2ADZNHX991Power toothbrush

DiamondClean 9000 4 3 5 6 8 12 14 13 11 10 7 9 1 2 1 English 6 Español 35 Français (Canada) 66 English Introduction Congratulations on your new Philips Sonicare power toothbrush! Superior plaque removal, whiter teeth and healthier gums are at your fingertips. Using Sonicare’s combination of gentle sonic technology and clinically developed and proven features, you can be confident that you’re getting the very best clean, every time. Further support and product registration are available to you at: http://www.philips.com/welcome. Welcome to the Philips Sonicare family! Intended Use DiamondClean series power toothbrushes are intended to remove adherent plaque and food debris from the teeth to reduce tooth decay and improve and maintain oral health. DiamondClean series power toothbrushes are intended for consumer home use. Use by children should be with adult supervision. IMPORTANT SAFEGUARDS READ ALL INSTRUCTIONS BEFORE USE When using electrical products, especially when children are present, basic safety precautions should always be followed, including the following: 6 English DANGERS To reduce the risk of electrocution: - Do not place or store product where it can fall or be pulled into a tub or sink. - Do not place in or drop into water or other liquid. - Do not use while bathing. - Do not immerse the charger in water or any other liquid. - After cleaning, make sure the charger is completely dry before you connect it to a power outlet. - Do not reach for a product that has fallen into water. Unplug immediately. WARNINGS To reduce the risk of burns, electrocution, fire or physical injury: - Do not clean the brush head, the handle or the charger in the dishwasher. - Do not use attachments other than those recommended by Philips Sonicare. - Never use a charger with a damaged cord or plug. - Always replace the charger with one of the original type in order to avoid a hazard. - Do not plug into an outlet with a voltage other than specified on the bottom of the product. This product is designed to operate within a range of 100 to 240 volts. Voltage converters do not warrant voltage compatibility. - Never force the plug into an outlet; if the plug does not easily fit into the outlet, discontinue use. - Discontinue use if the product appears damaged in any way (brush head, handle or charger, etc.). 7 English - The power cord cannot be replaced. If the power cord is damaged, discard the charger. - Keep the power cord away from heated surfaces. - This product contains no user-serviceable parts. Refer to ‘Warranty and support’ if the product no longer works properly or needs repair. - Do not use the charger outdoors. - Do not use the charger if dropped into water - This product is designed to clean your teeth, gums and tongue only. Use this product only for its intended use as described in this booklet. Discontinue use of this product and contact a physician/dentist if discomfort or pain is experienced. - This product is not intended for use by persons (including children) with reduced physical, sensory, or mental capabilities, or lack of experience and knowledge, unless they have been given supervision or instruction concerning use of the appliance by a person responsible for their safety. - Children should be supervised to ensure that they do not play with the product. - Philips Sonicare is a personal care device and is not intended for use on multiple patients in a dental office or institution. - This appliance contains no serviceable parts. If the appliance is damaged, contact the Consumer Care Center in your country (see chapter 'Warranty and support'). - For connection to a supply not in the U.S.A., use a charger of the proper configuration for the power outlet. - Use a UL-listed computer, USB Hub, or USB duplex receptacle when charging the handle in the travel case. - Avoid direct contact with products that contain essential oils or coconut oil. Contact may result in bristle tufts dislodging. 8 English - If your toothpaste includes peroxide, baking soda or other bicarbonate (common in whitening toothpastes), thoroughly clean your brush head and handle with soap and water after each use. Otherwise plastic cracking may occur. MEDICAL WARNINGS 1Consult your dental professional before you use this product if you have had oral or gum surgery in the previous 2 months. 2Contact your dental professional if excessive bleeding occurs after using this product or bleeding continues to occur after 1 week of use. 3Discontinue use of this product and contact a physician/dentist if discomfort or pain is experienced. 4This product complies with the safety standards for electromagnetic devices. If you have a pacemaker or other implanted device, contact your physician or the device manufacturer prior to use. 5Consult your physician if you have other medical concerns. SAVE THESE INSTRUCTIONS Your Philips Sonicare (Fig. 1) 1 Hygienic travel cap 2 Smart brush heads* 3 Handle 4 Power on/off button 5 Intensity light 6 Mode/intensity button 7 Modes 8 Brush head replacement reminder light 9 Battery indication 9 English 10 Charging glass 11 Charging stand 12 Charging base 13 (Charging)Travel case* 14 USB wall adapter* * Note: The content of the box may vary based on the model purchased. Sonicare app – Getting Started The Sonicare app pairs with your toothbrush to provide you a connected experience. By connecting your toothbrush to your Sonicare app account, you will be able to: - Easily review your progress report for ways to improve your brushing routine - Receive personalized tips and recommendations for managing your oral health To start using the Sonicare app: 1Download the Sonicare app to your phone 2Open the app and follow the guided steps 3Pair your toothbrush with the app 4Create your account 5Complete firmware update, if prompted, to access the latest improvements and features. 6Brush regularly You are ready to start your connected experience. Be sure to brush regularly. You can receive updates to help improv…

