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2 REV 1.1 - U8006182
NEDERLANDS
UK The features described in this manual are published with reservation to modifications.
NL De in deze handleiding beschreven mogelijkheden worden gepubliceerd onder
voorbehoud van wijzigingen.
F Les possibilités décrites dans ce manuel sont publiées sous réserve de modifications.
D Die in dieser Bedienungsanleitung umschriebenen Möglichkeiten, werden vorbehaltlich
Änderungen publiziert.
S Funktionerna i denna bruksanvisning publiceras med reservation för ändringar.
DK Vi forbeholder os retten til ændringer af de specifikationer, der er beskrevet i denne
brugsanvisning.
N Funksjoner beskrevet i denne manualen kan endres uten nærmere informasjon.
SF
Tässä ohjekirjassa julkaissut tiedot voivat muuttua ilman ennakkoilmoitusta.
Distributor:
Topcom Europe NV,
Grauwmeer 17, 3001 Heverlee, Belgium,
Manufacturer
Health & Life Co., Ltd.
9F No.186, Jian Yi Road, Chung Ho City, Taipei, Taiwan
Represented in Europe by:
EMERGO EUROPE
Molenstraat 15, 2513 BH, The Hague, The Netherlands
TEL : +31-70-3458570 FAX : +31-70-3467299
EC
REP
This Blood Pressure Monitor complies with the EC Directives and bears the CE
Mark "CE 0197".
This blood pressure monitor als complies with mainly the following standards,
(including but not limited)
Safety standards
EN 60601-1 - Medical electrical equipment part 1:General requirements for safety
EN 60601-1-2 - Medical electrical equipment part 1-2: Collateral standard:
Electromagnetic compatibility-Requirements and tests
Performance standards:
EN 1060-1 Non-invasive sphygmomanometers - General requirements
EN 1060-3 Non-invasive sphygmomanometers - Supplementary requirements for
electromechanical blood pressure measuring systems.
EN 1060-4 Non-invasive sphygmomanometers - Test procedures to determine
the overall system accuracy of automated non-invasive sphygmomanometers.
The declaration of conformity can be found on:
http://www.topcom.net/support/cedeclarations.php
HL_BPMArm6331.book Page 2 Thursday, December 17, 2009 10:39 AM
2


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