Nano Masks ~ The Details
Protect youreself from Avian Flu, SARS, Tuberculosis, and other AirBorne Diseases... According to the:
Click here for more Avian Influenza information from the Centers for Disease Control and Prevention (CDC)
Recommendations for Avian Influenza include:

Use of a fit-tested respirator, at least as protective as a National Institute of Occupational Safety and Health (NIOSH)-approved N-95 filtering facepiece (i.e., disposable) respirator, when entering the room.


OUR RECOMMENDATIONS... 


PREVENTATIVE PRODUCTS: Masks, Barriers, and filters for Airborne Pathogen Protection

Nano Mask - This enhanced filtration media has a .027 microns filtration capability, which provides protection against SARS, Avian Flu (H5N1), and other viruses. Nanoparticles absorb and destroy viruses and bacteria in both inhaled and exhaled breath

 

ADULT SIZE NanoMasks:


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CHILD SIZE NanoMasks:


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See Nano Mask Filter Replacements below and to the right...

 

NanoMask
SKUS: WP-NM1-102 (B,R,Y,M,G) / WP-NM5-FP1

CHILD SIZE SKUS: WP-NM2-100 (B,R,Y,P,G) / WP-NM5-FP2

A higher level of protection (Click here for NanoMask FAQs)

1. What is filtration efficiency?
Filtration efficiency is the measurement of a filters capacity to remove particulates, such as virus and bacterium, from air as it flows through the filter. Filtration efficiency is stated as a percentage of efficiency and is affected by such factors as size of the particulates to be filtered, volume of air and duration of use. An N-95 rated mask, for example, is 95% efficient at removing particles with a median diameter of approximately 0.3 microns at a volume of 85 liters per minute. Duration of use is a critical factor because virus and bacterium can infest the filter for extended periods of time. Bacteria can reproduce on their own while virus can survive for days before infecting a living host. Virus and bacterium can also move through filters over time resulting in an erosion of filtration efficiency and increase in the associated risk factors. 
2. What is the filtration efficiency of the NanoMask?
The filtration efficiency of the filter material used in the NanoMask is 99%. We enhance this intrinsic filtration efficiency with a coating of nano-particles. The nano-particles counteract the ability of pathogens to live and/or reproduce on the filter by eradicating virus and bacterium that come into contact with the filter surface.
3. How do the nano-particles work?
Nano-particles act as a destructive agent on the surface of the filter. The particles are positively or negatively charged and effectively break down the microbial structure of pathogens coming into contact with the filter.
4. How often do you have to replace the filters?
The active life of the nano-particles is approximately 48 continuous hours. We are recommending replacement at that time.
5. What is the shelf life of the filter?
The shelf life is currently two years. We will continue to adjust shelf life as we are able to test aged inventory for efficacy.
6. Have the filters been tested by a reputable testing facility?
Yes, the filters are tested at Nelson Laboratories in Salt Lake City, UT. Nelson Labs has provided high quality test services to manufacturers in the medical device, pharmaceutical and nutraceutical industries since 1985. They manage a 62,000 sq. ft. FDA registered facility in Salt Lake City, UT where they maintain 80 labs along with a custom-built 3,000 sq. ft. cleanroom and employ over 170 scientists and staff. Among their more than 75 degreed scientists are over 25 registered and specialist microbiologists (National Registry of Microbiologists). They currently offer more than 400 microbiological and analytical tests and are third-party
certified to ISO 9001 (BSI) and EN 45001/IEC/ISO 17025 standards accredited (AMTAC).
7. Has the NanoMask been approved by NIOSH?
The NanoMask is not yet validated by NIOSH. It was important to validate our nano-particle enhanced filter against bacterial and viral contaminates and NIOSH was not able to provide this biological validation. They currently test against a challenge of sodium chloride which is not able to measure the effectiveness of the nano-particle enhancement. We are developing the nano-particle technology in conjunction with the U.S. Military and sodium chloride testing was not sufficient for our purposes. We are registered with NIOSH and intend to submit the mask for certification in the near future but found it necessary to validate the bacterial and viral efficacies of the technology prior to a submission to NIOSH. Please refer to the ‘NIOSH Testing” PDF posted in our web site
for a more detailed explanation.
8. Does the NanoMask fit small children?
The NanoMask is currently available only in an adult size. We are developing a children’s size and hope to have it available by late November.
9. How do you disinfect the NanoMask?

