2AHLC01856Gateway

MoMe ® ARC Physician’s Guide #30815 rB InfoBionic, Inc. - 2 - MoMe ® Arc Physician’s Guide 30815 rB June 20, 2023 - 3 - Copyright, Technical Support, Trademark, and Contact Information Contact Information: InfoBionic, Inc. 312 Billerica Rd. Office Link #5 Chelmsford, MA 01824 USA Email: [email protected] Technical Support: 1 (844) 401-9725 8:00 a.m. – 8.00 p.m. EST Monday - Saturday 9:00 a.m. – 6:00 p.m. EST Sunday Email: [email protected] InfoBionic’s MoMe ® ARC System may be covered under one or more United States and International Patents. Please see the website: www.infobionic.com to satisfy the virtual patent marketing provisions including the America Invents Act and 35 U.S.C. § 287(a). Additional patents may be issued or pending in the US and elsewhere. © 2023 InfoBionic, Inc. and the MoMe ® ARC logo are registered trademarks of InfoBionic, Inc.  InfoBionic, Inc. - 4 - Table of Contents Chapter 1. Welcome to MoMe ® ARC ...................................................................................... 6 1.1 Features & Benefits ....................................................................................................... 6 1.2 MoMe® Arc Components .............................................................................................. 7 1.3 Indications ..................................................................................................................... 7 1.4 Contraindications ........................................................................................................... 7 1.5 Symbols......................................................................................................................... 8 1.6 Essential Performance .................................................................................................. 8 1.7 Cellular Coverage Considerations ................................................................................. 9 1.7.1 Device Indicators ........................................................................................................... 9 1.7.2 MoMe® Software Platform Indicators ............................................................................ 9 Chapter 2. Safety .................................................................................................................. 10 2.1 Warnings ..................................................................................................................... 10 2.2 Cautions ...................................................................................................................... 12 Chapter 3. Specifications and Components .......................................................................... 13 3.1 Specifications .............................................................................................................. 13 3.2 Components ................................................................................................................ 14 3.3 Service Life.................................................................................................................. 14 Chapter 4. Device Configuration, Patient Setup and Monitoring ........................................... 15 4.1 Device Configuration ................................................................................................... 15 4.2 Initial Patient Setup ..................................................................................................... 15 Step 1: Locate the kit components and ensure contents includes: ..................................... 15 Step 2: Prepare the Skin ..................................................................................................... 16 Step 3: Apply Gel Pads to Patient’s Chest and Connect Electrode Wires .......................... 16 Step 4: MoMe ® Arc System Activation and Baseline Recording ......................................... 16 4.3 Patient Monitoring ....................................................................................................... 17 4.4 Patient Reminders ....................................................................................................... 17 Chapter 5. Device Controls and User Interface..................................................................... 18 5.1 Event Record Button - Reporting Cardiac Symptoms ................................................. 18 5.2 Low Battery Alert ......................................................................................................... 19 5.3 Leads Off Alert ............................................................................................................ 20 5.4 Sensor Disconnected Alert .......................................................................................... 20 5.5 System Error ............................................................................................................... 21 5.6 Sensor Vibration .......................................................................................................... 21 5.7 LED Indicators ............................................................................................................. 21 5.8 Charging the MoMe® Arc Gateway and Sensor ......................................................... 22 Chapter 6. Service, Cleaning, and Disposal.......................................................................... 24 6.1 Service ........................................................................................................................ 24 6.2 Cleaning ...................................................................................................................... 24 6.3 Disposal of Waste ....................................................................................................... 24 6.4 Software Updates ........................................................................................................ 24 Chapter 7. Electromagnetic Emissions Compliance and…

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321 Billerica Road OfficeLink #5 Chelmsford, MA 01824 www.infobionic.com Date: 6/19/2023 Federal Communications Commissions Authorization and Evaluation Division 7435 Oakland Mills Road Columbia, MD 21046 RE: CFR 47 §2.911 (d)(5) Attestation FCC ID: 2AHKC01856,2AHLC01857,2AHKC01858 1. InfoBionic Inc. (“the applicant”) certifies that the equipment for which authorization is sought is not “covered” equipment prohibited from receiving an equipment authorization pursuant to section 2.903 of the FCC rules. 2. InfoBionic Inc(“the applicant”) certifies that, as of the date of the filing of the application, the applicant is not identified on the Covered List as an entity producing “covered” equipment and is not an affiliate or subsidiary of an entity identified on the Covered List . Sincerely yours, Name: David MacCutcheon Job Title: COO Company Name: InfoBionic. Inc.

