iHealth BP5S Guía De Usuario página 72

the following measures:
—Reorient or relocate the receiving antenna.
—Increase the separation between the equipment and receiver.
—Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
—Consult the dealer or an experienced radio/TV technician for help.
This product complies with Industry Canada. IC: RSS-210
IC NOTICE
This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject
to the following two conditions:
(1) This device may not cause interference, and this device must accept any interference,
including interference that may cause undesired operation of the device.
The CE Mark applies to products regulated by certain European health, safety and environmental
protection legislation. The CE Mark is obligatory for products it applies to: the manufacturer affixes
the marking in order to be allowed to sell his product in the European market.
Hereby, [ANDON HEALTH CO., LTD] declares that the radio equipment type [BP5S] is in compli-
ance with Directive 2014/53/EU.
The full text of the EU declaration of conformity is available at the following internet address:
https://ihealthlabs.eu/en/content/189-DoC-RED
OTHER STANDARDS AND COMPLIANCES
The Wireless Blood Pressure Monitor corresponds to the following standards:
IEC 60601-1Edition 3.1 2012-08/EN 60601-1:2006/A1:2013 (Medical electrical equipment -- Part
1: General requirements for basic safety and essential performance);
IEC 60601-1-2:2014/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
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