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Fiki Miki Matrace Latex/pěna Sensitive MS11 120/60/12 cm Antyalergic covers

Sensitive MATTRESS MS1 antyalergic covers (latex pad/PUR foam)

• very good elasticity and stable back support,
• hardness of providing smooth change of the position for children in infancy,
• secure edges facilitate STANDING position and making the first steps,
• excellent air circulation,
• multilayer antyalergic cover very easy to keep clean,
• high resistance when it comes to usage, tearing and demages.

Sensitive Mattress MS1 antyalergic covers is recommended for use on the selected or the entire bed's surface during sleeping and restiing. In normal use the mattress is intended to use for children:

• to prevent spine disorders that may come from forced body position during sleep,
• to prevent faulty posture,
• to support combating sleep disorders,
• with dysfunctions in the locomotor system of the neuromuscular system diseases (eg. brachial plexus birth injury, cerebral palsy).

Sensitive Mattress MS1 antyalergic covers (latex pad/PUR foam) is a double-side mattress with 12 cm thickness consisting of 4 layers:

4 layers cover (4W construction)

Cover is made of mattres fibre (100% poliester) B finished with SANITIZED protector A linked with poliester fibre C and flat polipropylen fibre D.

SANITIZED protector protects the mattress against house dust, mites and prevents against the mold's formation and unpleasant odors caused by bacteria and fungi. It enables long-term preservation of the freshness of the cover. It meets strict requirements and obtained positive results in quality tests. The design of the cover provides free air circulation and improves the quality of sleep. The cover protects the mattress' filling from dirt, polutions and damages of the inside of the mattress.

According to international standards and guidelines, treatment and prevention of allergic diseases the independent cover can be easily removed and replaced. The cover is adapted for washing at 60 ° C.

Latex foam pad(20% natural latex, 80% synthetic latex)

Perforated latex foam is designed to be used by children from birth (O +). This extremely durable and comfortable material links natural latex with a synthetic latex. It is subjected to a foaming process, secondly followed by vulcanization. It is characterized by: a perfect matching to the shape of the body. Excellent point-elasticity provides very comfortable body support during relax, great air circulation and humidity control, high resistance to dirt and tearing, lack of deformations. Latex foam is certified O & euml; co-Tex Standard 100, National Institute of Hygiene and certified by ASTM anti-fungal properties.

The latex foam pad can be easily removed. It is adapted to bending, so it can be formed into a small roll can be put to most freezers in homes. Low temperature inhibits the multiplication of microorganisms and the viruses that cause many types of infections and diseases. 24h spent in a temperature of -18 kills the majority of house dust mites.

Polyurethane foam (PUR) with longitudinal and transverse ventilation canals

Polyurethane foam (PUR) is a proven, used for many years solution to fill mattresses for children. High-quality PUR foam used in mattresses Fiki Miki is approved by strict endurance tests. The core of the mattress is made of polyurethane foam that providies a stable and elastic back support and allows the child to change the position comfortably. Transverse and longitudinal canals and multipoint back support provide a unique comfort during sleep and rest.

Strengthen edges of polyurethane foam

Hard "Safe Edge" improves security and facilitates the first steps. It is environment friendly and made entirely of foam coming from recycling.

Certificates and approvals​:

Sensitive Mattress MS1 antyalergic covers (PUR foam) received a possitive opinion from Mother and Child Institute in Warsaw (no Op-4860-64/2016), Certified by the National Institute of Hygiene (H-HŻ-6071-0346/14/C), utility model is registered in the Patent Office RP (nr. 63616). It is a medical 1st class product complies with the requirements of Council Directive 93/42/EWG of 14 June 1993 Concerning medical prodct changed by Directive 2007/47/WE of the European Parliament and of the Council of 5 September 2007 and met the standards: PN-EN ISO 14971:2012, PN-EN 1041+A1:2013-12, PN-EN ISO 15523-1:2012 and the Act of 20 May 2010 about medical products( Dz.U. 2010 Nr 107 Poz. 679) and Regulation of the Minister of Health of 12 January 2011 on the essential requirements and conformity assessment procedures for medical products (Dz.U. 2011 Nr 16 Poz. 74). The assessment of conformity of the product was conducted in accordance with Annex VII of the Minister of Health of 12 January 2011 on the essential requirements and conformity assessment procedures for medical products.