江西[Yujiang District] Jiangxi Mingya Tendering Agency Co., Ltd. Announcement on Electronic Non Face to Face Public Bidding for the Procurement of Operating Room Equipment for the New Campus of Yujiang District Traditional Chinese Medicine Hospital (Tender No.: JXMY2025-YJCG-GK001)

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Jiangxi Mingya Tendering Agency Co., Ltd. Regarding the Electronic Non Face to Face Public Tendering and Bidding Announcement for the Procurement of Operating Room Equipment in the New Campus of Yujiang District Traditional Chinese Medicine Hospital (Tender No.: JXMY2025-YJCG-GK001) Project Overview Potential bidders for the Yujiang District Traditional Chinese Medicine Hospital New Campus Operating Room Equipment Procurement Tendering Project should be listed on the Jiangxi Provincial Public Resource Trading Platform (website: https://www.jxsggzy.cn/ )Obtain the bidding documents and submit the bid documents before 9:30 am on May 15, 2025 (Beijing time). 1、 Project Basic Information: Project Number: JXMY2025-YJCG-GK001 Project Name: Procurement of Operating Room Equipment in the New Campus of Yujiang District Traditional Chinese Medicine Hospital Procurement Method: Public Bidding Budget Amount: 2079000.00 yuan Maximum Price Limit: 1614500.00 yuan Procurement Requirements: Procurement Item Number Procurement Item Name Quantity Unit Procurement Budget (RMB) Technical Requirements or Service Requirements Yu Purchase 2024F001293792 Yu Jiang District Traditional Chinese Medicine Hospital New Campus Operating Room Equipment Procurement Batch 1: 2079000.00 yuan Please refer to the attached announcement Contract Performance Period: Execute according to the requirements of the bidding documents. This project does not accept consortium bidding. 2、 Qualification requirements for applicants: 1. Meet the provisions of Article 22 of the Government Procurement Law of the People's Republic of China; 1.1. Capable of independently assuming civil liability; 1.2. Have a good business reputation and sound financial accounting system; 1.3. Possess the necessary equipment and professional technical capabilities to fulfill the contract; 1.4. Have a good record of paying taxes and social security funds in accordance with the law; Within the three years prior to participating in government procurement activities, there has been no significant record of illegal activities in business operations; 1.6 Other conditions stipulated by laws and administrative regulations. 1.6.1. Different bidders with the same unit leader or direct controlling or management relationships shall not participate in procurement activities under the same contract. 1.6.2 Bidders who provide overall design, specification preparation, project management, supervision, testing and other services for the procurement project shall not participate in the procurement activities of the procurement project. 1.6.3 Bidders who are listed as dishonest persons subject to enforcement and major tax violation cases (major tax violation dishonest subjects) by the "Credit China" website, or listed as serious illegal and dishonest behavior records in government procurement by the "China Government Procurement Network" website (punishment period has not yet expired), shall not participate in government procurement activities of this project. (On site verification by the purchaser or procurement agency during bid opening) 2. Qualification requirements for implementing government procurement policies: This project implements government procurement policies for small and medium-sized enterprises, prison enterprises, welfare units for people with disabilities, energy-saving, environmental protection products, etc. For specific regulations, please refer to the bidding documents. 3. Specific qualification requirements for this project: (1) For Class I, II, and III medical device products used in clinical practice, Class II and III medical device products must have a medical device registration certificate and registration form (new certificates do not require a registration form), and Class I medical device products must have a product filing registration certificate; (2) Class I, II, and III medical devices produced within the territory of the People's Republic of China
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