iHealth BP7 Руководство пользователя - Страница 13

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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

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

RF emissions

CISPR 11

Table 1

For all ME EQUIPMENT and ME SYSTEMS

Compliance

The Wireless Blood Pressure Wrist Monitor uses RF energy

Group 1

only for its internal function. Therefore, its RF emissions are

very low and are not likely to cause any interference in

Electromagnetic environment - guidance