* for human samples validated by qPCR. The defined threshold is Ct ≤ 30.
CE and ISO 13485 certified product.
• SPECIFICITY: 100%
• SENSITIVITY: 97%
• RESULT: 4-10 MINUTES
• COVERS ABOUT 99% OF 2.500.000+ MUTANTS
Due to the procedure not previously used in practice, the test can provide uniquely reliable results, eliminating false positives and false negatives by focusing on the detection of infectious individuals, thus helping to avoid unnecessary restrictions for those, who are not in fact contagious. Its accurate and extremely rapid SARS-COV-2 RNA detection method can thus offer an advantage over other PCR methods.
“Conclusions: Until the 9th day after the onset of symptoms, RT-LAMP had the same diagnostic accuracy as RT-qPCR. These findings suggest that RT-LAMP can be used as a diagnostic tool for COVID-19 as an alternative to RT-qPCR in the acute symptomatic phase of COVID-19.”
Diagnostic accuracy of LAMP versus PCR over the course of SARS-CoV-2 infection, Inaba et al. IJID, 2021.
“The FEMTO-ID LAMP kit digital genetic test for SARS-COV-2 detection proved to be incredibly successful during independent tests. Its specificity surpasses that of classic PCR-based tests, and which is a real advantage, it covers all new, emerging virus strains – it can also be swiftly adapted to any infectious agent leading to bacterial or viral infections. It is ultrafast, highly sensitive, and budget-friendly, which is a neverseen significant benefit. I really think that this test can revolutionize medical fields in a way!”
Balázs Rózsa, Assist. Prof, MD, PhD and physicist
Group leader, Institute of Experimental Medicine
Head of the Laboratory of Neural Circuits and Computation,
Group leader, Pázmány Péter University
If the FEMTO-ID LAMP kit digital genetic test has raised your interest, we are happy to assist you!