NIOSH recommends the following for cleaning and sanitation:
• Remove the filter.
• Wash the frame in warm (43°C/110°F maximum) water with a mild detergent.
• Rinse the mask thoroughly in clean, warm (43°C/110°F maximum), preferably running water.
• If the detergent used does not contain a disinfecting agent immerse the mask for two minutes in a disinfectant water solution such as:
• Quaternary ammonia disinfectant (one packet per 2 gallons or per manufacturer's recommendation).
• Hypochlorite solution (50 ppm of chlorine) made by adding approximately 2 ml of laundry bleach to 1 liter of water at 43°C/110°F.
• Aqueous solution of iodine (50 ppm of iodine) made by adding approximately 0.8 ml of tincture of iodine (approximately 7% ammonium and potassium iodide, 45% alcohol, and 48% water) to 1 liter of water at 43°C/110°F.
• Other commercially available cleansers of equivalent disinfectant quality when used as directed.
• Rinse components thoroughly in clean, warm (43°C/110°F maximum), preferably running water. The importance of thorough
rinsing cannot be overemphasized. Detergents or disinfectants that dry on the frame may result in dermatitis. In addition, some
disinfectants may cause deterioration of rubber if not completely removed.
• Allow the respirator to air dry in a non-contaminated environment.


20 Pack of ADULT SIZE Nano Mask filters ~
Stock up now on Extra Filters

ADULT MULTI PACK includes a mask in each color - Blue, Red, Green, Yellow and Magenta. Comes with two easy-to-insert, replaceable filters. Available in five colors. Protect the whole business with the Adult Multi-Pack (featuring 5 Adult Masks and 90 filters.)

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20 Pack of CHILD SIZE Nano Mask filters
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FAMILY PACK Each Mask Comes with two easy-to-insert, replaceable filters. Available in five colors. Protect your whole household with the Family Pack (featuring 3 Adult Masks with Filters and 2 Child Masks.)

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NEW 100 PACK ASSORTED COLOR ADULT SIZE!
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MORE INFORMATION FROM THE CDC on Avian Flu Prevention & Protection:

How are avian, pandemic, and seasonal flu different?
Avian flu is caused by avian influenza viruses, which occur naturally among birds.
Pandemic flu is flu that causes a global outbreak, or pandemic, of serious illness that spreads easily from person to person. Currently there is no pandemic flu.
Seasonal flu is a contagious respiratory illness caused by influenza viruses.

What You Should Know

Specific Topics

Information for Specific Groups

Interim Recommendations for Infection Control in Health-Care Facilities Caring for Patients with Known or Suspected Avian Influenza

Note: CDC is revising its interim guidance for infection control precautions for avian influenza. The revised recommendations will be posted on this website as soon as they are finalized.

Objective

This document provides interim guidance for protection of health-care workers involved in the care of patients in the United States with known or suspected avian influenza. Depending upon where avian influenza is active in the world, such patients may be recently returning travelers entering U.S. health-care facilities or individuals who have had close contact with domestic poultry infected with avian influenza in the United States. For information regarding the clinical and epidemiologic criteria to be used in screening patients for possible avian influenza, see the “Update on Influenza A(H5N1) and SARS: Interim Recommendations for Enhanced U.S. Surveillance, Testing, and Infection Control” and “Interim Recommendations for Persons with Possible Exposure to Avian Influenza During Outbreaks Among Poultry in the United States .”

Background

Influenza viruses that infect primarily birds are called “avian influenza viruses.” These type A influenza viruses are genetically distinguishable from influenza viruses that usually infect people. There are many subtypes of avian influenza A viruses, including H7 and H5. Avian influenza viruses can be distinguished as “low pathogenic” and “highly pathogenic” forms based on genetic features of the virus and the severity of the illness they cause in poultry.

