2AYVT-E3PROEye Massager

90*100mm 128g C2S, 印刷颜色3252C+Black+连线哑油 风琴5折 This device was tested for typical body‐worn operations. To comply with RF exposure requirements, a minimum separation distance of 0cm must be maintained between the user’s body and the handset, including the antenna. Third‐party belt‐clips, holsters, and similar accessories used by this device should not contain any metallic components. Body‐worn accessories that do not meet these requirements may not comply with RF exposure requirements and should be avoided. Use only the supplied or an approved antenna. This device in compliance with the essential requirements and other relevant provisions of Directive 2014/53/EU. All essential radio test suites have been carried out. 1. CAUTION : RISK OF EXPLOSION IF BATTERY IS REPLACED BY AN INCORRECT TYPE. DISPOSE OF USED BATTERIES ACCORDING TO THE INSTRUCTIONS 2. The device complies with RF specifications when the device used at 0mm form your body EU Compliance Statement: SKG Health technology Co.,Ltd. Here by declares that this device is in compliance with essential requirements and other relevant provisions of the Directive 2014/53/EU. A copy of the EU Declaration of Conformity is available online at https://www.skg.com/pages/skg-declaration-of-conformity. This device complies with part 15 of the FCC Rules. Operation is subject to the condition that this device does not cause harmful interference (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Any changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment. NOTE: 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 off 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 different from that to which the receiver is connected. -- Consult the dealer or an experienced radio/TV technician for help. The device has been evaluated to meet general RF exposure requirement. The device can be used in portable exposure condition without restriction. - English: This device complies with Industry Canada licence-exempt RSS standard(s). Operation is subject to the following two conditions: (1) This device may not cause interference, and (2) This device must accept any interference, including interference that may cause undesired operation of the device. - French: Le présentappareilestconforme aux CNR d'Industrie Canada applicables aux appareils radio exempts de licence. L'exploitationestautorisée aux deux conditions suivantes: (1) l'appareil ne doit pas produire de brouillage, et (2) l'utilisateur de l'appareildoit accepter tout brouillageradioélectriquesubi, mêmesi le brouillageest susceptible d'encompromettre le fonctionnement. Old electrical appliances must not be disposed of together with the residual waste, but have to be disposed of separately. The disposal at the communa collecting point via private persons is for free. The owner of old appliances is responsible to bring the appliances to these collecting points or to similar collection points. With this little personal effort, you contribute to recycle valuable raw materials and the treatment of toxic substances. Caution: lf you experience skin irritation when using the body massager, please refrain from using it, and wait two to three days to see if your symptoms ease. lf symptoms persist or worsen, please consult a physician. lf you have eczema, allergies or asthma, you may be more likely to experience a skin irritation or allergy from using the massager. * The appliance it must only be supplied at safety extra low voltage corresponding to the marking on the appliance. * This appliance can be used by children aged from 8 years and above and persons with reduced physical, sensory or mental capabilities or lack of experience and knowledge if they have been given supervision or instruction concerning use of the appliance in a safe way and understand the hazards involved. *Children shall not play with the appliance. * Cleaning and user maintenance shall not be made by children without supervision. Product Disposal Precautions Please support the recycling of rechargeable batteries (lithium-ion batteries) Danger Warning Place the removed rechargeable battery out of the reach of infants to prevent accidental ingestion The lithium-ion battery used in this product is a valuable recyclable resource. Please remove the lithium-ion battery prior to disposal and hand over it to a professional organization capable of recycling and processing rechargeable batteries. The battery must be removed from the device before discarding the appliance. The device must be turned off before removing the battery. The battery should be disposed of safely. 1. Pry open the main unit's inner and outer shells using professional tools. 2. Unscrew the fixed screws of the internal bracket using a screwdriver. 3. Unscrew the screws at the circuit board. 4. Cut the battery leads using scissors. 5. Remove the battery. Do not throw into the fire or expose to excessive heat. Do not puncture with nails, subject to heavy imp…