321 Billerica Road OfficeLink #5 Chelmsford, MA 01824 www.infobionic.com Date: 6/19/2023 Federal Communications Commissions Authorization and Evaluation Division 7435 Oakland Mills Road Columbia, MD 21046 RE: CFR 47 §2.911 (d)(7) Agent Designation Attestation FCC ID: 2AHKC01856,2AHLC01857,2AHKC01858 To whom it may concern: InfoBionic, Inc (“the applicant”) as required by section 2.911(d)(7), will also serve as the agent for service of process for the above referenced FCC ID. The applicant acknowledges that they will maintain an agent for no less than one year after the grantee has terminated all marketing and importation or the conclusion of any Commission-related proceeding involving the equipment. The applicant further acknowledges their responsibility to inform the FCC whenever the agent information changes. Dave MacCutcheon InfoBionic FCC FRN: 0025354739 321 Billerica Road OfficeLink #5 Chelmsford, MA 01824 [email protected] Sincerely yours, Dave MacCutcheon InfoBionic 321 Billerica Road OfficeLink #5 Chelmsford, MA 01824 [email protected]

321 Billerica Road Office Link #5 Chelmsford, MA 01824 www.infobionic.com Date: 4/3/2023 UL LLC 12 Laboratory Dr. Research Triangle Park, NC 27709 USA To whom it may concern: I, the undersigned, hereby authorize UL LLC to act on our behalf in all manners relating to application for equipment authorization, including signing of all documents relating to these matters. Any and all acts carried out by UL Verification Services Inc. on our behalf shall have the same effect as acts of our own. I, the undersigned, hereby certify that we are not subject to a denial of federal benefits, that includes FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 853(a). In authorizing UL LLC as our representative, we still recognize that we are responsible to: a) fulfill the requirements for the scope of certification requested, including implementing any appropriate changes requested by UL Verification Services Telecommunications Certification Body (TCB) and / or the FCC; b) supply any and all information needed for the evaluation of the products for which certification is sought; c) make claims regarding certification only in respect of the scope for which certification has been granted; d) not use our product certification in such a manner as to bring the TCB or FCC into disrepute and to not make any statement regarding product certification which the TCB or FCC may consider misleading or unauthorized; e) discontinue use of all advertising matter that contains any reference thereto and complies with any and all actions required by the FCC upon suspension or cancellation of certification; f) use certification only to indicate that products are certified in conformity with specified standards; g) endeavor to ensure that no certificate or report or any part thereof is used in a misleading manner, and any copies of the grants/certificates shall be reproduced in their entirety; h) comply with the requirements of the TCB and FCC, including the use of marks and label information prescribed for the scope of certification, when making reference to product certification in communication media such as documents, brochure or advertisements; i) comply with the requirements for certification, supply any information needed for evaluation of products to be certified and, where applicable, make provision for the participation of observers; j) ensure that products marketed under the scope of the requested certification continue to comply with the certification requirements; k) provide a sample of a production unit for testing within 30 days of the request should this product be selected as part of either the TCB’s or the FCC’s market surveillance requirements; l) keep a record of all complaints relating to product’s compliance with requirements of relevant standard; make records available to UL or FCC when requested; take appropriate action with respect to such complaints and any deficiencies found in the product that affect compliance with requirements for certification; document the actions taken with respect to complaints and/or deficiencies; m) inform the TCB immediately of any changes that may affect its ability to comply with the certification requirements. This authorization is valid until further written notice from the applicant. Sincerely Yours, David MacCutcheon, COO InfoBionic Inc.

321 Billerica Road OfficeLink #5 Chelmsford, MA 01824 www.infobionic.com Date: 11/21/2023 Attn: FCC Office of Engineering and Technology / UL Verification Services TCB Subject: Request for Confidentiality FCC ID: 2AHLC01856,2AHLC01857,2AHLC01858 To Whom It May Concern: Pursuant to the provisions of Sections 0.457 and 0.459 of the Commission’s rules (47 CFR §§ 0.457, 0.459), we are requesting the Commission to withhold the following attachments as confidential document from public disclosure indefinitely.  Schematic Diagram  Operational Description and Block Diagram Above mentioned document contains detailed system and equipment description are considered as proprietary information in operation of the equipment. The public disclosure of above documents might be harmful to our company and would give competitor an unfair advantage in the market. In additional to above mentioned documents, pursuant to Public Notice DA 04-1705 of the Commission’s policy, in order to comply with the marketing regulations in 47 CFR §2.803 and the importation rules in 47 CFR §2.1204, while ensuring that business sensitive information remains confidential until the actual marketing of newly authorized devices. We are requesting the commission to grant short-term confidentiality request on the following attachments until November 30, 2023  External Photos  Internal Photos  Test Setup Photos  User Manual It is our understanding that all measurement test reports, FCC ID label format and correspondent during certification review process cannot be granted as confidential documents and those information will be available for public review once the grant of equipment authorization is issued. Best Regards, Dave MacCutcheon COO InfoBionic Inc

