Innova Medical Group, Inc was formed 3/27/2020 in
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Posted On: 08/12/2020 4:30:09 PM
Innova Medical Group, Inc was formed 3/27/2020 in Nevada by Charles Huang. California Registration
Quote:
COVID-19 RAPID DIAGNOSTIC TESTS
Device: BIOTIME SARS-CoV-2 IgG/IgM Rapid Qualitative Test
Manufacturer: Xiamen Biotime Biotechnology Co., Ltd.
an Innova Medical Group Inc. company, (CALIFORNIA)?
Authorized, Global Manufacturer's Representative: COVIDSignals™
(MAINE and GERMANY), a Nano LiquiTec Group company.
COVIDSignals
Quote:
Nano LiquiTec® pivoted in March 2020 from operating the green nanotech manufacturing/distribution co., Deutsche Nano LiquiTec GmbH (www.nanoliquitec.com) to become COVIDSignals™ (Maine, US) and serve as a trusted supply conduit between healthcare institutions, airlines, pro sports organizations, industries, and governments, to leading biotech makers of COVID-19 rapid test kits (antibody and antigen).
COVIDSignals™ (www.covidsignals.com) is the strategic partner, manufacturer's rep., and global distributor of the Biotime SARS-CoV-2 RDT IgG/IgM antibody test - a rapid, qualitative, and convenient in-vitro assay using the Colloidal Gold Immunochromatography Method (nanoparticles) for the detection of COVID-19 IgM and IgG virus antibodies in human serum, plasma, or whole blood samples. It delivers a superior, high-accuracy in specificity and sensitivity of 98+%, and utilizes a German Nitrocellulose membrane, the world's most advanced.
COVIDSignals™ also offers the Biotime Rapid (30-minute) Antigen Test - the first in the world.
Biotime SARS-CoV-2 testing holds a CE Rating, anticipates receiving an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA)(submission number: PEUA200265, with data evaluated with an FDA, in-house lab - completed 6/20), and has been evaluated by an MD within Britain's National Health Service (NHS), who reported, “We have performed tests using the Biotime COVID-19 serology test on 50 PCR confirmed patients. The test picked up every, single infected patient. To further elaborate, the test picked up IgM positives in early-stage disease, IgG positives in later-stage disease, and IgM/IgG positive in mid-stage. We are very pleased with these findings and are recommending the service approve these tests.”
Biotime has shipped over 80 million tests to 30+ countries and is the chosen test of a premier international airline, contracted to provide 51 million tests for passengers.
And the manufacturer:Xiamen Biotime Biotechnology Co., Ltd. Letter to Natalie Huang. Wonder if she is related to Innova's Charles Huang?
---
Above re--posted from Ihub BigE1960
Quote:
COVID-19 RAPID DIAGNOSTIC TESTS
Device: BIOTIME SARS-CoV-2 IgG/IgM Rapid Qualitative Test
Manufacturer: Xiamen Biotime Biotechnology Co., Ltd.
an Innova Medical Group Inc. company, (CALIFORNIA)?
Authorized, Global Manufacturer's Representative: COVIDSignals™
(MAINE and GERMANY), a Nano LiquiTec Group company.
COVIDSignals
Quote:
Nano LiquiTec® pivoted in March 2020 from operating the green nanotech manufacturing/distribution co., Deutsche Nano LiquiTec GmbH (www.nanoliquitec.com) to become COVIDSignals™ (Maine, US) and serve as a trusted supply conduit between healthcare institutions, airlines, pro sports organizations, industries, and governments, to leading biotech makers of COVID-19 rapid test kits (antibody and antigen).
COVIDSignals™ (www.covidsignals.com) is the strategic partner, manufacturer's rep., and global distributor of the Biotime SARS-CoV-2 RDT IgG/IgM antibody test - a rapid, qualitative, and convenient in-vitro assay using the Colloidal Gold Immunochromatography Method (nanoparticles) for the detection of COVID-19 IgM and IgG virus antibodies in human serum, plasma, or whole blood samples. It delivers a superior, high-accuracy in specificity and sensitivity of 98+%, and utilizes a German Nitrocellulose membrane, the world's most advanced.
COVIDSignals™ also offers the Biotime Rapid (30-minute) Antigen Test - the first in the world.
Biotime SARS-CoV-2 testing holds a CE Rating, anticipates receiving an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA)(submission number: PEUA200265, with data evaluated with an FDA, in-house lab - completed 6/20), and has been evaluated by an MD within Britain's National Health Service (NHS), who reported, “We have performed tests using the Biotime COVID-19 serology test on 50 PCR confirmed patients. The test picked up every, single infected patient. To further elaborate, the test picked up IgM positives in early-stage disease, IgG positives in later-stage disease, and IgM/IgG positive in mid-stage. We are very pleased with these findings and are recommending the service approve these tests.”
Biotime has shipped over 80 million tests to 30+ countries and is the chosen test of a premier international airline, contracted to provide 51 million tests for passengers.
And the manufacturer:Xiamen Biotime Biotechnology Co., Ltd. Letter to Natalie Huang. Wonder if she is related to Innova's Charles Huang?
---
Above re--posted from Ihub BigE1960
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