2A7ZX2002BIO1Contactless vital sign detection sensor

Let’s get sleeping. Allons dormir. Set up your RemWave Sleep Sensor. Configurez votre capteur de sommeil RemWave. 2. 3. 4. 1. Create an account. Créer un compte. Download the RemWave Sleep app in the App Store or Google Play store. Téléchargez l’application RemWave Sleep. Tap Add Sensor. Appuyez sur Ajouter un capteur. Follow the in-app instructions to setup your sensor. Suivez les instructions de l’application pour configurer votre capteur What’s included. Ce qui est inclu 1 RemWave Sleep Sensor 1 capteur de sommeil RemWave 1 Power Supply and cord 1 Alimentation et câble 4 | EN We’re here for you. Online help and support: biofi.com/help Requirements, Safety, Warranty & Regulatory Guide for RemWave Sleep REQUIREMENTS The RemWave Sleep sensor requires a 2.4 GHz Wi-Fi network, a working broadband internet connection with at least 2 Mbps upload speed (DSL may not qualify), a compatible mobile device, the free RemWave Sleep app, and a RemWave account Minimum requirements are available at biofi.com/ requirements. Live biometric data, phone alerts, and history may be subject to interruptions or failures for reasons beyond Praesidium’s control, like intermittent Wi-Fi or service provider outages. Subscription(s) may be required for some features, and terms, conditions, and/or charges may apply. All features, functionality, and other product specifications are subject to change without notice or obligation. SAFETY Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment. This device should be operated with a minimum separation distance of 20 cm (8 inches) between the equipment and a person’s body and minimum separation distance of 7 cm (3 inches) between the sensor and any object. EN | 5 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: 1. Reorient or relocate the receiving antenna. 2. Increase the separation between the equipment and receiver. 3. Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. 4. Consult the dealer or an experienced radio/TV technician for help. For additional safety information visit: biofi.com/safety WARRANTY For warranty information visit: biofi.com/warranty 6 | EN REGULATORY INFORMATION (E-LABEL) Details about your devices regulatory certifications are viewable in the RemWave Sleep app. To view your device details and regulatory certifications follow these steps after adding the device to your account: Tap Account > Devices > Select a device from the list to view the regulatory information. FCC COMPLIANCE STATEMENT 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 CANADA COMPLIANCE STATEMENT This device complies with ISED 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. MEDICAL DEVICE INTERFERENCE This device contains components and radios that emit electromagnetic fields. These electromagnetic fields may interfere with medical devices, such as pacemakers and defibrillators. Consult your physician and medical device manufacturer for information specific to your medical device and whether you need to maintain a safe distance of separation between your medical device and this device. Stop using this device if you suspect it is interfering with your medical device. NOT A MEDICAL DEVICE This device is not a medical device and should not be used as a substitute for professional medical judgment. It is not designed or intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment, or prevention of any condition or disease. Please consult your healthcare provider prior to making any decisions related to your health. 8 | FR Exigences, sécurité, garantie et guide réglementaire pour RemWave Sleep CONDITIONS Le capteur de sommeil RemWave nécessite un réseau 2.4 GHz Wi-Fi, une connexion Internet haut débit fonctionnelle avec une vitesse de téléchargement d’au moins 2 Mbps (DSL peut ne pas être admissible), un appareil mobile compatible, l’application gratuite RemWave Sleep et un compte RemWave. Les exigences minimales sont disponibles sur biofi.com/requirements. Les données biométriques en direct, les alertes téléphoniques et l’historique peuvent faire l’objet d’interruptions ou de pannes pour des raisons indépendantes de la volonté de Praesidium, telles que des interruptions intermittentes du Wi-Fi ou des fournisseurs de services. Un ou plusieurs abonnements peuvent être requis pour certaines fonctionnalités, et des termes, conditions et/ou frais peuvent s’appliquer. Toutes les caractéristiques, fonctionnalités et autres spécifications du produit sont susceptibles d’être modifiées sans préavis ni obligation. SÉCURITÉ Les changements ou modifications non expressément approuvés par la partie responsable de la conformité pourraient annuler l’…

