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: UT 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 PVd]5.3[1= PEd]5.3[1=  80MHz to 800MHz PEd]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
PVd]5.3[1= PEd]5.3[1= PEd]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.

Navigation menu