2AGNA-20400Facial Toning Device

Proyecto Gosling_ Manual de estudio de usabilidad DESCRIPTION ‘Petite Facial Toning Device’ DESCRIPCIÓN 'Pequeño dispositivo de tonificación facial' ‘USER MANUAL ENSURE YOUR BEST RESULTS’ 'MANUAL DEL USUARIO ¡OBTENGA LOS MEJORES RESULTADOS!' Proyecto Gosling_ Manual de estudio de usabilidad ENGLISH ESPAÑOL TABLE OF CONTENTS TABLA DE CONTENIDO GETTING TO KNOW YOUR DEVICE CONOCIENDO SU DISPOSITIVO WELCOME BIENVENIDO IMPORTANT INFORMATION INFORMACIÓN IMPORTANTE CONTRAINDICATIONS FOR USE CONTRAINDICACIONES DE USO WARNINGS ADVERTENCIAS PRECAUTIONS PRECAUCIONES GETTING STARTED CÓMO EMPEZAR HOW TO USE YOUR Mini DEVICE CÓMO UTILIZAR SU DISPOSITIVO Mini TREATMENT FREQUENCY FRECUENCIA DE TRATAMIENTO RESULTS RESULTADOS CARING FOR YOUR Mini DEVICE CUIDADOS DE SU DISPOSITIVO Mini WARRANTY GARANTÍA SYMBOLS SÍMBOLOS GENERAL SPECIFICATIONS ESPECIFICACIONES GENERALES CONOCIENDO SU DISPOSITIVO Proyecto Gosling_ Manual de estudio de usabilidad 1) Spheres (electrodes) 2) Intensity Level Indicator 3) Dual Function Power Button: ON/OFF + Intensity Control Up/Down 4) NuFACE Microcurrent Gel 1.69 fl oz / 50 mL ESPAÑOL 1. Esferas (electrodos) 2. Indicador de nivel de intensidad 3. Botón de encendido doble función: ENCENDIDO/APAGADO + Control de intensidad Arriba/Abajo 4. NuFACE Cloud Gel 1.69 fl oz / 50 mL 1 3 2 4 Proyecto Gosling_ Manual de estudio de usabilidad ENGLISH ESPAÑOL WELCOME TO NuFACE® Congratulations on receiving your Mini Device! BIENVENIDO A NuFACE® ¡Felicitaciones por recibir su Mini Dispositivo! We’re excited that you’ll now be able to enjoy the powerful benefits of a 5-Minute Facial-Lift® — anytime, anywhere. Nos complace saber que a partir de ahora podrá disfrutar de los poderosos beneficios de un 5-Minute Facial- Lift® en cualquier momento, en cualquier lugar. Mini’s results are both instant and cumulative, so don’t forget to track your progress. We recommend taking before and after photos and sharing your results by tagging us at @MyNuFACE so we can follow in your skincare journey. Los resultados del Mini son instantáneos y acumulativos, por lo que no olvide de hacer un seguimiento de su progreso. Recomendamos tomar fotos antes y después y compartir sus resultados etiquetándonos en @MyNuFACE para que podamos acompañarle en el cuidado de su piel. Have an uplifting day, Your NuFACE Family ¡Que tenga un día tonificante! Su familia NuFACE Proyecto Gosling_ Manual de estudio de usabilidad ENGLISH ESPAÑOL INTENDED USE USO PREVISTO The NuFACE Mini Device is intended for facial and neck stimulation and is indicated for over-the- counter cosmetic use. El dispositivo NuFACE Mini está diseñado para la estimulación del rostro y del cuello y está indicado para uso cosmético sin receta. IMPORTANT INFORMATION INFORMACIÓN IMPORTANTE • Use the Mini Device only as described within this User Manual. The risks and dangers of using the Mini Device in any way that does not follow this User Manual might be unknown. • Utilice el dispositivo Mini solo como se describe en este Manual del usuario. Se desconocen los riesgos y peligros de usar el dispositivo Mini de cualquier otro modo diferente al consignado en este manual. • Your NuFACE Mini Device has two unique serial number located on the bottom of the device. Record your serial number and register your device online at www.MyNuFACE.com. A registration link can be found at the bottom of the webpage. • Su dispositivo Mini NuFACE tiene dos números de serie únicos ubicados en la parte inferior del mismo. Tome nota de su número de serie y registre su dispositivo en línea en www.MyNuFACE.com. Encontrará un enlace de registro en la parte inferior de la página web. CONTRAINDICATIONS FOR USE CONTRAINDICACIONES PARA EL USO • Do not use this device if you have a history of epilepsy or seizures. • No use este dispositivo si tiene antecedentes de epilepsia o convulsiones. • Do not use if you have had recent surgery or other surgical procedures. • No lo use si ha tenido una cirugía reciente u otros procedimientos quirúrgicos. • Do not use if you have an electronic implanted device such as a defibrillator, neurostimulator, • No lo use si tiene un dispositivo electrónico implantado, como un desfibrilador, neuroestimulador, pacemaker, or ECG Monitor. If you use a body-worn medical device, such as an insulin pump, marcapasos o monitor de ECG. Si usa un dispositivo médico en el cuerpo, tal como una bomba de insulina, consult your healthcare provider. consulte a su médico. • Do not use if you have any active cancer or over any suspicious or cancerous lesion. • No lo use si tiene algún cáncer activo o sobre cualquier lesión sospechosa o cancerosa. • Do not use if you are pregnant. The safety of electrical stimulation during pregnancy has not • No lo use si está embarazada. No se ha probado la seguridad de la estimulación eléctrica been established. durante el embarazo. Proyecto Gosling_ Manual de estudio de usabilidad • Do not use on infants and children under the age of 18. • No lo use en bebés y menores de 18 años. *Consult your healthcare provider if any of the contraindications above apply to you. * Consulte a su médico si se aplica a su caso alguna de las contraindicaciones anteriores. WARNINGS ADVERTENCIAS • If you are under the care of a physician, consult your physician before using this device. • Si está bajo el cuidado de un médico, consúltelo antes de usar este dispositivo. • Discontinue using the device and consult your healthcare provider if you experience an adverse • Deje de usar el dispositivo y consulte a su médico si experimenta una reaction from using the device. reacción adversa al utilizarlo. • Apply stimulation only to normal, intact, clean, healthy skin. Do not use over swollen, infected, • Aplique estimulación solo a la piel normal, sin lesiones, limpia y saludable. No lo use sobre áreas de piel hinchadas, infectadas, or inflamed areas or skin eruptions, e.g., phlebitis, thrombophlebitis, broken capillaries, varicose inflamadas o sobre erupciones cutáneas tales…

