2AAZF-POTPIEX01POTPIEX01

CONFIDENTIAL AND PROPRIETARY – Intuitive Surgical Inc. Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com User manual for POTPIEX01 module (WPT) The POTPIEX01 module is WPT transmitter module manufactured by Intuitive Surgical, Inc. to be installed in host product, da Vinci system, which is also manufactured by Intuitive Surgical, Inc. The intended use of the POTPIEX01 module is to provide wireless power to endoscope that is plugged into da Vinci system. The POTPIEX01 module is to be installed inside receptacle of Endoscope System Controller (ESC) integrated inside da Vinci system and provide wireless power in frequency range 120 – 148.5 kHz to endoscope. The POTPIEX01 module has permanently attached coil antenna (53 mm x 53 mm) that is not accessible or replaceable by the end user. For RF exposure, the compliance distance for both thermal effects and nerve stimulation is 0 cm. FCC The host product must be labeled with the following: Contains FCC ID: 2AAZF-POTPIEX01 The host product user manual must include the following statements: This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.” ISED The host product must be labeled with the following: Contains IC: 11508A-POTPIEX01 The host product user manual must include the following statements: Under Industry Canada regulations, this radio transmitter may only operate using an antenna of a type and maximum (or lesser) gain approved for the transmitter by Industry Canada. To reduce potential radio interference to other users, the antenna type and its gain should be so chosen that the equivalent isotropically radiated power (eirp) is not more than necessary for successful communication. This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Conformément à la réglementation d'Industrie Canada, cet émetteur radio peut fonctionner uniquement à l'aide d'une antenne de type et de gain maximum (ou moindre) approuvés pour l'émetteur par Industrie Canada. Pour réduire le risque d'interférence aux autres utilisateurs, le type d'antenne et son gain doivent être choisis afin que la puissance isotrope rayonnée équivalente (PIRE) n‘excède pas celle nécessaire à une communication réussie. CONFIDENTIAL AND PROPRIETARY – Intuitive Surgical Inc. Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com Cet appareil est conforme au(x) standard(s) des CNR d’Industrie Canada pour appareils radio exempt(s) de licence . Son fonctionnement est soumis aux deux conditions suivantes: (1) ce dispositif ne doit pas causer d'interférences nuisibles, et (2) cet appareil doit accepter toute interférence reçue, y compris les interférences qui peuvent provoquer un fonctionnement indésirable.

