ZLZ-TEARQDiagnostic Ultrasound System

TE Air Diagnostic Ultrasound System Operator's Manual For FCC ID application only! For FCC ID application only! 3 ©2022-2024 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All Rights Reserved. For this Operator’s Manual, the issue date is 2024-08. Intellectual Property Statement SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray) owns the intellectual property rights to this Mindray product and this manual. This manual may refer to information protected by copyright or patents and does not convey any license under the patent rights or copyright of Mindray, or 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, adaptation, translation or any other derivative work of this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden. is the trademarks, registered or otherwise, of Mindray in China and other countries. All other trademarks that appear in this manual are used only for informational or editorial purposes. They are the property of their respective owners. This posting serves as notice under 35 U.S.C.§287(a) for Mindray patents: http://www.mindrayna.com/ patents. Responsibility on the Manufacturer Party Contents of this manual are subject to change without prior notice. All information contained in this manual is believed to be correct. Mindray shall not be liable for errors contained herein or 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; and the product is used in accordance with the instructions for use. NOTE This equipment must be operated by skilled/trained clinical professionals. WARNING 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. Warranty THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR FITNESS FOR ANY PARTICULAR PURPOSE. For FCC ID application only! 4 Exemptions Mindray’s obligation or liability under this warranty does not include any transportation or other charges or liability for direct, indirect or consequential damages or delay resulting from the improper use or application of the product or the use of parts or accessories not approved by Mindray or repairs by people other than Mindray authorized personnel. This warranty shall not extend to: • Malfunction or damage caused by improper use or man-made failure. • Malfunction or damage caused by unstable or out-of-range power input. • Malfunction or damage caused by force majeure such as fire and earthquake. • Malfunction or damage caused by improper operation or repair by unqualified or unauthorized service people. • Malfunction of the instrument or part whose serial number is not legible enough. • Others not caused by instrument or part itself. Customer Service Department Manufacturer:Shenzhen Mindray Bio-Medical Electronics Co., Ltd. Address: Mindray Building, Keji 12th Road South, High-Tech Industrial Park, Nanshan, Shenzhen, 518057, P.R. China Website:www.mindray.com E-mail Address: [email protected] Tel:+86 755 81888998 Fax:+86 755 26582680 Manufacturer:Mindray DS USA, Inc. Address: 800 MacArthur Blvd. Mahwah, NJ 07430-0619 USA Tel:+1(201) 995-8000 Toll Free:+1 (800) 288-2121 Fax:+1 (800) 926-4275 Important Information • It is the customer’s responsibility to maintain and manage the system after delivery. • The warranty does not cover the following items, even during the warranty period: – Damage or loss due to misuse or abuse. – Damage or loss caused by Acts of God such as fires, earthquakes, floods, lightning, etc. – Damage or loss caused by failure to meet the specified conditions for this system, such as inadequate power supply, improper installation or environmental conditions. – Damage or loss due to use of the system outside the region where the system was originally sold. – Damage or loss involving the system purchased from a source other than Mindray or its authorized agents. • This system shall not be used by persons other than fully qualified and certified medical personnel. • DO NOT make changes or modifications to the software or hardware of this system. For FCC ID application only! 5 • In no event shall Mindray be liable for problems, damage, or loss caused by relocation, modification, or repair performed by personnel other than those designated by Mindray. • The purpose of this system is to provide physicians with data for clinical diagnosis. The physician is responsible for the results of diagnostic procedures. Mindray shall not be liable for the results of diagnostic procedures. • Important data must be backed up on external memory media. • Mindray shall not be liable for loss of data stored in the memory of this system caused by operator error or accidents. • This manual contains warnings regarding foreseeable potential dangers, but you shall also be continuously alert to dangers other than those indicated. Mindray shall not be liable for damage or loss resulting from negligence or ignorance of the precautions and operating instructions described in this operator’s manual. • If a new manager takes over this system, be sure to hand over this operator’s manual to the new manager. About This Manual This operator’s manual describes the operating procedures for…

