Based on the clinical needs of our hospital, we plan to conduct market research on the following goods/services. Qualified suppliers are welcome to participate. 1、 Procurement Project Content: Project Number, Project Name, Quantity, 98 Low Temperature Therapy Device, 2 Parameter Requirements: (See Attachment 1 for details) 2. Registration Requirements and Relevant Materials Required: (1) The specifications and models provided during registration must be consistent with those provided at the negotiation site. Belonging to consumables products, Jiangxi Province medical insurance prices and codes must be provided. As high-value consumables products, registration for products without medical insurance codes is not accepted; (2) If the product manufacturers or authorized agents who participated in the bidding of Nanchang First Hospital in the past 3 years have dishonest behavior or bad records, or have not strictly fulfilled the contract, the hospital will not accept applications; (3) For the convenience of review, please attach a list of the project name, equipment model, registrant name and registration certificate number of the registered equipment registration certificate on the first page of the registration document; (4) Suppliers with after-sales service issues will not be accepted for registration by hospitals; (5) All products submitted must hold a medical device registration certificate, except for special products. Medical device product registration certificate and registration form (for products not managed as medical devices, please refer to the website of the National Medical Products Administration for reference), and affix the official seal of the unit; Those providing Class II and III medical device products must have a medical device registration certificate and registration form, while those providing Class I medical device products must have a product filing registration certificate; Providing Class II and III medical device products produced within the territory of the People's Republic of China must have a medical device production license, and Class I medical device products must have a medical device production filing certificate; Those operating Class III medical devices must have a Medical Device Operating Enterprise License, while those operating Class II medical devices must have a Medical Device Operating Enterprise Registration Certificate; (Medical device registrants or manufacturing enterprises selling medical devices at their domicile or production address do not need to provide); (6) The original and photocopy of the legal representative's identity certificate or legal representative's authorization letter, ID card stamped with the company seal; (7) If the equipment (consumables) submitted by the bidder is not manufactured by the bidder itself, the bidder shall obtain the manufacturer's consent to provide a formal authorization letter or distribution authorization letter for the goods in this bid, stamped with the official seal of the production enterprise; Those who provide false materials will have their bid qualification cancelled. (This item is not required for maintenance and repair projects) (8) Suppliers need to provide screenshots and prints of the query results of the list of "Credit China" dishonest persons and parties involved in major tax violations, stamped with the official seal of the unit; (9) Suppliers are required to provide screenshots and prints of the query results for the list of serious illegal and dishonest behaviors in government procurement on the China Government Procurement Network, stamped with the official seal of the unit; (10) Copy of the Business License for Enterprise Legal Person, stamped with the official seal of the company; (11) If the manufacturer is a small and medium-sized enterprise, the supplier needs to provide a declaration letter from the manufacturer's small and medium-sized enterprise, stamped with the official seal of the unit; (12) If the registered product belongs to energy-saving products, supporting materials must be provided and stamped with the official seal of the unit; (13) If the registered product belongs to environmental labeling products, supporting materials must be provided and stamped with the official seal of the unit; (14) Suppliers must provide proof of enterprise scale (small and medium-sized enterprises)