Nano Air Mask is now DESAVO

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Independent Third-Party Test Results

 

  

DESAVO Pro-Line

This information is provided for informational purposes only and is not intended to suggest the safety or effectiveness of DESAVO for particulate filtration. 

DESAVO face masks have been tested by NPPTL (The National Personal Protective Technology Laboratory), the NIOSH laboratory that operates within the CDC to conduct scientific research, develop guidance and authoritative recommendations, and disseminate information to help prevent disease, injury, and death for millions of working men and women relying on equipment tested.  DESAVO is not an N95 mask (also known as a filtering facepiece respirator), and it is not NIOSH-approved. 

The complete NPPTL Assessment for DESAVO may be found on the CDC Website here; for ease of reference, see the PDF below:


 

CDC/NIOSH NPPTL Assessment
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DESAVO is being marketed as a face mask under the Emergency Use Authorization for use as source control by the general public as well as by HCP in healthcare settings as to help prevent the spread of infection or illness during the COVID-19 pandemic. It is not an N95 mask (also known as a filtering facepiece respirator), and it is not NIOSH-approved.

 

SHOP MASKS

Nano Air Classic / PURE-MSK

 

This information is provided for informational purposes only and is not intended to suggest the safety or effectiveness of PURE-MSK for particulate filtration.

 

COUGH SIMULATION - Florida Atlantic University

By Manhar Dhanak, Siddhartha Verma and John Frankenfield
Department of Ocean and Mechanical Engineering, FAU

Qualitative visualization of emulated coughs to examine the effectiveness of different mask materials in impeding the dispersal of droplets that are 10 microns in diameter on average. See visualization below.

 


NELSON LABS TESTING

PURE-MSK surgical masks have been tested by an independent third-party, Nelson Labs, a leading U.S. provider of microbiological and analytical lab testing.  Nelson Laboratories performs specific testing to assess the performance of materials and products, and it does not make claims about the overall safety and efficacy of a product. See full reports below:


Fluid Penetration Resistance Final Report
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PURE-MSK is FDA 510(k)-cleared for use as a surgical mask to provide a physical barrier to fluids and particulate materials.   It is intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from transfer of microorganisms, body fluids, and particulate matter. 

PURE-MSK is being marketed as a face mask under the Emergency Use Authorization for use as source control by the general public as well as by HCP in healthcare settings as to help prevent the spread of infection or illness during the COVID-19 pandemic.  It is not an N95 mask (also known as a filtering facepiece respirator), and it is not NIOSH-approved. 

 


SHOP MASKS
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