
Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.
User Manual NANJING MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. HyBase RFID Module-3 I Copyright © Copyright 2026 Nanjing Mindray Bio-Medical Electronics Co., Ltd. All rights reserved. Release time: 2026-04 Revision: 1.0 WARNING • Federal Law (USA) restricts this device to sale by or on the order of a physician or other practitioner licensed by U.S. state law to use or order the use of this device. Intellectual Property Statement NANJING MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray) owns the intellectual property rights to this Mindray device and this manual. This manual can refer to information protected by copyrights or patents and does not convey any license under the patent rights or copyright of Mindray, nor the rights of others. Mindray intends to maintain the contents of this manual as confidential information. Disclosure of the information in this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden. Release, amendment, reproduction, distribution, rental, adaption and translation of this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden. ,,are the registered trademarks II or trademarks owned by Mindray in China and other countries. All other trademarks that appear in this manual are used only for editorial purposes without the intention of improperly using them. They are the property of their respective owners. Responsibility on the Manufacturer Party Contents of this manual are subject to changes without prior notice. All information contained in this manual is believed to be correct. Mindray shall not be liable for errors contained herein nor for incidental or consequential damages in connection with the furnishing, performance, or use of this manual. Mindray is responsible for the effects on safety, reliability and performance of this product, only if: ■ all installation operations, expansions, changes, modifications and repairs of this product are conducted by Mindray authorized personnel; ■ the electrical installation of the relevant room complies with the applicable national and local requirements; ■ the product is used in accordance with the instructions for use. WARNING • This equipment must be operated by skilled/trained clinical professionals. • It is important for the hospital or organization that employs this equipment to carry out a reasonable service/maintenance plan. Neglect of this may result in machine breakdown or personal injury. III Service Mindray maintains a network of service representatives and factory-trained distributors. Prior to requesting service, perform a complete operational check of the instrument to verify proper control settings. If operational problems continue to exist, contact Mindray service. In North America contact the Service Department at (800) 288-2121, ext: 8116 for Technical Support or (201) 995-8000 for assistance in determining the nearest field service location. Please include the instrument model number, the serial number, and a description of the problem with all requests for service. Any questions regarding the warranty should be directed to the local sales or service representative. IV Company Contact Manufacture:Nanjing Mindray Bio-Medical Electronics Co., Ltd. Address: 666# Middle Zhengfang Road, Jiangning, 211111 Nanjing, Jiangsu, P.R.China Website: www.mindray.com E-mail Address: [email protected] Tel:+86 755 81888998 Fax:+86 755 26582680 Distributor: Mindray DS USA, Inc. Address: 800 MacArthur Boulevard, Mahwah, New Jersey, 07430 USA Tel: 1.800.288.2121, 1.201.995.8000 Website: www.mindray.com V Preface Manual Purpose This manual contains the instructions necessary to operate the product safely and in accordance with its function and intended use. Observance of this manual is a prerequisite for proper product performance and correct operation and ensures patient and operator safety. This manual is based on the maximum configuration and therefore some contents may not apply to your product. If you have any question, please contact us. This manual is an integral part of the product. It should always be kept close to the equipment so that it can be obtained conveniently when needed. Intended Audience This manual is geared for clinical professionals who are expected to perform daily operations of the product, maintain and troubleshoot the product and learn how to use the product. Illustrations All illustrations in this manual serve as examples only. They may not necessarily reflect the setup or data displayed on your equipment. Conventions ■ Italic text is used in this manual to quote the referenced chapters or sections. ■ Bold text is used to indicate the screen texts. ■ →is used to indicate operational procedures. VI FCC 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. Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment. Part §15.21 of the FCC rules states that users must be advised that 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…
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Project No.: 2603C130 Page 1 of 7 ATTACHMENT PHOTOGRAPHS OF EUT Project No.: 2603C130 Page 2 of 7 Project No.: 2603C130 Page 3 of 7 Project No.: 2603C130 Page 4 of 7
Label: FCC ID:2BHFC-RFID3 IC:32747-RFID3 Module: HyBase RFID Module-3 Location: 1.分别拧下上盖上方、前侧和后侧的6颗螺钉。打开上盖板露出板卡。 Remove the 6 screws located on the top, front and back of the upper cover respectively. Open the upper cover to expose the board. 2.标贴位于板卡的红色方块处 The label is located in the red solid square of the board.
