Lanaform ABPM-100 Manuel D'instructions page 10

EN
•
All the packaging is composed of materials that
pose no hazard for the environment and which can
be disposed of at your local sorting centre to be
used as secondary raw materials. The cardboard
may be disposed of in a paper recycling bin. The
packaging film must be taken to your local sorting
and recycling centre.
When you have finished using the device, please
dispose of it in an environmentally friendly way and
in accordance with the law. Prior to disposal, please
remove the battery and dispose of it at a collection
point so that it can be recycled.
10 / 68
M-ABPM100-Lot003.indd 10 M-ABPM100-Lot003.indd 10
FR NL DE SL SV
(Medical electrical equipment -- Part 1:
General requirements for basic safety and es-
sential performance), IEC60601-1-2:2014/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), IEC80601-2-30:2009+AMD1:2013/
EN 80601-2-30:2010/A1: 2015(Medical electrical
equipment –Part 2-30: Particular requirements
for the basic safety and essential performance of
automated non-invasive sphygmomanometers)
EN 1060-1: 1995 + A2: 2009 (Non-invasive sphy-
gmomanometers - Part 1: General requirements),
EN 1060-3: 1997 + A2: 2009 (Non-invasive sphyg-
momanometers - Part 3: Supplementary require-
ments for electro-mechanical blood pressure
measuring systems);ISO81060-2: 2013(Non-In-
vasive Sphygmomanometers - Part 2: Clinical
Validation Of Automated Measurement Type).
The accuracy of this blood pressure monitor has
been tested correctly and its durability has been
designed for long-term use. Technical meas-
urement checks must be carried out using the
appropriate methods when the device is used for
medical purposes. For accurate information on
how to check the accuracy of the device, you can
send a request by post to the after-sales service.
ADVICE REGARDING
THE DISPOSAL OF WASTE
ABPM-100 EN Instruction manual
Under no circumstances should
spent batteries be disposed of
with household waste.
EC 0197 DECLARATION DE CONFORMITY
Medical device
Category IIa.
We, LANAFORM,
hereby declare that the medical device
"ABPM-100" Lot001 LA090206 complies with European
Directive 93/42/EC concerning medical devices and
its most recent amendment 2007/47/EC.
LIMITED WARRANTY
LANAFORM guarantees this product against any
material or manufacturing defect for a period of
two years from the date of purchase, except in the
circumstances described below.
The LANAFORM guarantee does not cover damage
caused as a result of normal wear to this product. In
addition, the guarantee covering this LANAFORM
product does not cover damage caused by abusive
or inappropriate or incorrect use, accidents, the use
of unauthorized accessories, changes made to the
product or any other circumstance, of whatever sort,
that is outside LANAFORM's control.
LANAFORM may not be held liable for any type of
circumstantial, indirect or specific damage.
All implicit guarantees relating to the suitability of
the product are limited to a period of two years from
the initial date of purchase as long as a copy of the
proof of purchase can be supplied.
On receipt, LANAFORM will repair or replace your
appliance at its discretion and will return it to you.
The guarantee is only valid through LANAFORM's
Service Centre. Any attempt to maintain this product
by a person other than LANAFORM's Service Centre
will render this guarantee void.
202112LA090207003 15/11/2021
ELECTR
Table 1 - E
Phenomen
RF emissio
Harmonic d
Voltage flu
Table 2 - E
Phenomen
Electrostat
Discharge
Radiated R
Proximity fi
communic
Rated pow
Table 3 –
Test frequ
(MHz)
385
450
710
745
780
810
870
930
1720
1845
1970
•
2450
5240
5500
5785
15/11/2021 15:41:25 15/11/2021 15:41:25