Q6ZHEM7340TSBlood Pressure Monitor

HEM-7341T-Z_Cover.pdf 3787131-6E Made in Vietnam / Fabriqué au Vietnam OMRON HEALTHCARE Co., Ltd. 53, Kunotsubo, Terado-cho, Muko, Kyoto, 617-0002 JAPAN Distributed by / Distribué par : OMRON HEALTHCARE, INC. 2895 Greenspoint Pkwy. Hoffman Estates, IL 60169 USA / É.-U. For USA - OmronHealthcare.com For Canada - OmronHealthcare.ca © 2023 OMRON HEALTHCARE, INC. Gold Upper Arm Blood Pressure Monitor / Or partie supérieure du bras tensiomètre Model / Modèle BP5350 Instruction Manual / Guide de l’utilisateur EN FR 3787131-6E © 2023 OMRON HEALTHCARE, INC. 1 Table of Contents Introduction ................................................2 Safety Instructions ...............................2 Intended Use .......................................2 Receiving and Inspection .....................2 Symbols Glossary ................................2 Important Safety Information ....................3 1. Know Your Monitor ...............................7 1.1 Contents/Product Includes ..........7 1.2 Monitor and Arm Cuff ..................7 1.3 Display and Symbols ...................9 1.4 Classification of BP (Blood Pressure) ...................................13 2. Preparation ..........................................14 2.1 Installing Batteries .....................14 2.2 Setting the Date and Time .........15 2.3 Blood Pressure Measurement Tips ............................................17 2.4 Applying the Arm Cuff ................18 2.5 Sitting Correctly .........................20 2.6 Selecting a User ID ...................21 3. Using Your Monitor without a Smart Device ..................................................22 3.1 Taking a Measurement ..............22 4. Using Your Monitor with a Smart Device ..................................................25 4.1 Pairing Your Monitor with a Smart Device .......................................25 4.2 Taking a Measurement ..............27 4.3 Disabling/Enabling Bluetooth ....27 5. Using Memory Function .....................29 5.1 Viewing the Readings Stored in Memory .....................................29 5.2 Viewing the Average Reading ...30 5.3 Viewing Morning Weekly Averages ...................................31 6. Other Settings .....................................33 6.1 Deleting All Readings Stored in Memory .....................................33 6.2 Restoring Your Monitor to the Default Settings .........................34 7. Error Messages and Troubleshooting .................................36 8. Maintenance ........................................41 8.1 Maintenance ..............................41 8.2 Storage ......................................41 8.3 Cleaning ....................................42 8.4 Disposal ....................................42 9. Optional Accessories .........................43 Using the AC Adapter (optional accessory) .........................................44 10.Specifications .....................................45 11. FCC/ISED Statement ..........................48 12.Limited Warranty ................................50 13.Guidance and Manufacturer’s Declaration ..........................................52 2 Introduction Thank you for purchasing the OMRON BP5350 Blood Pressure Monitor. This monitor can be used by multiple users. This blood pressure monitor uses the oscillometric method of blood pressure measurement. This means this monitor detects your blood movement through your brachial artery and converts the movements into a digital reading. Safety Instructions This instruction manual provides you with important information about the OMRON BP5350 Blood Pressure Monitor. To ensure the safe and proper use of this monitor, READ and UNDERSTAND all of these instructions. If you do not understand these instructions or have any questions, contact 1-800-634-4350 before attempting to use this monitor. For specific information about your own blood pressure, consult with your physician. Intended Use This device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult patient population. The device detects the appearance of irregular heartbeats during measurement and gives a warning signal with readings. Environments of Use: Home Patient Population: Adult Receiving and Inspection Remove this monitor and other components from the packaging and inspect for damage. If this monitor or any other components is damaged, DO NOT USE and contact 1-800-634-4350. Symbols Glossary For symbol information, visit: OmronHealthcare.com/symbols-glossary Contraindications •This monitor is contraindicated for use in ambulatory environments. •This monitor is contraindicated for use on aircraft. 3 Important Safety Information Read the Important Safety Information in this instruction manual before using this monitor. Follow this instruction manual thoroughly for your safety. Keep for future reference. For specific information about your own blood pressure, CONSULT WITH YOUR PHYSICIAN. Warning Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury. •DO NOT use this monitor on infants, toddlers, children or persons who cannot express themselves. •DO NOT adjust medication based on readings from this blood pressure monitor. Take medication as prescribed by your physician. ONLY a physician is qualified to diagnose and treat high blood pressure. •DO NOT use this monitor on an injured arm or an arm under medical treatment. •DO NOT apply the arm cuff on your arm while on an intravenous drip or blood transfusion. •DO NOT use this monitor in areas containing high frequency (HF) surgical equipment, magnetic resonance imaging (MRI) equipment, computerized tomography (CT) scanners. This may result in incorrect operation of the monitor and/or cause an inaccurate reading. •DO NOT use this monitor in oxygen rich environments or near flammable gas. •Consult with your physician before using this monitor if you have common arrhythmias such as atrial or ventricular premature beats or a…

