Jawbone CORE User Manual

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Visit up.jawbone.com
Get the app. Connect your armband. Start living better.
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SENSOR MODULE
To remove the sensor module from the strap, press down evenly on both sides of the front face of the sensor module until it comes out of the strap. To reattach the sensor module, align the large indentation on the inside of the strap with the tab on the sensor module. Press evenly on both sides until the sensor module firmly snaps into place.
GET THE APP
Go to up.jawbone.com
Already using UP?
Make sure you have the latest version of the app.
CONNECT YOUR ARMBAND
Follow the instructions to pair your armband and create your profile.
Already using UP?
Tap the icon in the top right corner of the home
screen, “Add new band” and follow the instructions.
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STATUS BUTTON
STRAP
SENSOR MODULE
ADJUSTERS
STATUS LIGHT
STATUS INDICATORS
Sound
3 Beeps
Single Alert tone
None
Alert tone every 15 seconds
Status Light
Solid Light for a few Seconds
Slow blinking light
Fast blinking light
None
Status
Armband Collecting Data*
Low Battery
Battery Depleted
Armband not configured to app
*It may take up to 10 minutes for the armband to begin collecting data after it is placed on the arm.
KEEP YOUR ARMBAND CHARGED
Your armband should last at least four days when fully charged. The UP app will notify you when the battery is low. To charge your armband, remove the sensor module from the strap, place the sensor module into the dock and plug it into a USB port.
The status light will flash two times when fully charged. This may take up to two hours.
DOCK
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Questions? Support? jawbone.com/support/core
HOW TO WEAR CORE
Wear on the back of your left tricep (your arm and CORE should be clean, dry, and free of lotion or oil). Make sure the sensors touch your skin and the logo on the button points up toward the right.
Use the adjusters to tighten and loosen the strap, before putting it on your arm. Make sure the strap is not too tight—you should be able to place three fingers beneath it. Once the strap is adjusted to a comfortable fit, there is no need to readjust it. Simply slide the armband on and o your arm by stretching the strap.
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WARNINGS
• Always con sult a physician befo re starting any new d iet or exercise progr am.
• This sys tem (CORE device and UP a pp) is not to be used for diag nostic purpose s and is not intended to b e a substitute for the medic al advice or super vision of your pers onal physician.
• Becaus e everyone’s skin is dif ferent you may experi ence irritation or re dness after wear ing the armband. I f this occurs, d iscontinue use and c onsult your physicia n.
• If you have know n metal allergies , consult your physici an prior to wearing.
• Do not wear o n an open wound, sore , burn, blister or ra sh.
• To reduce po tential for skin irri tation, limit wear ing the device to a maxim um of 23 hours per day.
• To reduce the pote ntial risk of skin irri tation, dry your ar m and the armband th oroughly before wea ring.
• To avoid skin bur ns, do not wear whe n it has been exposed to exc essively hot tempe ratures includi ng direct sun expos ure.
• Choking h azard. This produ ct contains small p arts. Keep out of th e reach of children un der 3 years.
• Be caref ul not to over-tighten the stra p while on your arm. If yo u feel constrictio n or loss of circulatio n at any time, loosen th e adjustable stra p and readjust it to a mor e comfortable set ting. If you experie nce pain, bruisin g, swelling, or discolor ation of the arm, disc ontinue use and cons ult a physician.
CAUTIONS
• Check COR E for sharp edges or d amage before eac h use.
• The armba nd and dock shoul d not be used in airpla nes, hospitals , or any location that pr ohibits cellular t elephones or electr onic devices.
• Do not plac e the CORE in close proxi mity to other devices th at can cause elec tromagnetic inter ferences of any natu re.
• Do not inci nerate.
• Rough handling can break internal components.
• Never drop or shoc k the armband and do ck and always store it in a sa fe and dry place whe n not in use.
• If the ar mband is droppe d, ensure that it is wor king properly an d not physically dam aged before relyi ng on readings.
• Do not attem pt to open the armban d or dock yourself. It co ntains no user-ser viceable parts . Refer all servic ing to qualifi ed Service Perso nnel. Opening th e armband or dock yo urself will void the war ranty.
• Do not use un approved accessor ies.
• This prod uct is not defibrill ation proof.