Project No.: 2603C130 Page 1 of 7 ATTACHMENT PHOTOGRAPHS OF EUT Project No.: 2603C130 Page 5 of 7 Project No.: 2603C130 Page 6 of 7 Project No.: 2603C130 Page 7 of 7
Report No.: BTL-FCCP-2-2603C130 Report Version: R00 Page 1 of 7 FCC RF EXPOSURE REPORT FCC ID: 2BHFC-RFID3 Project No. : 2603C130 Equipment : RFID Module Brand Name : Test Model : HyBase RFID Module-3 Model Name : HyBase RFID Module-3 Applicant : Nanjing Mindray Bio-Medical Electronics Co., Ltd. Address : 666 Middle Zhengfang Road, Jiangning, 211111 Nanjing, Jiangsu,P.R.China Manufacturer : Nanjing Mindray Bio-Medical Electronics Co., Ltd. Address : 666 Middle Zhengfang Road, Jiangning, 211111 Nanjing, Jiangsu,P.R.China Factory : Nanjing Mindray Bio-Medical Electronics Co., Ltd. Address : 666 Middle Zhengfang Road, Jiangning, 211111 Nanjing, Jiangsu,P.R.China Date of Receipt : Mar. 12, 2026 Date of Test : Mar. 13, 2026 ~ Mar. 22, 2026 Issued Date : Apr. 22, 2026 Test Sample : Engineering Sample No.: DG920260312346 Standard(s) : FCC Guidelines for Human Exposure IEEE C95.1 & KDB 447498 D04 v01 The above equipment has been tested and found compliance with the requirement of the relative standards by BTL Inc. (Dongguan) Prepared by : Chella Zheng Approved by : Chay Cai No.3, Jinshagang 1st Road, Dalang, Dongguan, Guangdong People’s Republic of China. Te l : + 8 6-769-8318-3000 Web: www.newbtl.com Service mail: [email protected] Report No.: BTL-FCCP-2-2603C130 Report Version: R00 Page 2 of 7 Declaration BTL represents to the client that testing is done in accordance with standard procedures as applicable and that test instruments used has been calibrated with standards traceable to international standard(s) and/or national standard(s). BTL's reports apply only to the specific samples tested under conditions. It is manufacture’s responsibility to ensure that additional production units of this model are manufactured with the identical electrical and mechanical components. BTL assumes no responsibility for the data provided by the customer, any statements, inferences or generalizations drawn by the customer or others from the reports issued by BTL. This report is the confidential property of the client. As a mutual protection to the clients, the public and ourselves, the test report shall not be reproduced, except in full, without our written approval. BTL is not responsible for the sampling stage, so the results only apply to the sample as received. The information, data and test plan are provided by manufacturer which may affect the validity of results, so it is manufacturer’s responsibility to ensure that the apparatus meets the essential requirements of applied standards and in all the possible configurations as representative of its intended use. Limitation For the use of the authority's logo is limited unless the Test Standard(s)/Scope(s)/Item(s) mentioned in this test report is (are) included in the conformity assessment authorities acceptance respective. Please note that the measurement uncertainty is provided for informational purpose only and are not use in determining the Pass/Fail results. Report No.: BTL-FCCP-2-2603C130 Report Version: R00 Page 3 of 7 REVISION HISTORY Report No. Version Description Issued Date Note BTL-FCCP-2-2603C130 R00 Original Report. Apr. 22, 2026 Valid Report No.: BTL-FCCP-2-2603C130 Report Version: R00 Page 4 of 7 1. GENERAL CONCULUSION According to FCC §§1.1307 and KDB 447498 D04 v01, the available maximum time-averaged power or effective radiated power (ERP), whichever is greater, is less than or equal to the threshold P th (mW). 