OXJBP40Smart Arm Blood Pressure Monitor

English Smart Arm Blood Pressure Monitor Simple Operation High Measuring Accuracy USER MANUAL 1 English NantCare LLC, 2929 N 44th Street Phoenix, Arizona, 85018-7239 - USA 1-855-NANTCARE - Email: [email protected] www.nantcare.com Copyright© Revision 06 2012 Smart Arm Blood Pressure Meter 2 English 1 English Table of Contents 1Table of Contents 1.1 Introduction P 4 1.2 Intended Use P 4 1.3 Safety Information P 4-5 1.3.1 Operating the device - WARNINGS P 5 1.3.2 Cautions P 6 1.4 Before taking a measurement P 6 2Operating Instructions P 7 2.1 Know your NantLife Blood Pressure Meter P 7 2.2 Unit Display P 7 2.3 Display symbols P 8 2.4 Battery installation P 8 2.5 Battery Replacement P 8 2.6 Applying the arm cuff P 9 2.7 Taking a measurement P 9-10 2.8 Bluetooth Activation P 10 2.9 Bluetooth Pairing P 10 2.10 Data Transmission P 10 2.11 Using the software P 11 2.12 Evaluation by your care provider P 11 3Care and Maintenance P 12 3.1 Cleaning P 12 3 4Troubleshooting P 12 4.1 Error Indicators P 12 4.2 Troubleshooting tips P 13 5Warranty P 14 6Specifications P 15-16 7Manufacturer P 16 4 1.1 Introduction Thank you for purchasing the NantLife Smart Blood Pressure Monitor. Your new digital blood pressure meter uses the oscillometric method of blood pressure measurement. This means the monitor detects your blood’s movement through your brachial artery and converts the movements into digital reading. With its unique wireless integrated technology, the NantLife Smart Blood Pressure meter enables you to perform first-class, comfortable and extremely gentle blood pressure measurements. You have chosen the most up-to-date form of healthcare management. Measured values are transmitted automatically to a secured database via a Bluetooth-enabled mobile phone and/or the HBox® hub. Choose between 2 basic configurations: 1) Smart Medical Home with NantLife HBox® 2) Mobile Health with your Bluetooth-enabled smartphone or Bluetooth-enabled tablet The NantLife Smart Blood Pressure Monitor comes with the follow- ing components: • Monitor with LCD display • Standard Adult Cuff • User Manual • Quick User Guide • Warranty card Thank you for your trust; we are available at any time for service and product questions. More information at: www.NantLife.com SAVE THESE INSTRUCTIONS 1.2 Intended Use • NantLife Smart Blood Pressure Monitor is intended for home monitoring of blood pressure and pulse. • NantLife Blood Pressure Monitor is not intended to be a diagnostic device. • Never change your medication on the basis of results you have obtained. The evaluation of the measurements and the treatment based on them may only be carried out by the treating physician. • This device is intended for use in measuring blood pressure and pulse rate in the adult population. Do not use this device in infants or person who cannot express their intention. 1.3 Safety Information To assure the correct use of the monitor, basic safety measures should always be followed including the warnings and cautions lifted in this instruction manual. 1.3.1 Operating the device - WARNINGS ! Read all of the information in the instruction manual and any other instruction in the box before operating the unit. If you experience discomfort during a measurement: Press the inside button to deflate the cuff immediately. Remove the cuff and stop using the monitor. Please contact our Customer Service at [email protected] English 5 in addition, please note: • If you suffer from heartbeat irregularities, you should consult your doctor about whether blood pressure monitoring with the NantLife blood pressure meter is appropriate for you. Self- diagnosis and treatment using measured results may be dan- gerous. Follow the instructions of your physician or licensed healthcare provider. • Please also consult your doctor if you are taking anticoagulants (e.g. Marcumar, Coumadin, aspirin) • To produce precise readings, the device should be placed on a hard and leveled surface. The cuff should be fixed around the bare upper left arm • The device is suitable by default for standard adult upper arm with a circumference of 25-35 cm [9.84 - 13.77 inches] when using the default cuff, more sizes are available at www. NantLife.com: - 33-47 cm [12.99 - 18.5 inches] when using for Large Adult. • The custom large adult and small adult cuffs can be obtained directly from the NantLife website. • Do not under any circumstances use the device in the bath or the shower. If, however, liquid gets into the device, you must remove the batteries immediately and refrain from further use. Contact our service department (see page 17). • The device may not be used near a nuclear magnetic tomo- graphic resonance. • Using components that are not part of the scope of delivery can produce faulty measurements (Exception: battery replace- ment). • DO NOT subject the monitor to strong shocks such as dropping the unit on the floor. • DO NOT damage the batteries. If battery fluid gets in your eyes, immediately rinse with plenty of clean water and contact a physician immediately. • Keep away from source of fire and/or heat. • Store the device in a clean, safe location. • DO NOT disassemble the blood pressure meter or its acces- sories. • DO NOT use the blood pressure meter in the proximity of a MRI or CT. • DO NOT use the blood pressure meter in the presence of flam- mable anesthetics. • Explosion hazard: DO NOT use the blood pressure meter in an explosive atmosphere. • Chemicals from LCD display panel are toxic if ingested. Use caution if the blood pressure meter display screen is broken. • The blood pressure meter is intended only as an adjunct in patient assessment. It must be used in conjunction with other methods of assessing clinical signs and symptoms. • Check the blood pressure meter cuff application site frequent- ly to determine skin sensitivity of the patient. • Prolonged use or the patient’s condition may require chang- ing the site periodically. Change arm and check skin integrity, circul…

