Please read these instructions carefully
before
using the device.
This device has been developed by iHealth together with a team of medical specialists
and engineers. We have taken the utmost care to manufacture a device that is user-
friendly and clinically accurate. If you have any suggestions so that we can improve
our products, please send us a mail at [email protected].
This device bears the CE conformity mark. The quality of this wireless device has been
verified and conforms to the provisions of the IEC 60601-1:2005 (Medical electrical
equipment – Part 1: General requirements for safety); IEC 60601-1-2:2007 (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: Sup-
plementary requirements for electro-mechanical blood pressure measuring systems);
ANSI/AAMI SP-10:2002 + A1:2003 + A2:2006; AAMI/ANSI 80601-2-30:2009/IEC 80601-
2-30:2009 + Cor.2010/EN 80601-2-30:2010 (Medical electrical equipment –Part 2-30:
Particular requirements for the basic safety and essential performance of automated
non-invasive sphygmomanometers).
This device should give you years of excellent service. However, we recommend that
you have the device tested for accuracy every 2 years or after any major mechanical
impact (e.g. being dropped).
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