InfoBionic Chelmsford, MA, USA IP22 Read Manual First FCC ID: 2AHLC01856 *+B690MK20/$ $+7MIA03127C* MIA03127 SCALE 1:1 MANUFACTURE NOTES: 1. SERIALIZATION REQUIRED IN TWO PLACES, ‘03127’ AND BARCODE SHOWN AS PLACEHOLDER 3. ‘C’ DENOTES CHECKSUM TO BE CALCULATED PER ABOVE STANDARD. 2 SERIAL NUMBER STRING: *+B690MK20/$$+7MIA#####C* TO BE ENCODED IN 2D AZTEC BARCODE PER ANSI/HIBC 2.6 ‐ 2016 THE HEALTH INDUSTRY SUPPLIER LABELING STANDARD FOR PATIENT SAFETY & UNIQUE DEVICE IDENTIFICATION (UDI) . REVISIONS DCO#REV.DESCRIPTIONDATEAPPROVED TBD1INITIAL RELEASE 10/06/2021 D C B A A B C D 1 2 3 4 5 6 7 8 8 7 6 5 4 3 2 1 TITLE B REVPART NUMBERSIZESCALE 301RL-GATEWAY REGULATORY LABEL DRAWING FILE NAME MODEL FILE NAME DO NOT SCALE DRAWING DIMENSIONS ARE IN MILLIMETERS TOLERANCES UNLESS OTHERWISE SPECIFIED: X.X 0.2 X.XX 0.13 ANGULAR: 1 7301RL-ART 1:1 SHEET 1 OF 1 INFOBIONIC GATEWAY REGULATORY LABEL PROPRIETARY NOTICE: THIS DOCUMENT CONTAINS CONFIDENTIAL AND PROPRIETARY INFORMATION OF INFOBIONIC. IT MUST NOT BE REPRODUCED, DISCLOSED, OR USED AS THE BASIS FOR THE MANUFACTURE OR SALE OF ANY ITEM OTHER THAN THAT FOR WHICH IT WAS PROVIDED WITHOUT PRIOR WRITTEN PERMISSION OF INFOBIONIC. ALL RIGHTS RESERVED BY INFOBIONIC, COPYRIGHT (C) 301RL-GATEWAY REGULATORY LABEL THIRD ANGLE PROJECTION 200 Fifth Avenue Suite 4030 Waltham, MA 02451 TBD2UPDATE SIZE AND COLORS10/20/2021 TBD3REMOVED “MOME K3”07/26/2022 TBD4UPDATED READ MANUAL ICON11/03/2022 TBD5UPDATED MFG ICON, PLACEHOLDER SERIAL NUMBER01/17/2023 TBD6 UPDATED MFG LOCATION03/14/2023 TBD7 UPDATED FCC ID10/09/2023 4. MAGENTA LINE INDICATES PARTS OUTLINE ONLY - DO NOT PRINT. WhitePantone Cool Gray 9 C RAL 5005 Signal Blue

Proprietary and Confidential | November 9th, 2023 Label Construction ●Graphics indelibly printed on back (internal) surface of clear polycarbonate ●Permanent adhesive backing Gateway Proprietary and Confidential | November 9th, 2023 Label Graphics and Placement ●Graphics as shown, serialized ●Adhered into a matching recess with permanent adhesive Gateway Label image enlarged for clarity Placement on device

