Disposal Procedure - Laica BP-2220 Instrucciones Y Garantía

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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.
WARRANTY
This equipment is covered by a 2-year warranty starting from the purchase date, which has to be proven by
means of the stamp or signature of the dealer and by the fiscal payment receipt that shall be kept
enclosed to this document. This warranty period complies with the laws in force and applies only in case
the consumer is an individual. Laica products are designed for domestic use only; therefore, their use for
commercial purposes is forbidden. The warranty covers only production defects and does not apply, if the
damage is caused by accidental events, misuse, negligence or improper use of the product. Use the supplied
accessories only; the use of other accessories invalidate the warranty cover. Do not open the equipment for
any reason whatsoever; the opening or the tampering of the equipment, definitely invalidate the warranty.
Warranty does not apply to parts subject to tear and wear along the use, as well as to batteries, when they are
included. Warranty decays after 2 years from the purchase date. In this case, technical service interventions
will be carried out against payment. Information on technical service interventions, under warranty terms or
against payment, may be requested by writing at info@laica.com. Repair or replacement of products covered
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by the warranty terms are free of charge. In case of faults, refer to the dealer; DO NOT send anything directly
to LAICA. All interventions covered by warranty (including product replacement or the replacement of any of
its parts) shall not be meant to extend the duration of the original warranty period of the replaced product. The
manufacturer cannot be made liable for any damages that may be caused, directly or indirectly, to people, things
and pets resulting from the inobservance of the provisions contained in the suitable user manual, especially with
reference to the instructions related to installation, use and maintenance of the equipment.
Being constantly involved in improving its own products, Laica reserves the right to modify its product, totally
or partially, with reference to any production need, without that this involves any responsibility whatsoever by
Laica or its dealers.
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: Hangzhou Sejoy Electronics & Instruments Co., Ltd. Building 2, No. 202, Zhenzhong
Road, West Lake Economy & Technology Zone, 310030 Hangzhou, China
Shanghai International Corp. GmbH (Europe) Eiffestrasse 80, 20537 Hamburg, Germany
Distributed by: Laica S.p.A.
Viale del lavoro, 10 – Fraz. Ponte - 36021 Barbarano Vicentino (VI) – Italy
Phone: +39.0444.795314 - www.laica.com
Made in China
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