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150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Letter of Authorization and Anti- Drug Statement Applicant Name: Praesidium Inc. Address: 150 N 200 E, Ste 200, St. George, UT 84770 Product Name: BioFi Sleep Sensor Model Number: 2002BIO1 FCC ID: 2A7ZX2002BIO1 We authorize: CETECOM Inc., to act on our behalf on all matters concerning the above named equipment. We declare that CETECOM Inc. is allowed to forward all information related to the approval project to the Federal Communications Commission and discuss any issues concerning the approval application. The applicant must certify that neither the applicant nor any party to the application is subject to a denial of Federal benefits, that include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. § 862 because of a conviction for possession or distribution of a controlled substance. See 47 CFR 1.2002(b) for the definition of a "party" for these purposes. Does the applicant or authorized agent so certify? ☒ Yes I certify that I am authorized to sign this application. All of the statements herein and the exhibits attached hereto, are true and correct to the best of my knowledge and belief. In accepting a Grant of Equipment Authorization as a result of the representations made in this application, the applicant is responsible for (1) labeling the equipment with the exact FCC ID specified in this application, (2) compliance statement labeling pursuant to the applicable rules, and (3) compliance of the equipment with the applicable technical rules. If the applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production units of this equipment will continue to comply with the FCC's technical requirements. Authorizing an agent to sign this application, is done solely at the applicant's discretion; however, the applicant remains responsible for all statements in this application. If an agent has signed this application on behalf of the applicant, a written letter of authorization which includes information to enable the agent to respond to the above section 5301 (Anti-Drug Abuse) Certification statement has been provided by the applicant. It is understood that the letter of authorization must be submitted to the FCC upon request, and that the FCC reserves the right to contact the applicant directly at any time. Signature of Authorized Person Filing: Title: Date: VP of Operations 2/17/2023

150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Praesidium Inc. 150 N 200 E Suit e 200 St. George, Utah 84770 Federal Communication Commission 7435 Oakland Mills Road Columbia, MD 21046 13 February 2023 Attestation Statement according to 2.911(d)(5)(i) and 2.911(d)(5)(ii) FCC ID: 2A7ZX2002BIO1 TO WHOM IT MAY CONCERN: Hereby we certify 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. Further we certify that, as of the date of the filing of the application, Praesidium Inc. is not identified on the Covered List as an entity producing “covered” equipment. Sincerely, _______________ (signature & company stamp) Praesidium Inc. 150 N 200 E, Suite 200 St. George, Utah 84770 Kelli Klunder [email protected] 435-237-0530 For information on Covered equipment, refer: • 986446 D01 Covered Equipment v01 • FCC 22-84

150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Praesidium Inc. 150 N 200 E S uit e 200, St. George, Utah 84770 Federal Communication Commission Authorization and Evaluation Division 7435 Oakland Mills Road Columbia, MD 21046 USA 29 March 2023 Attestation Statement according to 2.911(d)(7) FCC ID: 2A7ZX2002BIO1 TO WHOM IT MAY CONCERN: Praesidium Inc. with FCC Registration Number (FRN) 0032683732 Certifies that, as of the date of this filing of the application with the TCB, Praesidium Inc. is our designated US agent for service of process for the above referenced FCC ID. Praesidium Inc. accepts 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 equipment. Praesidium Inc. with FCC Registration Number (FRN) 0032683732 Accepts, as of the date of the filing of the application, the obligation of the designated US agent for service of process for the above referenced FCC ID. Sin cerely, _______________ (signature & company stamp) P raesidium Inc. 150 N 200 E, Suite 200 St. George, Utah 84770 Kelli Klunder [email protected] 435-237-0530

150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Federal Communications Commission Equipment Authorization Division 7435 Oakland Mills Road Columbia, MD 21048 Date: 16 September 2022 Subject: Request for Permanent Confidentiality FCC ID: 2A7ZX2002BIO1 To Whom It May Concern: In accordance with §0.457(d) and §0.459 of CFR 47, and KDB 726920, Praesidium Inc. hereby requests permanent confidentiality for documents filed under the following exhibit types: 1. Block Diagram 2. Schematic Diagram 3. Part List 4. Operational Description These items contain detailed system and equipment description and related information about the product which Praesidium Inc. considers to be proprietary, confidential and a custom design which otherwise would not be released to the general public. Since this design is a basis from which future technological products will evolve, Praesidium Inc. also feels that this information would be of benefit to its competitors, and that the disclosure of the information in these exhibits would give our competitors an unfair advantage in the market. We are aware that exhibit types cover letters, attestations, label document, test reports, RF exposure information (SAR and MPE reports), cannot be requested to be classified confidential and are thus subject to publication, as will be documents of all other exhibits types for which we have not requested a confidentiality classification. Best Regards, Signature: ________________________ Name: Kelli Klunder Title: VP of Operations Company Name: Praesidium Inc. Address: 150N 200 E, Ste 200, St. George, UT 84770

