FCC ID: 2A86D-PD11 WiFi and Bluetooth Module

WARNING:pdfminer.pdfpage:The PDF <_io.BufferedReader name='/Volumes/Scratch/Incoming/eg-scratch/6804044.pdf'> contains a metadata field indicating that it should not allow text extraction. Ignoring this field and proceeding. Use the check_extractable if you want to raise an error in this case Rego PID Wireless Module Users Manual Applicable FCC and IC Rules:

This module was tested to be compliant with the following standards/agency listings. Reports and/or certificates of compliance are available upon request:

> This module complies with CFR 15.247 and RSS-247. Hosts are required to be evaluated for intentional emissions according to the above listed specifications. Hosts are also required to be tested for unintentional emissions according to:

Radiated Emissions, Part 15.109(b) Class B or A Conducted Emissions, Part 15.107(b), Class B or A Canada ICES-003, Class B or A RF Exposure Considerations:

The module has met RF exposure requirements for portable use; use of this module in any other host device requires antenna to user separation distance of at least 20cm. Specific Absorption Rate (SAR) refers to the rate at which the body absorbs radio frequency (RF) energy. The module was tested within Curbell Rego product using highest transmitter power and closest distance of separation

(0mm) and found to be below regulatory compliance requirements on all sides. Curbell will determine applicable testing modes should any additional testing be required. This module will only be used in Curbell s Rgo product and only Curbell is allowed to make changes. Module Approved antennas list:

Manufacturer Antenna Description Type Peak Gain

(dBI) Pulse Electronics (a Yageo Company) W3006 Dual Band Monopole 2.2 for 2.4Ghz 5.2-5.85 for 5Ghz 50 Connector Type Notes 1 SMD Mount Ceramic Antenna Notes:

1 Antenna was tested for compliance. Label and Compliance Information:

The module must be properly installed in host. The host is to include the following text on exterior of host:

Contains FCC ID: 2A68D-PD11 Contains IC: 29644-PD11 CAN ICES-003(B)/NMB-003(B). DFU-WMD-10000 REV.A Curbell must include the following statements on the exterior of the finished product unless the product is too small (e.g less than 4 x 4 inches):

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 any interference that may cause undesired operation. The above statement applies also to the module. For hosts in field, software updates to the Bluetooth module are delivered via our proprietary Android Operating System update mechanism (Airwatch). A Bluetooth module software update is included in a new build of the operating system. Android Operating System updates are signed using a secure key generated by Curbell Medical. Updates will not apply to a host should an update package become compromised, as the package signature would differ and not be verified and thus not applied to the host. Updates can be seen on host display. To access Regulatory Information on host proceed to Home screen then press Settings icon in top right corner of screen then proceed to Regulatory Information to access regulatory statements. Manual Statements:

The following statements apply to the module and are also required to be placed in host products user manual:

