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Ihealth bp5 Инструкция по эксплуатации онлайн [13/17] 167324
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13
EC REP
Lotus Global Co.,
L
td.
15 Alexandra Road,
L
ondon
U
K,
N
W8
0
DP
Tel: +0044-20-75868010
F
ax:
+
0044-20-79006187
ANDON HEALTH CO., LTD.
No. 3 Jinping Street,
Y
a
A
n
R
oad,
N
ankai
D
istrict, Tianjin
300190, China
Tel: 86-22-60526161
IMPORTANT INFORMATION REQUIRED BY THE FCC
This device complies with Part 15 of the FCC Rules. Its operation is
subject to the following two conditions:
(1)This device may not cause harmful interference, and
(2)this device must accept any interference received, including
interference that may cause undesired operation.
Changes or modifications not expressly approved by iHealth Lab Inc.
would void the user’s authority to operate the product.
Note: This product has been tested and found to comply with the limits for
a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits
are designed to provide reasonable protection against harmful interference
in a residential installation. This product generates, uses, and can radiate
radio frequency energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to radio communications. However,
there is no guarantee that interference will not occur in a particular
installation. If this product does cause 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
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.
This product is approved in accordance to R&TTE directive transmitter.
OTHER STANDARDS AND COMPLIANCES
The Wireless Blood Pressure Monitor corresponds to the following
standards:
IEC 60601-1:2006 (Medical electrical equipment – Part 1: General
requirements for safety);
Содержание
- Body posture sitting comfortably during measurement a be seated with your feet flat on the floor without crossing your legs b place your hand palm side up in front of you on a flat surface such as a desk or a table c the middle of the cuff should be at the level of the right atrium of your heart 4
- Connect to ios device via bluetooth 4
- Measurement procedures blood pressure can be affected by the position of the cuff and your physiologic condition it is very important that the cuff should be placed at the same level as your heart 4
- Monitor status bluetooth indicator 4
- Battery handling and usage 9
- Do not change the battery if the battery can no longer be charged please contact customer service 9
- Do not plug or unplug the power cord into the electrical outlet with wet hands 9
- Do not pull out the adapter when you are using the monitor 9
- Do not use any other type of ac adapter as it may harm the monitor 9
- If the ac adapter is abnormal please change the adapter 9
- Lithium battery replacement by inadequately trained personnel could result in a hazard such as a fire or explosion 9
- Monitor status status indicator charging flashing green light fully charged steady green light low battery flashing red light for a few seconds abnormal state steady red light 9
- Overcharging the battery may reduce its lifetime 9
- Problem possible cause solution 9
- The monitor cable battery and cuff must be disposed of according to local regulations at the end of their usage 9
- Troubleshooting 9
- Electromagnetic compatibility information 14
- 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 aami ansi 80601 2 30 2009 iec 80601 2 30 2009 cor 010 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 14
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