Portwest FFP2 Valved Fold Flat Respirator, White

Standards and labels

• EN 149:2001+A1:2009

  EN 149:2001+A1:2009 is a European standard for filtering half masks for protecting against particles and it is an amendment of EN 149:2001. It outlines additional requirements for mask design and performance testing. The mask must be able to filter a certain percentage of particles, have good breathability, and fit securely to the face. The test results shows how well the mask filters and how easy it is to breathe through, also it includes a test for the mask's ability to fit securely to the face. It also specifies the mask's ability to filter out specific airborne particles like dust, mist, and fumes. It includes additional requirements for the performance of the mask, such as the ability to seal against the face and the mask's durability.

  Test results

  Reusability NR - Not Reusable

  The standard EN 149:2001+A1:2009 designates a classification for filtering half masks, distinguishing between those that are re-usable (R) and non-reusable (NR). When a mask is classified as NR - Not Reusable, as per the result identified for EN 149:2001+A1:2009 NR, it implies that the mask is intended for single use only and should not be used more than once. The test method for determining reusability under this standard involves assessing the mask's material integrity, filter efficiency, and structural stability after simulated use, which might include cleaning, disinfection, and aging procedures. The practical implications of this result are significant; masks labeled as NR must be discarded after one use, highlighting a critical consideration for procurement professionals in terms of inventory, cost management, and usage protocols to ensure safety and compliance.

• 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.

• PPE Category 3

  PPE stands for "personal protective equipment." PPE Category 3 refers to equipment that is complex and provide the highest level of protection such as powered respirators, SCBA, and full body suits. In Europe, PPE Category 3 must meet certain safety standards set by the European Union, which means that it must be designed and manufactured to protect the user without causing harm. Companies that make or sell PPE must prove that it meets these standards. They also must have a quality management system in place, have to be audited regularly by a notified body and have to have a technical documentation.