FCC Part 1 Subpart I FCC Part 2 Subpart J TEST REPORT FOR AMBULATORY ELECTROCARDIOGRAM CHARGING BASE & GATEWAY MODEL NO: MOME ARC CHARGER, MOME ARC GATEWAY FCC ID: 2AHLC01858 (Charger), 2AHLC01856 (Gateway) REPORT NUMBER: R14275554-E10 v5 ISSUE DATE: 2024-01-08 Prepared for INFOBIONIC, INC 400 TOTTEN POND RD STE 315 WALTHAM, MA 02451, U.S.A. Prepared by UL LLC 12 LABORATORY DR. RESEARCH TRIANGLE PARK, NC 27709 USA TEL: (919) 549-1400 REPORT NO: R14275554-E10 v5 DATE: 2024-01-08 EUT: Charger, Gateway MODEL NAME: MoMe ARC Charger, MoMe ARC Gateway Page 2 of 21 UL LLC FORM NO: CCSUP4701I 12 Laboratory Dr., RTP, NC 27709 TEL: (919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC Revision History Rev. Issue Date Revisions Revised By V1 2023-10-03 Initial Issue Niklas Haydon V2 2023-10-13 Added E-Field measurements for configuration 4 to §8.3. Richard Jankovics V3 2023-11-21 Removed setup photos Added setup photos exhibit reference. Brian Kiewra V4 2024-01-02 §5.2 Added diagram for the device separation under the Measurement Setup. §8.3 Updated data and explanation of duty cycle for Configuration 4 – Portable use RF Exposure. Richard Jankovics V5 2024-01-08 §8.2 Added clarification of probe distances for portable configuration. §8.3 Added clarification of test conditions. Updated measurement data for Configuration 4 – Portable use RF Exposure. Richard Jankovics REPORT NO: R14275554-E10 v5 DATE: 2024-01-08 EUT: Charger, Gateway MODEL NAME: MoMe ARC Charger, MoMe ARC Gateway Page 3 of 21 UL LLC FORM NO: CCSUP4701I 12 Laboratory Dr., RTP, NC 27709 TEL: (919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC TABLE OF CONTENTS 1. ATTESTATION OF TEST RESULTS .................................................................................... 4 2. TEST METHODOLOGY ........................................................................................................ 5 3. FACILITIES AND ACCREDITATION .................................................................................... 5 4. DECISION RULES AND MEASUREMENT UNCERTAINTY ................................................ 6 4.1. METROLOGICAL TRACEABILITY ................................................................................ 6 4.2. DECISION RULES ......................................................................................................... 6 4.3. MEASUREMENT UNCERTAINTY ................................................................................. 6 5. EQUIPMENT UNDER TEST ................................................................................................. 7 5.1. DESCRIPTION OF EUT ................................................................................................. 7 5.2. DESCRIPTION OF TEST SETUP .................................................................................. 7 6. TEST AND MEASUREMENT EQUIPMENT ....................................................................... 11 7. DUTY CYCLE ...................................................................................................................... 12 8. MAXIMUM PERMISSIBLE RF EXPOSURE TEST RESULTS ........................................... 15 8.1. FCC LIMITS .................................................................................................................. 15 8.2. SUMMARY OF TEST RESULTS ................................................................................. 15 8.3. DETAILED TEST RESULTS ........................................................................................ 17 9. SETUP PHOTO ................................................................................................................... 21 END OF REPORT ...................................................................................................................... 21 REPORT NO: R14275554-E10 v5 DATE: 2024-01-08 EUT: Charger, Gateway MODEL NAME: MoMe ARC Charger, MoMe ARC Gateway Page 4 of 21 UL LLC FORM NO: CCSUP4701I 12 Laboratory Dr., RTP, NC 27709 TEL: (919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC 1. ATTESTATION OF TEST RESULTS COMPANY NAME: InfoBionic, Inc 400 Totten Pond Rd STE 315 Waltham, MA 02451, U.S.A EUT DESCRIPTION: Ambulatory Electrocardiogram Charging Base & Gateway MODEL NUMBER: MoMe ARC Charger, MoMe ARC Gateway SERIAL NUMBER: Charger (MIB2007), Gateway(MIB2008) DATE TESTED: 2022-11-14 to 2022-11-30, 2023-06-06 APPLICABLE STANDARDS STANDARD TEST RESULTS FCC PART 1 SUBPART I & PART 2 SUBPART J Complies UL LLC tested the above equipment in accordance with the requirements set forth in the above standards. The test results show that the equipment tested is capable of demonstrating compliance with the requirements as documented in this report. The results documented in this report apply only to the tested sample, under the conditions and modes of operation as described herein. It is the manufacturer's responsibility to assure that additional production units of this model are manufactured with identical electrical and mechanical components. All samples tested were in good operating condition throughout the entire test program. Measurement Uncertainties are published for informational purposes only and were not taken into account unless noted otherwise. This document may not be altered or revised in any way unless done so by UL LLC and all revisions are duly noted in the revisions section. Any alteration of this document not carried out by UL LLC will constitute fraud and shall nullify the document. Approved & Released For UL LLC By: Prepared By: Francisco de Anda Staff Engineer Niklas Haydon Operations Leader Consumer Technology Division Consumer Technology Division UL LLC UL LLC REPORT NO: R14275554-E10 v5 DATE: 2024-01-08 EUT: Charger, Gateway MODEL NAME: MoMe ARC Charger, MoMe ARC Gateway Page 5 of 21 UL LLC FORM NO: CCSUP4701I 12 Laboratory Dr., RTP…