150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Federal Communications Commission Equipment Authorization Division 7435 Oakland Mills Road Columbia, MD 21048 Date: 16 September 2022 Subject: Request for Short Term Confidentiality FCC ID: 2A7ZX2002BIO1 To Whom It May Concern: In accordance with §0.457(d) and §0.459 of CFR 47, Praesidium Inc. hereby requests short term confidentiality for documents filed under the following exhibit types: 1. External Photographs 2. Internal Photographs 3. User / Instruction Manual 4. Test Set-up Photographs Until the product will be publicly announced. Short term confidentiality release date / period: 180 days from grant issue date. These items contain detailed system and equipment description and related information about the product which Praesidium Inc. considers to be proprietary, confidential and a custom design which otherwise would not be released to the general public. Since this design is a basis from which future technological products will evolve, Praesidium Inc. also feels that this information would be of benefit to its competitors, and that the disclosure of the information in these exhibits would give our competitors an unfair advantage in the market. We are informed and aware of our obligation that we have to inform the involved TCB in written and in due time if we intend to market the product prior to the above specified confidentiality release date so that the short term confidentiality classification can be reset prior to product launch. We are aware that exhibit types cover letters, attestations, label document, test reports, RF exposure information (SAR and MPE reports), cannot be requested to be classified confidential and are thus subject to publication, as will be documents of all other exhibits types for which we have not requested a confidentiality classification. Page 2 Best Regards, Signature: __________________________ Name: Kelli Klunder Title: VP of Operations Company Name: Praesidium Inc. Address: 150N 200 E, Ste 200, St. George, UT 84770

150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Company Name: Praesidium Inc. Address: 150 N 200 E Suit e 200 St. George, Utah 84770 Model: 2002BIO1 FCC: 2A7ZX2002BIO1 IC: 28837-2002BIO1 External Photos Page 2 Page 3 Page 4 Page 5 Page 6 Page 7

