四川Market research on research equipment - human posture information acquisition system
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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: Please 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 a company can only apply for one brand.) Attachment Project 1: Human posture information retrieval system 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 number: 19983137845 Deadline: May 21, 2023 Manufacturer registration materials (each page needs to be stamped with the company seal) 1. "Business License" (three in one) of the production enterprise and the operating enterprise 2. "Medical Device Production Enterprise License" of the production enterprise Or "Medical Device Manufacturing Enterprise Filing Certificate" (only applicable to medical equipment and consumables) 3 The "Medical Device Operation License" or "Medical Device Operation Filing Certificate" of the operating enterprise may not be provided for the sale of Class I medical devices (only for medical equipment and consumables). 4. The sales authorization letter from the production enterprise to the operating enterprise. 5. The manufacturer or agent authorizes the business personnel, and both parties sign and provide copies of the legal representative and business personnel's ID cards (format to be drafted). 6. The Medical Device Registration Certificate or Class I Medical Device Filing. 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