User Manual

FCC ID: SLRHS6

Users Manual

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FCCID_2485672

          iHealth®
Wireless Body Analysis Scale




   OWNER’S MANUAL


TABLE OF CONTENTS
INTENDED USE........................................................................................................................................... 2
IMPORTANT NOTE FOR USERS .............................................................................................................. 2
CONTRAINDICATION ............................................................................................................................... 2
OFFLINE MEMORY .................................................................................................................................... 3
SPECIFICATIONS........................................................................................................................................ 3
GENERAL SAFETY AND PRECAUTIONS............................................................................................... 3
EXPLANATION OF SYMBOLS ................................................................................................................. 5




INTENDED USE

The iHealth 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 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.


OFELINE MEMORY


"The Scal can store up to 200 weight cesuls foreach user. When each user‘s memagy is full, any new
amessirements willovercie toldest ones


SPECIFICA TIONS


 1. Poduct name: Meallh Wieeless Body Aalysis Sele
2.  Motet: HSs
3.  Clisifiction:interrlly powered, type BP ppled pact (four lectes)
4.  Pover:dx1 SV          ==AMAbateres
     ‘Baterylife: appcos. 3 months wdaly usage
5. Measurement cinge
       Fody Welght: 11 1400 1b3 ke—180ky
       Fody Pus 5.0%.55.0%
       Tenpeatie: 5C —400(P—I0CD)
       Humidiy: 20— 590
       Scal cesoluton:0.2100.tkg
6. Accuriey
       Hodly Welght 21.1 15.5 kaCt o1 10 b/—5 ke—56k);
                      198 (110—400 t /50 ke—180 ky)
       Rody us at%
7. Opectingtemperatie: 41°P—I0i*F (SC —40°C)
8. Operating humidy: 20 853R
9. Storige and teensportemperatice: 4—131°P (20°C—53C)
 10. Slomge and ransporthueridiy: 9ORIT



GENERAL SAFETY AND PRECAUTIONS


1. Do 10tuse the Scale on an uneven floos, a softsudios oa carpetosdoing so may ceultin uncefuble
dn
2. This Wieeless Body Analysis Seais designed foraduls. Trfants or young chiléren or any pecson who
eannorsand sillwilhout asistance,should not us it
3 Aveld using this Scale neasvong magnelic felds, such asmicmowave ovens, lc


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.


WARRANTY INFORMATION
The iHealth 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.



Document Created: 2014-12-09 05:31:44
Document Modified: 2014-12-09 05:31:44

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