• The equip ment is not suitabl e for use in the presenc e of a flammable ane sthetic mixture with a ir or with oxygen or nitro us oxide .
• Medical electrical equipment requires special precautions regarding electromagnetic environments (EMC) and must be instal led and put into serv ice according to the EM C information provid ed in the User Manua l. Portable and m obile radio frequency (RF) communications equipment can affect medical electrical equipment.
• The equip ment of the system sho uld not be used adja cent to or stacked with oth er equipment.
• Avoid exposin g the equipment to ext reme temperature s like saunas, dire ct sunlight, mois ture, sand, dust , leaving in freezing c onditions, or mec hanical shock .
• All refere nces to the equipmen t have been replaced by th e product name, C ORE.
ACCESSORIES
• Addition al strap sizes and acces sories available a t jawbone.com/core
CORE CARE
Clean the a rmband regular ly after sweating or wh en it becomes notice ably moist or dirt y. Failure to keep the armb and clean, o r improper cleani ng may irritate the skin a nd affect the sen sor performanc e. Minimize use of solve nts, cleaners or other ch emicals and do not s terilize any part(s).
• To clean the sen sor module, use a clo th or towel moistened wit h mild soap and water to wi pe the metal sensor s that touch the sk in. Remove any excess soa p and dry with a cloth or towe l completely before w earing.
• To clean the stra p, hand wash with mild s oap and warm water, rinse , then air dry. For optim al performance a nd lifespan o f the strap, avoid machi ne drying.
• The senso rs may be disinfecte d by wiping with a soft clot h dampened with 70% is opropyl alcohol. A llow 5-10 minutes for dryin g before wearing. Al ways disinfect the se nsor module and rep lace the armband s trap prior to use by other s.
• Though th e armband was desig ned for wearabilit y and long-term use , it is a sensitive monito ring device. Rough handling can break internal components.
SAFE DISPOSAL
Dispose of t he CORE armband , battery, and this pa ckaging in accorda nce with local regul ations. Do not dispo se of the battery i n the sensor modul e with regular house hold waste.
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SN
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SYMBOL DEFINITIONS
Consult instructions for use FCC Decla ration of Conformit y
Non-ionizing radiation Batter y Charger System Com pliance
Type B Applied P art Bluetooth® Wireless Technology
Date of Manu facture
Manufacturer
CAUTION Serial Number
The Waste Electrical and Electronic Equipment Regulations indicates separate collection for electrical and electronic equipment
Electrical Safety Armband tested to applicable safety standards by MET Laboratories
Recyclable
SYSTEM ACCURACY (PER DAY, ADULTS)
• Total calori es/METs for free livin g activities: mean e rror < 10%
• Total minutes of p hysical activity : mean error < 5%
• Total step count : mean error < 9%
PRODUCT SPECIFICATIONS
SENSORS
• Accelerom eter (3-axis)
• Heat Flux
• Skin Temperature
• Galvani c Skin Response (GSR)
MATERIALS
• Sensor M odule: PC/PBT, ther moplastic uretha ne, 316L grade s tainless steel
• Adjusta ble strap/wing assem bly: Nylon, elas tane, silicone, 3 16L stainles s steel, PC/PBT an d rubber coating
Batter y power: At least 4 days Batter y type: Internal lith ium polymer cell Radio Frequency: 2.4GHz Contains a class 2 Bluetooth wireless technology transceiver Transmitter o utput power: <2. 5mW Sensor M odule size: (l) 26mm x (w) 36mm x ( h) 13mm [1 .0” x 1.4” x 0.5” ] Armban d weight (with adjustab le strap): 30g (1.1oz) Water resist ance: IPX5 classif ied Operati ng temperature/h umidity: +5°C - 40° C (40°F to 10 4°F)/ 5 - 95% RH non- condensing Storage tem perature/humi dity: -20°C - 55°C (-4°F to 13 1°F) / 5 - 95% RH non -condensing
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USER ENVIRONMENT
1.5m 1.5m
2.5m
1.5m
Computer and Wireless Communicator
Diagram n ot to scale.
GUIDANCE AND MANUFACTURER’S DECLARATION - EMISSIONS
The Armba nd is intended for us e in the electromag netic environment s pecified below. Th e customer or user of the Armb and should ensure th at it is used in such an env ironment.