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3608691-7K Made in Vietnam OMRON HEALTHCARE Co., Ltd. 53, Kunotsubo, Terado-cho, Muko, Kyoto, 617-0002 JAPAN Distributed by: OMRON HEALTHCARE, INC. 2895 Greenspoint Pkwy. Hoffman Estates, IL 60169 USA OmronHealthcare.com © 2023 OMRON HEALTHCARE, INC. HEM-7340T-Z_Cover.pdf 7 series Upper Arm Blood Pressure Monitor Model BP7350 Instruction Manual 3608691-7K © 2023 OMRON HEALTHCARE, INC. 1 Table of Contents Introduction ................................................2 Safety Instructions ...............................2 Intended Use .......................................2 Receiving and Inspection .....................2 Symbols Glossary ................................2 Important Safety Information ....................3 1. Know Your Monitor ...............................7 1.1 Contents/Product Includes ..........7 1.2 Monitor and Arm Cuff ..................7 1.3 Display and Symbols ...................9 1.4 Classification of BP (Blood Pressure) ...................................13 2. Preparation ..........................................14 2.1 Installing Batteries .....................14 2.2 Setting the Date and Time .........15 2.3 Blood Pressure Measurement Tips ............................................17 2.4 Applying the Arm Cuff ................18 2.5 Sitting Correctly .........................20 2.6 Selecting a User ID ...................21 3. Using Your Monitor without a Smart Device ..................................................22 3.1 Taking a Measurement ..............22 4. Using Your Monitor with a Smart Device ..................................................25 4.1 Pairing Your Monitor with a Smart Device .............................25 4.2 Taking a Measurement ..............27 4.3 Disabling/Enabling Bluetooth ....27 5. Using Memory Function .....................29 5.1 Viewing the Readings Stored in Memory .....................................29 5.2 Viewing the Average Reading ...30 6. Other Settings .....................................31 6.1 Deleting All Readings Stored in Memory .....................................31 6.2 Restoring Your Monitor to the Default Settings .........................32 7. Error Messages and Troubleshooting .................................34 8. Maintenance ........................................39 8.1 Maintenance ..............................39 8.2 Storage ......................................39 8.3 Cleaning ....................................40 8.4 Disposal ....................................40 9. Optional Accessories .........................41 Using the AC Adapter (optional accessory) .........................................42 10.Specifications .....................................43 11. FCC Statement ....................................46 12.Limited Warranty ................................47 13.Guidance and Manufacturer’s Declaration ..........................................49 2 Introduction Thank you for purchasing the OMRON BP7350 Blood Pressure Monitor. This monitor can be used by multiple users. This blood pressure monitor uses the oscillometric method of blood pressure measurement. This means this monitor detects your blood movement through your brachial artery and converts the movements into a digital reading. Safety Instructions This instruction manual provides you with important information about the OMRON BP7350 Blood Pressure Monitor. To ensure the safe and proper use of this monitor, READ and UNDERSTAND all of these instructions. If you do not understand these instructions or have any questions, contact 1-800-634-4350 before attempting to use this monitor. For specific information about your own blood pressure, consult with your physician. Intended Use This device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult patient population. The device detects the appearance of irregular heartbeats during measurement and gives a warning signal with readings. Environments of Use: Home Patient Population: Adult Receiving and Inspection Remove this monitor and other components from the packaging and inspect for damage. If this monitor or any other components is damaged, DO NOT USE and contact 1-800-634-4350. Symbols Glossary For symbol information, visit: OmronHealthcare.com/symbols-glossary Contraindications •This monitor is contraindicated for use in ambulatory environments. •This monitor is contraindicated for use on aircraft. 3 Important Safety Information Read the Important Safety Information in this instruction manual before using this monitor. Follow this instruction manual thoroughly for your safety. Keep for future reference. For specific information about your own blood pressure, CONSULT WITH YOUR PHYSICIAN. Warning Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury. •DO NOT use this monitor on infants, toddlers, children or persons who cannot express themselves. •DO NOT adjust medication based on readings from this blood pressure monitor. Take medication as prescribed by your physician. ONLY a physician is qualified to diagnose and treat high blood pressure. •DO NOT use this monitor on an injured arm or an arm under medical treatment. •DO NOT apply the arm cuff on your arm while on an intravenous drip or blood transfusion. •DO NOT use this monitor in areas containing high frequency (HF) surgical equipment, magnetic resonance imaging (MRI) equipment, computerized tomography (CT) scanners. This may result in incorrect operation of the monitor and/or cause an inaccurate reading. •DO NOT use this monitor in oxygen rich environments or near flammable gas. •Consult with your physician before using this monitor if you have common arrhythmias such as atrial or ventricular premature beats or atrial fibrillation; arterial sclerosis; poor perfusion; diabetes; pregnancy; pre-eclampsia or renal disease. NOTE that any of these conditions in addition to patient motion, trembling, or shivering may affect the measurement reading. •NEVER diagno…