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Changes or modications not expressly approved by Philips Oral Heathcare could void the user's authority to operate the equipment. 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. This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment o and on, the user is encouraged to try to correct the interference by one or more of the following measures: -- Reorient or relocate the receiving antenna. -- Increase the separation between the equipment and receiver. -- Connect the equipment into an outlet on a circuit dierent from that to which the receiver is connected. -- Consult the dealer or an experienced radio/TV technician for help” SIZE: 5.5 W X 4.12 H (In) P/N: 300003804381 DFU, LEAFLET FCC RULES AND REGULATIONS, NA 300003804381 ARTWORK D#: D000347343 Canada: This device contains licence-exempt transmitter(s)/receiver(s) that comply with Innovation, Science and Economic Development Canada’s licence-exempt RSS(s). Operation is subject to the following two conditions: 1. This device may not cause interference. 2. This device must accept any interference, including interference that may cause undesired operation of the device. L’émetteur/récepteur exempt de licence contenu dans le présent appareil est conforme aux CNR d’Innovation, Sciences et Développement économique Canada applicables aux appareils radio exempts de licence. L’exploitation est autorisée aux deux conditions suivantes : 1. L’appareil ne doit pas produire de brouillage; 2. L’appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage est susceptible d’en compromettre le fonctionnement 300003804381 SIZE: 5.5 W X 4.12 H (In) P/N: 300003804381 DFU, LEAFLET FCC RULES AND REGULATIONS, NA ARTWORK D#: D000347343

Philips Oral Healthcare 22100 Bothell Everett Hwy Bothell, WA 98021 December 9, 2019 Federal Communications Commission 445 12 th Street SW Washington, DC 20554 Subject: Limited Agency Agreement Philips Oral Healthcare, Inc. FCC ID: 2ADZNHX991 To Whom It May Concern: We, Philips Oral Healthcare, Inc., hereby authorized Intertek Testing Services to act as our Agent for the purpose of preparing application for FCC ID number 2ADZNHX991 under all applicable parts of the FCC rules and regulations. The effective date of this limited agency agreement is December 9, 2019. The Limited Agency Agreement expires on July 9, 2020 unless sooner terminated or extended by written notice to Intertek Testing Services and the Federal Communications Commission. This is to advise that we are in full compliance with the Anti-Drug Abuse Act. The applicant is not subject to a denial of federal benefits pursuant to Section 5301 of the Anti-Drug Act of 1988, 21 U.S.C. 862, and no party to the application is subject to a denial of federal benefits pursuant to that section. If you have any questions or comments, please do not hesitate to contact me. Sincerely, Matthew Vasa Engineer, Safety and Approbations,