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- SKG Health Technologies Co., Ltd. - The information provided in this letter is based on the referenced rule parts of Title 47 of the CFR as well as KDB 986446 D01. An expiration date for this letter does not exist. In case the U.S. agent changes, the grantee is obligated to notify the FCC within 30 days via the granting TCB. Federal Communications Commission Authorization and Evaluation Division Equipment Authorization Branch 7435 Oakland Mills Road Columbia, MD 21046 10/30/2023 U.S. Agent Designation [SKG Health Technologies Co., Ltd.] acknowledges their consent for the following contact located in the United States to act as their agent for service of process for the equipment for which authorization is sought (FCC ID: [2AYVT-E3PRO]): Name and company of U.S. agent: AOCE Corporation Inc. Physical U.S. address of agent: 6547 N Academy Bivd #2266，Colorado Springs， CO, 80918 United States FRN of U.S. agent: 0033401381 Email address of U.S. agent: [email protected] [AOCE Corporation Inc.] acknowledges their obligation to accept service of process on behalf of [SKG Health Technologies Co., Ltd.]. [SKG Health Technologies Co., Ltd.] with the FRN [0030525117] accepts its obligation to maintain an agent for service of process in the United States for no less than one year after either the grantee has permanentl y te rminated all marketing and importation of the applicable equipment within the U.S., or the conclusion of any Commission-related administrative or judicial proceeding involving the equipment, whichever is later. By signing this form, we confirm th e above and that we are aware of the application requirements listed under § 2.911(d)(7). Sincerely, Signature [Name] Henry Li [Title] Manager [Company] SKG Health Technologies Co., Ltd. Signature [Name of U.S. agent] Johnson.wang [Title of U.S. agent] Manager [Company of U.S. agent] AOCE Corporation Inc. 48_[mo del] US_Agent_2.911(d)(7) - U, V04

SKG Health Technologies Co., Ltd. The information provided in this letter is based on the referenced rule parts of Title 47 of the CFR as well as KDB 986446 D01. Federal Communications Commission Authorization and Evaluation Division Equipment Authorization Branch 7435 Oakland Mills Road Columbia, MD 21046 10/30/2023 To whom it may concern: We, [SKG Health Technologies Co., Ltd.], hereby certif y that the equipment for which authorization is sought (FCC ID: [2AYVT-E3PRO]) is not “covered” equipment prohibited from receiving an equipment authorization pursuant to § 2.903 of the FCC rules. We also certify that, as of the date of the fi lin g of the application, we are not identified on the Covered List (https://www.fcc.gov/supplychain/coveredlist ) as an entity producing “covered” equipment. By signing this form, we confirm the above and that we are aware of the application requirements listed under § 2.911(b) and (d)(5) and (6). Sincerely, Signature [Name] Henry Li [Title] Manager [Company] SKG Health Technologies Co., Ltd. 62_[model] CoveredEqu_2.911(d)(5)(i) and (ii) - U, V02

FCC ID: 2AYVT-E3PRO External ---------------- End ----------------

Label Location On EUT Label

FCC ID: 2AYVT-E3PRO Internal PCB ANT ---------------- End ----------------

RF EXPOSURE EVALUATION FCC ID: 2AYVT-E3PRO According to FCC 1.1310: The criteria listed in the following table shall be used to evaluate the environment impact of human exposure to radio frequency(RF) Radiation as specified in §1.1307(b): Routine SAR eva luation refers to that specifically required by §2.1093, using measurements or computer simulation. When routine SAR evaluation is not required, portable transmitters with output power greater than the applicable low threshold require SAR evaluation to qualify for TCB approval. Channel (MHz) Maximum output power (dBm) Tune up tolerance (dBm) Max Tune Up Power (dBm) Distance (mm) Calculation results Limit Operating Mode 2402 -4.23 -4.23±1 -3.23 5 0.147 3 BDR&EDR 2441 -4.35 -4.35±1 -3.35 5 0.144 3 2480 -3.25 -3.25±1 -2.25 5 0.188 3 2402 -3.37 -3.37±1 -2.37 5 0.180 3 2441 -3.47 -3.47±1 -2.47 5 0.177 3 2480 -2.41 -2.41±1 -1.41 5 0.228 3 2402 -2.98 -2.98±1 -1.98 5 0.196 3 2441 -3.10 -3.10±1 -2.10 5 0.193 3 2480 -2.07 -2.07±1 -1.07 5 0.246 3 Test Results: PASS.

