This document is an official authorization letter from Lumicare Medtech Co., Ltd, dated March 27, 2025. It formally appoints Shenzhen Huatongwei International Inspection Co., Ltd. as their agent for the purpose of FCC equipment certification. The designated agent is located at Building 7, Baiwang Idea Factory, No.1051, Songbai Road, Yangguang Community, Xili Subdistrict, Nanshan District, Shenzhen, Guangdong, China, and is represented by Xu Yang.
The letter confirms that all submitted documentation accurately describes the device or system seeking certification. It also certifies that each manufactured, imported, or marketed unit will bear a label identical to the one submitted for approval. Furthermore, the applicant affirms that they are not subject to any denial of Federal benefits, including FCC benefits, as per Section 5301 of the Anti-Drug Abuse Act of 1988.
Lumicare Medtech Co., Ltd acknowledges full responsibility for complying with all terms and conditions for certification, as specified by Nemko North America Inc., even with the agent's involvement. The letter is signed by Tong Liu.
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The letter confirms that all submitted documentation accurately describes the device or system seeking certification. It also certifies that each manufactured, imported, or marketed unit will bear a label identical to the one submitted for approval. Furthermore, the applicant affirms that they are not subject to any denial of Federal benefits, including FCC benefits, as per Section 5301 of the Anti-Drug Abuse Act of 1988.
Lumicare Medtech Co., Ltd acknowledges full responsibility for complying with all terms and conditions for certification, as specified by Nemko North America Inc., even with the agent's involvement. The letter is signed by Tong Liu.
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