)

● Paul-Ehrlich-Institut proof

● HSC common list (Device-ID: 2109)

● PZN: 17394138

 

We look forward to your enquiry for larger quantities

 

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PRODUCT DESCRIPTION DOWNLOADS

GREEN SPRING

Rapid Test

GREEN SPRING

Rapid Test

Clungene

Schnelltest

 

 

 

 

Advantages

• BfArM Zulassung

• easy to handle

• fast and reliable test results in only 15 minutes

• 4 sampling methods

• Room temperature storage

• no cross-reactivity with different Coronaviren wie MERS, 229E, NL63, KHU1 oder Influenza A, B

Sensitivity 96,77%

describes how well a test actually detects infected persons and how many infected persons pass through its meshes. In statistics, this is referred to as false-negative results. The closer the value is to 100 percent, the more reliably the test detects all infected persons.

specificity 100,00%

describes how rarely a test falsely classifies people as infected. This is about the statistically false-positive results. Again, the closer the value is to 100 per cent, the better.

 

 

 

Purpose of use

The Green Spring® SARS-CoV-2 Antigen Rapid Test is for the rapid qualitative detection of SARS-CoV-2 nucleocapsid protein antigen in human saliva, nasal, nasopharyngeal or throat swab specimens. The results are used for the detection of SARS-CoV-2 antigen. The antigen is generally detectable in upper respiratory tract specimens during the acute phase of infections. Positive results do not rule out bacterial infection or co-infection with other viruses. The pathogen detected may not be the sole cause of the disease.

 

Principle of testing

The Green Spring® SARS-CoV-2 Antigen Rapid Test is a qualitative, membrane-based immunoassay for the detection of SARS-CoV-2 nucleocapsid protein antigens. The test line region is coated with SARS-CoV-2 antibody. The sample reacts with the SARS-CoV-2 antibody in the test line region. If the sample contains SARS-CoV-2 antigens, a coloured line appears in the test line area (T) as a relevant result. As a procedural control, a coloured line appears in the control line area (C), indicating that the correct volume of sample has been added and membrane wetting has occurred correctly.