(Second) Competitive Negotiation Announcement: Our hospital issued a negotiation announcement for the procurement of Mycoplasma pneumoniae RNA testing reagents for Shaanxi Nuclear Industry 215 Hospital on April 15, 2025. As the number of applicants was less than three, we are now issuing a second competitive negotiation announcement to social enterprises. Any company that can meet the requirements of this announcement can participate as required after the announcement is released. The relevant information is announced as follows: 1. Project Name: Shaanxi Nuclear Industry 215 Hospital Mycoplasma pneumoniae RNA Testing Reagent Procurement (Second) 2. Project Number: XY21520250407 3. Specific Content: Mycoplasma pneumoniae RNA Testing 4. Supplier Qualification Requirements: 1. A person with independent legal personality and independent ability to bear civil liability; 2. Suppliers must have the corresponding business scope and capability to undertake and implement this project; 3. Having a good business reputation and a sound financial accounting system, not included in the "Credit China" website (www.creditchina. gov.cn) "list of dishonest persons subject to enforcement or parties involved in major tax violations, or serious illegal and dishonest behavior in government procurement" record list; 4. Having a good record of lawfully paying social security funds; 5. Having the necessary equipment and professional technical capabilities to fulfill the contract; 5、 Requirements for qualification materials for registration: Applicants who come to register must bring the following documents (stamped with the bidder's official seal on each page) to the hospital's bidding and procurement office for inspection by their legal representative or authorized representative. Only after passing the examination can they register to participate. 1. Supplier's business license (three in one), business license, and keep copies of the original documents for reference; 2. Original Certificate of Authorization and Entrustment from the Legal Person (including the name, phone number, email number of the contact person, and the signature and official seal of the legal person); 3. Copy of the ID card of the legal representative and authorized person; 4. Provide performance in the past three years; 5. A commitment letter from a company free from commercial bribery and unfair competition; 6. Suppliers who are manufacturers must provide a valid business license (three in one), medical device production license (not provided for imported products), medical device registration certificate for the equipment they invest in (imported products require a "import" registration certificate), filing certificate, and attachments; 7. Suppliers who are distributors must provide valid business licenses (three in one), medical device operating licenses (Class II and III medical devices may not be provided), valid business licenses of manufacturers (three in one), medical device production licenses or filing certificates (imported products do not need to provide the first four items), medical device registration certificates for the products they invest in (imported products need to provide "import" registration certificates), authorizations and attachments. If the invested products are imported products, a complete authorization chain product authorization letter must be provided; 8. Provide proof of social security payment (in any year from 2022 to 2024); 9. Provide financial audit reports for any year from 2022 to 2024; 10. Please provide a screenshot of the list of individuals who have not been included in the "Credit China" website (www.creditchina. gov.cn) and are not listed in the "Record of Dishonest Persons Subject to Enforcement or Major Tax Illegal Cases, or Serious Illegal and Dishonest Behaviors in Government Procurement". 6、 Registration method: 1. Offline registration, carried by its legal representative or authorized representative