EMISSIONS TEST
RF Emissi ons CISPR 11
Harmon ics IEC 6100-3 -2
Flicker IEC 6 100-3-3
COMPLIANCE
Class B, G roup 1
N/A
N/A
ELECTROMAGNETIC ENVIRONMENT–GUIDANCE
The Armba nd uses RF energy o nly for its internal functio n. Therefore, its R F emissions are ver y low and are not l ikely to cause any inter ference in nearby electronic equipment
The Armba nd is suitable for us e in all establishm ents, including domestic, and those directly connected to the publi c low-voltage power sup ply network that supplies buildings used for domestic purposes
GUIDANCE AND MANUFACTURER’S DECLARATION - IMMUNITY
The Armba nd is intended for us e in the electromag netic environment s pecified below. Th e customer or user of the Armb and should ensure th at it is used in such an env ironment.
IMMUNITY TEST
ESD IEC 61 000-4-2
EFT IEC 61 000-4-4
Voltage Dips/ Drop out IEC 61000-4-11
Power Frequency 50/60H
Magneti c Field IEC 61000-4-8
IEC 60601 TEST LEV EL
COMPLIANCE LEVEL
±6kV Contact ±8kV Air
±2kV Mains ±1kV I/O s
±1kV Differential ±2kV Common
>95% Dip fo r
0.5 Cycles 60% Dip for 5 Cycles 30% Dip for 2 5 Cycles >95% Dip fo r 5 Seconds
3A/m
±6kV Contact ±8kV Air
N/A
N/A
N/A
3A/m
ELECTROMAGNETIC ENVIRONMENT–GUIDANCE
Floors sh ould be wood, concr ete, or ceramic tile. I f floors a re synthetic, they r/h sho uld be at least 30%
Mains powe r quality should b e that of a typical commercial or hospital environment
Mains powe r quality should b e that of a typical commerci al or hospital envir onment. If the user o f the Armband requires continued operation during power mains inte rruptions, it is rec ommended that the Armban d be powered from an uni nterruptible power supply or b attery.
Power freq uency magnetic fi elds should be that o f a typical c ommercial or hosp ital environment .
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GUIDANCE AND MANUFACTURER’S DECLARATION - EMISSIONS
The Armba nd is intended for us e in the electromag netic environment s pecified below. Th e customer or user of the Armb and should ensure th at it is used in such an env ironment.
IMMUNITY TEST
Conducted RF IEC 61000-4-6
Radiated RF IEC 61000-4-3
IEC 60601 TEST LEV EL
COMPLIANCE LEVEL
3 Vrms 150 kHz to 80 MHz
3 V/m 80 MHz to
2.5 GHz
3 Vrms 150 kHz to 80 MHz
3 V/m 80 MHz to
2.5 GHz
ELECTROMAGNETIC ENVIRONMENT–GUIDANCE
Portable and mobile communications equipment should be s eparated from Arm band by no less than the distances calculated/listed below:
D=(3.5/V1)(Sqrt P)
D=(3. 5/E1)(Sqrt P) 8 0 to 800 MHz
D=(7/EI)(Sqrt P) 800 MHz to 2 .5 GHz
Where P is th e max power in watts and D i s the recommended separation distance in meters.
Field stre ngths from fixed tran smitters, as dete rmined by an electr omagnetic site sur vey, should be less than the compli ance levels (V1 an d E1).
Interfe rence may occur in the vi cinity of equipme nt containing a transmitter.
RECOMMENDED SEPARATION DISTANCES FOR THE PRODUCT
The Armba nd is intended for us e in the electromag netic environment s pecified below. Th e customer or user of the Armb and can help prevent e lectromagnetic i nterference by mai ntaining a minimum d istance between portable and mobile RF Communications Equipment and the Armband as recommended below, according to the maximum output power of the communications equipment.
