Opharm Face Mask FFP2 Green

Medical devices with the EN 1041:2008+A1:2013 rating are tested for the adequacy and clarity of information supplied by the manufacturer. This ensures you receive clear, complete, and understandable instructions for safe and effective use, helping you operate the device correctly and safely.

Medical devices with the ISO 15223-1 rating are tested for clear and consistent communication of important information using standardized symbols. This means you can easily understand crucial safety and usage details on your medical products, regardless of language.

Medical devices with the EN 13485:2016 rating are tested via a comprehensive quality management system for their safety, performance, and regulatory compliance. This ensures the products you use are reliably made and safe for your health.

Medical face masks with the EN 14683:2019+AC:2019 rating are tested for bacterial filtration efficiency, breathability, splash resistance, and microbial cleanliness. This ensures they effectively help reduce the spread of infectious agents and are safe and comfortable for general use.

Products from companies with the EN ISO 9001:2015 rating are tested for the company's systems for consistently providing quality products and services and meeting customer needs. This means the company is committed to consistent quality, aiming to meet your needs and improve its offerings, leading to more reliable products and better customer experience.

Medical devices with the EN 14971 rating are tested for potential hazards and associated risks throughout their entire lifecycle. This means manufacturers have systematically identified and reduced possible dangers, ensuring the products are safer for you to use.

"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.