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HEM-7340T-CA_Cover.pdf EN FR 3787149-9D 7 Series Upper Arm / Au Bras Série 7 Blood Pressure Monitor / Tensiomètre Model / Modèle BP7350CAN Instruction Manual / Guide de l’utilisateur Made in Vietnam / Fabriqué au Vietnam OMRON HEALTHCARE Co., Ltd. 53, Kunotsubo, Terado-cho, Muko, Kyoto, 617-0002 JAPAN / JAPON Distributed by / Distribué par : OMRON HEALTHCARE, INC. 2895 Greenspoint Pkwy. Hoffman Estates, IL 60169 USA / É.-U. OmronHealthcare.ca © 2023 OMRON HEALTHCARE, INC. 3787149-9D © 2023 OMRON HEALTHCARE, INC. 1 Table of Contents Introduction ................................................2 Safety Instructions ...............................2 Intended Use .......................................2 Receiving and Inspection .....................2 Symbols Glossary ................................2 Important Safety Information ....................3 1. Know Your Monitor ...............................7 1.1 Contents/Product Includes ..........7 1.2 Monitor and Arm Cuff ..................7 1.3 Display and Symbols ...................9 1.4 Classification of BP (Blood Pressure) ...................................13 2. Preparation ..........................................14 2.1 Installing Batteries .....................14 2.2 Setting the Date and Time .........15 2.3 Blood Pressure Measurement Tips ............................................17 2.4 Applying the Arm Cuff ................18 2.5 Sitting Correctly .........................20 2.6 Selecting a User ID ...................20 3. Using Your Monitor without a Smart Device ..................................................21 3.1 Taking a Measurement ..............21 4. Using Your Monitor with a Smart Device ..................................................24 4.1 Pairing Your Monitor with a Smart Device .............................24 4.2 Taking a Measurement ..............26 4.3 Disabling/Enabling Bluetooth ....26 5. Using Memory Function .....................28 5.1 Viewing the Readings Stored in Memory .....................................28 5.2 Viewing the Average Reading ...29 6. Other Settings .....................................30 6.1 Deleting All Readings Stored in Memory .....................................30 6.2 Restoring Your Monitor to the Default Settings .........................31 7. Error Messages and Troubleshooting .................................33 8. Maintenance ........................................38 8.1 Maintenance ..............................38 8.2 Storage ......................................38 8.3 Cleaning ....................................39 8.4 Disposal ....................................39 9. Optional Accessories .........................40 Using the AC Adapter (optional accessory) .........................................41 10.Specifications .....................................42 11. FCC/ISED Statement ..........................45 12.Limited Warranty ................................47 13.Guidance and Manufacturer’s Declaration ..........................................49 2 Introduction Thank you for purchasing the OMRON BP7350CAN Blood Pressure Monitor. This monitor can be used by multiple users. This blood pressure monitor uses the oscillometric method of blood pressure measurement. This means this monitor detects your blood movement through your brachial artery and converts the movements into a digital reading. Safety Instructions This instruction manual provides you with important information about the OMRON BP7350CAN Blood Pressure Monitor. To ensure the safe and proper use of this monitor, READ and UNDERSTAND all of these instructions. If you do not understand these instructions or have any questions, contact 1-800-634-4350 before attempting to use this monitor. For specific information about your own blood pressure, consult with your physician. Intended Use This device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult patient population. The device detects the appearance of irregular heartbeats during measurement and gives a warning signal with readings. Receiving and Inspection Remove this monitor and other components from the packaging and inspect for damage. If this monitor or any other components is damaged, DO NOT USE and contact 1-800-634-4350. Symbols Glossary For symbol information, visit: OmronHealthcare.ca/symbols-glossary Contraindications •This monitor is contraindicated for use in ambulatory environments. •This monitor is contraindicated for use on aircraft. 3 Important Safety Information Read the Important Safety Information in this instruction manual before using this monitor. Follow this instruction manual thoroughly for your safety. Keep for future reference. For specific information about your own blood pressure, CONSULT WITH YOUR PHYSICIAN. Warning Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury. •DO NOT use this monitor on infants, toddlers, children or persons who cannot express themselves. •DO NOT adjust medication based on readings from this blood pressure monitor. Take medication as prescribed by your physician. ONLY a physician is qualified to diagnose and treat high blood pressure. •DO NOT use this monitor on an injured arm or an arm under medical treatment. •DO NOT apply the arm cuff on your arm while on an intravenous drip or blood transfusion. •DO NOT use this monitor in areas containing high frequency (HF) surgical equipment, magnetic resonance imaging (MRI) equipment, computerized tomography (CT) scanners. This may result in incorrect operation of the monitor and/or cause an inaccurate reading. •DO NOT use this monitor in oxygen rich environments or near flammable gas. •Consult with your physician before using this monitor if you have common arrhythmias such as atrial or ventricular premature beats or atrial fibrillation; arterial sclerosis; poor perfusion; diabetes; pregnancy; pre-eclampsia or renal disease. NOTE that any of these conditions in addition to patient mot…