Philips Oral Healthcare 22100 Bothell Everett Hwy Bothell, WA 98021 1(2) December 9, 2019 Attention: Application Examiner RE: Request for Confidentiality Applicant: Philips Oral Healthcare, Inc. FCC ID: 2ADZNHX991 ISED ID: 20109-HX991 To Whom It May Concern: Permanent Confidentiality Request is hereby submitted by Philips Oral Healthcare, Inc. to withhold permanently from public review certain portions of the application for equipment certification for the referenced FCC identifiers. This request for confidentiality is made pursuant to 47 CFR 0.457(d) and 0.459 of the FCC Rules. In particular, the following sections of the application are to be kept permanently confidential:  Schematics  Detailed Block Diagrams  Detailed Operational/Functional Description  Tune up procedure  Parts list Short-term Confidentiality Request is hereby submitted by Philips Oral Healthcare, Inc. to withhold from public review for a period of 45 days from the date of the Grant of Equipment Authorization and prior to marketing, certain portions of the application for equipment certification for the referenced FCC identifiers. This request for confidentiality is made pursuant to 47 CFR 0.457(d) and 0.459 of the FCC Rules. In particular, the following sections of the application are to be kept confidential for a period of 45 days from the date of Authorization:  Test setup photos  External photos  Internal photos  User manual Philips Oral Healthcare 22100 Bothell Everett Hwy Bothell, WA 98021 2(2) Rationale for request for confidentiality: Philips Oral Healthcare, Inc. has invested considerable time and materials in research and development to produce the referenced product. Permanent confidentiality: Disclosure of the permanently confidential portions of this application to competitors would not only give them significant competitive advantages in developing similar products, but would also disclose successful implementation of unpublished, leading edge technology developed by us. Short term confidentiality: Disclosure of the short-term confidential portions of this application during the period of importation and/or distribution would reveal key aspects of proprietary technology to competitors and diminish the value of our investment in research and development. If you have questions or need further information, please contact the undersigned. Sincerely, Matthew Vasa Engineer, Safety and Approbations, Philips Oral Healthcare

External Photos FCC ID: 2ADZNHX991 IC:20109-HX991

SCALE 1:1 HX991B 200401 11 Made in China | Fabriqué en Chine Hecho en China FCC ID: 2ADZNHX991 IC: 20109-HX991 SCALE 1:1 HX991W 200401 11 Made in China | Fabriqué en Chine Hecho en China FCC ID: 2ADZNHX991 IC: 20109-HX991 SCALE 1:1 HX991R 200401 11 Made in China | Fabriqué en Chine Hecho en China FCC ID: 2ADZNHX991 IC: 20109-HX991 SCALE 1:1 HX991P 200401 11 Made in China | Fabriqué en Chine Hecho en China FCC ID: 2ADZNHX991 IC: 20109-HX991 SCALE 1:1 HX991S 200401 11 Made in China | Fabriqué en Chine Hecho en China FCC ID: 2ADZNHX991 IC: 20109-HX991 SCALE 1:1 HX991L 200401 11 Made in China | Fabriqué en Chine Hecho en China FCC ID: 2ADZNHX991 IC: 20109-HX991