CONFIDENTIAL AND PROPRIETARY – Intuitive Surgical Inc. Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com POTPIEX01 modular integration instruction in host device The POTPIEX01 (WPT module) is manufactured by Intuitive Surgical, Inc. to be installed in host products manufactured by Intuitive Surgical, Inc. The intended use of the POTPIEX01 module is to provide wireless power to an endoscope (client device) that is plugged into the module. The POTPIEX01 module will provide wireless power in frequency range 120 – 148.5 kHz to endoscope. The POTPIEX01 module has permanently attached coil antenna (53 mm x 53 mm) that is not accessible or replaceable by the end user. Per FCC KDB 996369, host product manufacturers shall follow modular integration instructions of this document when they integrate POTPIEX01 in a host product. The reason that POTPIEX01 has limited modular approval is because the module does not have its own shielding per FCC §15.212 (a) (1) (i) and it cannot be tested stand-alone. 1. List of applicable FCC rules that are applicable to the modular transmitters 47 CFR FCC §15.207 and §15.209. 2. Summary of specific operational use conditions POTPIEX01 has a built-in, integral loop/coil antenna. Host product manufacturer is not allowed to make changes to the built-in antenna. 3. Limited module procedures Full testing per FCC §15.207 and §15.209 and a Class II permissive change are required on the module grant of POTPIEX01 to register the host device as a specific host approved with the POTPIEX01 module. Full testing includes fundamental, spurious, out of band and band edge radiated emissions as well as conducted emissions on AC power port and an RF exposure assessment. The RF exposure shall be evaluated in portable condition in accordance with FCC KDB 680106 or latest guidance. 4. Trace antenna designs Not applicable. POTPIEX1 has a built-in, integral loop/coil antenna. Host product manufacturer is not allowed to make changes to trace antenna designs. CONFIDENTIAL AND PROPRIETARY – Intuitive Surgical Inc. Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com 5. RF exposure considerations POTPIEX01 may be installed such that it can be operated as close as 0 cm to users or nearby persons. The use condition applies for portable use. If integration is such that the user would be 20 cm or farther, then mobile use is applied. 6. Antennas POTPIEX01 Inductance: 10 uH Number of turns: 12 Ferrite shield: 53mm x 53mm x 1.5mm Dimensions in mm: 48mm x 48mm 7. Label and compliance information FCC The host product must be labeled with the following: Contains FCC ID: 2AAZF-POTPIEX01 The host product user manual must include the following statements: This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.” ISED The host product must be labeled with the following: Contains IC: 11508A-POTPIEX01 CONFIDENTIAL AND PROPRIETARY – Intuitive Surgical Inc. Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com The host product user manual must include the following statements: Under Industry Canada regulations, this radio transmitter may only operate using an antenna of a type and maximum (or lesser) gain approved for the transmitter by Industry Canada. To reduce potential radio interference to other users, the antenna type and its gain should be so chosen that the equivalent isotropically radiated power (eirp) is not more than necessary for successful communication. This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Conformément à la réglementation d'Industrie Canada, cet émetteur radio peut fonctionner uniquement à l'aide d'une antenne de type et de gain maximum (ou moindre) approuvés pour l'émetteur par Industrie Canada. Pour réduire le risque d'interférence aux autres utilisateurs, le type d'antenne et son gain doivent être choisis afin que la puissance isotrope rayonnée équivalente (PIRE) n‘excède pas celle nécessaire à une communication réussie. Cet appareil est conforme au(x) standard(s) des CNR d’Industrie Canada pour appareils radio exempt(s) de licence. Son fonctionnement est soumis aux deux conditions suivantes: (1) ce dispositif ne doit pas causer d'interférences nuisibles, et (2) cet appareil doit accepter toute interférence reçue, y compris les interférences qui peuvent provoquer un fonctionnement indésirable. 8. Information of test modes and additional testing requirements Host product with POTPIEX01 installed shall have endoscope plugged into the module. A host product requiring FCC approval shall be tested to FCC Part 15 Subpart B to check for emissions that may occur due to the intermixing of emissions with digital circuitry or due to enclosure of the host product. Full testing per FCC §15.207 and §15.209 includes fundamental, spurious, out of band and band edge radiated emissions as well as conducted emissions on AC power port and an RF exposure assessment. Any changes in the receiving WPT coil and its circuits in the endoscope plug (client device) will require a Class 2 Permissive Change. The receiving WPT coil is Wurth Elektronik P/N 760308102207 and the controller is Renesas Electronics P/N P9221-R. 9. Additional testing, part 15 Subpart B disclaimer POTPIEX01 is only FCC authorized for specific rule parts listed on the grant, and the host product manufacturer is responsible for compliance to any other FCC rules that apply to the host not covered by the modular transmitter g…

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Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com US Agent Attestation Letter TO: Federal Communications Commission Authorization and Evaluation Division 7435 Oakland Mills Road Columbia, Maryland 21046 Re: section 2.911(d)(7) filing To whom it may concern, This letter is to confirm that Intuitive Surgical, Inc. has accepted responsibility to act as the agent for service of process as acknowledged by the applicant, Intuitive Surgical, Inc. Intuitive Surgical, Inc. confirms he is not associated with or part of any TCB or test lab. U.S. Agent: Bryan Blair Title: Manager, Hardware Compliance and PCB Design Company Name: Intuitive Surgical, Inc. Address: 1266 Kifer Road, Sunnyvale, CA 94086 Telephone No: +1-408-523-7373 Email: [email protected] FRN (FCC Registration Number): 0022966345 The applicant accepts and acknowledges the obligation to 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. Signature of Applicant (must be signed by the contact of record in the FCC database for the applicant grantee code): Signature of U.S. Agent (if different from applicant): Name: Name: Date: 09/29/2023 Date:

Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com Attestation Statement Date: 09/29/2023 Federal Communications Commission Authorization and Evaluation Division 7435 Oakland Mills Road Columbia, Maryland 21046 Re: Attestation regarding ‘covered’ equipment and the Covered List FCC ID: 2AAZF-POTPIEX01 To whom it may concern, Per 2.911(d)(5)(i), Intuitive Surgical, Inc. 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. Per 2.911(d)(5)(ii), Intuitive Surgical, Inc. 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. Sincerely, Name: Bryan Blair Job Title: Manager, Hardware Compliance and PCB Design

41039 Boyce Road Fremont, CA. 94538 Phone: 510-578-3500 Page 1 of 1 October 27, 2023 Federal Communications Commission Office of Engineering and Technology Laboratory Division 7435 Oakland Mills Road Columbia, MD 21046 Innovation Science and Economic Development Canada Certification and Engineering Bureau 3701 Carling Avenue, Building 94 Ottawa, Ontario K2H 8S2 FCC ID: 2AAZF-POTPIEX01 IC: 11508A-POTPIEX01 To whom it may concern: The enclosed documents constitute a formal submittal and application for FCC Equipment Authorization and ISED Canada Certification for a RF Module (limited modular app rova l due to no shi elding ) that is designed to provide power wirelessly (WPT) pursuant to the following rules: Subpart C of Part 15 of FCC Rules (CFR 47), §15.209 RSS-Gen Issue 5, April 2018, “General Requirements for Compliance of Radio Apparatus” RSS-216, Issue 2, Sept embe r 2020, “Wireless Power Transfer Devices” The EUT is unmodulated whi le chargi ng and us ed FSK modulation to communicate charge status . National Technical Systems, as duly authorized agent prepared this submittal. A copy of the letter of our appointment as agent is included with the application. If there are any questions or if further information is needed, please contact National Technical Systems for assistance. Sincerely, Davi d W. Bare Chi ef E ngineer DWB/dmg

Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com Request for Confidentiality Letter Date: 09/29/2023 Federal Communications Commission Authorization and Evaluation Division 7435 Oakland Mills Road Columbia, Maryland 21046 Re: Request for confidentiality FCC ID: 2AAZF-POTPIEX01 To whom it may concern, We hereby respectfully request that under the provision of §§ 0.457(d) and 0.459 the documents listed below and attached with this application for certification be provided with confidential status. Exhibit Type of Confidentiality Frequency Block Diagrams Permanent Operational Description Permanent Schematics Permanent Part List & Placement/BOM Permanent External Photos Short Term Internal Photos Short Term Test Setup Photos Short Term User’s Manual Short Term Intuitive Surgical, Inc. has spent effort in developing this product and it is one of the first of its kind in industry. Having the subject information easily available to competition would negate the advantage we have achieved by developing this product. Not protecting the details of the design will result in financial hardship. Permanent Confidentiality: The applicant request that exhibits listed as permanently confidential be permanently withheld from public review due to materials that contain trade secrets and proprietary information not customarily released to the public. Short-Term Confidentiality: The applicant requests the exhibits selected above as short term confidential be withheld from public view for a period of 180 days from the date of the Grant of Equipment Authorization and prior to marketing. This is to avoid premature release of sensitive information prior to marketing or release of the product to the public. Any exhibit / information for which we have requested confidentiality, but which may not be accorded such treatment by the FCC, should be returned to us. Sincerely, Name: Tony Permsombut Job Title: Senior Hardware Compliance Engineer

Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com Agent Authorization Letter Date: 11/15/2023 Federal Communications Commission Office of Engineering and Technology Laboratory Division 7435 Oakland Mills Road Columbia, MD 21046 Certification and Engineering Bureau Innovation, Science and Economic Development Canada (ISED) 3701 Carling Avenue (Building 94) Ottawa, Ontario K2H 8S2 To whom it may concern, We, the undersigned, hereby authorize David Bare or David Guidotti of NTS Labs, LLC. to act on our behalf, as our agent, in the following matters related to the FCC and/or Innovation Science and Economic Development Canada approval of our products: report submittal, related correspondence, the signing of all documents relating to these matters, and any other lawful activity necessary to obtain such certification. Any act carried out by NTS Labs, LLC. within the scope of this authorization shall have the same affect as our own. This authorization shall expire 12 months from original date. Sincerely, Name: Bryan Blair Job Title: Senior Manager, Hardware Compliance and PCB Design

CONFIDENTIAL AND PROPRIETARY – Intuitive Surgical Inc. Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com FCC/IC Label placement of POTPIEX01 module ( WPT) The label contains FCC ID: 2AAZF-POTPIEX01, IC: 11508A-POTPIEX01 and Regulatory Model name POTPIEX01 for identification. The material of the label is fine textured LEXAN Polycarbonate, 0.010” thick with adhesive 3M#9672 having white background and black text with minimum font size 4 pt. See Figure 1. The label is affixed to the left side of the POTPIEX01 module in a manner such that it will remain adhered to the module during the expected life of the product. Refer to the external photos for label placement. Figure 1: Label of POTPIEX01 module

© 2024 RF Exposure Lab, LLC This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. 802 N. Twin Oaks Valley Road, Suite 105 • San Marcos, CA 92069 • U.S.A. TEL (760) 471-2100 • FAX (760) 471-2121 http://www.rfexposurelab.com CERTIFICATE OF COMPLIANCE RF EXPOSURE & NERVE STIMULATION EVALUATION Intuitive Surgical, Inc. Dates of Test: January 12, 2024 1020 Kifer Road Test Report Number: SAR.20240107 Sunnyvale, CA 94086 Lab Designation Number: US1195 This wireless mobile device has been shown to meet the requirements for RF exposure testing and Nerve Stimulation for uncontrolled environment/general exposure limits specified in above listed standards. The device has also been shown to meet the simultaneous requirements of each standard as well (See test report). I attest to the accuracy of the data. I assume full responsibility for the completeness of these calculations and vouch for the qualifications of all persons making them. Jay M. Moulton Vice President Testing Certificate # 2387.01 FCC ID: 2AAZF-POTPIEX01 Model(s): POTPIEX01 Serial Number: FNW22430532 Equipment Type: Wireless Power Transfer Classification: WPT Transmitter TX Frequency Range: 120-148.5 kHz Frequency Tolerance: ± 2.5 ppm Maximum RF Output: 120 kHz – -34.67 dBm EIRP Signal Modulation: FSK Antenna Type: Internal Application Type: Certification Standard(s): KDB680106 D01 v04 Maximum E-Field 38.72 V/m Maximum H-Field 1.43 A/m Distance Calculated: 0 mm Report No.: SAR.20240107 © 2024 RF Exposure Lab, LLC Page 2 of 11 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Table of Contents 1. Introduction ........................................................................................................................... 4 2. Radiation Sources ................................................................................................................. 