Therma Bright Inc V.THRM

Alternate Symbol(s): TBRIF

Healthcare Medical Devices

Therma Bright Inc. is a developer and partner in a range of diagnostic and medical device technologies. It focuses on providing consumers and medical professionals with solutions that address medical and healthcare challenges. It is involved in developing, acquiring, manufacturing, and marketing proprietary healthcare and medical devices for the consumer and institutional marketplace. Its product offerings include Covid-19 diagnostic test product line, such as AcuVid COVID-19 Rapid Antigen Saliva Test and AcuVid COVID-19 Rapid Antibody Test; Sores & Bite Inflammation Therapy product line, such as InterceptCS Cold Sore Prevention System and TherOZap, and Muscle Pain & Blood Circulation Health Therapy product line, such as Venowave, which is a circulation booster designed to improve circulation in the lower extremities. The Venowave is a medical compression pump that is lightweight, compact, battery operated, designed to treat and alleviate the symptoms associated with poor circulation.

TSXV:THRM - Post by User

Therma Bright Inc > THRM - Going to be Epic 💥

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Comment by Smokey1958on May 04, 2021 1:40pm

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Post# 33124406

RE:RE:RE:RE:THRM - Going to be Epic 💥

Thank you, TheeRock! Didn't know how they got around not doing their own approval which is very different from authorization .....which they clearly make as a distinction between approving a device and authorizing it (EUA) without the more rigorous testing that would exist when approving.

Cheers!

TheeRook wrote: Something like the LoD u should know.
the FDA is all about the Lod.

NDU/mL = NAAT Detectable Units/mL

https://www.fda.gov/medical-devices/coronavirus-covid-19-and-medical-devices/sars-cov-2-reference-panel-comparative-data

Smokey1958 wrote:
To what approvals are you referring? THRM already has CE approval for the EU.

I expect you're referring to the Limit Of Detection required for HC and FDA approval. I'm not sure Canada is much of a consideration as Rob Fia clearly stated in a recent NR that a HC application was the last one on the list. As for FDA approval I'm not certain, but I don't believe that a Limit of Detection is required for an EUA.

Brazil would also have something similar to an EUA ....is that the same for the rest of the South American and African countries???

THRM essentially guaranteed the manufacture of 100,000 devices by June to their new European partner ....pending the results of the current testing in Brazil. Seems to me most of the pieces required for THRM to set up manufacturing and distributing devices is now ongoing or is already in place.

GLTE!!!