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Hubei Yijiantang Technology Co., Ltd
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Hubei Yijiantang Technology Co., Ltd. is registered at Room 1-4, 8th Floor, Building 7, Guannan Fuxing Pharmaceutical Park, No. 58 Guanggu Avenue, Donghu New Technology Development Zone, Wuhan (Wuhan Free Trade Zone Wuhan Area). The registration authority is the Market Supervision and Administration Bureau of Donghu New Technology Development Zone, with Feng Yonghua as the legal representative. The company's business scope includes general projects such as technical services, technical development, technical consulting, technical exchange, technology transfer, technology promotion, IoT technology research and development, sales of Class II medical devices, cloud computing equipment technology services, production of protective equipment for medical staff (Class I medical devices), production of Class I medical devices, sales of Class I medical devices, production of daily masks (non-medical), retail of protective equipment for medical staff, and service consumption robots. Manufacturing, sales of consumer robots, research and development of intelligent robots, sales of electronic products, Internet of Things technical services, Internet of Things application services, software development, cloud computing equipment sales, cloud computing equipment manufacturing, health consulting services (excluding diagnostic services), remote health management services, marketing planning, food sales (only pre packaged food sales), health food (pre packaged) sales, food Internet sales (only pre packaged food sales), general merchandise sales, goods import and export, Chinese medicine health care services (non-medical), veterinary equipment sales. (In addition to the licensed business, it can independently operate items not prohibited or restricted by laws and regulations) Licensed items: Internet information services, production of Class II medical devices, Internet information services for medical devices, production of medical masks, production of protective articles for medical personnel (Class II medical devices). (For projects that require approval by law, business activities can only be carried out after approval by relevant departments. The specific business projects shall be subject to the approval documents or licenses issued by the relevant departments.)