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EMC Report for Philips Oral Healthcare, LLC on the Philips Sonicare DiamondClean File: 103985132MPK-001 Page 1 of 51 TEST REPORT Report Number: 103985132MPK-001 Project Number: G103985132 Original Issue Date: August 07, 2019 Revision Issue Date: March 26, 2020 Testing performed on Philips Sonicare DiamondClean Model Tested: HX991B, HX991W FCC ID: 2ADZNHX991 IC: 20109-HX991 to FCC Part 15 Subpart C (15.247) Industry Canada RSS-247 Issue 2 FCC Part 15, Subpart B Industry Canada ICES-003 For Philips Oral Healthcare LLC Test Performed by: Test Authorized by: Intertek 1365 Adams Court Menlo Park, CA 94025 USA Philips Oral Healthcare LLC 22100 Bothell Everett Highway Bothell, WA 98021 USA Prepared by: Date: August 07, 2019 Minh Ly Reviewed by: Date: August 07, 2019 Krishna K Vemuri This report is for the exclusive use of Intertek's Client and is provided pursuant to the agreement between Intertek and its Client. Intertek's responsibility and liability are limited to the terms and conditions of the agreement. Intertek assumes no liability to any party, other than to the Client in accordance with the agreement, for any loss, expense or damage occasioned by the use of this report. Only the Client is authorized to copy or distribute this report and then only in its entirety. Any use of the Intertek name or one of its marks for the sale or advertisement of the tested material, product or service must first be approved in writing by Intertek. The observations and test results in this report are relevant only to the sample tested. This report by itself does not imply that the material, product, or service is or has ever been under an Intertek certification program. This report must not be used to claim product endorsement by A2LA, NIST nor any other agency of the U.S. Government. EMC Report for Philips Oral Healthcare, LLC on the Philips Sonicare DiamondClean File: 103985132MPK-001 Page 2 of 51 Report No. 103985132MPK-001 Equipment Under Test: Philips Sonicare DiamondClean Trade Name: Philips Oral Healthcare LLC Model Tested Number: HX991B, HX991W Applicant: Philips Oral Healthcare LLC Contact: Matthew Vasa Address: Philips Oral Healthcare LLC 22100 Bothell Everett Highway Bothell, WA 98021 Country: USA Tel. Number: (425) 482-8367 Email: [email protected] Applicable Regulation: FCC Part 15 Subpart C (15.247) Industry Canada RSS-247 Issue 2 FCC Part 15, Subpart B Industry Canada ICES-003 Issue 6 Date of Test: July 11 – 26, 2019 We attest to the accuracy of this report: Mih Ly Project Engineer Krishna K Vemuri Engineering Team Lead EMC Report for Philips Oral Healthcare, LLC on the Philips Sonicare DiamondClean File: 103985132MPK-001 Page 3 of 51 TABLE OF CONTENTS 1.0 Summary of Tests .......................................................................................................................... 4 2.0 General Information ...................................................................................................................... 5 2.1 Product Description ............................................................................................................ 5 2.2 Related Submittal(s) Grants ................................................................................................ 6 2.3 Test Facility ........................................................................................................................ 6 2.4 Test Methodology ............................................................................................................... 6 2.5 Measurement Uncertainty ................................................................................................... 6 3.0 System Test Configuration ............................................................................................................ 7 3.1 Support Equipment ............................................................................................................. 7 3.2 Block Diagram of Test Setup .............................................................................................. 7 3.3 Justification ......................................................................................................................... 8 3.4 Software Exercise Program................................................................................................. 8 3.5 Mode of Operation during Test........................................................................................... 8 3.6 Modifications Required for Compliance ............................................................................ 8 3.7 Additions, Deviations and Exclusions from Standards ....................................................... 8 4.0 Measurement Results..................................................................................................................... 9 4.1 6- dB Bandwidth and 99% Occupied Bandwidth ................................................................ 9 4.2 Maximum Peak Conducted Output Power at Antenna Terminals .................................... 16 4.3 Maximum Power Spectral Density ................................................................................... 20 4.4 Out of Band Antenna Conducted Emission ...................................................................... 24 4.5 Transmitter Radiated Emissions ....................................................................................... 29 4.6 Radiated Emissions on Digital Parts ................................................................................. 43 4.7 AC Line Conducted Emission .......................................................................................... 48 5.0 List of Test Equipment ................................................................................................................ 49 6.0 Document History ........................................................................................................................ 50 Annex A - Duty Cycle Measurement .…