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Date: July 27,2023

Federal Communications Commission Authorization and Evaluation Division 7435 Oakland Mills Road Columbia, MD 21046 RE: CFR 47 §2.911 (d)(7) FCC US Agent Letter of Attestation FCC ID: Q6ZHEM7340TS Grantee FRN: 0021928791 To whom it may concern: FCC US Agent Contact Person: Lisa Fields Company Name: Omron Healthcare, Inc FRN: 0033512021 Company Address: 2895 Greenpoint Parkway Hoffman Estates ILLINOIS 60169 USA Email: [email protected] This letter is to confirm that we have accepted the responsibility to act as US Agent on behalf of OMRON HEALTHCARE Co.,Ltd (“the applicant”) for the above referenced FCC ID. We are aware of the requirements and responsibilities of the applicant’s agent for service of process as outlined in the FCC section §2.911(d)(7) and Report and Order FCC 22-84 paragraph 63. Sincerely yours, Signature: Ms. Lisa Fields Omron Healthcare, Inc Date: July 31, 2023

Date:July 27, 2023

( 1 / 3 ) Product Photographs（BP5350） Main Unit Top Bottom The label design is a draft. See label diagram for final label. ( 2 / 3 ) Front Back ( 3 / 3 ) Left side Right side

( 1 / 3 ) Product Photographs（BP7350） Main Unit Top Bottom The label design is a draft. See label diagram for final label. ( 2 / 3 ) Front Back ( 3 / 3 ) Left side Right side

( 1 / 3 ) Product Photographs（BP7350CAN） Main Unit Top Bottom The label design is a draft. See label diagram for final label. ( 2 / 3 ) Front Back ( 3 / 3 ) Left side Right side

BP5350(HEM-7341T-Z) , BP7350 (HEM-7340T-Z) and BP7350CAN (HEM-7340T-CA) _Label Design and Location Bottom view FCCID:Q6ZHEM7340TS FCCID:Q6ZHEM7340TS FCCID:Q6ZHEM7340TS XXXXXXXXXXXXX XXXXXXXXXXXXX 50.7 28.5 BP7350 (HEM-7340T-Z) BP5350 (HEM-7341T-Z) *Due to the size of product, the statement required by FCC 15.19(a) will be printed on users manual. The FCC Identifier “FCC ID” is 4.0 point or larger. The labels are laser-engraved, so the letters do not XXXXXXXXXX BP7350CAN (HEM-7340T-CA) XXXXXXXXXXXX XXXXXXXXXXXX

( 1 / 2 ) Product Photographs （ BP5350 ） Main Unit （ internal ） pattern antenna RF Part ( 2 / 2 ) PWB （ internal ） Rear Front 裏面 RF Part pattern antenna

UL Japan, Inc. Ise EMC Lab 4383-326 Asama-cho, Ise-shi, Mie 516-0021 Japan T:: +81.596.24.8999 / F:: +81.596.24.8124 / W:: japan.ul.com July 26, 2023 FCC ID: Q6ZHEM7340TS To whom it may concern, We, UL Japan, Inc, hereby declare that Blood Pressure Monitor, model: BP5350 (FCC ID: Q6ZHEM7340TS) of OMRON HEALTHCARE Co., Ltd. is exempt from RF exposure SAR evaluation as its output power meets the exclusion limits stated in KDB 447498D01(v06). KDB 447498D01(v06) has the following exclusion for portable devices: The 1g and 10g SAR test exclusion thresholds for 100 MHz to 6 GHz at test separation distances ≤ 50 mm are determined by: [(max. power of channel, including tune-up tolerance, mW)/(min. test separation distance, mm)] ꞏ[√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 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 is applied to determine SAR test exclusion. This device has f = 2.48 GHz and distance = 5 mm (minimum separation distance: 5 mm was used in the calculation) and the maximum average output power (Burst power average) was 1 mW So for this device: 1 mW[maximum average output power]/5 mm[minimum separation distance]*√2.48 = 0.3 *This is less than 3.0, so no SAR is required. Even taking into account the tolerance, this device can be satisfied with the limits. Thank you for your attention to this matter. Takumi Shimada Engineer

