Aj Pro FFP2 with Neck Strap

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.

  Test results

  Reusability NR - Not Reusable

  This filtering facepiece protects against particles like dusts, mists, and aerosols. It is marked "NR" for "Non-Reusable," meaning it is intended for single-shift use only and should be discarded after one use.

• 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.

• MD Label

  MD stands for "Medical Device." It refers to any instruments, apparatus, machines, implants, or other similar or related articles that are intended to be used for human beings for the purpose of diagnosis, prevention, monitoring, treatment or alleviation of disease, injury or disability. In Europe, a MD Label is a special label that must be on all Medical Devices that are sold or used in the European Union (EU). The label must include information about the product, such as the name of the manufacturer, the intended use of the product and CE mark. To be able to sell or use a Medical Device in the EU, the device must meet certain standards and requirements set by the European Union and notified body.