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EMC Report for Philips Oral Healthcare, LLC on the Philips Sonicare DiamondClean File: 103985132MPK-002 Page 1 of 25 TEST REPORT Report Number: 103985132MPK-002 Project Number: G103985132 August 02, 2019 Testing performed on the Philips Sonicare DiamondClean Model(s) Tested: HX991B, HX991W FCC ID: 2ADZNHX991 IC: 20109-HX991 to FCC Part 15 Subpart C (15.225) Industry Canada RSS-210 Issue 9 For Philips Oral Healthcare LLC Test Performed by: Test Authorized by: Intertek 1365 Adams Court Menlo Park, CA 94025 USA Philips Oral Healthcare LLC 22100 Bothell Everett Highway Bothell, WA 98021 Prepared by: Date: August 02, 2019 Minh Ly Reviewed by: Date: August 02, 2019 Krishna Vemuri This report is for the exclusive use of Intertek's Client and is provided pursuant to the agreement between Intertek and its Client. Intertek's responsibility and liability are limited to the terms and conditions of the agreement. Intertek assumes no liability to any party, other than to the Client in accordance with the agreement, for any loss, expense or damage occasioned by the use of this report. Only the Client is authorized to copy or distribute this report and then only in its entirety. Any use of the Intertek name or one of its marks for the sale or advertisement of the tested material, product or service must first be approved in writing by Intertek. The observations and test results in this report are relevant only to the sample tested. This report by itself does not imply that the material, product, or service is or has ever been under an Intertek certification program. This report must not be used to claim product endorsement by A2LA, NIST nor any other agency of the U.S. Government. EMC Report for Philips Oral Healthcare, LLC on the Philips Sonicare DiamondClean File: 103985132MPK-002 Page 2 of 25 Report No. 103985132MPK-002 Equipment Under Test: Philips Sonicare DiamondClean Trade Name: Philips Oral Healthcare LLC Model Tested: HX991B, HX991W Applicant: Philips Oral Healthcare LLC Contact: Matthew Vasa Address: Philips Oral Healthcare LLC 22100 Bothell Everett Highway Bothell, WA 98021 Country: USA Tel. Number: (425) 482-8367 Email: [email protected] Applicable Regulation: FCC Part 15 Subpart C (15.247) Industry Canada RSS-247 Issue 2 Date of Test: July 11 – 19, 2019 We attest to the accuracy of this report: Minh Ly Project Engineer Krishna K Vemuri Engineering Team Lead EMC Report for Philips Oral Healthcare, LLC on the Philips Sonicare DiamondClean File: 103985132MPK-002 Page 3 of 25 TABLE OF CONTENTS 1.0 Summary of Tests .......................................................................................................................... 4 2.0 General Description ....................................................................................................................... 5 2.1 Product Description ............................................................................................................ 5 2.2 Related Submittal(s) Grants ................................................................................................ 6 2.3 Test Methodology ............................................................................................................... 6 2.4 Test Facility ........................................................................................................................ 6 2.5 Measurement Uncertainty ................................................................................................... 6 3.0 System Test Configuration ............................................................................................................ 7 3.1 Support Equipment and description .................................................................................... 7 3.2 Block Diagram of Test Setup .............................................................................................. 7 3.3 Justification ......................................................................................................................... 8 3.4 Software Exercise Program ................................................................................................. 8 3.5 Mode of Operation during test ............................................................................................ 8 3.6 Modifications required for Compliance .............................................................................. 8 3.7 Additions, deviations and exclusions from standards ......................................................... 8 4.0 Measurement Results ..................................................................................................................... 9 4.1 Field Strength of Fundamental and Radiated Emissions Outside the band ........................ 9 4.1.1 Requirements ......................................................................................................... 9 4.1.2 Procedure ............................................................................................................. 10 4.1.3 Test Results .......................................................................................................... 11 4.2 Frequency Tolerance ......................................................................................................... 18 4.2.1 Requirement ........................................................................................................ 18 4.2.2 Procedure ............................................................................................................ 18 4.2.3 Test Results .......................................................................................................... 19 4.3 Occupied Bandwidth ......................................................................................................... 20 4.3.1 Requirements ....................................................................................................... 20 4.3.2 Procedure ..........................................…

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Test Setup Photo 15.247 Test Setup Photo ‐ FCC Part 15, Subpart B Test Setup Photo 15.225