Total or partial reproduction of this document without permission of the Laboratory is not allowed. Page 1 of 97 BTF Testing Lab (Shenzhen) Co., Ltd. F101, 201 and 301, Building 1, Block 2, Tantou Industrial Park, Tantou Community, Songgang Street, Bao'an District, Shenzhen, China RF Te st Report For Applicant Name: SKG Health Technologies Co., Ltd. Address: 23A Floor, Building 3, Zhongke R&D Park, No.009 Gaoxin South 1st Rd, High-tech Zone Community Yuehai Street, Nanshan District, Shenzhen, China EUT Name: Eye Massager Brand Name: N/A Model Number: E3 Pro Series Model Number: Refer to section 2 Issued By Company Name: BTF Testing Lab (Shenzhen) Co., Ltd. Address: F101, 201 and 301, Building 1, Block 2, Tantou Industrial Park, Tantou Community, Songgang Street, Bao'an District, Shenzhen, China Report Number: BTF230911R00101 Test Standards: 47 CFR Part 15.247 FCC ID: 2AYVT-E3PRO Test Conclusion: Pass Test Date: 2023-08-29 to 2023-09-14 Date of Issue: 2023-10-24 Prepared By: Chris Liu / Project Engineer Date: 2023-10-24 Approved By: Ryan.CJ / EMC Manager Date: 2023-10-24 Note: All the test results in this report only related to the testing samples. Which can be duplicated completely for the legal use with approval of applicant; it shall not be reproduced except in full without the written approval of BTF Testing Lab (Shenzhen) Co., Ltd., All the objections should be raised within thirty days from the date of issue. To validate the report, you can contact us. Test Report Number: BTF230911R00101 Total or partial reproduction of this document without permission of the Laboratory is not allowed. Page 2 of 97 BTF Testing Lab (Shenzhen) Co., Ltd. F101, 201 and 301, Building 1, Block 2, Tantou Industrial Park, Tantou Community, Songgang Street, Bao'an District, Shenzhen, China Revision History Version Issue Date Revisions Content R_V0 2023-10-24 Original Note: Once the revision has been made, then previous versions reports are invalid. Test Report Number: BTF230911R00101 Total or partial reproduction of this document without permission of the Laboratory is not allowed. Page 3 of 97 BTF Testing Lab (Shenzhen) Co., Ltd. F101, 201 and 301, Building 1, Block 2, Tantou Industrial Park, Tantou Community, Songgang Street, Bao'an District, Shenzhen, China Table of Contents 1 INTRODUCTION ..........................................................................................................................................5 1.1 Identification of Testing Laboratory ...............................................................................................5 1.2 Identification of the Responsible Testing Location ......................................................................5 1.3 Announcement .................................................................................................................................5 2 PRODUCT INFORMATION..........................................................................................................................6 2.1 Application Information ...................................................................................................................6 2.2 Manufacturer Information ................................................................................................................6 2.3 Factory Information .........................................................................................................................6 2.4 General Description of Equipment under Test (EUT) ................................................................... 6 2.5 Technical Information ......................................................................................................................6 3 SUMMARY OF TEST RESULTS .................................................................................................................7 3.1 Test Standards .................................................................................................................................. 7 3.2 Uncertainty of Test ...........................................................................................................................7 3.3 Summary of Test Result ..................................................................................................................7 4 TEST CONFIGURATION .............................................................................................................................8 4.1 Test Equipment List .........................................................................................................................8 4.2 Test Auxiliary Equipment ..............................................................................................................13 4.3 Test Modes ......................................................................................................................................13 5 EVALUATION RESULTS (EVALUATION) .................................................................................................14 5.1 Antenna requirement .....................................................................................................................14 5.1.1 Conclusion: ...........................................................................................................................14 6 RADIO SPECTRUM MATTER TEST RESULTS (RF) ...............................................................................15 6.1 Conducted Emission at AC power line ........................................................................................15 6.1.1 E.U.T. Operation: ..................................................................................................................15 6.1.2 Test Setup Diagram: .............................................................................................................15 6.1.3 Test Data: .............................................................................................................................16 6.2 Occup…

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version01 SKG Health Technologies Co., Ltd. Declaration concerning Antenna Specification It i s hereby declared that the product Model No.: E3 Pro FCC ID: 2AYVT-E3PRO fulfill s the requirement in FCC test relating to the antenna type. The device specified above confirms to the FCC recommendations for PCB antenna type(s) described below: Model No. of antenna: 2.4G ANT Type of antenna: PCB Antenna Gain of the antenna: -0.68 dBi Frequency range: 2400-2500 MHz The mounting of the antenna is fixed to the radio module and no other antenna should be used. Company name: SKG Health Technologies Co., Ltd. Address: 23A Floor, Building 3, Zhongke R&D Park, No.009 Gaoxin South 1st Rd, High-tech Zone Community Yuehai Street, Nanshan District, Shenzhen, China City: Shenzhen ZIP / Postal code: Country: China Place: Place: Date: 2023-10-30 Signature:

InvertedFAntennaSpecification Summary AntennaPhoto&Length(mm) ITEMANTSPEC ModelName2.4GANT Center Frequency HorizontalVertical 2400MHz2450MHz2500MH2400MHz2450MHz2500MH -1.20-0.75-0.68-5.20-2.40-1.85 MAX.Gain-0.68dB PolarizationHorizontalandVertical Horizontaland Vertical Omni-directional Impedance0Ohm AntennaLength27.8mm ManufactureHuizhouhuiqielectronicsCO.,LTD Horizontal:2400MHz2450MHz2500MHz Power(dBm) Max:0Min:-40Scale:5/div Vertical:2400MHz2450MHz2500MHz Power(dBm) Max:0Min:-30Scale:5/div

FCC ID: 2AYVT-E3PRO Conducted Emission at AC power line Emissions in restricted frequency bands (below 1GHz) Emissions in restricted frequency bands (above 1GHz)