150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Company Name: Praesidium Inc. Address: 150 N 200 E Suit e 200 St. George, Utah 84770 Model: 2002BIO1 FCC: 2A7ZX2002BIO1 IC: 28837-2002BIO1 Description of E-Label This model is applied E-label, please find description of E-label below. 1. FCC ID(E-label): Account > Devices > [Device Name] Page 2 2. Instruction of E-label in the User Manual (printed manual) 150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Company Name: Praesidium Inc. Address: 150 N 200 E Suit e 200 St. George, Utah 84770 Model: 2002BIO1 FCC: 2A7ZX2002BIO1 IC: 28837-2002BIO1 S UBJECT: E- Label Statement To Whom it May Concern: We hereby provide the following attestations according to CFR 2.935 and FCC KDB 784748 D02: At the time of purchase, the FCC ID is readily and physically visible to the purchaser on the exterior package per 2.935(d). The FCC ID will be readily legible without the aid of magnification according to 2.935(a). The literature in the package describes how to access the electronic display to find the FCC ID per 2.935(e) and FCC KDB 784748. The user will be able to access this information within a maximum of 3 steps. We, Praesidium Inc. have programmed the e-label and it is not able to be modified by any third party. The user will be able to access this information without a SIM card, special accessories, or supplemental plug-ins. The FCC ID will be able to survive normal shipping and handling, so it is visible for inspection at the time of import. Should you have any questions or comments concerning the above, please contact the undersigned. Sincerely, Signature: __________________________ Name: Kelli Klunder Title: VP of Operations Company Name: Praesidium Inc. Address: 150N 200 E, Ste 200, St. George, UT 84770 150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Company Name: Praesidium Inc. Address: 150 N 200 E Suit e 200 St. George, Utah 84770 Model: 2002BIO1 FCC: 2A7ZX2002BIO1 IC: 28837-2002BIO1 Label and Location 38.1mm x 12.7mm 38.1mm x 12.7mm DURABLE PORTFOLIO Product Data Sheet Fasson® 2 Mil White Polyester TC/S8001/50#SCK Spec#: 78385 Facestock Facestock physical properties 2 Mil White Polyester TC is a homogeneously pigmented white facestock featuring excellent tear strength, heat resistance, dimensional stability, opacity, and chemical resistance. Imperial Value Units Metric Value Units Caliper: ASTM D1000 0.0020 inches 50.80 micron Tensile: ASTM D882 MD 21,300 PSI 1,497 kg/cm2 CD 28,400 PSI 1,997 kg/cm2 Adhesive Adhesive physical properties S8001 is a high performance, clear permanent emulsion acrylic pressure sensitive adhesive with balanced adhesion to a wide variety of substrates, including low surface energy plastics, engineering grade plastics, bare, coated, or painted metals, including powder coat and enamel paints. It features medium tack and excellent chemical and UV resistance for outdoor industrial applications. Imperial Value Units Metric Value Units Type:Emulsion Acrylic Caliper: ASTM D1000 0.0010 inches 25.40 microns Standard Coat Wt:27 g/sq m Minimum Appl Temp:50 F 10 C Service Temp Range: Min -40 F -40 C Max 302 F 150 C Loop Tack Stainless Steel: PSTC11 32.0 oz/inch 35.2 N/100 mm Liner Liner physical properties 50# SCK is a bleached, super calendered paper stock with very good die-cutting and matrix stripping properties. Used for standard roll-to-roll applications. Not recommended for sheeting. Imperial Value Units Metric Value Units Caliper: ASTM D1000 0.0032 inches 81.2800 micron Basis Wt: TAPPI T410 * (24" x 36" 500 sheets) 54.5 lbs/ream87.2 g/sq m Tensile: ASTM D882 MD 48.0 lbs/inch 211.2 N/25 mm CD 26.0 lbs/inch 114.4 N/25 mm Tear: TAPPI T414 MD 1.8 ounces 51.1 grams CD 2.1 ounces 59.6 grams Liner Release: TMLI 90 o removal of Liner from Facestock. Total Construction Caliper (approximate): Rate of Removal Grams/2" Width 400 inches/min. 30 0.006 inches (6 mils; 152 microns) Page 1 of 7Durable Form 08/05/2013http://na1.fasson.com/frna/Prod_sht.nsf/FRNA/Prod_sht.nsf/A847FCD076183FB288257 ... Features and Benefits Opaque white facestock with very good hiding power and physical strength Glossy clear top coat that accepts most flexographic, letterpress, and rotary screen inks. Excellent thermal transfer printability with some resin enhanced wax, and most resin based ribbons. Excellent chemical resistance and good outdoor durability UL and c-UL Recognized. See files MH8212 and MH17205 for specific details on recognized conditions Applications and Uses Suitable for a variety of durable labeling applications such as: Product identification Barcodes WIP (Work-in-process) tracking labels Asset tags Printing and Converting The top coat is designed for printing by most solvent, UV cured, and water-based flexographic inks; UV cured letterpress and rotary screen inks. Specially formulated inks are not normally necessary, however, testing is recommended prior to final ink system selections. The following press inks are UL Recognized at 150ºC (302ºF) without the need for overlaminations. Color recognitions or restrictions and additional chemical resistances are noted for each ink system: ► Water-based flexogrphic inks with lube oil resistance: Environmental Inks & Coatings' "DR III FR" {recognized in all colors for indoor use, blue and black for outdoor use}, "Aqua Plus" and "Aqua Film III" {recognized for indoor use in blue, black, and red, for outdoor use in blue and black}; Flint Ink's "HydroFilm ACE" {recognized in blue, black, and red for indoor and outdoor use}; and ACTEGA WIT, Inc. "Versifilm Plus ULF" {recognized in all colors for indoor and outdoor use}, and "Water Gloss" {recognized in all colors for indoor and outdoor use}. ► UV flexographic inks with lube oil and gas splash resistance: Environmental Inks & Coatings' "UltraFlex III SFR" {recognized in all colors for indoor use; blue, black an…

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150 N 200 E, Suite 200, St George, Utah 84770 www.Biofi.Tech 435.237.0530 [email protected] Company Name: Praesidium Inc. Address: 150 N 200 E Suit e 200 St. George, Utah 84770 Model: 2002BIO1 FCC: 2A7ZX2002BIO1 IC: 28837-2002BIO1 Internal Photos Page 2 Page 3 Page 4 Page 5 Page 6

