Mattresses can not be withdrawned because of hygenic reasons (Article 38 p.5 of the Consumer Rights Act)

Antiallergic, healthy latex mattress for babies and children.
Medium-hard H2 double-sided cot mattress made of one latex foam block.
High content of natural latex.
Provides flexibility and proper support for the child's spine.

Latex plate from a uniform perforated block 8 cm high, 1st hardness zone, inner cotton cover. Latex with a content of min. 20% natural latex resin. Medical Device Class I Outer quilted cover 100g, removable.
Medica fabric - cotton 40% / pe 60% breathable fabric based on natural cotton.

3-sided zip tape. Latex with Euro-Latex certificate and PZH Hygienic Certificate. Knitted fabric with a child safe certificate.
Mattress weight 5kg (120/60 cm) -6 kg (130/70, 140/70).
Height about 9 cm.
Latex mattresses from the Hevea collection have the CE mark and the status of Medical Item.
Analyzes carried out in laboratory conditions and available clinical test results confirmed the increased breathability and vapor permeability of this type of mattress insert.
This is especially important for babies and children prone to prosecution.
Hevea mattresses from the above collections reduce the risk of ordinary and red prickly heat.

APPLICATION: baby cots, baby weight up to 40 kg, age without restrictions.

NOTES: double-sided mattress, two usable sides, latex insert is recommended to be turned over every few months.

GUARANTEE: 2 years for the product, 5 years for the mattress insert
HARDNESS: H2 (medium hard)
HEIGHT: 10cm
MEDICAL PRODUCT: YES

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