26
7.Technical Data
• Disposal of this product and used batteries should
be carried out in accordance with the national
regulations for the disposal of electronic products
.
This device fulfils the previsions of EC directive 93/42/EEC
(Medical Device Directive). This blood pressure monitor is
designed according to the European Standard EN1060, Non-
invasive sphygmomanometers Part 1: General Requirements and
Part 3: Supplementary requirements for electromechanical blood
pressure measuring systems.
Caution: Please read the instruction manual
carefully before using the device.
Subsidiary
OMRON HEALTHCARE UK LTD.
Opal Drive
Fox Milne, Milton Keynes MK 15 0DG, United
Kingdom
Subsidiary
OMRON Medizintechnik
Handelsgesellschaft m.b.H.
Windeckstraße 81a D-68163 Mannheim,
Germany
www.omron-medizintechnik.de
Subsidiary
OMRON SANTÉ FRANCE
14, rue de Lisbonne, F-93561 Rosny-sous-Bois
Cedex, France
Manufacturer
OMRON HEALTHCARE CO.,
LTD.
24, Yamanouchi Yamanoshita-
cho, Ukyo-ku, Kyoto, 615-0084
Japan
EU-representative
OMRON
HEALTHCARE
EUROPE B.V.
Kruisweg 577
2132NA Hoofddorp
The Netherlands
www.omron-healthcare.com
= Type B
EC REP
HEM6021-E.book Page 26 Friday, July 22, 2005 11:08 AM
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