A2LA Accredited IC recognized # 3462B CETECOM Inc. 411 Dixon Landing Road  Milpitas, CA 95035  U.S.A. Phone: + 1 (408) 586 6200  Fax: + 1 (408) 586 6299  E-mail: [email protected]  http://www.cetecom.com CETECOM Inc. is a Delaware Corporation with Corporation number: 2905571 © Copyright by CETECOM Radio Frequency Exposure Evaluation Report For: Praesidium Inc. Model Name: 2002BIO1 Product Description: Contactless vital sign detection sensor FCC ID: 2A7ZX2002BIO1 IC: 28837-2002BIO1 Applied Rules and Standards: CFR Part1 (1.1307 & 1.1310), Part 2 (2.1091), FCC KDB 447498 D01 General RF Exposure Guidance v06 Report #: EMC_PRAES_002-23001_MPE_FCC_ISED DATE: 2023-03-30 Test Report #: EMC_PRAES_002-23001_MPE_FCC_ISED FCC ID: 2A7ZX2002BIO1 Date of Report 2023-03-30 Page 2 of 8 IC: 28837-2002BIO1 Page 2 of 8 TABLE OF CONTENTS 1 Assessment ................................................................................................................................................ 3 2 Administrative Data .................................................................................................................................... 4 2.1 Identification of the Testing Laboratory Issuing the Test Report ..................................................... 4 2.2 Identification of the Client / Manufacturer .................................................................................... 4 2.3 Identification of the Manufacturer ............................................................................................... 4 3 Equipment under Assessment .................................................................................................................... 5 4 RF Exposure Limits and FCC Basic Rules ................................................................................................. 6 4.1 FCC 1.1310((3)(i)(C) Table 1 – Exemption Threshold .................................................................. 6 4.2 RSS-102 2.5.2 Exemption Limits for Routine Evaluation — RF Exposure Evaluation ...................... 6 4.3 RF Exposure Estimation (MPE Estimation) ................................................................................. 6 5 Evaluation .................................................................................................................................................. 7 5.1 Analysis to Exclude Routine RF Exposure evaluation for Co-transmission Operation ...................... 7 6 Revision History ......................................................................................................................................... 8 Test Report #: EMC_PRAES_002-23001_MPE_FCC_ISED FCC ID: 2A7ZX2002BIO1 Date of Report 2023-03-30 Page 3 of 8 IC: 28837-2002BIO1 Page 3 of 8 1 Assessment This RF Exposure evaluation report, provides evidence for compliance of the below identified device, with the RF Exposure limits for mobile devices, as defined in FCC CFR Part1 (1.1307 & 1.1310), Part 2 (2.1091), under worst case conditions (measured or rated RF output power, antenna gain, distance towards human body. Multiple transmitter information as presented by the applicant). In addition, maximum antenna gain, or minimum distance towards the human body calculated respectively where relevant. The device meets the limits as stipulated by the above given FCC and IC rule parts based on available specifications for worst case conditions at 20 cm distance to the body. Company Description Model Name Praesidium Inc. Contactless vital sign detection sensor 2002BIO1 Responsible for Testing Laboratory: 2023-03-30 Compliance Stoecker, Arndt (Director of Regulatory Services) Date Section Name Signature Responsible for the Report: 2023-03-30 Compliance Huang, Guangcheng (Senior EMC Engineer) Date Section Name Signature Test Report #: EMC_PRAES_002-23001_MPE_FCC_ISED FCC ID: 2A7ZX2002BIO1 Date of Report 2023-03-30 Page 4 of 8 IC: 28837-2002BIO1 Page 4 of 8 2 Administrative Data 2.1 Identification of the Testing Laboratory Issuing the Test Report Company Name: CETECOM Inc. Department: Compliance Street Address: 411 Dixon Landing Road City/Zip Code Milpitas, CA 95035 Country USA Telephone: +1 (408) 586 6200 Fax: +1 (408) 586 6299 Director of Regulatory Services: Stoecker, Arndt Responsible Project Leader: Saman, Rami 2.2 Identification of the Client / Manufacturer Applicant’s Name: Praesidium Inc. Street Address: 150 N 200 E City/Zip Code St. George, Utah 84770 Country USA 2.3 Identification of the Manufacturer Manufacturer’s Name: Same as client. Manufacturers Address: -------------------- City/Zip Code -------------------- Country -------------------- Test Report #: EMC_PRAES_002-23001_MPE_FCC_ISED FCC ID: 2A7ZX2002BIO1 Date of Report 2023-03-30 Page 5 of 8 IC: 28837-2002BIO1 Page 5 of 8 3 Equipment under Assessment Model No: 2002BIO1 Marketing name: BioFi FCC ID: 2A7ZX2002BIO1 IC: 28837-2002BIO1 HW Version : 2002BIO1 SW Version : V1.0.0 HVIN: 2002BIO1 PMN: RemWave Sleep Product description: Contactless vital sign detection sensor Power Supply / Rated Operating Voltage Range: (V DC) Vmin: 4.25 / Vnom: 5 / Vmax: 5.75 Operating Temperature range: 32 °F to 104 °F (0 °C to 40 °C) Integrated Module Info:  Radar:  Manufacturer: Texas Instruments  Part Number: IWR6843AQGABL  Description: Single-chip 60-64 GHz intelligent mmWave sendor  WLAN (Wi-Fi): 802.11 b/g/n  Manufacturer: WIZnet H.K. LTD  Model: WIZFI360PA  FCC ID: 2ATUB-WIZFI360PA  IC: 20560-WIZI360PA Regulatory Band:  Radar: 60-64 GHz  WLAN (Wi-Fi) 2.4:  2.4 GHz: 802.11 b/g/n  2.412 GHz to 2.462 GHz: Channel 1 – 11 Antenna Type and Peak gain:  Radar: PCB embedded 60-64 GHz antenna array, 15 dBi gain  WLAN: PCB embedded 2.4 GHz Wi-Fi antenna, 2 dBi gain Maximum Conducted Output Power (dBm):  Radar: -10 dBm  WLAN (Wi-Fi) 2.4: 19 dBm ± 1 dB Sample Revision:  Prototype Unit;  Production Unit;  Pre-Production Device category: Fixed installation Exposure Category: public/uncontrolled Test Report #: EMC_PRAE…

