iHealth Labs HS5S Vista User Manual HS5S OM EN
iHealth Lab Inc. Vista HS5S OM EN
User Manual
iHealth®
iHealth Vista
Wireless Body Analysis Scale
OWNER’S MANUAL
TABLE OF CONTENTS
INTENDED USE ........................................................................................................................................... 1
IMPORTANT NOTE FOR USERS .............................................................................................................. 1
CONTRAINDICATION ............................................................................................................................... 1
OFFLINE MEMORY .................................................................................................................................... 2
SPECIFICATIONS ........................................................................................................................................ 2
GENERAL SAFETY AND PRECAUTIONS ............................................................................................... 3
EXPLANATION OF SYMBOLS ................................................................................................................. 6
INTENDED USE
The iHealth Vista Wireless Body Analysis Scale is a precision electronic instrument intended for adult use.
The Scale utilizes full electronic methodology and pressure sensors to non-invasively measure body
composition components automatically. The measurements are displayed and stored on an iPod touch,
iPhone, or iPad with a date and time stamp.
IMPORTANT NOTE FOR USERS
Pregnant women need to consult their healthcare provider before use. Some physical conditions could
affect hydration levels that may lead to inaccurate results. Please consult your healthcare provider for more
information.
Always store the iHealth Vista Wireless Body Analysis Scale in a dry place. To ensure accurate results,
keep the Scale away from magnetic fields as these may adversely affect results or possibly damage the
Scale.
CONTRAINDICATION
Never use this product in combination with medical electronic devices such as:
(1) Medical electronic implants such as pacemakers.
(2) Electronic life support systems such as artificial heart/lungs.
(3) Portable electronic medical devices such as electrocardiographs.
This product could cause these devices to malfunction posing a considerable health risk to users of these
devices.
OFFLINE MEMORY
The Scale can store up to 200 weight results for each user. When each user’s memory is full, any new
measurements will overwrite the oldest ones.
SPECIFICATIONS
1. Product name: iHealth Vista Wireless Body Analysis Scale
2. Model: HS5
3. Classification: internally powered, type BF applied part (four electrodes)
4. Power: 4×1.5V AA alkaline batteries
Battery life: approx. 3 months with daily usage
5. Measurement range:
Body Weight: 11 lb-330 lb/5 kg-150 kg
Body Fat: 5.0%-65.0%
Humidity: 20 - 85%RH
Scale resolution:0.2lb/0.1kg
6. Accuracy:
Body Weight: ±1.1 lb/0.5 kg(5 kg-40 kg / 11-88 lb);
±1%+ 0.2 lb / 0.1 kg(40 kg-150 kg / 88-330 lb)
Body Fat: ±1%
7. Operating temperature: 10℃ - 35℃(50°F-95°F)
8. Operating humidity: 20 - 85%RH
9. Storage and transport temperature: -20℃ - 60℃(-4°F-140°F)
10. Storage and transport humidity:10 - 95%RH
GENERAL SAFETY AND PRECAUTIONS
1. Do not use the Scale on an uneven floor, a soft surface or a carpet as doing so may result in unreliable
data.
2. This Wireless Body Analysis Scale is designed for adults. Infants or young children or any person who
cannot stand still without assistance, should not use it.
3. Avoid using this Scale near strong magnetic fields, such as microwave ovens, etc.
4. The Scale will maintain its safety and performance features for at least 10,000 measurements or two
years of use.
5. 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.
Cet appareil est conforme à la section 15 des réglementations de la FCC. Le fonctionnement de l’appareil est
sujetaux deux conditions suivantes :
(1) cet appareil ne doit pas provoquer d’interférences néfastes, et
(2) cet appareil doit tolérer les interférences reçues, y compris celles qui risquent de provoquer un
fonctionnement indésirable.
6. Changes or modifications not expressly approved by iHealth Lab Inc. invalidate the user’s warranty for
this equipment.
7. This equipment 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 equipment 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 equipment 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.
8. Please take attention that changes or modification not expressly approved by the party responsible for
compliance could void the user’s authority to operate the equipment.
9. 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
(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
radioexempts 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.
10. Under Industry Canada regulations, this radio transmitter may only operate using an antenna of a type
and maximum (or lesser) gain approved for the transmitter by Industry Canada. To reduce potential radio
interference to other users, the antenna type and its gain should be so chosen that the equivalent
isotropically radiated power (e.i.r.p.) is not more than that necessary for successful communication.
Conformément à la réglementation d'Industrie Canada, le présent émetteur radio peut fonctionner avec une
antenne d'un type et d'un gain maximal (ou inférieur) approuvé pour l'émetteur par Industrie Canada. Dans
le but de réduire les risques de brouillage radioélectrique à l'intention des autres utilisateurs, il faut choisir
le type d'antenne et son gain de sorte que la puissance isotrope rayonnée équivalente (p.i.r.e.) ne dépasse
pas l'intensité nécessaire à l'établissement d'une communication satisfaisante.