This equipment has been tested and found to comply with the limits for a Class A digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference when the equipment is operated in a commercial environment. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instruction manual, may cause harmful interference to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference in which case the user will be required to correct the interference at his expense. WARNING: The Federal Communications Commission warns that changes or modifications of the radio module within this device not expressly approved by Curbell Medical Products Inc. could void the users authority to operate the equipment. 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 interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. Le prsent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radio exempts de licence. L'exploitation est autorise aux deux conditions suivantes : (1) l'appareil ne doit pas produire de brouillage, et (2) l'utilisateur de l'appareil doit accepter tout brouillage radiolectrique subi, mme si le brouillage est susceptible d'en compromettre le fonctionnement. The modular transmitter is only FCC authorized for the specific rule parts listed on the grant. The product manufacturer is responsible for compliance to any other FCC rules that apply to the host not covered by the modular transmitter certification. DFU-WMD-10000 REV.A Additional testing, Part 15 subpart B and ICES-003 disclaimer The final host/module combination must be evaluated against the FCC Part 15B for unintentional radiators, and IC Interference-Causing Equipment Standard for Digital Apparatus in order to be properly authorized for operation as a Part 15 digital device. The host integrator installing this module into their product must ensure that the final composite product complies with the FCC/IC requirements by a technical assessment or evaluation to the FCC/IC rules, including the transmitter operation and should refer to guidance in KDB 996369. For host products including a certified modular transmitter, the frequency range of investigation of the composite system is specified by rule in Sections 15.33(a)(1) through (a)(3), or the range applicable to the digital device, as shown in Sections 15.33(b)(1), whichever is the higher frequency range of investigation. When testing the host product, all the transmitters must be operating. The transmitters can be enabled by using publicly available drivers and turned on, so the transmitters are active. In certain conditions, it might be appropriate to use a technology-specific call box (test set) where accessory 50 devices or drivers are not available. When testing for emissions from the unintentional radiator, the transmitter shall be placed in the receive mode or idle mode, if possible. If receive-mode only is not possible, then the radio shall be passive (preferred) and/or active scanning. In these cases, this would need to enable activity on the communication BUS (i.e., PCIe, SDIO, USB) to ensure the unintentional radiator circuitry is enabled. Testing laboratories may need to add attenuation or filters depending on the signal strength of any active beacons (if applicable) from the enabled radio(s). See ANSI C63.4, ANSI C63.10, and ANSI C63.26 for further general testing details. DFU-WMD-10000 REV.A

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Curbell Medical Products, Inc. hereby delegates CKC Certification Services, LLC (CKC CS) as our power of attorney to act on our behalf in matters pertaining to U.S. Federal Communications Commission and also matters pertaining to ISED Canada Certification filings for Curbell Medical Products, Inc. Rgo Patient Interactive Device. The actions of CKC CS shall be considered the same as our own on such matters. Sincerely, Gregory Walczak Sr. Compliance/Application Engineer Curbell Medical Products Inc.

WARNING:pdfminer.pdfpage:The PDF <_io.BufferedReader name='/Volumes/Scratch/Incoming/eg-scratch/6804036.pdf'> contains a metadata field indicating that it should not allow text extraction. Ignoring this field and proceeding. Use the check_extractable if you want to raise an error in this case CKC Certification Services, LLC CB: US0103; NB/AB: 0976 5046 Sierra Pines Drive Mariposa, CA 95338 Phone: 1 800-500-4EMC (4362) Fax: 209-787-5568 Email: tcbadmin@ckc.com APP-FCC-A Applicant Attestation Applicant Information Check here if there is a change in contact details. Company Name:

Contact Name:

Contact Title:

Company Address:

Telephone No:

Facsimile No:

Email Address:

Curbell Medical Products Inc. Gregory Walczak Sr. Compliance/Applications Engineer 20 Centre Drive, Orchard Park, New York 14127 1-800-235-7500 ext. 7248 gwalczak@curbellmedical.com Certification Type / Equipment Identification Certification Program:

Type of Service Requested:

Certification Number:

Radio Certification Class II permissive change 2A86D-PD11 The equipment identified above is / is not prohibited from receiving an equipment authorization under certification pursuant to 47 CFR Part 2, Subpart J, 2.903. The applicant identified above is / is not identified on the FCCs Covered List as an entity, affiliate, or subsidiary which produces equipment on the Covered List or identified as an entity which has rebranded or relabeled equipment produced by entities identified on the Covered List. I (the applicant), hereby attest that the below statements are true and correct regarding the herein identified equipment subject to US equipment authorization under certification in accordance with 47 CFR Part 2 Subpart J. Signature of Authorized Individual: 1 Printed Name:

Title of authorized signature:

