Laica DBP-2220 Instrucciones Y Garantía página 17

English
EN
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.
WARRANTY
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
32
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 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.
STANDARDS
The product corresponds to the below standards: IEC 60601-1:2005 +A1:2012(E)/EN 60601-1:2006/
A11:2011 (Medical electrical equipment - Part 1:General requirements for basic safety and essential
performance), IEC 60601-1-2:2007/EN 60601-1-2:2007/AC:2010 (Medical electrical equipment - Part
1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic
compatibility - Requirements and tests), IEC 80601-2-30:2009+AMD1:2013/EN 80601-2-30:2010/
A1:2015 (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).
Manufactured by:
JOYTECH Healthcare Co., Ltd., No.365, Wuzhou Road, Yuhang Economic Development Zone,
311100, Hangzhou, China
Shanghai International Corp. GmbH
(Europe) Eiffestrasse 80, 20537
Hamburg, Germany
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
English
EN
MedEnvoy Switzerland
Gotthardstrasse 28
6302 Zug - Switzerland
33