Bioconfort® Memory foam hypoallergenic mattresses have been designed around these fundamental principles and are made up of a sheet of Bioconfort® material, a latest-generation self-modelling visco-elastic polymer, which deforms differently according to the pressure points, following the profile of the body in order to ergonomically support the spine, ensuring constant relaxation of the joints and promoting blood circulation.
The top layer of Bioconfort® is supported by a highly non-deformable breathable polyurethane base, which supports and prevents sagging.
The elimination of water vapor generated during sleep is guaranteed by hundreds of ventilation channels that cross the base.
The sensation is that of an enveloping embrace that follows every curve of the body; a soft cloud that supports and shapes itself, in real time, depending on the position assumed.
Bioconfort® EVO: 4 mattresses in 1!
Bioconfort® EVO is a very flexible “evolved” mattress, in fact by combining the stratification of the core and the mattress topper you can obtain 4 different levels of rigidity, (0-2-4-6 cm of Bioconfort® material), allowing everyone to choose the most suitable shape while maintaining the constant breathability of the mattress.
The mattress topper can also be easily sanitized, exposed to the sun and aired. Bioconfort® EVO is the ideal product to fully enjoy the unique qualities of Bioconfort®.
Mattress Structure
The mattress core, made up of a 2 cm layer of exclusive self-modeling viscoelastic Bioconfort® Material on a 17 cm base of high resilience polyurethane foam, (exclusive through-cutting for effective ventilation and sanitization of the mattress), is combined with a mattress topper made up of a 5 cm slab of self-modeling viscoelastic Bioconfort® Material. Height 23 cm
Lining
The completely removable and washable lining covers are made of Naturalcare®, a totally hypoallergenic fiber that generates a sensation of prolonged freshness, allowing you to fully appreciate the high standard of comfort guaranteed by Bioconfort® Hypoallergenic Mattresses.
Certifications
The ability to allow a uniform distribution of body weight combined with high breathability means that Bioconfort® products meet the requirements of the CE regulations relating to Class 1 medical devices for the prophylaxis of bedsores. This Certification guarantees the conformity of the products to the directive 93/42/EEC making them suitable for use in the field of health protection.
Guarantees
All Bioconfort® Hypoallergenic Mattresses have a "30-day guarantee". You will have the opportunity to try Bioconfort® mattresses at home for 30 days and if you are not satisfied at the end of this period you can return the product and receive a refund of the amount spent*.
The use of innovative, totally hypoallergenic materials, high breathability and self-modelling properties, brings Bioconfort® Hypoallergenic Mattresses to the attention of those who want to operate an effective prevention in the field of indoor allergies without sacrificing a superior quality rest.
Bioconfort® Mattresses can be used indifferently on slatted bases and well-ventilated static or adjustable bed bases.
10-year guarantee (pro rata)
* The refund will be paid upon receipt of the product which must be intact and is intended net of shipping costs.
What is meant by “Medical Device”?
According to the definition contained in Legislative Decree No. 46 of 1997, which transposed EU Directive 93/42 into Italian law, a medical device is:
an instrument
an apparatus
an implant
a substance
another product
used alone or in combination, including computer software intended for proper functioning, and designated by the manufacturer to be used in humans for the purposes of:
diagnosis, prevention, monitoring, treatment, or alleviation of a disease
diagnosis, monitoring, treatment, alleviation, or compensation for an injury or disability
study, replacement, or modification of anatomy or of a physiological process
control of conception
provided that it does not achieve its principal intended action in or on the human body by pharmacological or immunological means, nor by metabolic process, but whose function may be assisted by such means.
What guarantees are implied by the CE marking of medical devices?
This marking demonstrates compliance with the essential requirements of Legislative Decree 46/97 (implementation of EU Directive 93/42/EEC) for medical devices, and therefore serves as a product certification ensuring:
functional quality and quality of materials
control of the manufacturing process and testing phases
traceability of the device throughout its entire circulation path, from the factory to the final customer
The purchase of a Class 1 medical device allows eligible individuals to benefit from a tax deduction for healthcare expenses (Art. 15, paragraph 1, letter C of the Italian Income Tax Code – TUIR – and Resolution of the Italian Revenue Agency No. 253 of 29/09/2009).
Therefore, the expense incurred for the purchase of such products may be deducted as a healthcare expense for an amount equal to 19% (for the portion exceeding the deductible threshold of €129.11, applied to the total amount of all healthcare expenses incurred) in the income tax return relating to the tax period in which the purchase was made.
To take advantage of this benefit, the following documentation is required:
A prescription on the letterhead of the attending physician (and/or specialist) certifying the necessity of using the aforementioned products.
An invoice made out to the taxpayer to whom the expense refers, or a fiscal receipt containing the following data: nature, quality, and quantity of the goods purchased, and the tax code of the recipient.
This documentation must be kept together with the income tax return for at least 5 years.
It should be emphasized that the condition for deducting the expenses incurred must be linked to a pathology proven by the medical prescription, certifying the necessity that justified the expense.
It should also be noted that the purchased product must be included in List 2 of Ministerial Decree No. 332 of 27 August 1999, issued by the Ministry of Health.
Regular testing of materials allows us to maintain the high quality standards of our products, ensuring the peace of mind of our customers.
Recent studies report a positive allergy test rate for latex of approximately 3.5% in the general population, rising to 26% among asthmatics. (Source: FDA)
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Medical Devices