Date Gregory Walczak Sr. Compliance/Applications Engineer 1/6/2023 Note this attestation shall be signed by the applicant or their direct appointee within the same legal entity. A third party agent is not permitted to sign on behalf of the applicant. 1 Signature is subject to the FCCs authorized individual policy; see KDB 852134 APP-FCC-A Page 1 of 2 Rev 0 CKC Certification Services, LLC CB: US0103; NB/AB: 0976 5046 Sierra Pines Drive Mariposa, CA 95338 Phone: 1 800-500-4EMC (4362) Fax: 209-787-5568 Email: tcbadmin@ckc.com Attachment A Additional Information The FCCs Covered List includes certain telecommunications equipment and video surveillance equipment produced by specific manufacturers, their Affiliates or Subsidiaries and including any products produced by these entities which are rebranded or relabeled by other entities. (191, 184, 185, 188) 2 The FCC claims the identified equipment poses an unacceptable risk to United States national security. Telecommunications Equipment (195):

Any equipment used in fixed or mobile networks that provides advanced communications service, provided the equipment includes or uses electronic components, as defined under section 1.50001(c). Video Surveillance Equipment (205):

Any equipment that is used in fixed and mobile networks that provides advanced communications service in the form of a video surveillance service, provided the equipment includes or uses electronic components. Advanced Communications Service (195, 205) Any equipment that can be used in such a fixed or mobile broadband network to enable users to originate and receive high quality voice, data, graphics, and video telecommunications service using any technology with connection speeds of at least 200 kbps in either direction. Affiliate (183):

An entity that (directly or indirectly) owns or controls, is owned or controlled by, or is under common ownership or control with, another entity, where the term own means to have, possess, or otherwise control an equity interest (or the equivalent thereof) of more than 10 percent. Subsidiary (184):

Any entity in which such named entity directly or indirectly (1) holds de facto control or (2) owns or controls more than 50% of the total voting power of the entitys outstanding voting stock. Useful Links:

FCC Covered List https://www.fcc.gov/supplychain/coveredlist 47 CFR Part 2 Subpart J (including 2.903 and 2.911) https://www.ecfr.gov/current/title-47/chapter-I/subchapter-A/part-2/subpart-J FCC KDB System:

https://apps.fcc.gov/oetcf/kdb/index.cfm FCC Report and Order 22-84 https://docs.fcc.gov/public/attachments/FCC-22-84A1.pdf 2 Parenthetical references are citations of paragraph numbers in FCC Report and Order FCC 22-84 (ET Docket 21.232). APP-FCC-A Page 2 of 2 Rev 0

WARNING:pdfminer.pdfpage:The PDF <_io.BufferedReader name='/Volumes/Scratch/Incoming/eg-scratch/6770381.pdf'> contains a metadata field indicating that it should not allow text extraction. Ignoring this field and proceeding. Use the check_extractable if you want to raise an error in this case July 19, 2023 Curbell Medical Products 20 Centre Drive Orchard Park, New York 14127 To Whom It May Concern, This letter is to request Single Modular Approval in accordance with under FCC Rule Part 15.212(a)(1) for certification request under FCC ID: 2A86D-PD11. This product is a Bluetooth WIFI Module and is used in Curbell Medical Products Rego Patient Interactive Device (PD11). Declaration of conditions. Y/N Y Y Y Y Y Y Y Y 15.212(a)(1) Condition

(i) The radio elements of the module have their own shielding. The physical crystal and tuning capacitors may be located external to the shielded radio elements

(ii) The module has buffered modulation/data inputs (if such inputs are provided) to ensure that the module will comply with part 15 requirements under conditions of excessive data rates or over-

modulation.

(iii) The module has its own power supply regulation.

(iv) The module complies with the antenna and transmission system requirements of 15.203, 15.204(b) and 15.204(c). The antenna(s) are either permanently attached or employ a unique antenna coupler (at all connections between the module and the antenna, including the cable).

(v) The module was tested in a stand-alone configuration, i.e., the module was not inside another device during testing for compliance with part 15 requirements. Unless the transmitter module will be battery powered, it complies with the AC line conducted requirements found in 15.207. AC or DC power lines and data input/output lines connected to the module do not contain ferrites, unless they will be marketed with the module (see 15.27(a)). The length of these lines was the length typical of actual use or, if that length is unknown, at least 10 centimeters was used to insure that there is no coupling between the case of the module and supporting equipment. Any accessories, peripherals, or support equipment connected to the module during testing were unmodified and commercially available (see 15.31(i)).