Text truncated - open the document above for the full version.

English Smart Arm Blood Pressure Monitor Simple Operation High Measuring Accuracy USER MANUAL 1 English NantCare LLC, 2929 N 44th Street Phoenix, Arizona, 85018-7239 - USA 1-855-NANTCARE - Email: [email protected] www.nantcare.com Copyright© Revision 06 2012 Smart Arm Blood Pressure Meter 2 English 1 English Table of Contents 1Table of Contents 1.1 Introduction P 4 1.2 Intended Use P 4 1.3 Safety Information P 4-5 1.3.1 Operating the device - WARNINGS P 5 1.3.2 Cautions P 6 1.4 Before taking a measurement P 6 2Operating Instructions P 7 2.1 Know your NantLife Blood Pressure Meter P 7 2.2 Unit Display P 7 2.3 Display symbols P 8 2.4 Battery installation P 8 2.5 Battery Replacement P 8 2.6 Applying the arm cuff P 9 2.7 Taking a measurement P 9-10 2.8 Bluetooth Activation P 10 2.9 Bluetooth Pairing P 10 2.10 Data Transmission P 10 2.11 Using the software P 11 2.12 Evaluation by your care provider P 11 3Care and Maintenance P 12 3.1 Cleaning P 12 3 4Troubleshooting P 12 4.1 Error Indicators P 12 4.2 Troubleshooting tips P 13 5Warranty P 14 6Specifications P 15-16 7Manufacturer P 16 4 1.1 Introduction Thank you for purchasing the NantLife Smart Blood Pressure Monitor. Your new digital blood pressure meter uses the oscillometric method of blood pressure measurement. This means the monitor detects your blood’s movement through your brachial artery and converts the movements into digital reading. With its unique wireless integrated technology, the NantLife Smart Blood Pressure meter enables you to perform first-class, comfortable and extremely gentle blood pressure measurements. You have chosen the most up-to-date form of healthcare management. Measured values are transmitted automatically to a secured database via a Bluetooth-enabled mobile phone and/or the HBox® hub. Choose between 2 basic configurations: 1) Smart Medical Home with NantLife HBox® 2) Mobile Health with your Bluetooth-enabled smartphone or Bluetooth-enabled tablet The NantLife Smart Blood Pressure Monitor comes with the follow- ing components: • Monitor with LCD display • Standard Adult Cuff • User Manual • Quick User Guide • Warranty card Thank you for your trust; we are available at any time for service and product questions. More information at: www.NantLife.com SAVE THESE INSTRUCTIONS 1.2 Intended Use • NantLife Smart Blood Pressure Monitor is intended for home monitoring of blood pressure and pulse. • NantLife Blood Pressure Monitor is not intended to be a diagnostic device. • Never change your medication on the basis of results you have obtained. The evaluation of the measurements and the treatment based on them may only be carried out by the treating physician. • This device is intended for use in measuring blood pressure and pulse rate in the adult population. Do not use this device in infants or person who cannot express their intention. 1.3 Safety Information To assure the correct use of the monitor, basic safety measures should always be followed including the warnings and cautions lifted in this instruction manual. 1.3.1 Operating the device - WARNINGS ! Read all of the information in the instruction manual and any other instruction in the box before operating the unit. If you experience discomfort during a measurement: Press the inside button to deflate the cuff immediately. Remove the cuff and stop using the monitor. Please contact our Customer Service at [email protected] English 5 in addition, please note: • If you suffer from heartbeat irregularities, you should consult your doctor about whether blood pressure monitoring with the NantLife blood pressure meter is appropriate for you. Self- diagnosis and treatment using measured results may be dan- gerous. Follow the instructions of your physician or licensed healthcare provider. • Please also consult your doctor if you are taking anticoagulants (e.g. Marcumar, Coumadin, aspirin) • To produce precise readings, the device should be placed on a hard and leveled surface. The cuff should be fixed around the bare upper left arm • The device is suitable by default for standard adult upper arm with a circumference of 25-35 cm [9.84 - 13.77 inches] when using the default cuff, more sizes are available at www. NantLife.com: - 33-47 cm [12.99 - 18.5 inches] when using for Large Adult. • The custom large adult and small adult cuffs can be obtained directly from the NantLife website. • Do not under any circumstances use the device in the bath or the shower. If, however, liquid gets into the device, you must remove the batteries immediately and refrain from further use. Contact our service department (see page 17). • The device may not be used near a nuclear magnetic tomo- graphic resonance. • Using components that are not part of the scope of delivery can produce faulty measurements (Exception: battery replace- ment). • DO NOT subject the monitor to strong shocks such as dropping the unit on the floor. • DO NOT damage the batteries. If battery fluid gets in your eyes, immediately rinse with plenty of clean water and contact a physician immediately. • Keep away from source of fire and/or heat. • Store the device in a clean, safe location. • DO NOT disassemble the blood pressure meter or its acces- sories. • DO NOT use the blood pressure meter in the proximity of a MRI or CT. • DO NOT use the blood pressure meter in the presence of flam- mable anesthetics. • Explosion hazard: DO NOT use the blood pressure meter in an explosive atmosphere. • Chemicals from LCD display panel are toxic if ingested. Use caution if the blood pressure meter display screen is broken. • The blood pressure meter is intended only as an adjunct in patient assessment. It must be used in conjunction with other methods of assessing clinical signs and symptoms. • Check the blood pressure meter cuff application site frequent- ly to determine skin sensitivity of the patient. • Prolonged use or the patient’s condition may require chang- ing the site periodically. Change arm and check skin integrity, circul…