1) Option A. 1-mW Test Exemption Per § 1.1307(b)(3)(i)(A), a single RF source is exempt RF device (from the requirement to show data demonstrating compliance to RF exposure limits, as previously mentioned) if the available maximum time-averaged power is no more than 1 mW, regardless of separation distance. This exemption applies to all operating configurations and exposure conditions, for the frequency range 100 kHz to 100 GHz, regardless of fixed, mobile, or portable device exposure conditions. This is a standalone exemption, and it cannot be applied in conjunction with any other test exemption. 2) Option B. SAR-Based Exemption A more comprehensive exemption, considering a variable power threshold that depends on both the separation distance and power, is provided in § 1.1307(b)(3)(i)(B). This exemption is applicable to the frequency range between 300 MHz and 6 GHz, with test separation distances between 0.5 cm and 40 cm, and for all RF sources in fixed, mobile, and portable device exposure conditions. Accordingly, a RF source is considered an RF exempt device if its available maximum time-averaged (matched conducted) power or its effective radiated power (ERP), whichever is greater, are below a specified threshold. This method shall only be used at separation distances (cm) from 0.5 centimeters to 40 centimeters and at frequencies from 0.3 GHz to 6 GHz (inclusive). Pth is given by: Report No.: BTL-FCCP-2-2603C130 Report Version: R00 Page 5 of 7 Table B2-Example Power Thresholds (mW) Frequency (MHz) Distance(mm) mW 5 10 15 20 25 30 35 40 45 50 300 39 65 88 110 129 148 166 184 201 217 450 22 44 67 89 112 135 158 180 203 226 835 9 25 44 66 90 116 145 175 207 240 1900 3 12 26 44 66 92 122 157 195 236 2450 3 10 22 38 59 83 111 143 179 219 3600 2 8 18 32 49 71 96 125 158 195 5800 1 6 14 25 40 58 80 106 136 169 3) Option C MPE-Based Exemption An alternative to the SAR-based exemption is provided in § 1.1307(b)(3)(i)(C), for a much wider frequency range, from 300 kHz to 100 GHz, applicable for separation distances greater or equal to λ/2π, where λ is the free-space operating wavelength in meters. The MPE-based test exemption condition is in terms of ERP, defined as the product of the maximum antenna gain and the delivered maximum time-averaged power. For this case, a RF source is an RF exempt device if its ERP (watts) is no more than a frequency-dependent value, as detailed tabular form in Appendix B. These limits have been derived based on the basic specifications on Maximum Permissible Exposure (MPE) considered for the FCC rules in §…
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Report No.: BTL-FCCP-1-2603C130 Report Version: R00 Page 1 of 30 FCC Radio Test Report FCC ID: 2BHFC-RFID3 This report concerns: Original Grant Project No. : 2603C130 Equipment : RFID Module Brand Name : Model Name : HyBase RFID Module-3 Applicant : Nanjing Mindray Bio-Medical Electronics Co., Ltd. Address : 666 Middle Zhengfang Road, Jiangning, 211111 Nanjing, Jiangsu,P.R.China Manufacturer : Nanjing Mindray Bio-Medical Electronics Co., Ltd. Address : 666 Middle Zhengfang Road, Jiangning, 211111 Nanjing, Jiangsu,P.R.China Factory : Nanjing Mindray Bio-Medical Electronics