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no bacteria CE certification facemask China

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China. HS Code. 63079000. Product Description. Ce FDA Approval Disposable Anti Bacteria 3 Ply Face Mask. 1.Disposable Face Mask Advantages: 3 layers of filtration, no odor, anti-allergic materials, sanitary packaging, good. breathability. 2.

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Apr 05, 2020 · CE certification, as a necessary document for the legal sale of Chinese products in the European Union, has recently become the focus of the market. CE certificates issued by various certification agencies and intermediary companies have dazzled Chinese companies. Below, we will teach you how to verify CE certification. 1.

Jul 24, 2020 · Although both face mask types are designed to protect against the transmission of bacteria, they fall under different regulatory scrutiny. Respirator masks are considered personal protective equipment (PPE) products by both the European Union and US Food and Drug Administration (FDA), while surgical face masks are classified as a medical device.

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- With the bacteria resistance rate up to 99% - Individual sealed packaging, sterile - It can be recycled for 20 times - 800,000 production capacity per day - CE, FDA certification Packaging 2 pieces in one sealed packaging bag 8 bags in one box 36 boxes in one carton. Totally 576 pieces in one carton

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The company has perfect quality supervision and management mechanism, with the State Foreign Economic and Trade approved the import and export rights, has passed the ISO9001 quality certification, the European CE certification. Our company offers variety of products which can meet your multifarious demands.

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Jun 16, 2020 · Suggestion: Watch the 20 minutes video tutorial before reading this article. Click Here to Get the Starter Package: All Categories. Importing products from China to the European Union? Depending on the product, importers are required to ensure full compliance with all relevant CE directives – a process that is far more complex than requesting a test report from your supplier.

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Jul 24, 2020 · Although both face mask types are designed to protect against the transmission of bacteria, they fall under different regulatory scrutiny. Respirator masks are considered personal protective equipment (PPE) products by both the European Union and US Food and Drug Administration (FDA), while surgical face masks are classified as a medical device.

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