Page 1 of 19 Control No. 23130-2101 JQA File No. : KL80230312 Issue Date : July 20, 2023 T E S T R E P O R T Applicant : OMRON HEALTHCARE Co.,Ltd. Address : 53, Kunotsubo, Terado-cho, Muko,Kyoto,617-0002 JAPAN Products : Blood pressure PWB pattern antenna for Bluetooth HEM-73xxT series Model No. : HEM-MAIN-VGRCK4S Serial No. : R3A-1 Test Standard : Antenna gain measurements related to the Radio Law Test Results : Refer to Summary Date of Receipt : March 9, 2023 Date of Test : March 26, 2023 and April 4, 2023 Kosei Shibata Deputy Director Japan Quality Assurance Organization Kitakansai Testing Center Saito EMC Branch 7-3-10, Saito-asagi, Ibaraki-shi, Osaka 567-0085, Japan ● The test results in this test report was made by using the measuring instruments which are traceable to national standards of measurement in accordance with ISO/IEC 17025. ● The applicable standard, testing condition and testing method which were used for the tests are based on the request of the applicant. ● The test results presented in this report relate only to the offered test sample. ● The contents for the equipment under test (EUT) such as identification information in clause 2 and 6 of this report were provided by the applicant. JQA is not responsible for the test results affected by the incorrect information. ● The contents of this test report cannot be used for the purposes, such as advertisement for consumers. ● This test report shall not be reproduced except in full without the written approval of JQA. JQA File No. : KL80230312 Issue Date : July 20, 2023 Page 2 of 19 Control No. 23130-2101 Table of Contents Page 1 Summary of Test Results ............................................................................................................ 4 2 Description of the Equipment Under Test (EUT) ........................................................................ 5 3 Test Location ............................................................................................................................... 6 4 Accreditation of Test Laboratory ................................................................................................. 6 5 Setup of EUT .............................................................................................................................. 7 5.1 Test Configuration ..................................................................................................................... 7 5.2 Test Arrangement (Drawings) ................................................................................................... 7 5.3 Operating Condition .................................................................................................................. 7 6 Test Item ..................................................................................................................................... 8 6.1 Antenna gain measurements .................................................................................................... 