Text truncated - open the document above for the full version.

Date: 05/28/20 Carol Cole Company dba NuFACE 1325 Sycamore Ave Suite A Vista, CA 92081, USA FCC ID: 2AGNA-20400 IC ID: 25861-20400 REQUEST FOR CONFIDENTIALITY Pursuant to Sections §§ 0.457(d) and 0.459 of the FCC Rules and Industry Canada Regulations, the applicant hereby requests that the following documents be held under confidentiality. LONG TERM: 1. Schematics 2. Block Diagram 3. Operational Description 4. Parts List / Tune Up 5. Internal Photos Special Conditions: Internal Photos are requested to be held long term confidential as the circuit board and internal components are sealed within the enclosure with a weld and are not accessible to users. SHORT TERM: for the period of 180 days (not to exceed 180). 1. External Photos 2. Test Setup Photos The above information contains trade secrets and proprietary information not customarily released to the public. The public disclosure of this information might be harmful to the applicant and provide unjustified benefits to its competitors. Sincerely, ___________________ Bryan Miller CFO/COO Carol Cole Company dba NuFACE

External Photos – Front, Back, Right side, Left side, bottom and top ,

ONE WORLD  OUR APPROVAL www.nemko.com KDB 447498 D01 General RF Exposure Guidance v06 (October 23, 2015) 1. Declaration of RF exposure compliance for exemption from routine evaluation limits FCC ID: 2AGNA-20400 Model number: 20400 Manufacturer: Carol Cole Company 4.3.1. Standalone SAR test exclusion considerations: During normal operation, user extremities can come within 20 cm of the internal antenna and therefore product is considered as “Portable”. The 1-g and 10-g SAR test exclusion thresholds for 100 MHz to 6 GHz at Test separation distances ≤ 50 mm are determined by: [(max. power of channel, including tune-up tolerance, mW) ÷ (min. test separation distance, mm)] × [ √ 퐹(퐺퐻푧)] ≤ 3.0 for 1-g SAR and ≤ 7.5 for 10-g extremity SAR, where f(GHz) is the RF channel transmit frequency in GHz Power and distance are rounded to the nearest mW and mm before calculation The result is rounded to one decimal place for comparison The test exclusions are applicable only when the minimum test separation distance is ≤ 50 mm and for transmission frequencies between 100 MHz and 6 GHz. When the minimum test separation distance is < 5 mm, a distance of 5 mm according to 5) in section 4.1 is applied to determine SAR test exclusion Calculation based on the above formula: Separation Distance = 5 mm EIRP Output Power = 4.87 dBm = 3.07 mW Frequency = 2402 GHz Calculation = (3.07÷5)× √ 2.402 = .952 < 3 The calculation is below the threshold, therefore the product exempt from the SAR test requirements 2. Attestation ATTESTATION: I attest that the testing was performed or supervised by me; that the test measurements were made in accordance with the above-mentioned departmental standard(s), and that the radio equipment identified in this application has been subject to all applicable test conditions specified in the departmental standards and all of the requirements of the standards have been met. Signature: Date: July 23, 2020 Name: Chip Fleury, Wireless and Certification Supervisor SAR Exclusion