(vi) The module is equipped with either a permanently affixed label or is capable of electronically displaying its FCC identification number.

(vii) The module complies with any specific rules or operating requirements that ordinarily apply to a complete transmitter and the applicant has provided adequate instructions along with the module to explain any such requirements.

(viii) The module complies with any applicable RF exposure requirements in its final configuration. The instructions provided with the module adequately explain any usage conditions or restrictions. I acknowledge on behalf of the applicant that compliance of this module in all final configurations is the responsibility of the applicant under the condition that the integrator follows all provided installation instructions. Sincerely, Gregory Walczak Sr. Compliance/Applications Engineer Curbell Medical Products Curbell Medical Products, Inc. 20 Centre Drive Orchard Park, NY 14127 Tel: 716-667-3377 or 800-235-7500 Fax: 716-667-7508 www.curbellmedical.com

WARNING:pdfminer.pdfpage:The PDF <_io.BufferedReader name='/Volumes/Scratch/Incoming/eg-scratch/6804040.pdf'> contains a metadata field indicating that it should not allow text extraction. Ignoring this field and proceeding. Use the check_extractable if you want to raise an error in this case 7/19/2023 Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 To whom it may concern:

Curbell Medical Products Inc., hereby requests a Permissive Change Class II of the radio equipment certification for the WIFI Wi Link Network Controller certification number, FCC ID: 2A86D-PD11. This product differs from the originally approved product in the following manor:

(a) Associated digital circuitry. No changes made to this section.

(b) Functional capabilities. No changes to this section.

(c) Antenna Characteristics. No changes to Characteristics, just orientation on PCB for our use.

(d) Cosmetic differences No changes to this section.

(e) Other SAR testing done for use closer than 20cm from human body I do attest that the Field strength and/or RF Output readings remained the same or are lower than the originally approved product and that they did not increase therefore qualifying this product for this application type. Sincerely, Gregory Walczak Sr. Compliance/Applications Engineer Curbell Medical Products Inc.

WARNING:pdfminer.pdfpage:The PDF <_io.BufferedReader name='/Volumes/Scratch/Incoming/eg-scratch/6770377.pdf'> contains a metadata field indicating that it should not allow text extraction. Ignoring this field and proceeding. Use the check_extractable if you want to raise an error in this case Attestation For United States Agent for Service of Process Self-Designation for US Based Manufacturers Only Applicant / Equipment Manufacturer Information Company Name:

Grantee Code:

FRN:

Curbell Medical Products Inc. 2A86D 0033035361 Applicant Attestation The undersigned hereby consents:

a) b) c) d) to self-designation as US Agent for Service of Process; and to accept responsibility and obligation to maintain self-designation for no less than one year after either all marketing and importation of the applicable equipment within the U.S has been permanently terminated, or the conclusion of any Commission-related administrative or judicial proceeding involving the equipment, whichever is later; and to accept service of process in the US for matters related to the applicable equipment and at the physical address and email address identified in the applicants grantee code registration for equipment authorization applications under certification pursuant to 47 CFR Part 2 Subpart J; and to maintain current grantee code information on file in accordance with 47 CFR Part 2.929. Signature of Applicant:

Printed Name:

Date:

Gregory Walczak 4/5/2023 CKC CS PUB FCC AFSOP Self Designation v4

WARNING:pdfminer.pdfpage:The PDF <_io.BufferedReader name='/Volumes/Scratch/Incoming/eg-scratch/6770380.pdf'> contains a metadata field indicating that it should not allow text extraction. Ignoring this field and proceeding. Use the check_extractable if you want to raise an error in this case December 7, 2022 Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 To whom it may concern:

This letter is to inform you that we, Curbell Medical Products Inc., are requesting Change in FCC ID for the new certification(s), FCC ID: 2A86D-PD11. The device to be certified is identical in design and construction to the originally approved product(s). In order to ensure continued compliance of the product, we have employed the following:

The product is still manufactured by the same company using the same design specifications as the original. The same PCB design, layouts and parts list will be used to manufacture the product. We have a QMS program in place to ensure compliance of the product through regular testing. Sincerely, Gregory Walczak Sr. Compliance/Applications Engineer Curbell Medical Products Inc.

