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Nov 24, 2020 · These assessments were developed as an assessment of the filter efficiency for those respirators represented as certified by an international certification authority, other than NIOSH, to support the availability of respiratory protection to US healthcare workers and other workers due to the respirator shortage associated with COVID-19.

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Surgical N95 Respirator Face Mask under FDA Product Code MSH must undergo NIOSH Certification prior to FDA 510k application and clearance. General N95 face mask (without Virus/ Bacteria protection claim ) under product code MSH can be directly registered and listed without 510k and NIOSH.

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Single-use Medical Face Mask: Regulations for the Supervision and Administration of Medical Devices: YY/T 0969-2013: Surgical Mask: YY 0469-2011: EU: Type I, Type II, Type IIR: Directive 93/42/EEC: EN 14683-2019+AC:2019: United States: Level 1, Level 2, Level 3: 21 CFR Subchapter H: ASTM F2100-19

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CEL Data last Updated: November 3, 2020 11:12 AM Page last reviewed: November 13, 2020 Page last updated: November 13, 2020 Content source: National Institute for Occupational Safety and Health (NIOSH)

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Medical face masks are considered as medical devices and regulated by national medical device regulations. Regulations will define the legal obligations, to ensure that medical face masks provide the minimum level of protection against intended risks. Specific requirements by classification are cited in the referenced performance standards.

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