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Rapid immunochromatographic test for the qualitative detection of human cardiac Troponin I (cTnI), Myoglobin, CK-MB and in whole blood, serum or plasma as an aid in the diagnosis of myocardial infarction (MI).

Myoglobin

Relative sensitivity: 54/54=>99.9% (95% CI*: 94.6%-100.0%)

Relative specificity: 379/390=97.2% (95% CI*: 95.0%-98.6%)

Accuracy: (54+379)/(54+11+379)=97.5% (95% CI*:95.6%-98.8%)
* Confidence Intervals

Cardiac Troponin I 

Relative sensitivity: 172/173=99.4% (95% CI*: 96.8%-99.9%)

Relative specificity: 472/477=99.0% (95% CI*: 97.6%-99.7%)

Accuracy: (172+472)/(172+1+5+472)=99.1% (95% CI*: 98.0%-99.7%)
* Confidence Intervals

CK-MB

Relative sensitivity: 62/62=>99.9% (95% CI*: 95.3%-100.0%)

Relative specificity: 468/471=99.4% (95% CI*: 98.1%-99.9%)

Accuracy: (62+468)/(62+3+468)=99.4% (95% CI*: 98.4%-99.9%)
* Confidence Intervals

Rapid immunochromatographic test for the qualitative detection of IgM antibody to Rubella in serum or plasma to aid in the diagnosis of Rubella infection.

Relative Sensitivity: 94.3% (95% CI*: 80.8%-99.3%) 

Relative Specificity: 98.9% (95% CI*: 96.7%-99.8%) 

Overall Accuracy: 98.3% (95% CI*: 96.2%-99.5%) 

* Confidence Interval

Rapid immunochromatographic test for the qualitative detection of human C-reactive protein (CRP) in whole blood, serum or plasma as an aid in the diagnosis of inflammatory condition. The cut-off of the test is 10 μg/ml.

Relative sensitivity: 96.7% (95% CI*: 82.8%-99.9%)

Relative specificity: 98.5% (95% CI*: 95.7%-99.7%)

Overall accuracy: 98.3% (95% CI*: 95.6%-99.5%)

* Confidence Intervals 

Rapid immunochromatographic test for the qualitative detection of SARS-CoV-2, Influenza A and Influenza B virus antigens in nasopharyngeal swab specimens from individuals with suspected SARS-CoV-2 / Influenza infection in conjunction with clinical presentation and the results of other laboratory tests.

SARS-CoV-2 Ag
Relative Sensitivity: 96.4% (95% CI*: 89.8% - 99.2%)

Relative Specificity: 99.2% (95% CI*: 95.5% - 99.9%)

Accuracy: 98.0% (95% CI*: 95.1% - 99.5%)
* Confidence Intervals

Influenza type A

Relative Sensitivity: 94.1% (95% CI*: 71.3% - 99.9%)

Relative Specificity: 98.4% (95% CI*: 91.5% - >99.9%)

Accuracy: 97.5% (95% CI*: 91.3% - 99.7%) 98.8%
* Confidence Intervals

Influenza type B
Relative Sensitivity: 91.7% (95% CI*: 61.5% - 99.8%)

Relative Specificity: 100.0% (95% CI*: 95.7% - 100.0%)

Accuracy: 98.8% (95% CI*: 93.2% - >99.9%)

* Confidence Intervals

Rapid immunochromatographic test for the qualitative detection of SARS-CoV-2 virus antigens in nasopharyngeal swab specimens as an aid in rapid diagnosis of Coronavirus (Covid-19) infection.

Relative Sensitivity: 96.4% (95% CI*: 89.8% - 99.2%)

Relative Specificity: 99.2% (95% CI*: 95.5% - 99.9%)

Accuracy: 98.0% (95% CI*: 95.1% - 99.5%)
* Confidence Intervals

The ViroQ SARS-FluA/B-RSV Kit is used for qualitative detection of SARS-CoV-2, Influenza A, Influenza B and RSV (Respiratory Syncytial Virus) RNA in the samples taken from the throat-nasal swab based on reverse transcription of the RNA and subsequent amplification in real-time PCR.