Text truncated - open the document above for the full version.

Aug Fed Aut FCC Re: Pur s requ 1: B 2: C 3: O 4: P Th e rele app Th e all a app Sin c Nan Con g. 9, 2012 deral Comm thorization C ID: OXJB : Confiden suant to Se uests confid Block Diagra Circuit Diagra Operational D Parts List e above mat ased to the licant and p e Applicant u accompanyi lication. cerely, ntCare LLC ntact Peop munication and Evalu BP40 ntiality Re ctions 0.457 ential treatm m am Description terials conta e public. The rovide unjus understands ng docume n C ple: Rechar n Commiss uation Divis quest 7 and 0.459 ment of infor ain trade se e public dis stified benef that pursua ntation will rd Binier sion sion 9 of the Com rmation appl ecrets and p sclosure of t fits to its com nt to Rules 0 not be mad mmission’s R ied this app proprietary these matte mpetitors. 0.457, disclo e before th Rules, the a lication as o information ers might be osure of this e date of th applicant he outlined belo not custom e harmful to s Application he Grant for ereby ow: marily o the n and r this

Aug Fed Aut FCC Re: Pur s requ 1: B 2: C 3: O 4: P Th e rele app Th e all a app Sin c Nan Con g. 9, 2012 deral Comm thorization C ID: OXJB : Confiden suant to Se uests confid Block Diagra Circuit Diagra Operational D Parts List e above mat ased to the licant and p e Applicant u accompanyi lication. cerely, ntCare LLC ntact Peop munication and Evalu BP40 ntiality Re ctions 0.457 ential treatm m am Description terials conta e public. The rovide unjus understands ng docume n C ple: Rechar n Commiss uation Divis quest 7 and 0.459 ment of infor ain trade se e public dis stified benef that pursua ntation will rd Binier sion sion 9 of the Com rmation appl ecrets and p sclosure of t fits to its com nt to Rules 0 not be mad mmission’s R ied this app proprietary these matte mpetitors. 0.457, disclo e before th Rules, the a lication as o information ers might be osure of this e date of th applicant he outlined belo not custom e harmful to s Application he Grant for ereby ow: marily o the n and r this

PHOTOGRAPHS OF THE EUT TOTAL VIEW OF EUT TOP VIEW OF EUT BOTTOM VIEW OF EUT LEFT VIEW OF EUT RIGHT VIEW OF EUT FRONT VIEW OF EUT BACK VIEW OF EUT

PHOTOGRAPHS OF THE EUT TOTAL VIEW OF EUT TOP VIEW OF EUT BOTTOM VIEW OF EUT LEFT VIEW OF EUT RIGHT VIEW OF EUT FRONT VIEW OF EUT BACK VIEW OF EUT

