iHealth BP7, Owner'S Manual, Page: 13 / 16

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harmful interference to radio or television reception, which can be determined by turning the
equipment off and on, the user is encouraged to try to correct the interference by one or more of 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
This product is approved in accordance to R&TTE directive transmitter.
IC NOTICE
This device complies with Industry Canada licence-exempt RSS standard(s). Operation is
subject
to the following two conditions: (1) this device may not cause interference, and (2) this device
must accept any interference, including interference that may cause undesired operation of the
device.
Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radio
exempts de licence. L'exploitation est autorisée aux deux conditions suivantes : (1) l'appareil ne
doit pas produire de brouillage, et (2) l'utilisateur de l'appareil doit accepter tout brouillage
radioélectrique subi, même si le brouillage est susceptible d'en compromettre le
fonctionnement.
OTHER STANDARDS AND COMPLIANCES
The Wireless Blood Pressure Wrist Monitor corresponds to the following standards: IEC
60601-1:2006 (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: Supplementary requirements for
electro-mechanical blood pressure measuring systems),ANSI/AAMI
SP-10:2002+A1:2003+A2:2006, ANSI/AAMI/IEC 80601-2-30:2009 (Medical electrical equipment
– Part 2-30: Particular requirements for the basic safety and essential performance of automated
non-invasive sphygmomanometers)
ELECTROMAGNETIC COMPATIBILITY INFORMATION
Table 1
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration - electromagnetic emissions
The Wireless Blood Pressure Wrist Monitor is intended for use in the electromagnetic environment
specified below.
The customer or the user of the monitor should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1
The Wireless Blood Pressure Wrist Monitor uses RF energy
only for its internal function. Therefore, its RF emissions are
very low and are not likely to cause any interference in