Sun Yat sen University Affiliated Third Hospital Yuedong Hospital Laboratory Reagent Research Announcement Release Time: May 20, 2025 Click Count: 4 Author: admin Sun Yat sen University Affiliated Third Hospital Yuedong Hospital intends to conduct market demand research on the following reagents and their supporting equipment. The research period is from May 20, 2025 to May 26, 2025. Qualified suppliers and distributors are welcome to submit their materials for registration. 1、 Project Overview (see attachment for details): 2. Supplier Qualification Requirements: 1. The supplier shall meet the conditions stipulated in Article 22 of the Government Procurement Law. 2. Suppliers who are not included in the list of dishonest persons subject to enforcement, parties involved in major tax violations, records of serious illegal and dishonest behavior in government procurement, or other non compliant conditions on the "Credit China" website (www.creditchina. gov.cn) and the China Government Procurement Network (www.ccgp. gov.cn). 3. Suppliers should be independent legal entities established in accordance with the law; 4. Suppliers should have legal and valid authorization for the medical device business scope and reagent manufacturers corresponding to the products they sell. 5. If any of the following situations exist between different suppliers, they will not be accepted as suppliers participating in the same project competition: A. If there is an investment and invested relationship between each other; B、 Members of each other's operators, board of directors (or similar management organizations) are in direct family or spousal relationships; C、 The legal representative or unit head is the same person or different units with controlling or management relationships. 3、 The materials required for supplier registration are: (1) Reagent Information 1. Cover Sheet (prepared according to Attachment 1); 2. Market survey form (prepared according to Annex 2); 3. Detailed quotation table (prepared according to Attachment 3, ensuring that the quotation can create agreements, place orders, and receive payments normally in the Guangdong Province Drug and Medical Consumables Procurement Management System); 4. List of product users and market prices (in principle, copies of invoices from at least 3 hospitals in the past 2 years should be provided); 5. A copy of the business license of the participating company, a copy of the medical device operating license, and a power of attorney from the legal representative, all of which must be stamped with the official seal of the participating company; 6. Copy of the business license, medical device production license, medical device registration certificate, customs declaration form (for imported products), authorization letter, product description (instructions, color pages, functional features, etc.), and user list of the enterprises participating in the project products. The above documents must be stamped with the official seals of the distributor and the product manufacturing enterprise; On the day of registration, if the credit results are checked on the "Credit China" website and the China Government Procurement Network, and the relevant records of dishonesty have become invalid, the service provider needs to provide relevant supporting documents. Note: The above submitted materials are sorted into a booklet in order, and all registration materials are in PDF electronic format (Attachment 2 and Attachment 3 need to be accompanied by an Excel version, and the filling content can refer to Attachment 4). Please send them to the email address: zssyydyysjb@163.com The email title naming format is: project name+project number+registered company name. （2） Supporting equipment information (if no equipment is needed, this item can be ignored) 1. Supply