Smart Arm Blood Pressure Monitor Model Name：BP4.0 Brand Name：NantLife FCC ID: OXJBP40

Smart Arm Blood Pressure Monitor Model Name：BP4.0 Brand Name：NantLife FCC ID: OXJBP40

OPEN VIEW OF EUT-1 OPEN VIEW OF EUT – 2 INTERNAL VIEW OF SAMPLE – 1 INTERNAL VIEW OF SAMPLE – 2 Bluetooth Antenna

OPEN VIEW OF EUT-1 OPEN VIEW OF EUT – 2 INTERNAL VIEW OF SAMPLE – 1 INTERNAL VIEW OF SAMPLE – 2 Bluetooth Antenna

FCC PART 15&RSS­210 Test Report Report No.: AGC026120602‐1F2 FCC ID : OXJBP40 IC : 10549A‐BP40 PRODUCT DESIGNATION : Smart Arm Blood Pressure Monitor BRAND NAME : NantLife TEST MODEL : BP4.0 CLIENT : NantCare LLC DATE OF ISSUE : Aug.08, 2012 STANDARD(S) : FCC Part 15 Rules& RSS‐210 REPORT VERSION : V 1.0 Attestation of Global Compliance (Shenzhen) Co., Ltd. CAUTION: This report shall not be reproduced except in full without the written permission of the test laboratory and shall not be quoted out of context. Report No.: AGC026120602-1F2 Page 1 of 39 VERIFICATION OF COMPLIANCE Applicant NantCare LLC 2929 N. 44th Street, Suite 110 Phoenix, AZ 85018 Manufacturer Shenzhen Jian Lang Technology Ltd. C202, 2F, Blook 1, Nanyou Tian'an Industry Town, SZ. R.P.C Product Designation Smart Arm Blood Pressure Monitor Brand Name NantLife Model Name BP4.0 FCC ID OXJBP40 IC 10549A-BP40 Report Number AGC026120602-1F2 Date of Test Jul.30, 2012 to Aug.03, 2012 WE HEREBY CERTIFY THAT: The above equipment was tested by Attestation of Global Compliance (Shenzhen) Co., Ltd. The test data, data evaluation, test procedures, and equipment configurations shown in this report were made in accordance with the procedures given in ANSI C63.4 (2003) .The sample tested as described in this report is in compliance with the FCC Rules Part 15 and RSS-210 requirements The test results of this report relate only to the tested sample identified in this report. Tested By Bart Xie Aug.08, 2012 Reviewed By Forrest Lei Aug.08, 2012 Approved By Solger Zhang Aug.08, 2012 Report No.: AGC026120602-1F2 Page 2 of 39 TABLE OF CONTENTS 1. GENERAL INFORMATION ................................................................................................................................................. 4 1.1 PRODUCT DESCRIPTION ....................................................................................................................... 4 1.2 TABLE OF CARRIER FREQUENCYS ...................................................................................................... 4 1.3 RELATED SUBMITTAL(S) / GRANT (S) ................................................................................................... 5 1.4 TEST METHODOLOGY ............................................................................................................................ 5 1.5 TEST FACILITY ......................................................................................................................................... 5 1.6 SPECIAL ACCESSORIES ......................................................................................................................... 5 1.7 EQUIPMENT MODIFICATIONS ................................................................................................................ 5 2. SYSTEM TEST CONFIGURATION ................................................................................................................................... 6 2.1 CONFIGURATION OF TESTED SYSTEM ................................................................................................ 6 2.2 EQUIPMENT USED IN EUT SYSTEM ...................................................................................................... 6 3. SUMMARY OF TEST RESULTS ....................................................................................................................................... 7 4. DESCRIPTION OF TEST MODES .................................................................................................................................... 7 5. PEAK OUTPUT POWER ..................................................................................................................................................... 8 5.1 LIMITS ........................................................................................................................................................ 8 5.2 MEASUREMENT PROCEDURE ................................................................................................................ 8 5.3 TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) ....................................................................... 8 5.4 MEASUREMENT EQUIPMENT USED ....................................................................................................... 9 5.5 MEASUREMENT RESULT ......................................................................................................................... 9 6. DB BANDWIDTH ................................................................................................................................................................. 10 6.1 LIMITS ...................................................................................................................................................... 10 6.2 MEASUREMENT PROCEDURE ............................................................................................................. 10 6.3 TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) ..................................................................... 10 6.3 MEASUREMENT EQUIPMENT USED ................................................................................................... 10 6.5 MEASUREMENT RESULTS .................................................................................................................... 10 7. 99% BANDWIDTH ............................................................................................................................................................... 13 7.1 LIMITS ...................................................................................................................................................... 13 7.2 MEASUREMENT PROCEDURE .............................................................................................................. 13 7.3 TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) ..................................................................... 13 7.4 MEASUREMENT EQUIPMENT USED ........................…

