Getein Testing Kit
Rapid chromatographic immunoassay (lateral-flow) for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasopharyngeal swabs from individuals who are suspected of COVID-19 within the first seven days from the onset of symptoms.
Getein Covid-19 Testing Kits Box and Product inside
Getein Covid-19 Testing Kits
Getein Covid-19 Testing Kits Box and Product inside
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Specifications
Test Name
One Step Test for SARS-COV-2 Antigen
Test per Box
25
Available in
United Kingdom
Available for self-testing
Yes
ISO Certification
PHE approved
MHRA approved
CE Marked approved
ISO 13485
Yes
Yes but no CDTA
Yes
Government approval
Testing method
UK Government Approved
Nasal and saliva
Test accuracy
Nasal :
Sensitivity : 97.06%
Specificity: 98.71%
Accuracy: 98.13%
Saliva :
Sensitivity : 98.18%
Specificity: 100%
Accuracy: 98.72%
Result time
10-15 minutes
What’s included in the box
25 Test Cassettes
25 Sterilized Swabs
25 Extraction Tube
2 Sample Extraction Buffer
1 IFU
1 Tube Stand
Specifications
Test Name
One Step Test for SARS-COV-2 Antigen (For Self Test)
Test per Box
1/5/25
Available in
United Kingdom
Available for self-testing
ISO Certification
CE Marked approved
Testing method
Yes
ISO 13485
Yes
Nasal
Test accuracy
Nasal :
Sensitivity : 77.06%
Specificity: 98.71%
Accuracy: 98.13%
Result time
10-15 minutes
What’s included in the box
1/5/25 Test Cassettes
1/5/25 Sterilized Swabs
1/5/25 Extraction Buffer Tube
1 IFU
1 Tube Stand
Other Other Covid-19 Testing Kit
Intended to aid in the rapid diagnosis of SARS-CoV-2 infections, the Orient Gene Covid-19 Antigen Test is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in nasal swab specimens from individuals who are suspected of COVID-19 by their healthcare provider.
The IgA / IgM / IgG Antibody Combined Rapid Test can be used to evaluate the course of disease.
T1 indicates the detection results of IgA and (or) IgM, and the detection significance is to assist the diagnosis of early and present infection. T2 is the result of IgG detection, and the significance of detection is to assist the diagnosis of mid-term or previous infection.
Intended to aid in the rapid diagnosis of SARS-CoV-2 infections, the Healgen Covid-19 Antigen Test is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in nasal swab specimens from individuals who are suspected of COVID-19 by their healthcare provider.
A rapid test for the detection of SARS-CoV-2 antigens in anterior nasal specimens directly from individuals within 7 days of symptom onset or without symptoms or other epidemiological reasons to suspect COVID-19 infection.