11.Guidance and manufacturer’s declaration - electromagnetic emissions - for all ME
EQUIPMENT and ME SYSTEM.
Table 1:Guidance and manufacturer’s declaration – electromagnetic emissions
The HS5 is intended for use in the electromagnetic environment specified below. The customer or the user
of the HS5 should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1 The HS5 uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not
likely to cause any interference in nearby electronic
equipment
RF emissions
CISPR 11
Class B
The HS5 is suitable for use in all establishments,
including domestic establishments and those directly
connected to the public low-voltage power supply
network that supplies buildings used for domestic
purposes.
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations/
Flicker emissions
IEC 61000-3-3
Not applicable
Guidance and manufacturer’s declaration - electromagnetic immunity - for all ME
EQUIPMENT and ME SYSTEM.
Table 2:Guidance and manufacturer’s declaration – electromagnetic immunity
The HS5 is intended for use in the electromagnetic environment specified below. The customer or the user of
the HS5 should assure that it is used in such an environment.
Immunity test IEC 60601
Test level
Compliance
level
Electromagnetic environment - guidance
Electrostatic
Discharge(ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
±6 kV
contact
±8 kV air
Floors should be wood, concrete or
ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30%.
Power frequency
(50/60Hz) magnetic
field
IEC 61000-4-8
3A/m 3A/m Power frequency magnetic fields should
be at levels characteristic of a typical
location in a typical commercial or
hospital environment
Note: U
T
is the a.c. mains voltage prior to application of the test level.
Guidance and manufacturer’s declaration – electromagnetic immunity for ME EQUIPMENT
and ME SYSTEM that are not LIFE-SUPPORTING.
Table 3: Guidance and manufacturer’s declaration – electromagnetic immunity
The HS5 is intended for use in the electromagnetic environment specified below. The customer or the user of
the HS5 should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance
level
Electromagnetic environment-guidance
Radiated RF
IEC 61000-4-3
3 Vrms
80MHz to 2.5GHz
3V/m
Portable and mobile RF communications
equipment should be used no closer to any
part of the SYSTEM, including cables, than
the recommended separation distance
calculated from the equation applicable to the
frequency of the transmitter.
Recommended separation distance
P
V
d]
5.3
[
1
=
P
E
d]
5.3
[
1
= 80MHz to 800MHz
P
E
d]
7
[
1
= 800MHz to 2.5GHz
Where P is the maximum output power rating
of the transmitter in watts(W) according to
the transmitter manufacturer and d is the
recommended separation distance in metres
(m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey,
should be less than the compliance level in
each frequency range.
Interference may occur in the vicinity of
equipment marked wigh the following
symbol:
Recommended separation distances between portable and mobile RF communications equipment and the
ME EQUIPMENT and ME SYSTEM – for ME EQUIPMENT and ME SYSTEM that are not
LIFE-SUPPORTING.
Recommended separation distances between portable and mobile RF communications equipment and the
HS5
The HS5 is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the HS5 can help prevent electromagnetic interference by maintaining
a minimum distance between portable and mobile RF communications equipment (transmitters ) and the HS5
as recommended below, according to the maximum output power of the communications equipment.
Rated maximum
output power of
transmitter
W
Separation distance according to frequency of transmitter
m
150kHz to 80 MHz 80MHz to 800MHz 800MHz to 2.5GHz
P
V
d]
5.3
[
1
= P
E
d]
5.3
[
1
= P
E
d]
7
[
1
=
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
12.After the laboratory measurement, the max SAR value is 0.134W/Kg which fulfils the related
requirement.
WARRANTY INFORMATION
The iHealth Vista Wireless Body Analysis Scale is warranted to be free from defects in materials and
workmanship appearing within 1 year from the date of purchase, when used in accordance with the
instructions provided. The above warranties extend only to the original retail purchaser. We will, at our
option, repair or replace without charge any product covered by the above warranties. Repair or
replacement is our only responsibility and your only remedy under the above warranties.
EXPLANATION OF SYMBOLS
Symbol for “THE OWNER’S MANUAL MUST BE READ”
! Symbol for “CAUTION”
Symbol for “TYPE BF APPLIED PARTS”
Symbol for “ENVIRONMENT PROTECTION – Waste electrical products should not be
disposed of with house-hold waste. Please recycle where facilities exist. Check with your local Authority
or retailer for recycling advice”.
Symbol for “MANUFACTURER”
Symbol for “KEEP DRY”
Symbol for “Year of Manufacture”
Symbol for “COMPILES WITH RTTE
99/5/EC REQUIREMENTS”
ANDON HEALTH CO., LTD.
No. 3 Jinping Street, YaAn Road, Nankai District,
Tianjin 300190, China. Tel: 86-22-60526161
iHealth is a trademark of iHealth Lab Inc.
Other trademarks and trade names are those of their respective owners.