8 JQA File No. : KL80230312 Issue Date : July 20, 2023 Page 3 of 19 Control No. 23130-2101 REVISION HISTORY File No. Contents Issue Date KL80230312 Initial Issue July 20, 2023 JQA File No. : KL80230312 Issue Date : July 20, 2023 Page 4 of 19 Control No. 23130-2101 1 Summary of Test Results Applied Standard : Antenna gain measurements related to the Radio Law In the approval of test results, - No deviations were employed from the applied standard. - No modifications were conducted by JQA to achieve compliance to the limitations. Reviewed by Yasuhisa Sakai / Project Manager Tested by Yuji Shintaku / Assistant Manager JQA File No. : KL80230312 Issue Date : July 20, 2023 Page 5 of 19 Control No. 23130-2101 2 Description of the Equipment Under Test (EUT) Manufacturer OMRON HEALTHCARE Co.,Ltd. 53, Kunotsubo, Terado-cho, Muko,Kyoto,617-0002 JAPAN Products Blood pressure PWB pattern antenna for Bluetooth HEM-73xxT series Model No. HEM-MAIN-VGRCK4S Serial No. R3A-1 Product Type Pre-Production Date of Manufacture February 8, 2023 Power Rating -- EUT Grounding None JQA File No. : KL80230312 Issue Date : July 20, 2023 Page 6 of 19 Control No. 23130-2101 3 Test Location Japan Quality Assurance Organization (JQA) Kitakansai Testing Center Saito EMC Branch 7-3-10, Saito-asagi, Ibaraki-shi, Osaka 567-0085, Japan 4 Accreditation of Test Laboratory JQA is accredited under ISO/IEC 17025 by following accreditation bodies and the test facility of Testing Division is registered by the following bodies . Test Facility Accreditation or Registration Expiry Date Body Code/Number Saito EMC Branch VLAC VLAC-001-2 April 30, 2024 A2LA 5498.01 November 30, 2023 VCCI A-0002 April 30, 2024 FCC JP5008 April 30, 2024 ISED JP0014 November 30, 2023 BSMI SL2-IS-E-6006, SL2-IN-E-6006, SL2- R1/R2-E-6006, SL2-A1-E-6006 September 14, 2025 Conformity assessment body for Japan electrical appliances and material by METI February 22, 2025 JQA File No. : KL80230312 Issue Date : July 20, 2023 Page 7 of 19 Control No. 23130-2101 5 Setup of EUT 5.1 Test Configuration The EUT consists of : Sign Item Manufacturer Model No. Serial No. A Blood pressure PWB pattern antenna for Bluetooth HEM- 73xxT series OMRON HEALTHCARE Co.,Ltd. HEM-MAIN- VGRCK4S R3A-1 The AE used for testing : None Type of Cable: None 5.2 Test Arrangement (Drawings) 5.3 Operating Condition Operating Mode Transmission status by CW signal input to antenna A JQA File No. : KL80230312 Issue Date : July 20, 2023 Page 8 of 19 Control No. 23130-2101 6 Test Item 6.1 Antenna gain measurements 6.1.1 Test Site and Instruments Test Site : Anechoic Chamber A4 Type Model Serial No. (ID) Manufacturer Last Cal. Cal. Due Test Receiver ESU 26 100170 (A-6) Rohde & Schwarz 2022/06/08 2023/06/27 Horn Antenna 91889-2 560 (C-40-2) EATON 2022/05/25 2023/05/24 RF Cable SF126 MY4596/26 (C-78) HUBER+SUHNER 2023/02/03 2024/02/02 Double-Ridge Guide Horn Antenna 3115 00227684 (C-103) ETS LINDGREN 2022/05/26 2023/05/25 Attenuator 54A-10 W5713 (D-29) Weinschel …