Avian influenza viruses do not usually infect humans; however, several instances of human infections and outbreaks of avian influenza have been reported since 1997 (for more information, see “ Basic Information About Avian Influenza” ). In 2003, influenza A (H7N7) infections occurred in the Netherlands among persons who handled infected poultry and among their families during an outbreak of avian flu among poultry. More than 80 cases of H7N7 illness were confirmed by testing (the symptoms were mostly confined to eye infections, with some respiratory symptoms), and one patient died (a veterinarian who had visited an H7N7 influenza-affected farm). Although there was evidence of limited person-to-person spread of infection, sustained human-to-human transmission did not occur in this or other outbreaks of avian influenza. It is believed that most cases of avian influenza infection in humans have resulted from contact with infected poultry or contaminated surfaces. However, other means of transmission are also possible, such as the virus becoming aerosolized and landing on exposed surfaces of the mouth, nose, or eyes, or being inhaled into the lungs.

Infection and disease in people caused by highly pathogenic avian influenza H5N1 infection have been identified recently in Vietnam and Thailand. On February 1, 2004, the World Health Organization (WHO) reported that laboratory test results had confirmed two fatal cases of human H5N1 infection in Vietnam in which human-to-human transmission may have occurred. The cases occurred in two sisters who were part of a cluster of four cases of severe respiratory illness in a single family. According to WHO, a detailed investigation of this cluster concluded that limited human-to-human transmission was one possible explanation, but direct poultry-to-human transmission could not be ruled out.

The following interim recommendations are based on what are deemed optimal precautions for protecting individuals involved in the care of patients with highly pathogenic avian influenza from illness and for reducing the risk of viral reassortment (i.e., mixing of genes from human and avian viruses). The ability of low pathogenic avian influenza viruses to cause infection and serious disease is less well established, but appears to be lower than that of highly pathogenic viruses based on available information. Nonetheless, it is considered prudent to take all possible precautions to the extent feasible when caring for patients with known or possible avian influenza.

Rationale for Enhanced Precautions

Human influenza is thought to transmit primarily via large respiratory droplets. Standard Precautions plus Droplet Precautions are recommended for the care of patients infected with human influenza. However, given the uncertainty about the exact modes by which avian influenza may first transmit between humans additional precautions for health-care workers involved in the care of patients with documented or suspected avian influenza may be prudent. The rationale for the use of additional precautions for avian influenza as compared with human influenza include the following:

Recommendations for Avian Influenza

All patients who present to a health-care setting with fever and respiratory symptoms should be managed according to recommendations for Respiratory Hygiene and Cough Etiquette and questioned regarding their recent travel history.

Patients with a history of travel within 10 days to a country with avian influenza activity and are hospitalized with a severe febrile respiratory illness, or are otherwise under evaluation for avian influenza, should be managed using isolation precautions identical to those recommended for patients with known Severe Acute Respiratory Syndrome (SARS). These include:

For additional information regarding these and other health-care isolation precautions, see the Guidelines for Isolation Precautions in Hospitals. These precautions should be continued for 14 days after onset of symptoms or until either an alternative diagnosis is established or diagnostic test results indicate that the patient is not infected with influenza A virus. Patients managed as outpatients or hospitalized patients discharged before 14 days with suspected avian influenza should be isolated in the home setting on the basis of principles outlined for the home isolation of SARS patients (see http://www.cdc.gov/ncidod/sars/guidance/i/pdf/i.pdf).

Vaccination of Health-Care Workers against Human Influenza

health-care workers involved in the care of patients with documented or suspected avian influenza should be vaccinated with the most recent seasonal human influenza vaccine. In addition to providing protection against the predominant circulating influenza strain, this measure is intended to reduce the likelihood of a health-care worker’s being co-infected with human and avian strains, where genetic rearrangement could take place, leading to the emergence of potential pandemic strain.

Surveillance and Monitoring of Health-Care Workers

asteriskRespirators should be used in the context of a complete respiratory protection program as required by the Occupational Safety and Health Administration (OSHA). This includes training, fit-testing, and fit-checking to ensure appropriate respirator selection and use. To be effective, respirators must provide a proper sealing surface on the wearer's face. Detailed information on a respiratory protection program is provided at this OSHA web page.

This CDC Page last modified May 21, 2004