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Apr 17, 2020 · Counterfeit respirators are products that are falsely marketed and sold as being NIOSH-approved and may not be capable of providing appropriate respiratory protection to workers. When NIOSH becomes aware of counterfeit respirators or those misrepresenting NIOSH approval on the market, we will post
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Class 1 Medical Device as per EU MDR CE Marking. Most Class 1 medical device can be self Certified by EU MDR or even as per US FDA regulations. Class 1 Medical Device, CE marking, Notified Body involvement is not mandatory. Class 1 products manufactures ISO 13485 implementation and certification is not required.
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Apr 17, 2020 · Counterfeit respirators are products that are falsely marketed and sold as being NIOSH-approved and may not be capable of providing appropriate respiratory protection to workers. When NIOSH becomes aware of counterfeit respirators or those misrepresenting NIOSH approval on the market, we will post
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