
Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.
薉俒䧭ⱃ 勞餘 㼓⯕HꜤ晜紺 ⰻ곜兜鸑H⛼ⱗ 紺 㽯㼄 NN CONTACT INFORMATION Digital Blood Pressure Monitor B02T is legal manufactured by:Company name:Address: Website:Telephone: Shenzhen Jamr Technology Co., Ltd.2nd Floor, A-building, No.2 Guiyuan Road, Guihua community, Guanlan town, Longhua new district, 518100 Shenzhen, PEOPLE’S REPUBLIC OF CHINAwww.jiemeirui.com0086 755 85292057 Authorized European Representative:Company Name:Contact person:Address:E-mail: Shanghai International Holding Corp. GmbH (Europe) Mr JIN LIANG Eiffestrasse 80, 20537 Hamburg, [email protected] Fully Automatic Upper Arm Model Number: B02T USER’S MANUAL Blood Pressure Monitor Thank you for choosing a B02T blood pressure instrument. We're proud of the care and quality that goes into the manufacture of each and every item that bears our name. Only the finest materials are used to assure you of a timeless instrument designed for optimum performance. You'll quickly appreciate the results, for you now own one of the finest digital blood pressure instruments that money can buy. With proper care and maintenance, your B02T automatic blood pressure monitor is sure to provide you with many years of dependable service. Please read the following instructions and general information which will prove helpful in allowing you to enjoy your B02T of Digital In hospitals and physician's offices throughout the world, where accuracy and dependability are critical,B02T professional diagnostic products are the instruments of choice.Now you too can enjoy the benefits of B02T engineering and quality in the home. This feature rich instrument was designed to simplify the measurement of blood pressure and pulse rate at home and deliver consistent, dependable results.Your B02T digital blood pressure monitor is a fully automatic digital blood pressure measuring device for use on the upper arm. It enables very fast and reliable measurement of the systolic and diastolic blood pressure as well as the pulse by way of the oscillometric method. This device offers clinically proven accuracy and has been designed to be user friendly. Read this booklet thoroughly before attempting to use your new B02T Digital Blood Pressure Monitor.Thank you for your patronage. It is indeed our pleasure to serve you.Sincerely,Shenzhen Jamr Technology Co., Ltd. A Special Thank You... 1.Introduction and Intended Use This manual is for B02T models. It is a fully automatic digital blood pressure measuring device for use by adults on the upper arm at home or in your doctor’s/nurse’s office. It enables very fast and reliable measurement of systolic and diastolic blood pressure as well as pulse through the oscillometric method. This device offers clinically proven accuracy and has been designed to be user friendly.Before using, please read this instruction manual carefully and then keep it in a safe place. Please contact your doctor for further questions on the subject of blood pressure and its measurement.Warning Not suitable for neonatal and infants. Warning Not suitable for people who cannot express their ideas correctly. This device can not be used together with hf surgical equipment. 1.1 Remember... measurements. ! this device." before prescribing or making adjustments to any medications used to control hypertension. Under no circumstances should YOU alter the dosages of any drugs prescribed by your doctor. # ! before using this instrument on a child. $ ! instrument should only be evaluated after consultation with your doctor.%& ! * "+ 4 * on the dynamics of blood pressure readings and will help you to obtain the best results.; $ $ with local regulations after reaching the life cycle. 1.Introduction and Intended Use...........................................................2.Important Information on Blood Pressure and its Measurement.......3. Components of Your Blood Pressure Monitor..................................4. Using Your Monitor for the First Time..............................................5.Measurement Procedure..................................................................6.Care and Maintenance.....................................................................7. Warranty..........................................................................................8. Certifications....................................................................................9. Technical Specifications..................................................................10. EMC Declaration...........................................................................11. Warranty Card............................................................................... 3681012232424242530 CONTENTS NOTE!Warning = or electromagnetic fields in the direct vicinity of the device (e.g. mobile telephones, microwave ovens) during use. These can lead to erratic results.> ? occur, refer to local distributor or the manufacturer.1.Too frequent measurements can cause injury to the PATIENT due to blood flow interference.2.Don’t place the cuff over wound part.3.Pressurization of the CUFF can temporarily cause loss of function of simultaneously used monitoring ME EQUIPMENT on the same limb.Warning: The device contains sensitive electronic components. Avoid strong electrical or electrom…
Text truncated - open the document above for the full version.