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© TDK Corporation 2016 Wireless Charging page1 11,80 8,40 0,00 11,80 5,30 11,80 6,50 11,80 0,00 8,40 5,30 6,50 7,80 7,80 TDK Confidential TDK Datasheet for WT252512-8F2-SM = Dimension of coil unit = = Coil unit Assembly= = Electrical Characteristics=  Ls [ uH] : 2.76 uH +/- 5% @1.0MHz  Rs [ ohm] : 0.15 Ω +/- 10% @1.0MHz  Rdc [Ohm] : 0.07 Ω typ 1.Air Coil 2.Adhesive Tape 3.Ferrite Sheet 4.PET Tape

TEST REPORT Report Number. : R14275554-E11 Applicant : InfoBionic, Inc 400 Totten Pond Rd STE 315 Waltham, MA 02451, U.S.A. Model(s) : MoMe ARC Charger, MoMe ARC K3 Sensor & MoMe ARC Gateway FCC IDs : 2AHLC01858, 2AHLC01857, 2AHLC01856 EUT Description : Charger Base, Sensor & Gateway Test Standard(s) : FCC 47 CFR PART 15 SUBPART C: 2022 Date Of Issue: 2023-10-03 Prepared by: UL LLC 12 Laboratory Dr. Research Triangle Park, NC 27709 U.S.A. TEL: (919) 549-1400 REPORT NO: R14275554-E11 DATE: 2023-10-03 FCC ID: 2AHLC01858, 2AHLC01857, 2AHLC01856 Page 2 of 29 UL LLC 12 Laboratory Dr., RTP, NC 27709; USA TEL:(919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC Revision History Rev. Issue Date Revisions Revised By V1 2023-10-03 Initial Issue Noah Bennett REPORT NO: R14275554-E11 DATE: 2023-10-03 FCC ID: 2AHLC01858, 2AHLC01857, 2AHLC01856 Page 3 of 29 UL LLC 12 Laboratory Dr., RTP, NC 27709; USA TEL:(919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC TABLE OF CONTENTS 1. ATTESTATION OF TEST RESULTS ..................................................................................4 2. TEST RESULTS SUMMARY ...............................................................................................5 3. TEST METHODOLOGY ......................................................................................................5 4. FACILITIES AND ACCREDITATION ..................................................................................5 5. DECISION RULES AND MEASUREMENT UNCERTAINTY ...............................................6 METROLOGICAL TRACEABILITY ...............................................................................6 DECISION RULES ........................................................................................................6 MEASUREMENT UNCERTAINTY ................................................................................6 SAMPLE CALCULATION .............................................................................................6 6. EQUIPMENT UNDER TEST ................................................................................................7 DESCRIPTION OF EUT ...............................................................................................7 MAXIMUM OUTPUT POWER .......................................................................................7 SOFTWARE AND FIRMWARE .....................................................................................7 WORST-CASE CONFIGURATION AND MODE ...........................................................8 DESCRIPTION OF TEST SETUP .................................................................................9 7. TEST AND MEASUREMENT EQUIPMENT ......................................................................10 8. EMISSION BANDWIDTH ..................................................................................................12 9. RADIATED EMISSION TEST RESULTS...........................................................................14 LIMITS AND PROCEDURE ........................................................................................14 FCC TX FUNDAMENTAL AND SPURIOUS EMISSIONS FROM 9 kHz TO 30 MHz...15 CONFIG 1 ............................................................................................................15 CONFIG 2 ............................................................................................................16 CONFIG 3 ............................................................................................................17 FCC TX SPURIOUS EMISSION 30 TO 1000 MHz .....................................................18 CONFIG 1 ............................................................................................................18 CONFIG 2 ............................................................................................................20 CONFIG 3 ............................................................................................................22 10. AC MAINS LINE CONDUCTED EMISSIONS ................................................................24 CONFIG 1 ........................................................................................................25 CONFIG 2 ........................................................................................................27 11. SETUP PHOTOS ...........................................................................................................29 REPORT NO: R14275554-E11 DATE: 2023-10-03 FCC ID: 2AHLC01858, 2AHLC01857, 2AHLC01856 Page 4 of 29 UL LLC 12 Laboratory Dr., RTP, NC 27709; USA TEL:(919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC 1. ATTESTATION OF TEST RESULTS COMPANY NAME: InfoBionic, Inc 400 Totten Pond Rd STE 315 Waltham, MA 02451, U.S.A EUT DESCRIPTION: Charger Base MODEL: Mome ARC Charger, MoMe ARC K3 Sensor & MoMe ARC Gateway SERIAL NUMBER: SIA2008, MIB2008, MIB1033 SAMPLE RECEIPT DATE: 2022-08-15 DATE TESTED: 2022-11-14 Thru 2022-11-30 APPLICABLE STANDARDS STANDARD TEST RESULTS FCC PART 15 SUBPART C: 2022 Complies UL LLC tested the above equipment in accordance with the requirements set forth in the above standards. The test results show that the equipment tested is capable of demonstrating compliance with the requirements as documented in this report. The results documented in this report apply only to the tested sample, under the conditions and modes of operation as described herein. It is the manufacturer's responsibility to assure that additional production units of this model are manufactured with identical electrical and mechanical components. All samples tested were in good operating condition throughout the entire test program. Measurement Uncertainties are published for informational purposes only and were not taken into account unless noted otherwise. This document may not b…