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FCC PART 15&RSS­210 Test Report Report No.: AGC026120602‐1F2 FCC ID : OXJBP40 IC : 10549A‐BP40 PRODUCT DESIGNATION : Smart Arm Blood Pressure Monitor BRAND NAME : NantLife TEST MODEL : BP4.0 CLIENT : NantCare LLC DATE OF ISSUE : Aug.08, 2012 STANDARD(S) : FCC Part 15 Rules& RSS‐210 REPORT VERSION : V 1.0 Attestation of Global Compliance (Shenzhen) Co., Ltd. CAUTION: This report shall not be reproduced except in full without the written permission of the test laboratory and shall not be quoted out of context. Report No.: AGC026120602-1F2 Page 1 of 39 VERIFICATION OF COMPLIANCE Applicant NantCare LLC 2929 N. 44th Street, Suite 110 Phoenix, AZ 85018 Manufacturer Shenzhen Jian Lang Technology Ltd. C202, 2F, Blook 1, Nanyou Tian'an Industry Town, SZ. R.P.C Product Designation Smart Arm Blood Pressure Monitor Brand Name NantLife Model Name BP4.0 FCC ID OXJBP40 IC 10549A-BP40 Report Number AGC026120602-1F2 Date of Test Jul.30, 2012 to Aug.03, 2012 WE HEREBY CERTIFY THAT: The above equipment was tested by Attestation of Global Compliance (Shenzhen) Co., Ltd. The test data, data evaluation, test procedures, and equipment configurations shown in this report were made in accordance with the procedures given in ANSI C63.4 (2003) .The sample tested as described in this report is in compliance with the FCC Rules Part 15 and RSS-210 requirements The test results of this report relate only to the tested sample identified in this report. Tested By Bart Xie Aug.08, 2012 Reviewed By Forrest Lei Aug.08, 2012 Approved By Solger Zhang Aug.08, 2012 Report No.: AGC026120602-1F2 Page 2 of 39 TABLE OF CONTENTS 1. GENERAL INFORMATION ................................................................................................................................................. 4 1.1 PRODUCT DESCRIPTION ....................................................................................................................... 4 1.2 TABLE OF CARRIER FREQUENCYS ...................................................................................................... 4 1.3 RELATED SUBMITTAL(S) / GRANT (S) ................................................................................................... 5 1.4 TEST METHODOLOGY ............................................................................................................................ 5 1.5 TEST FACILITY ......................................................................................................................................... 5 1.6 SPECIAL ACCESSORIES ......................................................................................................................... 5 1.7 EQUIPMENT MODIFICATIONS ................................................................................................................ 5 2. SYSTEM TEST CONFIGURATION ................................................................................................................................... 6 2.1 CONFIGURATION OF TESTED SYSTEM ................................................................................................ 6 2.2 EQUIPMENT USED IN EUT SYSTEM ...................................................................................................... 6 3. SUMMARY OF TEST RESULTS ....................................................................................................................................... 7 4. DESCRIPTION OF TEST MODES .................................................................................................................................... 7 5. PEAK OUTPUT POWER ..................................................................................................................................................... 8 5.1 LIMITS ........................................................................................................................................................ 8 5.2 MEASUREMENT PROCEDURE ................................................................................................................ 8 5.3 TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) ....................................................................... 8 5.4 MEASUREMENT EQUIPMENT USED ....................................................................................................... 9 5.5 MEASUREMENT RESULT ......................................................................................................................... 9 6. DB BANDWIDTH ................................................................................................................................................................. 10 6.1 LIMITS ...................................................................................................................................................... 10 6.2 MEASUREMENT PROCEDURE ............................................................................................................. 10 6.3 TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) ..................................................................... 10 6.3 MEASUREMENT EQUIPMENT USED ................................................................................................... 10 6.5 MEASUREMENT RESULTS .................................................................................................................... 10 7. 99% BANDWIDTH ............................................................................................................................................................... 13 7.1 LIMITS ...................................................................................................................................................... 13 7.2 MEASUREMENT PROCEDURE .............................................................................................................. 13 7.3 TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) ..................................................................... 13 7.4 MEASUREMENT EQUIPMENT USED ........................…

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PHOTOGRAPHS OF THE TEST SETUP RADIATED SPURIOUS EMISSION

PHOTOGRAPHS OF THE TEST SETUP RADIATED SPURIOUS EMISSION