4 3. POTPIEX01 ........................................................................................................................... 5 4. RF Exposure Classifications ................................................................................................. 6 5. RF Exposure Limits ............................................................................................................... 7 FCC Requirements ................................................................................................................... 7 6. General Conditions ............................................................................................................... 8 7. Environmental Conditions ..................................................................................................... 8 8. Test Equipment ..................................................................................................................... 8 9. EUT Description .................................................................................................................... 8 10. Nerve Stimulation Evaluation Results ............................................................................... 9 Appendix A – Calibration Certificates ......................................................................................... 11 Report No.: SAR.20240107 © 2024 RF Exposure Lab, LLC Page 3 of 11 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Comment/Revision Date Original Release January 16, 2024 Note: The latest version supersedes all previous versions listed in the above table. The latest version shall be used. Report No.: SAR.20240107 © 2024 RF Exposure Lab, LLC Page 4 of 11 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. 1. Introduction This report shows the RF exposure evaluation of the Intuitive Surgical, Inc. Model POTPIEX01 Wireless Power Transfer with KDB680106 D01 v04. 2. Radiation Sources Radio Description FSK Frequency (MHz) 120-148.5 kHz Maximum Power (dBm) -34.67 dBm (EIRP) Maximum Duty Cycle (%) 100% Report No.: SAR.20240107 © 2024 RF Exposure Lab, LLC Page 5 of 11 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. 3.POTPIEX01 Photo Removed Report No.: SAR.20240107 © 2024 RF Exposure Lab, LLC Page 6 of 11 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. 4. RF Exposure Classifications Report No.: SAR.20240107 © 2024 RF Exposure Lab, LLC Page 7 of 11 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. 5. RF Exposure Limits FCC Requirements The RF exposure limits, as set forth in § 1.1310, do not cover the frequency range below 100 kHz for Specific Absorption Rate (SAR) and below 300 kHz for Maximum Permitted Exposure (MPE). In addition, present limitations of RF exposure evaluation systems prevent an accurate evaluation of SAR below 4 MHz. For these reasons, a specific MPE-based RF Exposure compliance procedure for devices operating in the aforementioned low-frequency ranges has been set in place. This procedure is applicable to Equipment Authorization of all RF devices, thus including, but not limited to, Part 18 and WPT devices. Accordingly, for § 2.1091-Mobile devices, the MPE limits between 100 kHz to 300 kHz are to be considered the same as those at 300 kHz in Table 1 of § 1.1310, that is, 614 V/m and 1.63 A/m, for the electric field and magnetic field, respectively. For § 2.1093-Portable devices below 4 MHz and down to 100 kHz, the MPE limits in § 1.1310 (with the 300 kHz limit applicable all the way down to 100 kHz) can be used for the purpose of equipment authorization in lieu of SAR evaluations. Report No.: SAR.20240107 © 2024 RF Exposure Lab, LLC Page 8 of 11 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. 6. General Conditions • Thi…