Report reference ID: 388354 - 1TRFWL Page 1 of 36 ONE WORLDOURAPPROVAL Test report 388354 – 1TRFWL Date of issue: January 7, 2020 Applicant: Carol Cole Company dba NuFace Product: Mini 2.0 (Facial Toning Device) Model: Variants: 20400 N/A FCC ID: 2AGNA-20400 IC ID: 25861-20400 Specifications:  FCC 47 CFR Part 15 Subpart C, §15.247 Operation in the 902–928 MHz, 2400–2483.5 MHz, 5725–5850 MHz  RSS-247, Issue 2, February 2017 Digital Transmission Systems (DTSs), Frequency Hopping Systems (FHSs) and License-Exempt Local Area Network (LE-LAN) Devices Report reference ID: 388354 - 1TRFWL Page 2 of 36 Test location: Company name Nemko USA, Inc. Address 2210 Faraday Ave, Suite 150 City Carlsbad Province California Postal code 92008 Country USA Telephone +1 760 444 3500 Website www.nemko.com Site number FCC: US5058; IC: 2040B-3 Tested by Andres Martinez, Wireless Engineer Reviewed by Chip Fleury, Wireless and Certification Supervisor. Review date January 7, 2020 Reviewer signature Limits of responsibility Note that the results contained in this report relate only to the items tested and were obtained in the period between the date of initial receipt of samples and the date of issue of the report. This test report has been completed in accordance with the requirements of ISO/IEC 17025. All results contain in this report are within Nemko USA’s ISO/IEC 17025 accreditation. This report must not be used by the client to claim product certification, approval, or endorsement by NVLAP, NIST, or any agency of the U.S. Government. Copyright notification Nemko USA Inc. authorizes the applicant to reproduce this report provided it is reproduced in its entirety and for use by the company’s employees only. Any use which a third party makes of this report, or any reliance on or decisions to be made based on it, are the responsibility of such third parties. Nemko USA Inc. accepts no responsibility for damages, if any, suffered by any third party as a result of decisions made or actions based on this report. © Nemko USA Inc. Report reference ID: 388354 - 1TRFWL Page 3 of 36 Table of contents Table of contents .......................................................................................................................................................................................................... 3 Section 1. Report summary ................................................................................................................................................................................. 4 1.1 Applicant and manufacturer .................................................................................................................................................................................... 4 1.2 Test specifications .................................................................................................................................................................................................... 4 1.3 Test methods ............................................................................................................................................................................................................ 4 1.4 Statement of Compliance ......................................................................................................................................................................................... 4 1.5 Exclusions ................................................................................................................................................................................................................. 4 1.6 Test report revision history ...................................................................................................................................................................................... 4 Section 2. Summary of test results ....................................................................................................................................................................... 5 2.1 FCC Part 15 Subpart C, general requirements test results ........................................................................................................................................ 5 2.2 FCC Part 15 Subpart C, intentional radiators test results.......................................................................................................................................... 5 2.4 IC RSS-GEN, Issue 5, test results ............................................................................................................................................................................... 5 2.5 IC RSS-247, Issue 2, test results ................................................................................................................................................................................ 6 Section 3. Equipment under test (EUT) details ..................................................................................................................................................... 7 3.1 Sample information .................................................................................................................................................................................................. 7 3.2 EUT information ....................................................................................................................................................................................................... 7 3.3 Technical information .............................................................................................................................................................................................. 7 3.4 Product description and theory of operation ........................................................................................................................................................... 7 3.5 EUT exercise details ..............…

Text truncated - open the document above for the full version.