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A2LA Accredited IC recognized # 3462B CABID: US0187 CETECOM Inc. 411 Dixon Landing Road  Milpitas, CA 95035  U.S.A. Phone: + 1 (408) 586 6200  Fax: + 1 (408) 586 6299  E-mail: [email protected]  http://www.cetecom.com CETECOM Inc. is a Delaware Corporation with Corporation number: 2905571 © Copyright by CETECOM FCC / ISED Test Report For: Praesidium Inc. Model Name: 2002BIO1 Product Description: Contactless vital sign detection sensor FCC ID: 2A7ZX2002BIO1 IC ID: 28837-2002BIO1 Applied Rules and Standards: 47 CFR Part 15.255 RSS-210 Issue 10 REPORT #: EMC_PRAES-002-23001_FCC15.255-Rev1 DATE: 2023-04-12 Test Report #: EMC_PRAES-002-23001_FCC15.255-Rev1 FCC ID: 2A7ZX2002BIO1 Date of Report 2023-04-12 Page 2 of 45 IC ID: 28837-2002BIO1 TABLE OF CONTENTS 1 ASSESSMENT .............................................................................................................................................................. 3 2 ADMINISTRATIVE DATA ............................................................................................................................................... 4 2.1 IDENTIFICATION OF THE TESTING LABORATORY ISSUING THE EMC TEST REPORT ........................................................................... 4 2.2 IDENTIFICATION OF THE CLIENT ............................................................................................................................................. 4 2.3 IDENTIFICATION OF THE MANUFACTURER ................................................................................................................................. 4 3 EQUIPMENT UNDER TEST (EUT) ................................................................................................................................... 5 3.1 EUT SPECIFICATIONS ......................................................................................................................................................... 5 3.2 EUT SAMPLE DETAILS ......................................................................................................................................................... 6 3.3 ACCESSORY EQUIPMENT (AE) DETAILS ................................................................................................................................... 6 3.4 TEST SAMPLE CONFIGURATION ............................................................................................................................................. 6 3.5 JUSTIFICATION FOR WORST CASE MODE OF OPERATION ............................................................................................................ 6 4 SUBJECT OF INVESTIGATION ...................................................................................................................................... 7 5 MEASUREMENT RESULTS SUMMARY .......................................................................................................................... 7 6 ME…

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