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Page: 1 of 15 TEST REPORT For FCC Part15B Report No. .......................................: CHTW24070029 Report verification: Project No. ..................................: SHT2404097802W FCC ID ............................................. : ZLZ-TEARQ Applicant’s name ........................... : Shenzhen Mindray Bio-Medical Electronics Co.,LTD. Address ............................................. : Mindray Building, Keji 12th Road South, High-tech Industrial Park, Nanshan,518057 Shenzhen,PEOPLE'S REPUBLIC OF CHINA Product Name ................................ : Diagnostic Ultrasound System Trade Mark ....................................... : Model No. ......................................... : TE Air Listed Model(s) ................................. : - Standard ......................................... : FCC CFR Title 47 Part 15 Subpart B Date of receipt of test sample...........: May.20, 2024 Date of testing..............................: May.20, 2024 - Jul.04, 2024 Date of issue.................................: Jul.05, 2024 Result .................. ........................: Pass Compiled by (position+printed name+signature) ... : File administrators Kiki Kong Supervised by (position+printed name+signature) ... : Project Engineer Kiki Kong Approved by (position+printed name+signature) ... : RF Manager Hans Hu Testing Laboratory Name ............. : Shenzhen Huatongwei International Inspection Co., Ltd. Address ............................................. : Building 7, Baiwang Idea Factory, No.1051, Songbai Road, Yangguang Community, Xili Subdistrict, Nanshan District, Shenzhen, Guangdong, China Shenzhen Huatongwei International Inspection Co., Ltd. All rights reserved. This publication may be reproduced in whole or in part for non-commercial purposes as long as the Shenzhen Huatongwei International Inspection Co., Ltd. is acknowledged as copyright owner and source of the material. Shenzhen Huatongwei International Inspection Co., Ltd. takes no responsibility for and will not assume liability for damages resulting from the reader's interpretation of the reproduced material due to its placement and context. The test report merely corresponds to the test sample. Report No.: CHTW24070029 Page: 2 of 15 Date of issue: 2024-07-05 Shenzhen Huatongwei International Inspection Co., Ltd. Report Template Version: V06 (2023-09) Contents 1. TEST STANDARDS AND REPORT VERSION ........................................... 3 1.1. Test Standards 3 1.2. Report version information 3 2. TEST DESCRIPTION .................................................................... 4 3. SUMMARY ............................................................................... 5 3.1. Client Information 5 3.2. Product Description 5 3.3. sting Laboratory Information 6 4. TEST CONFIGURATION ................................................................. 7 4.1. Descriptions of test mode 7 4.2. Environmental conditions 7 4.3. Statement of the measurement uncertainty 7 4.4. Equipments Used during the Test 8 5. TEST CONDITIONS AND RESULTS ..................................................... 9 5.1. Conducted Emissions 9 5.2. Radiated Emissions 10 6. TEST SETUP PHOTOS OF THE EUT .................................................. 14 7. EXTERNAL AND INTERNAL PHOTOS OF THE EUT .................................. 15 Report No.: CHTW24070029 Page: 3 of 15 Date of issue: 2024-07-05 Shenzhen Huatongwei International Inspection Co., Ltd. Report Template Version: V06 (2023-09) 1. TEST STANDARDS AND REPORT VERSION 1.1. Test Standards The tests were performed according to following standards: FCC CFR Title 47 Part 15 Subpart B - Unintentional Radiators ANSI C63.4: 2014 – American National Standard for Methods of Measurement of Radio-Noise Emissions from Low-Voltage Electrical and Electronic Equipment in the Range of 9 kHz to 40GHz 1.2. Report version information Revision No. Date of issue Description N/A 2024-07-05 Original Report No.: CHTW24070029 Page: 4 of 15 Date of issue: 2024-07-05 Shenzhen Huatongwei International Inspection Co., Ltd. Report Template Version: V06 (2023-09) 2. TEST DESCRIPTION Section Test Item Section in CFR 47 Result #1 Test Engineer 5.1 Conducted Emissions 15.107(a) N/A N/A 5.2 Radiated Emissions 15.109(a) PASS CHUANFENG LI Note: #1: The test result does not include measurement uncertainty value N/A: Not tested Report No.: CHTW24070029 Page: 5 of 15 Date of issue: 2024-07-05 Shenzhen Huatongwei International Inspection Co., Ltd. Report Template Version: V06 (2023-09) 3. SUMMARY 3.1. Client Information Applicant: Shenzhen Mindray Bio-Medical Electronics Co.,LTD. Address: Mindray Building, Keji 12th Road South, High-tech Industrial Park, Nanshan,518057 Shenzhen,PEOPLE'S REPUBLIC OF CHINA Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co.,LTD. Address: Mindray Building, Keji 12th Road South, High-tech Industrial Park, Nanshan,518057 Shenzhen,PEOPLE'S REPUBLIC OF CHINA Factory: Shenzhen Mindray Bio-Medical Electronics Co.,LTD. Address: Mindray Building, Keji 12th Road South, High-tech Industrial Park, Nanshan,518057 Shenzhen,PEOPLE'S REPUBLIC OF CHINA 3.2. Product Description Main unit information: Product Name: Diagnostic Ultrasound System Trade Mark: Model No.: TE Air Listed Model(s): - Power supply: DC 3.85V from battery Hardware version: 02 Software version: 02 Accessory unit information: Battery information: Model:LP11I003I 1ICP6/29/90 DC 3.85V 1650mAh 6.35Wh Te Note: #: Probe Model No.: e5M Listed Probe Model(s): i5M\z5M\z5Ms\z5Mt\e5M\e5Ms\e5Mt\a5Mx TE Air ultrasonic diagnostic system consists of TE Air application software and wireless probe. The general- purpose probes include i5M\z5M\z5Ms\z5Mt\e5M\e5Ms\e5Mt\a5Mx and they all base on a same electrical design. They are used as typical and representative model on the test base on the original difference information list received from design input which base on market requirement. After analysis tiny difference about additional software added whi…

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TEST SETUP PHOTOS Radiated Emission