Change in ID (FCC) / Change in Multiple Listing (ISED) Texas Instruments Incorporated 12500 TI Boulevard, Dallas Texas 75243 United States of America August 15th, 2023 Re: Change in ID / Change in Multiple Listing To Whom It May Concern:

Curbell Medical Products (Company) has contacted Texas Instruments Incorporated

(TI) regarding Companys intention to file applications for a change in identification in the United States pursuant to Section 2.933 of the Federal Communication Commissions (FCC) rules, and/or a multiple listing in Canada pursuant to Section 11.5 of Innovation, Science and Economic Development Canada (ISED) Certification of Radio Apparatus (RSP-100 Issue 12), with respect to the following:

TI Model Number /

HVIN (ISED) WL18MODGI Certification Number Z64-WL18DBMOD Original Grant Date 3/27/2018 WL18MODGI 451I-WL18DBMOD 4/4/2018 Model Name /

PMN (ISED) FCC WL18MODGI: 37 Grade: WiLink 8 Dual Band Combo 2x2 MIMO Wi-Fi, Bluetooth and Bluetooth low energy Module. 07 Grade:

WiLink 8 Dual Band Combo 2x2 MIMO Wi-

Fi Module ISED WL18MODGI: 37 Grade: WiLink 8 Dual Band Combo 2x2 MIMO Wi-Fi, Bluetooth and Bluetooth low energy Module. 07 Grade:

WiLink 8 Dual Band Combo 2x2 MIMO Wi-

Fi Module Company has requested TIs permission to reference, in Companys applications, certain documentation relating to the equipment identified in the table above. This letter is provided to permit Gregory Walczak, Curbell Medical Products, 20 Centre Dr, Orchard Park, NY, 14127; email: gwalczak@curbellmedical.com, phone: 1-800-235-7500 ext. 7248, to use the publicly available test data and application exhibits submitted to the FCC and to ISED on behalf of TI with respect to the equipment identified above pertaining to the grants of equipment certification covered by this letter. TI also gives authorization to both FCC & ISED officials to use DocuSign Envelope ID: 86C76C26-6687-43B2-BADB-1FDDF9908031 Change in ID (FCC) / Change in Multiple Listing (ISED) documents it has on file from the existing certification and also declare that the original certification on file with FCC & ISED remains unchanged. Company has represented to TI that its equipment submitted to ISED is identical in design and construction to the equipment approved by ISED as identified in the table above. Based on Companys representation to TI, TI understands that Company will market the above equipment under the following certification number:

Model / PMN FCC WL1837MODGIMOC ISED WL1837MODGIMOC HVIN

ECP-UW00-0001 Certification Number 2A86D-PD11 29644-PD11 Based on Companys representations to TI, TIs original certification test results continue to be applicable to the equipment bearing the changed identification and Company may list the existing certified product under Companys new certification number, subject to FCC and ISED rules. This permission to act using data and applications previously filed with the FCC and ISED on behalf of TI is limited to the matters set forth herein. This letter does not, and shall not be construed to, grant rights or permissions beyond those expressly granted to the party named herein. This permission expires automatically one year from the date of this letter. If you have any questions concerning this letter, please contact me by email at shmulik@ti.com or by phone at +97297906794. Respectfully, Texas Instruments Incorporated _______________________________ By:

Name: Shmulik Elgavi Title:

Product Line Manager, Wi-Fi Connectivity Solutions DocuSign Envelope ID: 86C76C26-6687-43B2-BADB-1FDDF9908031