Laica KD-7920 Instrucciones Y Garantía página 16

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DISPOSAL PROCEDURE
The symbol on the bottom of the device indicates the separated collection of electric and electronic equipment (Dir.
2012/19/Eu-WEEE).
At the end of life of the device, do not dispose it as mixed solid municipal waste, but dispose it referring to a specific
collection centre located in your area or returning it to the distributor, when buying a new device of the same type
to be used with the same functions.
If the appliance to be disposed of is less than 25 cm, it can be returned to a retail location that is over 400 m² without having to
purchase a new, similar device. This procedure of separated collection of electric and electronic devices is carried out forecasting
a European environmental policy aiming at safeguarding, protecting and improving environment quality, as well as avoiding
potential effects on human health due to the presence of hazardous substances in such equipment or to an improper use of
the same or of parts of the same. Caution! The wrong disposal of electric and electronic equipment may involve sanctions.
To correctly dispose of batteries (Dir. 2013/56/Eu) do not throw them into household waste but rather dispose of them as
special waste at specialised recycling centres. For more information about disposal of used batteries, contact the store where you
purchased the equipment containing the batteries, the municipality or the local waste disposal service.
This appliance is guaranteed for 2 years from the time of delivery of the goods, or another longer term envisaged by the
national legislation of the consumer's residence. This provision complies with Italian and European legislation. The Laica
products are designed for home use and must not be used in public venues. The warranty only covers manufacturing defects
and does not apply if the damage is caused by an accidental event, incorrect use, negligence or misuse of the product.
Use only the accessories supplied; the use of different accessories may result in invalidity of the warranty. Do not open the
unit for any reason; in the case of opening or tampering, the warranty is definitively voided. This warranty does not apply to
parts subject to wear or to the batteries when supplied. After 2 years from delivery, or another longer term envisaged by the
national legislation of the consumer's residence, the warranty expires; in this case, the technical assistance interventions
will be carried out against a fee. Information on technical assistance, whether under warranty or for a fee, can be requested
by contacting info@laica.com.
No payment will be due for repairs or replacements of products that fall within the terms of the warranty. In the event of
faults, contact the retailer. Do NOT send the appliance directly to LAICA. All the operations under warranty (including those
of replacement of the product or part thereof) will not prolong the duration of the original period of warranty of the product
replaced. The manufacturer declines any liability for any damage that may, directly or indirectly, be caused to persons,
property or animals as a result of the non-observance of all the requirements established in the relevant instructions manual
and concerning, especially, warnings relating to installation, use and maintenance of the appliance. Laica, in its constant
WARRANTY
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commitment to improving its products, is entitled to changing without any notice, in whole or in part, its products in relation to
production requirements, without this entailing any liability for Laica towards its dealers. For further information: www.laica.it.
The product corresponds to the below standards: IEC 60601-1 Edition 3.1.2012-08 EN 60601-1:2006/A1:2013 (Medical
electrical equipment - Part 1:General requirements for basic safety and essential performance), IEC 60601-1-2:2014 / EN
60601-1-2:2015 (Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance -
Collateral standard: Electromagnetic compatibility - Requirements and tests), IEC 80601-2-30:2018/EN IEC 80601-2-30:2019
(Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and ssential performance of automated
non-invasive sphygmomanometers) EN 1060-1:1995 + A2:2009 (Non-invasive sphygmomanometers - Part 1:General
requirements), EN 1060-3:1997+A2:2009 (Non-invasive sphygmomanometers - Part 3: Supplementary requirements for
electro-mechanical blood pressure measuring systems). ISO 81060-2:2013(Non-Invasive Sphygmomanometers - Part 2:
Clinical Validation of Automated Measurement)
Manufactured by:
ANDON HEALTH CO., LTD. No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, China.
iHealthLabs Europe SAS - 36 Rue de Ponthieu, 75008, Paris, France
Distributed by: Laica S.p.A.
Viale del lavoro, 10 - 36048 Barbarano Mossano (VI) – Italy
Phone: +39.0444.795314 - info@laica.com - www.laica.it
Made in China
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STANDARDS
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