Co., Ltd. Address : 666 Middle Zhengfang Road, Jiangning, 211111 Nanjing, Jiangsu,P.R.China Date of Receipt : Mar. 12, 2026 Date of Test : Mar. 13, 2026 ~ Mar. 22, 2026 Issued Date : Apr. 22, 2026 Test Sample : Engineering Sample No.: DG920260312346 Standard(s) : FCC CFR Title 47, Part 15, Subpart C The above equipment has been tested and found compliance with the requirement of the relative standards by BTL Inc. (Dongguan) Prepared by : Chella Zheng Approved by : Chay Cai No.3, Jinshagang 1st Road, Dalang, Dongguan, Guangdong People’s Republic of China. Te l : + 8 6-769-8318-3000 Web: www.newbtl.com Service mail: [email protected] Report No.: BTL-FCCP-1-2603C130 Report Version: R00 Page 2 of 30 Declaration BTL represents to the client that testing is done in accordance with standard procedures as applicable and that test instruments used has been calibrated with standards traceable to international standard(s) and/or national standard(s). BTL's reports apply only to the specific samples tested under conditions. It is manufacture’s responsibility to ensure that additional production units of this model are manufactured with the identical electrical and mechanical components. BTL assumes no responsibility for the data provided by the customer, any statements, inferences or generalizations drawn by the customer or others from the reports issued by BTL. The report must not be used by the client to claim product certification, approval, or endorsement by A2LA or any agency of the U.S. Government. This report is the confidential property of the client. As a mutual protection to the clients, the public and ourselves, the test report shall not be reproduced, except in full, without our written approval. BTL’s laboratory quality assurance procedures are in compliance with the ISO/IEC 17025: 2017 requirements, and accredited by the conformity assessment authorities listed in this test report. BTL is not responsible for the sampling stage, so the results only apply to the sample as received. The information, data and test plan are provided by manufacturer which may affect the validity of results, so it is manufacturer’s responsibility to ensure that the apparatus meets the essential requirements of applied standards and in all the possible configurations as representative of its intended use. Limitation For the use of the authority's logo is limited unless the Test Standard(s)/Scope(s)/Item(s) mentioned in this test report is (are) included in the conformity assessment authorities acceptance respective. Please note that the measurement uncertainty is provided for informational purpose only and are not use in determining the Pass/Fail results. Report No.: BTL-FCCP-1-2603C130 Report Version: R00 Page 3 of 30 Table of Contents Page REVISION HISTORY 5 1 . APPLICABLE STANDARDS 6 2 . SUMMARY OF TEST RESULTS 6 2.1 TEST FACILITY 7 2.2 MEASUREMENT UNCERTAINTY 7 2.3 TEST ENVIRONMENT CONDITIONS 7 3 . GENERAL INFORMATION 8 3.1 GENERAL DESCRIPTION OF EUT 8 3.2 DESCRIPTION OF TEST MODES 9 3.3 BLOCK DIAGRAM SHOWING THE CONFIGURATION OF SYSTEM TESTED 10 3.4 SUPPORT UNITS 10 4 . AC POWER LINE CONDUCTED EMISSIONS TEST 11 4.1 LIMIT 11 4.2 TEST PROCEDURE 11 4.3 DEVIATION FROM TEST STANDARD 11 4.4 TEST SETUP 12 4.5 EUT OPERATING CONDITIONS 12 4.6 TEST RESULTS 12 5 . RADIATED EMISSION TEST 13 5.1 LIMIT 13 5.2 TEST PROCEDURE 13 5.3 DEVIATION FROM TEST STANDARD 13 5.4 TEST SETUP 