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Test Report No. : 14694851H-A-R1 Page : 1 of 36 UL Japan, Inc. Ise EMC Lab. 4383-326 Asama-cho, Ise-shi, Mie-ken 516-0021 Japan / +81-596-24-8999 RADIO TEST REPORT Test Report No.: 14694851H-A-R1 Customer OMRON HEALTHCARE Co., Ltd. Description of EUT Blood Pressure Monitor Model Number of EUT BP5350 FCC ID Q6ZHEM7340TS Test Regulation FCC Part 15 Subpart C Test Result Complied (Refer to SECTION 3) Issue Date August 23, 2023 Remarks - Representative Test Engineer Approved By Junya Okuno Engineer Takumi Shimada Engineer CERTIFICATE 5107.02 The testing in which "Non-accreditation" is displayed is outside the accreditation scopes in UL Japan, Inc. There is no testing item of "Non-accreditation". Report Cover Page - Form-ULID-003532 (DCS:13-EM-F0429) Issue# 21.0 Test Report No. : 14694851H-A-R1 Page : 2 of 36 UL Japan, Inc. Ise EMC Lab. 4383-326 Asama-cho, Ise-shi, Mie-ken 516-0021 Japan / +81-596-24-8999 ANNOUNCEMENT REVISION HISTORY Original Test Report No.: 14694851H-A This report is a revised version of 14694851H-A. 14694851H-A is replaced with this repor t. Revision Test Report No. Date Page Revised Contents - (Ori ginal) 14694851H-A May 31, 2023 - 1 14694851H-A-R1 August 23, 2023 P.5 Correction of Operating Temperature (Lower temperature limi t 5 deg. C => 10 deg. C) 1 14694851H-A-R1 August 23, 2023 P.22, 24, 25 Correction of Distance factor: 1 GHz -10 GHz for No.3 Semi Anechoic Chamber (2.82 dB => 2.28 dB)  This test report shall not be reproduced in full or partial, without the written approval of UL Japan, Inc.  The results in this report appl y only to the sample tested. (Laboratory was not involved in sampling.)  This sample tested is in compliance with the limits of the above re gulation.  The test results in this test report are traceable to the national or international standards.  This test report must not be used by the customer to claim product certification, approval, or endorsement by the A2LA accredi tation body.  This test report covers Radio technical requirements. It does not cover administrative issues such as Manual or non-Radio test related Requirements. (if applicable)  The a…

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