Medical Device News Magazine

BluSense Diagnostics Releases a COVID-19 Antibody Test

Provides Lab-Grade Accuracy in Minutes

About Medical Device News Magazine

About Medical Device News Magazine. We are a digital publication founded in 2008 located in the United States.

Advertise with Medical Device News Magazine! Join Our #1 Family of Advertisers!

We pride ourselves on being the best-kept secret when it comes to distributing your news! Our unique digital approach enables us to circulate your...

BluSense Diagnostics CE-marked its blood test for the detection of the antibodies, which identifies if a person has had the coronavirus infection (COVID-19).

ViroTrack Sero COVID-19 IgA+IgM/IgG Ab has been evaluated in collaboration with Hvidovre hospital, demonstrating an exceptional laboratory-grade accuracy in 13 minutes.

“It is a great achievement, as we developed and CE-marked the diagnostics product in as little as three months. This would not have been possible without the hard work of our team and our patented technology – Immuno-Magnetic Assay (IMA), which can be scaled to almost any infectious disease”, – says BluSense Diagnostics CEO and founder Filippo Bosco.

“We are proud to provide an antibody test as it will identify who has had the virus and possibly is immune to it. The knowledge could also play a critical role in supporting the development of vaccines and surveillance efforts.”

During the clinical evaluation study in Hvidovre hospital, more than one hundred samples were tested with ViroTrack COVID-19 antibody test comparing the performance to the laboratory tests that are leading in the market. The results showed that the test developed by BluSense Diagnostics demonstrates above 90% accuracy in 8 days or more after the symptoms started as well as a very high performance during the early stage of the infection.

“Our product employs the best of two worlds – it has the convenience of the rapid diagnostics and the high accuracy of the laboratory tests. Because of that, we can deploy it in decentralized clinical settings, where time and great reliability are of paramount importance”, – says F. Bosco.

Today, when a hospital examines a patient for COVID-19, the sample is sent to the hospital’s laboratory for analysis, which takes a few hours or even a few days. The ViroTrack COVID-19 serology test, which runs on a fully automated and portable analyser BluBox, allows to shorten the testing time and provides automated on-the-spot sample processing.

ViroTrack COVID-19 serology test detects three COVID-19 antibodies (IgA, IgM and IgG) and helps determine a patient’s immune response as well as monitor all antibodies generated through disease progression.

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Other News

Shoulder Innovations Further Strengthens IP Portfolio in Key Areas with Recent Patent Grants

"These recent grants further strengthen key patent families that are foundational to our technology, and we are pleased the USPTO continues to recognize our meaningful innovation in the shoulder arthroplasty segment," said Rob Ball, CEO of Shoulder Innovations. "This noteworthy expansion of our IP position represents the culmination of over 10 years of research and development, and we are proud of our team for their continued dedication to creating practical solutions for shoulder surgeons and advancing patient outcomes."

Radical Catheter Technologies Presents Analysis of Disruptive, Recently FDA-Cleared Endovascular Technology at the Society of NeuroInterventional Surgery 21st Annual Meeting

This new catheter, the first product commercialized from this novel technology platform, is designed to enable access to the blood vessels in the brain for both femoral and radial access. A multi-center analysis of this disruptive technology is being presented today at Society of NeuroInterventional Surgery 21st annual meeting. In addition, the Company confirmed the closing of a $20 million financing round led by NeuroTechnology Investors, which will be used to scale the company and expand the Radical platform notes Radical Catheter Technologies.

Rapid Medical™ Completes Initial Neurovascular Cases in the USA Following FDA Clearance of Its Active Access Solution

“With DRIVEWIRE, our design goal was to bring new levels of access and control to the interventional suite while improving best-in-class guidewires,” comments Giora Kornblau, Chief Technology Officer at Rapid Medical. “When physicians are looking for technologies that increase the clinical possibilities and safety for the patient, we want Rapid to be the first place they look.”