FFP2 Mask
It is a respirator with active-passive protection, which filtration is ≥ 94.9% confirmed by tests with particles of 60-160 nanometers.
The product fits perfectly to the face thanks to a unique clasp, a soft foam sponge for the nose and a wire inserted in the upper part of the mask. Non-sensitizing, non-irritating.
The product is certified to EN 149, and also meets EN 14683 Type I, II, IIR.
Filtering half-mask BISAF BS2 FFP2
It is a novelty and a unique product on the market with a comfortable shape of a medical mask, which at the same time ensures high level of filtration previously attainable only in filtering half-masks!
Medical Device 1 class
EN 149:2001+A1:2009
Directive 93/42/EEC
Filtering half-mask BISAF BS2 FFP2
It is a novelty and a unique product on the market with a comfortable shape of a medical mask, which at the same time ensures high level of filtration previously attainable only in filtering half-masks!
Medical Device 1 class
EN 149:2001+A1:2009
Directive 93/42/EEC
Available color variants
In our offer there are masks of different colors. Currently, we have created, as many as 9 variants and each of them retains identical properties.
Compare our products and choose the one that meets your needs. Click on the button to go to the table.
Clic on the mask to view details
Properties
- Filtration ≥ 94,9% confirmed by tests with particles of 60-160 nanometres corresponding to the size of the coronavirus.
- Half-mask with active and passive protection.
- Microbiologically pure.
- Bendable and flexible.
- Unlike traditional FFP2 half-masks, this one is comfortable and does not obstruct breathing.
- Perfect facial fit possible due to unique clasp at the back of the head, soft foam sponge for the nose and a wire inserted in the lower part of the mask.
- Prevents glasses from fogging.
- Possibility of personalization in terms of colour as well as printings in case of large orders.
- Individually packaged product.
- It has an EU type examination certificate for compliance with EN 149:2001+A1:2009 Personal Protective Equipment and is a Class I medical device in accordance with Directive 93/42/EEC on medical devices, which allows it to be used both in industry and in health care – including hospitals and Health Care Centers!
- The device is subject to the conformity assessment procedure under the Act of 20 May 2010 “On Medical Devices” Journal of Laws of 2010. No. 107, item 679, as amended. and the Regulation of the Minister of Health of 17 February 2016.
Application
- Use as Personal Protective Equipment in workplaces and by health care workers, in operating rooms or other similar facilities.
- Use by patients to reduce the risk of spreading infection, especially in epidemic or pandemic situations.
- Use as Personal Protective Equipment, providing protection for the wearer and his or her surroundings from infectious agents in the fight against pandemics.
- Protection of the respiratory system from solid particle aerosols or water-based aerosols (dust, smoke), liquid aerosols (mists) and bioaerosols (microorganisms, fungi, viruses ), as long as the concentration of the dispersed phase of these aerosols in the air does not exceed the value of 10 x NDS.
- Protection of the respiratory system from harmful particles in the air, such as smog particles PM10 and PM 2.5.