The ViroQ SARS-FluA/B-RSV Kit is used for qualitative detection of SARS-CoV-2, Influenza A, Influenza B and RSV (Respiratory Syncytial Virus) RNA in the samples taken from the throat-nasal swab based on reverse transcription of the RNA and subsequent amplification in real-time PCR.

Rapid immunochromatographic test for the qualitative detection of C-reactive protein (CRP) in human whole blood, serum and plasma samples as an aid in diagnosis of acute inflammatory disorders.

The test is performed by applying the whole blood, serum or plasma sample to the sample well of the cassette and observing the formation of colored lines. CRP is detected by utilizing a combination of anti-CRP antibody coated particles and CRP antibody. The sample migrates by capillary effect along the membrane. If present in the sample, CRP reacts with anti-CRP antibody-coated particles and is captured by CRP antibody coated in the test (T) region.

Test sensitivity: > 99.9% (95.6% - 100.0%)*

Test specificity: 97.5% (96.3% - 98.7%)*

Overall Agreement: 97.8% (96.2% - 98.9%)*

* 95 % Confidence Interval

Rapid immunochromatographic test for the qualitative detection of C-reactive protein (CRP) in human whole blood, serum and plasma samples as an aid in diagnosis of acute inflammatory disorders.

The test is performed by applying the whole blood, serum or plasma sample to the sample well of the cassette and observing the formation of colored lines. CRP is detected by utilizing a combination of anti-CRP antibody coated particles and CRP antibody. The sample migrates by capillary effect along the membrane. If present in the sample, CRP reacts with anti-CRP antibody-coated particles and is captured by CRP antibody coated in the test (T) region.

Test sensitivity: > 99.9% (95.6% - 100.0%)*

Test specificity: 97.5% (96.3% - 98.7%)*

Overall Agreement: 97.8% (96.2% - 98.9%)*

* 95 % Confidence Interval

Rapid immunochromatographic test for the qualitative detection of C-reactive protein (CRP) in human whole blood, serum and plasma samples as an aid in diagnosis of acute inflammatory disorders.

The test is performed by applying the whole blood, serum or plasma sample to the sample well of the cassette and observing the formation of colored lines. CRP is detected by utilizing a combination of anti-CRP antibody coated particles and CRP antibody. The sample migrates by capillary effect along the membrane. If present in the sample, CRP reacts with anti-CRP antibody-coated particles and is captured by CRP antibody coated in the test (T) region.

Test sensitivity: > 99.9% (95.6% - 100.0%)*

Test specificity: 97.5% (96.3% - 98.7%)*

Overall Agreement: 97.8% (96.2% - 98.9%)*

* 95 % Confidence Interval

Rapid immunochromatographic test for the qualitative detection of Procalcitonin (PCT) in human whole blood, serum and plasma samples as an aid in diagnosis of systemic inflammation and sepsis.

The test is performed by applying the whole blood, serum or plasma sample to the sample well of the cassette and observing the formation of colored lines. PCT is detected by utilizing a combination of mouse anti-PCT antibody-coated particles and mouse anti-PCT antibody. The sample migrates by capillary effect along the membrane. If present in the sample, PCT reacts with mouse anti-PCT antibody coated particles and is captured by mouse anti-PCT antibody coated in the test (T) region.

Test sensitivity: 98.7% (96.3% - 99.7%)*

Test specificity: 98.9% (96.9% - 99.8%)*

Overall Agreement: 99.0% (97.8% - 99.7%)*

* 95% Confidence Interval

Rapid immunochromatographic test for the qualitative detection of Procalcitonin (PCT) in human whole blood, serum and plasma samples as an aid in diagnosis of systemic inflammation and sepsis.

The test is performed by applying the whole blood, serum or plasma sample to the sample well of the cassette and observing the formation of colored lines. PCT is detected by utilizing a combination of mouse anti-PCT antibody-coated particles and mouse anti-PCT antibody. The sample migrates by capillary effect along the membrane. If present in the sample, PCT reacts with mouse anti-PCT antibody coated particles and is captured by mouse anti-PCT antibody coated in the test (T) region.

Test sensitivity: 98.7% (96.3% - 99.7%)*

Test specificity: 98.9% (96.9% - 99.8%)*

Overall Agreement: 99.0% (97.8% - 99.7%)*

* 95% Confidence Interval