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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.
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.
On this scale, 1 is a completely ineffective respirator. Some respirator manufacturers, like 3M, complained that DM and DFM respirators with superior filtration, that would normally receive an APF well above 2, were being "held hostage" by poorly-performing respirators. [97]
The N95 respirator mask was developed by 3M and approved in 1972. [114] Due to its ability to filter viral particulates, its use was recommended during the COVID-19 pandemic but supply soon became short. [114] Much of the company's supply had already been sold prior to the outbreak. [115]
According to 3M, respirators made according to the following standards are equivalent to US N95 or European FFP2 respirators "for filtering non-oil-based particles such as those resulting from wildfires, PM 2.5 air pollution, volcanic eruptions, or bioaerosols (e.g. viruses)": [33] Chinese KN95 (GB2626-2006): similar to US.
This image is a work of the National Institute for Occupational Safety and Health, part of the Centers for Disease Control and Prevention in the United States Department of Health and Human Services, taken or made as part of an employee's official duties.
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