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During the COVID-19 pandemic, the mask and respirator market rapidly grew, along with counterfeit respirators. [1] NIOSH, on behalf of the Department of Health and Human Services, filed a trademark application on June 17, 2020, for various 42 CFR 84 trademarks, including the N95, allowing NIOSH to enforce rules on counterfeit masks outside of rules defined in 42 CFR 84.
For example, there is a list of over 500 harmful gases in the Respirator Selection Guide [21] and over 60 of them have no warning properties, and there is no such information for over 100 of them. So, if one uses warning properties to replace cartridges, this may lead to breathing air with an excess harmful gas concentration in some cases.
The European respirator standards refer to the filtering classification by EN 149, EN 14683, and EN 143, all European standards of testing and marking requirements for respirators. [1] FFP standard masks (where FFP stands for filtering facepiece) [ 2 ] cover the nose, mouth and chin and may have inhalation and/or exhalation valves.
Other problems include using a size other than the size the wearer was fit-tested on, using the wrong sort of cartridge, re-using a cartridge that is no longer good, not doing a positive- and negative-pressure seal check each time the mask is donned, failing to test the respirator (and perhaps inhaling the carbon from a broken cartridge), and ...
A respirator is a device designed to protect the wearer from inhaling hazardous atmospheres including lead fumes, vapors, gases and particulate matter such as dusts and airborne pathogens such as viruses.
An N95 respirator is a disposable filtering facepiece respirator or reusable elastomeric respirator filter that meets the U.S. National Institute for Occupational Safety and Health (NIOSH) N95 standard of air filtration, filtering at least 95% of airborne particles that have a mass median aerodynamic diameter of 0.3 micrometers under 42 CFR 84, effective July 10, 1995.