MAX OUTPUT POWER (WAT TS)
SEPARATION (M) 150KHZ TO 80MHZ
D=(3.5/V1)(SQRT P)
SEPARATIO N (M) 80 TO 800MHZ
D=(3.5/V1)(SQRT P)
SEPARATIO N (M) 800MHZ TO 2.5G HZ
D=(7/E1)(SQRT P)
0.01
0.1
1
10
100
0.1166
0.3689
1.1666
3.6893
11.6666
0.1166
0.3689
1.1666
3.6893
11.6666
0.2333
0.7378
2.3333
7.3 786
23.3333
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RE GUL AT OR Y S TATE M E NT
FCC Decla ration of Conformit y – We, BodyMedia, I nc., One Gateway Cen ter, 420 Fort Duquesn e Boulevard, Suite 1 900, Pittsbu rgh, PA 15222, a who lly owned subsidiar y of Jawbone, decl are under our sole re sponsibility tha t the products, BodyMe dia, Inc. and Bo dyMedia® Armba nd (Model AB200) an d Dock (Model CR 200), comply with par t 15 of the FCC rules. O peration is subjec t to the following two con ditions: (1) This d evice may not cause ha rmful interferen ce, and (2) This device m ust accept any inter ference received, i ncluding interf erence that may caus e undesired opera tion.
This equi pment has been test ed and found to comply w ith the limits for a Clas s B digital device, pu rsuant to part 15 of the FCC Rule s. These limits are d esigned to provide re asonable protect ion against harmf ul interference i n a residential install ation. This equip ment generates, u ses and can radiate r adio frequency e nergy and, if not ins talled and used in accorda nce with the instruc tions, may cause ha rmful interfere nce to radio communic ations. However, there i s no guarante e that interferen ce will not occur in a par ticular installa tion. If this equip ment does cause ha rmful interfere nce to radio or tel evision reception , which can be determ ined by turning the eq uipment off and on , the user is encour aged to try to corre ct the interferen ce by one or more of the foll owing measures:
• Reorien t or relocate the recei ving antenna.
• Increas e the separation bet ween the equipme nt and receiver.
• Connec t the equipment into a n outlet on a circuit se parate from the receive r.
• Consult th e dealer or an exper ienced radio/T V technician for hel p.
CAUTION : Changes or modi fications to this equ ipment not express ly approved by the part y responsible for complia nce could void the user ’s authority to oper ate the equipment.
RF Expos ure information: Se e 2.1093 of the FCC Rul es
This prod uct is a Type B Applied Par t complying with the sp ecified require ments of the Standa rd to provide protectio n against electric shock, particularly regarding allowable Leakage Current. IEC 6060 1-1, Edition 3.1, 2 012-08, Medi cal Electrical Eq uipment - Part 1: G eneral requirem ents for basic safe ty and essential performance IEC 6060 1-1-2, Third Edition , 2007-03, Medic al Electrical Equ ipment - Part 1-2: Ge neral requirem ents for basic safet y and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests AAMI 60601-1: ANSI /AAMI ES 60601-1:20 05, Medical Ele ctrical Equipme nt – Part 1: Genera l Requirements fo r Basic Safety an d Essential Perf ormance ANSI/I EC 60529, 2004 , Degrees of Protecti on Provided by Enclosu res (IP Code) IEC 6095 0-1, Edition 2.1 , 2012-05, Infor mation Technology Equ ipment - Safety - Pa rt 1: General Req uirements UL 1642 , Standard for Safet y, Lithium Batteries IEC 62133 , Edition 2.0, 2012 , Secondary cel ls and batteries con taining alkalin e or other non-acid e lectrolytes - Safe ty requirem ents for portab le sealed seconda ry cells, and for b atteries made from t hem, for use in por table applicati ons WEEE, 20 06 No. 3289, Enviro nmental Protecti on - The Waste Electric al and Electronic E quipment Regula tions Califor nia Energy Commis sion - 2012 Applian ce Efficiency Reg ulations, CEC-4 00-2012-019 -CMF
47CFR Part 1 5 Subpart B & ICES -003, Issue 4 Feb ruary 2004 for C lass B Digital Device s 47CFR Part 1 5 Subpart C 15. 247 & RSS-210, Issue 8 , December 2010 f or Intentional Radi ators ETSI EN 30 0 328 (Article 3. 2 of R&TTE Directive) ETSI EN 30 1 489-1 with ETSI EN 4 89-17 (Article 3 .1(b) of R&TTE Directive) RoHS requirements
BodyMedia, Inc. One Gateway C enter 420 Fort Du quesne Blvd. Suite 190 0 Pittsburgh, PA 15222 USA
10089 1_Rev1
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QUESTIONS? SUPPORT?
JAWBONE.COM/SUPPORT/CORE
CORE
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