Opharm Face Mask FFP2 Black

Standards and labels

• EN 149:2001+A1:2009

  Filtering half masks (respirators) with the EN 149:2001+A1:2009 rating are tested for their filtering efficiency against airborne particles, breathing resistance, and secure fit. This ensures the mask effectively protects your respiratory system and helps you choose the right level of filtration (FFP1, FFP2, FFP3) and reusability.

  Reach out to ask about the standard test results

• EN ISO 9001:2015

  Products with the EN ISO 9001:2015 rating are tested for the company's commitment to consistent quality and customer satisfaction through its management systems. This means you can expect reliable products and a focus on meeting your needs.

  Reach out to ask about the standard test results

• Made in Europe

  "Made in Europe" is a label used to indicate that a product has been manufactured or produced in Europe. The European Union (EU) has regulations that set the requirements for the "Made in" label. According to EU rules, products that are labeled as "Made in" must be entirely produced within the EU. This means that all the stages of production, from raw materials to the finished product, must take place within the EU. However, the EU does not have specific rules for labeling a product "Made in Europe" as a whole, because Europe is not a single country but a continent. Each country may have their own regulations for labeling a product "Made in Europe", and it's important to check the regulations of the country where the product will be sold.

• CE Marking

  CE Marking is a label that shows a product meets certain safety and environmental standards set by the European Union. To get the CE Marking, a company must test and certify their product meets these standards. CE Marking is required for many products sold in the EU, including electronics, machinery, toys and medical devices. It helps ensure that products are safe for consumers and the environment, and allows for easy trade within the EU.