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This standard is closer to international standards, such as EU standard en149, NIOSH certifi ion of the United States, as 1716 of Australia, js-t-8151 of Japan. 2. EU requirements for face mask Products sold in the EU market must obtain CE certifi ion.
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Both the Medical Device Directive 93/42 / EEC and the Medical Device Regulation EU 2017/745 specify the information that should appear on the packaging in which the medical face mask is supplied. The following information must be provided: a number of