We are now collecting relevant materials for the following materials. Please contact our department from suppliers who have relevant products and information and have legal and qualified qualifications. (Notice: Suppliers must first scan the QR code below to fill in the registration information and submit the paper version of the materials to the following address. Failure to scan the code or submit the paper version of the materials will be considered as unsuccessful registration, and each company can only apply for one brand per project. Only one complete registration material needs to be submitted, which should include all relevant materials for the registered projects. Suppliers who submitted the registration materials in the first round do not need to submit the materials again in the second round.) Attachment Project 1: Batch of Low Value Tools and Equipment for Cafeteria Registration Address: No. 1094, Water Tower Building, West China Hospital, Sichuan University Registration Time: Monday to Friday, 9:00-11:00 am, 2:00-5:00 pm Contact Person: Teacher Liu Contact Phone: 19983137845 Deadline: May 21, 2025.4.21 Manufacturer Registration materials (each page needs to be stamped with the company seal) 1. "Business License" of the manufacturing and operating enterprises (Three in one) 2. The "Medical Device Production Enterprise License" or "Medical Device Production Enterprise Filing Certificate" of the manufacturing enterprise (only applicable to medical equipment and consumables). If not involved, an official non-medical device description (only for medical equipment and consumables) is required. 7. For medical consumables, a screenshot of the Sichuan Provincial Medical Device Platform must be provided. 8. A copy of the webpage of this project on the official website of West China Hospital (please put it on the first page and indicate the registration project). Please prepare a complete set of registration materials separately according to the corresponding project you have registered for. This material only involves registration and supplier qualification preliminary review. Specific requirements will be subject to the subsequent process. This information is not authorized to be published through other channels. Specific requirements shall be subject to the content published on the official website by the Equipment and Materials Department