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Antiviral medical masks, certified, intended for hospitals, dentists, medical offices and for everyday use.
Adapted to sensitive skin, they are gentle and do not cause irritation. They do not have an unpleasant artificial smell.
Excellent bacterial filtration capacity, up to 98%, high wearing comfort thanks to increased air flow, the masks have an elastic band that prevents the mask from slipping off the face.
Increased security
Improved design
The masks have a 3-layer structure to better fulfill their role of additional protection against viruses and bacteria during periods of increased disease incidence.
Be careful with ordinary fabric masks that are popularly available for sale. They do not have any filtering capacity and are not certified in any way. The best masks are those chosen by doctors. Hundreds of thousands of people have already trusted us!
Excellent filtration
Compared to classic face masks, ours use an additional MeltBlown filtering layer with a filtering capacity of ≥ 98%
production: made in Poland
Features: 3-layer
material: non-sterile polypropylene non-woven fabric with rubber bands
mask: 173mm x 95mm
The medical device meets the requirements of Regulation (EU) 2017/745 OF THE EUROPEAN PARLIAMENT and OF THE COUNCIL of 5 April 2017 on medical devices.
The device, in accordance with Annex VIII of Regulation 2017/745, has been classified as a class I medical device, according to rule 1.
In order to demonstrate the safety and effectiveness of the medical device, the following standards were used to assess compliance:
EN 14683:2019+AC:2019
Medical masks - Requirements and test methods
EN ISO 13485:2016
Medical devices – Quality management systems – Requirements for legal purposes
EN 1041:2008
Information provided by the manufacturer of medical devices
EN ISO 15223-1:2016
Medical devices - Symbols for use in the labeling, labeling and information provided with medical devices - Part 1: General requirements
EN ISO 14971:2012
Medical devices – Application of risk management to medical devices
EN ISO 10993-1:2009
Biological assessment of medical devices – Part 1: Assessment and testing in the risk management process