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

Anti-allergic, healthy latex mattress for babies and children.
Medium-firm H2 double-sided crib mattress made of one block of latex foam.
High content of natural latex. Provides flexibility and proper support for the child's spine.
Latex board made of a uniform perforated block, 8 cm high, hardness zone I, cotton inner cover.
Latex with min. 20% natural latex resin. Medical Device Class I Outer cover quilted with 100g wool, removable.

Aegis Natural Care knit
The product made with Aegis Microbe Shield technology is health-promoting and anti-allergic.
Selective action against unwanted microorganisms puts AEGIS at the forefront of anti-allergic knitwear.
HEVEA AEGIS Natural Care knitwear is odorless, resistant to washing and repeated washing.
The cover can be washed at temperatures up to 60 degrees Celsius. Eko-Tex Standard 100 certificate. Composition: cotton 30%/polyester 70%, AEGIS finish.
Zipper tape on 3 sides. Latex with Euro-Latex certificate and PZH Hygienic Certificate. Knitted fabrics certified Safe for children.
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 a Medical Device.
Analyzes conducted in laboratory conditions and available clinical test results confirmed the increased breathability and vapor permeability of this type of mattress inserts.
This is especially important for infants and children prone to heat rash. Hevea mattresses from the above collections reduce the risk of heat rash and heat rash.
APPLICATION: slatted children's beds, child's weight up to 40 kg, age without limitation.

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

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

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