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Aerus ActivePure Technology Air Purifier Kills COVID-19 on Surfaces in Lab Results

Aerus is awaiting final approval from the FDA for Emergency Use Authorization (EUA) for the Aerus Hydroxyl Blaster with ActivePure Technology for use in reducing SARS-CoV-2 surface pathogens. The results have also been submitted by Acrus to the FDA-equivalent Canadian and European Union regulators, requesting that they clear Aerus ActivePure devices to combat the SARS-Covy-2 coronavirus. Aerus expects to receive clearances in all jurisdictions.

Additionally, Aerus is also ronning independent laboratory tests to demonstrate the efficacy of ActivePure Technology on airborne SARS-CoV-2 virus for FDA clearance.

Controlled, independent laboratory studies have established the efficacy of ActivePure Technology in Aerus products including:

  • 93% surface kill in three hours of live SARS-CoV-2, even when covered by a protective biofilm, with the Aerus Hydroxyl Blaster with ActivePure Technology
  • 98% surface kill in six hours of live SARS-CoV-2, even when covered by a protective biofilm, with the Aerus Hydroxyl Blaster with ActivePure Technology
  • 99.999% kill rate of airborne RNA viruses in just 30 minutes with the Aerus Medical Guardian with ActivePure Technology, an FDA 510(k) Cleared Class II Medical Device
  • 99.9999% kill rate of airborne RNA viruses in 60 minutes with the Aerus Medical Guardian with ActivePure Technology