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SETUP PHOTOS EXHIBIT Report Number. : R14275554-EP5 Applicant : InfoBionic, Inc 400 Totten Pond Rd STE 315 Waltham, MA 02451, U.S.A. Model : Mome ARC Charger, MoMe ARC K3 Sensor & MoMe ARC Gateway FCC IDs : 2AHLC01858, 2AHLC01857, 2AHLC01856 EUT Description : Charger Base, Sensor & Gateway Test Standard(s) : FCC 47 CFR PART 15 SUBPART C: 2022 Date Of Issue: 2022-11-30 Prepared by: UL LLC 12 Laboratory Dr. Research Triangle Park, NC 27709 U.S.A. TEL: (919) 549-1400 REPORT NO: R14275554-EP5 DATE: 2022-11-30 FCC ID: 2AHLC01858, 2AHLC01857, 2AHLC01856 Page 2 of 18 UL LLC 12 Laboratory Dr., RTP, NC 27709; USA TEL: (919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC REPORT REVISION HISTORY Rev. Issue Date Revisions Revised By V1 2022-11-30 Initial Issue Noah Bennett REPORT NO: R14275554-EP5 DATE: 2022-11-30 FCC ID: 2AHLC01858, 2AHLC01857, 2AHLC01856 Page 3 of 18 UL LLC 12 Laboratory Dr., RTP, NC 27709; USA TEL: (919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC TABLE OF CONTENTS REPORT REVISION HISTORY ..................................................................................................2 TABLE OF CONTENTS .............................................................................................................3 1. SETUP DIAGRAMS ............................................................................................................4 2. SETUP PHOTOS .................................................................................................................5 END OF TEST REPORT ..........................................................................................................17 REPORT NO: R14275554-EP5 DATE: 2022-11-30 FCC ID: 2AHLC01858, 2AHLC01857, 2AHLC01856 Page 4 of 18 UL LLC 12 Laboratory Dr., RTP, NC 27709; USA TEL: (919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC 1. SETUP DIAGRAMS Config 1 Config 2 Config 3 REPORT NO: R14275554-EP5 DATE: 2022-11-30 FCC ID: 2AHLC01858, 2AHLC01857, 2AHLC01856 Page 5 of 18 UL LLC 12 Laboratory Dr., RTP, NC 27709; USA TEL: (919) 549-1400 This report shall not be reproduced except in full, without the written approval of UL LLC 2. SETUP PHOTOS CONDUCTED MEASUREMENT SETUP REPORT NO: R14275554-EP5 DATE: 2022-11-30 FCC ID: 2AHLC01858, 2AHLC01857, 2AHLC01856 Page 6 of 18 UL LLC 12 Laboratory Dr., RTP, NC 2770…

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