Product description
Product Features:
- Disposable respirator with exhalation valve
- Integral seal on entire inner edge for insulation
- Charcoal layer prevents irritation from low concentrations of gases and acids
- Large exhalation valve for heavy-duty work
- Large cup surface area for excellent filtering capacity
- Large adjustable elastic bands for precise facial adhesion
- Latex-free
Technical Details:
- Standard: EN 149 FFP2 NR
- Respiratory Protection
- Antimicrobial Protection
- Medical Protection
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Standards and labels
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 ReusableThe 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.
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.
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.
SIR SAFETY SYSTEM delivery terms
Free delivery when you order more than 1 000,00 € from SIR SAFETY SYSTEM
Supplier shipping fee 50,00 €
Brand minimum 350,00 €
Sir Safety System FA1308 High-EFF Respirator FFP2 NR Carbon W/V, 10 pcs
32,93 € / package (VAT incl.)
26,24 €
A package contains 10 pcs
2,62 € / piece
In a package
10 pieces
In a carton
200 packages
2 000 pieces
SIR SAFETY SYSTEM
Delivery time: 1 business days
Orders from 350,00 €
Supplier shipping fee 50,00 €
Free shipping on orders over 1 000,00 €
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