14 5.5 EUT OPERATING CONDITIONS 15 5.6 TEST RESULT - 9 KHZ TO 30 MHZ 15 5.7 TEST RESULTS - 30 MHZ TO 1000 MHZ 15 6 . BANDWIDTH 16 6.1 LIMIT 16 6.2 TEST PROCEDURE 16 6.3 DEVIATION FROM STANDARD 16 6.4 TEST SETUP 16 6.5 EUT OPERATION CONDITIONS 16 6.6 TEST RESULTS 16 Report No.: BTL-FCCP-1-2603C130 Report Version: R00 Page 4 of 30 Table of Contents Page 7 . MEASUREMENT INSTRUMENTS LIST 17 APPENDIX A - AC POWER LINE CONDUCTED EMISSIONS 18 APPENDIX B - RADIATED EMISSION - 9 KHZ TO 30 MHZ 21 APPENDIX C - RADIATED EMISSION - 30 MHZ TO 1000 MHZ 26 APPENDIX D - BANDWIDTH 29 Report No.: BTL-FCCP-1-2603C130 Report Version: R00 Page 5 of 30 REVISION HISTORY Report No. Version Description Issued Date Note BTL-FCCP-1-2603C130 R00 Original Report. Apr. 22, 2026 Valid Report No.: BTL-FCCP-1-2603C130 Report Version: R00 Page 6 of 30 1. APPLICABLE STANDARDS According to the specifications of the manufacturer, the EUT must comply with the requirements of the following standard: ANSI C63.10-2020 2. SUMMARY OF TEST RESULTS Test procedures according to the technical standard(s): FCC CFR Title 47, Part 15, Subpart C Standard(s) Section Test Item Test Result Judgment Remark 15.207 AC Power Line Conducted Emissions APPENDIX A PASS ------ 15.209(a) Radiated Emissions APPENDIX B APPENDIX C PASS ------ 15.215(c) Bandwidth APPENDIX D PASS ------ 15.203 Antenna Requirement ------ PASS Note(2) NOTE: (1) “N/A” denotes test is not applicable to this device. (2) The device what use a permanently attached antenna were considered sufficient to comply with the provisions of 15.203. Report No.: BTL-FCCP-1-2603C130 Report Version: R00 Page 7 of 30 2.1 TEST FACILITY The test facilities used to collect the test data in this report is at the location of No.3, Jinshagang 1st Road, Dalang, Dongguan, Guangdong People’s Republic of China. BTL's Registration Number for FCC: 747969 BTL's Designation Number for FCC: CN1377 2.2 MEASUREMENT UNCERTAINTY ISO/IEC 17025 requires that an estimate of the measurement uncertainties ass…
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CXJFBCEM4305-D18 EM430518MM直径非标卡规格书 EM4305卡介绍:EM4305卡是一款低频的非接触式ID卡,主要功能是用来满足动物识别、 门锁访问控制及工业等领域的特定需求。EM4305特别适合于低成本的动物标签应用,符 合ISO11784/11785标准,有助于产品的一致性和设备的互通性。对大多数的动物识别 应用而言,ISO的数据完整性是很重要的。EM4305可避免发生未授权的修改。 产品参数 材质:PVC 芯片:低频(频率100~150KHZ,兼容ISO/IEC7814/7815) 颜色:白色PVC,可定制 读距:低频0.5~5cm(与客户读写器有关) 尺寸:18.0mm直径(±0.5mm)厚度1.0mm(±0.1mm) 温度:-20°C~60°C(如外封装耐高温材料另论) 防护等级:IP65 CXJFBCEM4305-D18 EM430518MM直径非标卡规格书 芯片信息/应用 EM4305卡主要性能指标: 1、512位EEPROM,分为16个扇区,每个扇区32bit 2、32bitUID 3、兼容ISO11784/11785协议 4、32位口令读和写保护 5、可使EEPROM扇区进入只读锁定状态 6、2种编码方式(曼彻斯特、Bi-phase) 7、多种数据传输速率(8、16、32、64个RF时钟) 8、具有读卡器先问询的特点 典型应用:感应式智能门锁、小区一卡通系统、门禁、通道系统等。 EM4305卡制作工艺: 可选材质:PVC/ABS环保材料/PET耐高温材料等; 可选尺寸:φ18*1.0MM(可定制); 可选印刷:双面彩色印刷、丝印、专色; 表面可选:哑面/磨砂/透明、加膜; 可选工艺:烫金/银、烫镭射金/银、金/银底、UV油、签名条、刮刮乐; 打码方式:激光码、金/银凸码、黑平码、金平码、喷码; 可选磁条:低抗磁条、高抗磁条; 可选条码:EAN13、Code39、Code128、二维码等; 写码服务; 可提供彩卡之外,还可提供白卡、个性卡、滴胶卡等。
Project No.: 2603C130 Page 1 of 4 EUT TEST PHOTO Project No.: 2603C130 Page 2 of 4 AC Power Line Conducted Emissions Test Photos Project No.: 2603C130 Page 3 of 4 Radiated Emissions Test Photos 9 kHz to 30 MHz Project No.: 2603C130 Page 4 of 4 Radiated Emissions Test Photos 30 MHz to 1000 MHz
3722 Illinois Avenue · Saint Charles, Illinois, 60174 · United States
| # | Rule Parts | Frequency Range | Power Output |
|---|---|---|---|
| 1 | 15C | 0.1275 MHz - 0.1275 MHz | - |