CONFIDENTIALITY REQUEST for Certification Service in USA Federal Communication Commission Equipment Authorization Division, Application Processing Branch 7435 Oakland Mills Road Columbia, MD 21046 Date: 2020/09/25 TO WHOM IT MAY CONCERN Pursuant to Paragraphs §0.457 and 0.459 of the Commission’s Rules (47 C.F.R.) and Section §552(b)(4) of the Freedom of Information Act, we requests confidentiality for the following products: Model No.: B02T FCC ID: 2AS8AB02T For the product stated above, we request that the following information be held confidential; Exhibits Long-Term Confidentiality Short-Term Confidentiality Short-Term Confidentiality Days External Photos Internal Photos Block Diagram Schematics Test Setup Photos User’s Manual Parts List Tune Up Operational Descriptions The long-term confidentiality exhibits contain our trade secrets and proprietary information that could be of benefit to our competitors. The short-term confidentiality on the basis of ensuring that business sensitive information remains confidential until the actual marketing of our new device. If you have any questions, please feel free to contact me at the address shown below. Sincerely, Name/Title: zero Luo/Manager Company: Shenzhen Jamr Technology Co., Ltd Address: 2nd Floor, A-building, No.2 Guiyuan Road, Guihua Community, Guanlan Town, Longhua New District, Shenzhen,China Phone: 075585292057 Fax: 0755-27980758 E-Mail: [email protected]
Shenzhen Jamr Technology Co., Ltd 2nd Floor, A-building, No.2 Guiyuan Road, Guihua Community, Guanlan Town, Longhua New District, Shenzhen,China Federal Communications Commission Authorization and Evaluation Division Equipment Authorization Branch 7435 Oakland Mills Road Columbia, MD 21046 2020/09/25 To whom it may concern: We, Shenzhen Jamr Technology Co., Ltd the undersigned, hereby authorize Eurofins Product Service GmbH to act on our behalf in all matters relating to applications for equipment authorization FCC ID: 2AS8AB02T including the signing of all documents related to these matters. Any and all acts carried out by Eurofins Product Service GmbH on our behalf shall have the same effect as acts of our own. We also hereby certify that no party to this application is subject to a denial of benefits, including FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 862. Sincerely, Name/Title: zero Luo/Manager Company: Shenzhen Jamr Technology Co., Ltd Address: 2nd Floor, A-building, No.2 Guiyuan Road, Guihua Community, Guanlan Town, Longhua New District, Shenzhen,China Phone: 075585292057 Fax: 0755-27980758 E-Mail: [email protected]
FCC ID: 2AS8AB02T FCC ID: 2AS8AB02T FCC ID: 2AS8AB02T
FCC ID: 2AS8AB02T FCC ID: 2AS8AB02T
FCC ID: 2AS8AB02T FCC ID: 2AS8AB02T
RF Exposure evaluation FCC ID: 2AS8AB02T 1.1. Applicable Standard According to §1.1307(b)(1), systems operating under the provisions of this section shall be operated in a manner that ensures that the public is not exposed to radio frequency energy level in excess of the Commission’s guidelines. According to §1.1310 and §2.1093 RF exposure requirement KDB447498 v06: Mobile and Portable Devices RF Exposure Procedures and Equipment Authorization Policies 1.2. Requirement According to KDB447498 D01 General RF Exposure Guidance v06 Section 4.3.1 Standalone SAR test exclusion considerations: “Unless specifically required by the published RF exposure KDB procedures, standalone 1-g head or body and 10-g extremity SAR evaluation for general population exposure conditions, by measurement or numerical simulation, is not required when the corresponding SAR Test Exclusion Threshold condition, listed below, is satisfied. These test exclusion conditions are based on source-based time-averaged maximum conducted output power of the RF channel requiring evaluation, adjusted for tune-up tolerance, and the minimum test separation distance required for the exposure conditions.22 The minimum test separation distance is determined by the smallest distance from the antenna and radiating structures or outer surface of the device, according to the host form factor, exposure conditions and platform requirements, to any part of the body or extremity of a user or bystander (see 5) of section 4.1). To qualify for SAR test exclusion, the test separation distances applied must be fully explained and justified by the operating configurations and exposure conditions of the transmitter and applicable host platform