HEVEA JUNIOR LATEXMATTRESS

CONSTRUCTION: Perforated 3-zone latex foam sheet - 9 cm thick (for size 160/70) and 10 cm (for other sizes). Inner cover of hygienic membrane, outer cover made of knitted fabric quilted with 200 g oats. Aegis Natural Care cotton fabric 30% / polyester 70%, AEGIS finish. The use of Aegis technology in the mattress cover gives it protective and preventive functions. The product is made with Aegis Microbe Shield technology is health-promoting and environmentally friendly for people and animals. Medica gray knitwear option - 40% cotton / 60% pe. Cover, zipper tape on 3 sides to keep the product clean and hygienic. Recommended washing at temperatures up to 60 ° C. The latex is certified Euro latex. Mattress weight 8 kg (160/70 cm) - 12 kg (200/90). Height 11-13 cm. Medical device class I. Robust and comfortable perforated latex mattress with moisture protection. The product is CE marked. It has 2 zones of different hardness.

APPLICATION: Children's and youth beds and sofas as well as bunk beds, child's weight up to 80 kg, age without restrictions. The variable hardness zones of the mattress are arranged symmetrically - it doesn't matter which of the zones is used by the head and which by the legs. It is recommended to change the sides of the mattress in the bed frame regularly (both top / bottom and head / legs).

NOTES: double sided mattress, two usable sides. The ability to make unusual sizes.

Class I medical devices in accordance with the requirements of Council Directive 93/42 / EEC of June 14, 1993 on medical devices, amended by Directives 2007/47 / EC PE and RE of September 5, 2007 and harmonized standards: PN-EN ISO 14971 : 2012, PN-EN 1041 A 1: 2013-12, PN-EN ISO 15523-1: 2012. and the law of May 20, 2010 on medical devices (Journal of Laws 2010 No. 107 point 679) and the regulation of the Minister of Health of January 12, 2011 on the basic requirements and procedures for assessing the conformity of medical devices (Journal of Laws 2011) No. 16, point 74). The product conformity assessment was carried out in accordance with No. VII of the Ordinance of the Minister of Health of January 12, 2011 on the basic requirements and procedures for assessing the conformity of medical devices.