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CONFIDENTIAL AND PROPRIETARY – Intuitive Surgical Inc. Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 T. 408 523 2100 F.408 523 1390 Intuitive.com Antenna Specification of POTPIEX01 module (WPT) Frequency range 120 – 148.5 kHz Type of antenna Coil antenna Description Inductance: 10 uH Number of turns: 12 Ferrite shield: 53mm x 53mm x 1.5mm Dimensions in mm:

41039 Boyce Road 510-578-3500 Phone Fremont, CA. 94538 510-440-9525 Fax File: FR-172107.02-NARF Rev 1 Page 1 EMC Test Report Application for Grant of Equipment Authorization Innovation, Science and Economic Development Canada RSS-Gen Issue 5 / RSS-216 Issue 2 FCC Part 15 Subpart C Model: POTPIEX01 ISED CERTIFICATION #: 11508A-POTPIEX01 FCC ID: 2AAZF-POTPIEX01 APPLICANT: Intuitive Surgical Inc. 1266 Kifer Road Building 101 Sunnyvale, CA 94086 TEST SITE(S): NTS Labs LLC 41039 Boyce Road. Fremont, CA. 94538-2435 IC SITE REGISTRATION #: 2845B-3; 2845B-4, 2845B-5, 2845B-7 PROJECT NUMBER: PR172107 REPORT DATE: August 7, 2023 RE-ISSUED DATE: November 28, 2023 FINAL TEST DATES: May 8, June 30, July 28, November 21 and 28, 2023 TOTAL NUMBER OF PAGES: 45 This report and the information contained herein represent the results of testing of only those articles / products identified in this document and selected by the client. The tests were performed to specifications and/or procedures selected by the client. NTS Labs LLC makes no representations expressed or implied that such testing fully demonstrates efficiency, performance, reliability, or any other characteristic of the articles being tested, or similar products. This report should not be relied upon as an endorsement or certification by NTS Labs LLC of the equipment tested, nor does it present any statement whatsoever as to its merchantability or fitness of the test article or similar products, for a particular purpose. This report shall not be reproduced except in full without written approval from NTS Labs LLC. NTS Labs LLC Project number PR172107 Report Date: August 7, 2023, Re-Issued Date: November 28, 2023 Test Report FR-172107.02-NARF Rev 1 Page 2 VALIDATING SIGNATORIES PROGRAM MGR _________________________ David W. Bare Chief Engineer TECHNICAL REVIEWER: _________________________ David W. Bare Chief Engineer FINAL REPORT PREPARER: _________________________ David Guidotti Senior Technical Writer QUALITY ASSURANCE DELEGATE _________________________ Gary Izard Senior Technical Writer NTS Labs LLC Project number PR172107 Report Date: August 7, 2023, Re-Issued Date: November 28, 2023 Test Report FR-172107.02-NARF Rev 1 Page 3 REVISION HISTORY Rev# Date Comments Modified By - August 7, 2023 First release 1 November 28, 2023 Updated RSS standard, updated operating frequency range, added Magnetic field strength results, added client device description, added additional details of the operation during testing. Added FSK modulation for control communication and OBW data. dwb NTS Labs LLC Project number PR172107 Report Date: August 7, 2023, Re-Issued Date: November 28, 2023 Test Report FR-172107.02-NARF Rev 1 Page 4 TABLE OF CONTENTS COVER PAGE ............................................................................................................................................................. 1 VALIDATING SIGNATORIES ................................................................................................................................. 2 REVISION HISTORY ................................................................................................................................................ 3 TABLE OF CONTENTS ............................................................................................................................................ 4 SCOPE .......................................................................................................................................................................... 5 OBJECTIVE ................................................................................................................................................................ 6 STATEMENT OF COMPLIANCE ........................................................................................................................... 6 DEVIATIONS FROM THE STANDARDS .............................................................................................................. 6 TEST RESULTS SUMMARY .................................................................................................................................... 7 DEVICES OPERATING UNDER THE GENERAL LIMITS ................................................................................. 7 GENERAL REQUIREMENTS APPLICABLE TO ALL BANDS .......................................................................... 7 MEASUREMENT UNCERTAINTIES .................................................................................................................... 8 EQUIPMENT UNDER TEST (EUT) DETAILS ...................................................................................................... 9 GENERAL ................................................................................................................................................................ 9 OTHER EUT DETAILS ........................................................................................................................................... 9 ANTENNA SYSTEM .............................................................................................................................................. 9 ENCLOSURE ........................................................................................................................................................... 9 MODIFICATIONS ................................................................................................................................................... 9 SUPPORT EQUIPMENT ......................................................................................................................................... 9 EUT INTERFACE PORTS .................................................................................................................................... 10 EUT OPERATION .............................................................................................................................................…

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EMC Test Data Immunity Standard(s): Tony PermsombutProject Engineer: David Bare Emissions Standard(s): Contact: Environment: Radio Class: - -FCC Part 15, RSS-210, KS X 3143, Japan ELP PR172107 Project Manager: T-Log Number: Deepa Shetty PR Number: TL172107-RA-POTPIE Date of Last Test: 7/20/2023 EMC Test Data For The Intuitive Surgical, Inc. POTPIEX01 Product Client: Intuitive Surgical, Inc. POTPIEX01 Tested as module with PIEX01 Product System Configuration: TL172107-RANA-POTPIEX01.xlsCoverPage 1 of 10 EMC Test Data Client: Contact: Standard: Tony PermsombutProject Engineer: David Bare FCC Part 15, RSS-210, KS X 3143, Japan ELPClass: - Intuitive Surgical, Inc.PR Number: PR172107 Model: POTPIEX01 T-Log Number: TL172107-RA-POTPIE Project Manager: Deepa Shetty Test Configuration Photograph #1 (Radiated Emissions - Below 30 MHz) TL172107-RANA-POTPIEX01.xlsRE FCC 30-Jun-23Page 2 of 10 EMC Test Data Client: Contact: Standard: Tony Per…

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