requirements, typically in the SAR measurement or SAR analysis report, according to the required published RF exposure KDB procedures. When no other RF exposure testing or reporting is required, a statement of justification and compliance must be included in the equipment approval, in lieu of the SAR report, to qualify for the SAR test exclusion. When required, the device specific conditions described in the other published RF exposure KDB procedures must be satisfied before applying these SAR test exclusion provisions; for example, handheld PTT two-way radios, handsets, laptops & tablets etc.23 “ [(max. power of channel, including tune-up tolerance, mW)/ (min. test separation distance, mm)] · [√f (GHz)] ≤ 3.0 for 1-g SAR and ≤ 7.5 for 10-g extremity SAR, where: • f (GHz) is the RF channel transmit frequency in GHz • Power and distance are rounded to the nearest mW and mm before calculation • The result is rounded to one decimal place for comparison • 3.0 and 7.5 are referred to as the numeric thresholds in the step 2 below The test exclusions are applicable only when the minimum test separation distance is ≤ 50 mm and for transmission frequencies between 100 MHz and 6 GHz. When the minimum test separation distance is < 5 mm, a distance of 5 mm according to 5) in section 4.1 is applied to determine SAR test exclusion. 1.3. Manufacturing tolerance GFSK(Peak) Channel Channel 00 Channel 19 Channel 39 Target (dBm) 1.0 1.0 1.0 Tolerance ±(dB) 1.0 1.0 1.0 2. E v a l u a t i o n R e s u l t Evaluation Results Band/Mode f (GHz) Antenna Distance (mm) RF output power (including tune-up tolerance) SAR Test Exclusion Threshold SAR Test Exclusion dBm mW BT 2.480 5 2.0 1.5849 0.50<3.0 Yes 3. C o n c l u s i o n The measurement results comply with the FCC Limit per 47 CFR 2.1093 for the uncontrolled RF Exposure and SAR Exclusion Threshold per KDB 447498 v06 .....................End of Report.........................
Shenzhen Global Test Service Co.,Ltd. No.7-101 and 8A-104, Building 7 and 8, DCC Cultural and Creative Garden, No.98, Pingxin North Road, Shangmugu Community, Pinghu Street, Longgang District, Shenzhen, Guangdong FCC PART 15 SUBPART C TEST REPORT FCC PART 15.247 Report Reference No. ..................... : FCC ID. ........................................... : GTS20200924006-1-1 2AS8AB02T Compiled by ( position+printed name+signature) .............................. : File administrators Jimmy Wang Supervised by ( position+printed name+signature) .............................. : Test Engineer Aaron Tan Approved by ( position+printed name+signature) .............................. : Manager Jason Hu Date of issue ..................................... : Sep.25,2020 Testing Laboratory Name ..............: Shenzhen Global Test Service Co.,Ltd. Address ............................................ : No.7-101 and 8A-104, Building 7 and 8, DCC Cultural and Creative Garden, No.98, Pingxin North Road, Shangmugu Community, Pinghu Street, Longgang District, Shenzhen, Guangdong Applicant’s name ............................ : Shenzhen Jamr Technology Co., Ltd Address ............................................ : 2nd Floor, A-building, No.2 Guiyuan Road, Guihua Community, Guanlan Town, Longhua New District, Shenzhen,China Test specification ...........................: Standard ........................................... : FCC Part 15.247 TRF Originator .................................. : Shenzhen Global Test Service Co.,Ltd. Shenzhen Global Test Service Co.,Ltd. All rights reserved. This publication may be reproduced in whole or in part for non-commercial purposes as long as the Shenzhen Global Test Service Co.,Ltd. is acknowledged as copyright owner and source of the material. Shenzhen Global Test Service Co.,Ltd. takes no responsibility for and will not assume liability for damages resulting from the reader's interpretation of the reproduced material due to its placement and context. Test item description ..................... : Blood Pressure Monitors Trade Mark ....................................... : N/A Manufacturer .................................... : Shenzhen Jamr Technology Co., Ltd Model/Type reference....................... : B02T Listed Models .................................. : N/A Modulation Type ............................... : GFSK Operation Frequency ........................ : From 2402MHz to 2480MHz Rating ............................................... : DC 6.0V From Battery and DC5V From Adapter Result................................................ : PASS Report No.: GTS20200924006-1-1 Page 2 of 35 T E S T R E P O R T Test Report No. : GTS20200924006-1-1 Sep.25,2020 ______________________________________________________________________________________________ Date of issue Equipment under Test : Blood Pressure Monitors Model /Type : B02T Listed Models : N/A Applicant : Shenzhen Jamr Technology Co., Ltd Address : 2nd Floor, A-building, No.2 Guiyuan Road, Guihua Community, Guanlan Town, Longhua New District, Shenzhen, China Manufacturer : Shenzhen Jamr Technology Co., Ltd Address : 2nd Floor, A-building, No.2 Guiyuan Road, Guihua Community, Guanlan Town, Longhua New District, Shenzhen, China Test Result: PASS The test report merely corresponds to the test sample. It is not permitted to copy extracts of these test result without the written permission of the test laboratory. Report No.: GTS20200924006-1-1 Page 3 of 35 Contents 1. T E S T S T A N D A R D S .................................................................. 4 2. S U M M A R Y ............................................................................. 5 2.1. General Remarks 5 2.2. Product Description 5 2.3. Equipment Under Test 5 2.4. Short description of the Equipment under Test (EUT) 5 2.5. EUT operation mode 6 2.6. Block Diagram of Test Setup 6 2.7. Related Submittal(s) / Grant (s) 6 2.8. EUT configuration 6 2.9. Modifications 6 3. T E S T E N V I R O N M E N T ............................................................... 7 3.1. Address of the test laboratory 7 3.2. Test Facility 7 3.3. Environmental conditions 7 3.4. Test Description 8 3.5. Statement of the measurement uncertainty 8 3.6. Equipments Used during the Test 9 4. T E S T C O N D I T I O N S AN D R E S U L T S ............................................ 10 4.1. AC Power Conducted Emission ................................................................................... 10 4.2. Radiated Emission ........................................................................................................ 13 4.3. Maximum Peak Output Power ...................................................................................... 19 4.4. Power Spectral Density ................................................................................................ 20 4.5. 6dB Bandwidth ............................................................................................................. 22 4.6. Band Edge Compliance of RF Emission ...................................................................... 24 4.7. Spurious RF Conducted Emission ............................................................................... 27 4.8. Antenna Requirement ................................................................................................... 29 5. T E S T S E T U P P H O T O S O F T H E E U T .......................................... 30 6. E X T E RN A L A N D I N T E R N A L P H O T O S O F T H E E U T ....................... 31 Report No.: GTS20200924006-1-1 Page 4 of 35 1. T E S T S T A N D A R D S The tests were performed according to following standards: FCC Rules Part 15.247: Frequency Hopping, Direct Spread Spectrum and Hybrid Systems that are in operation within the bands of 902-928 MHz, 2400-2483.5 MHz, and 5725-5850 MHz. ANSI C63.10-2013: American National Standard for Testing Unlicensed Wireless Devices KDB558074 D01 v05r02: Guidance for Compliance M…
Text truncated - open the document above for the full version.
FCC ID: 2AS8AB02T _______________________________________________________________________________________________ 1. TEST SETUP PHOTOGRAPHS 1.1. Photo of Radiated Emissions Measurement Fig. 1 Fig. 2 FCC ID: 2AS8AB02T _______________________________________________________________________________________________ 1.2. Photo of conducted Emissions Measurement Fig. 3
| # | Rule Parts | Frequency Range | Power Output |
|---|---|---|---|
| 1 | 15C | 2.40 GHz - 2.48 GHz | 1.30 mW |

Blood Pressure Monitor
Equipment Class
DTS - Digital Transmission SystemBlood Pressure Monitor
Equipment Class
DTS - Digital Transmission System
Blood Pressure Monitor
Equipment Class
DTS - Digital Transmission System
Blood Pressure Monitor
Equipment Class
DTS - Digital Transmission System
Upper Arm Type Blood Pressure Monitor
Equipment Class
DTS - Digital Transmission System