iHealth KN-550BT Bedienungsanleitung Seite 15

This device bears the CE conformity mark. The quality of this wireless device has been veri ed and
conforms to the provisions of the IEC 60601-1:2005 corr.1 (2006) + corr.2 (2007)/EN 60601-1:2006/AC:2010
(Medical electrical equipment – Part 1: General requirements for safety); IEC 60601-1-2:2007 /EN
60601-1-2:2007 /AC:2010 (Medical electrical equipment – Part 1: General requirements for safety; Collateral
Standard-Electromagnetic compatibility - Requirements and tests); EN 1060-1: 1995 + A1: 2002 + A2: 2009
(Non-invasive sphygmomanometers - Part 1: General requirements); EN 1060-3: 1997 + A1: 2005 + A2: 2009
(Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood
pressure measuring systems);IEC80601-2-30:2009+Cor.：2010 (Medical electrical equipment –Part 2-30:
Particular requirements for the basic safety and essential performance of automated non-invasive
sphygmomanometers).
R&TTE mention: Hereby, iHealth declares that the BP Track KN-550BT is in compliance with the essential
requirements and other relevant provisions of Directive 1999/5/EC. Directive 1999/5/EC Declaration of
Conformity and all iHealth certi cation and regulatory documents can be downloaded on the following
link: https://www.ihealthlabs.eu/support/certi cations.
For information regarding potential electromagnetic or other interference between the iHeath Track Blood
Pressure Monitor and other devices together with advice regarding avoidance of such interference, please
visit www.ihealthlabs.eu/support/electromagnetic. It is suggested that the Wireless Blood Pressure Monitor
should be operated at least 10 metres away from electric or wireless devices (e.g. routers, microwave oven,
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etc.).