Research Announcement for the Procurement of High-Performance Computing Clusters, Gynecological Examination Chairs, and Other Equipment at CITIC Xiangya Reproductive and Genetic Specialty Hospital

Release time:

2024/08/24

source：

CITIC Xiangya Reproductive and Genetic Specialty Hospital

A batch of equipment including a high-performance computing cluster and gynecological examination chairs Procurement Requirements

Research Announcement

According to the hospital's development, our hospital plans to procure A batch of equipment including a high-performance computing cluster and gynecological examination chairs Manufacturers with qualified qualifications, good reputation and after-sales service capabilities are welcome to Manufacturer actively participate Product Recommendation 。

I. Detailed List of Procurement Requirements

Equipment Procurement Plan List
Serial Number	Equipment Name	Unit	Quantity	Total Price (Ten Thousand Yuan)	Imported or Not	Remarks
1	High-performance computing cluster	Set	1	600	No Limit	Domestic products preferred
2	Gynecological examination chair	Set	1	15	No Limit	Suggested style as follows:

II. Registration Target: Equipment manufacturers or agents /Regional General Agent 。

III. III. Research Method: Offline Recommendation

IV. Registration Time: 2024 Year 8 Month 26 Day 8:00 to 2024 Year 9 Month 6 Day 17:00

V. Product Recommendation Time and Location: To be determined

VI. The content of the research materials includes but is not limited to the following materials:

Cover of Recommendation Letter ： Intended to recommend Product Name, Specification, Model, Manufacturer, Recommending Unit, Contact and Tel; and prepare the catalog and page numbers according to the following terms and affix the official seal of the registration unit.

Basic Information ： Recommended Product Information Registration Form: The recommending manufacturer needs to accurately fill in the product registration form of the recommended equipment (Attachment 1).

Product Structure Composition ： Recommended Product Technical Parameters and Configuration Details Table: The recommending manufacturer needs to accurately fill in the product technical parameters and configuration details table of the recommended equipment (Attachment 2).

Qualification and Qualification Documents:

Medical device products: Medical Device Production License, Medical Device Registration Certificate, Medical Device Registration Inspection Report, product brochures (original) and instructions of the recommended model, etc.
Non-medical device products: Provide relevant product qualification documents (if any) in this industry.

Product Comparison : What are the brands and models of similar and same-level products on the market, and what are the technical and characteristic differences of this equipment from similar and same-level products.

Installation Conditions : Detail the environment, conditions, auxiliary supporting facilities, water and electricity pipelines, etc. required for equipment installation and operation, and whether there are any special installation site requirements.

Main Users : Specify the main user list of this recommended model in China (Grade-A hospitals), focusing on providing Changsha City's Grade-A hospitals' bidding notices or contracts, and provide configuration lists and warranty period descriptions. 市内三甲医院的中标通知书或合同，同时要提供配置清单及质保年限说明。

VII Other Requirements:

Please participate in the research Manufacturer or authorized by the manufacturer agents submit the registration materials in order and prepare a catalog and page numbers, the format is self-defined. At 2024 Year 9 Month 6 Day 17:00, the electronic version of the materials received will be deemed as successfully submitted, and submissions will no longer be accepted after the deadline. In addition, After affixing the official seal on the paper version of the registration materials, you can choose to submit them on-site or mail them.

Email: zxxy403zzb@163.com ( Note the full name of the company and the Contact Tel)

Address: No. 567, Tongzippo West Road, Xiangjiang New Area, Changsha, Hunan Province CITIC Xiangya Reproductive and Genetic Specialty Hospital Lug Valley General Hospital Office Building 400 Asset Equipment Department

Contact: Peng Teacher 13467634984/ 0731-84566688 ext. 88468

Note: Electronic version (A copy of the Word version) and one copy of the paper version with an official seal. The content of both must be consistent. Application materials that do not meet the specified requirements will be considered invalid.

CITIC Xiangya Reproductive and Genetic Specialty Hospital Co., Ltd.

2024 Year 8 Month 24 Day

Attachment: 《 Product Recommendation Registration Form》、《Requirements for Recommendation Letter Format》

Attachment 1:

Product Recommendation Registration Form

Equipment Name
Manufacturer Name
Specification
Model
Imported or Not
Registration Number
Price
Warranty Period
Warranty Scope and Annual Maintenance Fee for the Whole Machine	The maintenance company needs to indicate whether it is the original manufacturer or a third party, and the annual maintenance fee should be filled in as a percentage.
Are there any consumable parts or accessories?	If so, a quotation sheet for consumable parts and accessories must be provided.
Applicant Name
Applicant Contact and Tel
Remarks:

Attachment 2: Recommendation Letter (Self-prepared)

Must include the following content:

1. Recommendation Letter Cover ： Intended to recommend Product Name, Specification, Model, Manufacturer, Recommending Unit, Contact and Tel; and prepare the catalog and page numbers according to the following terms and affix the official seal of the registration unit.

2. Basic Information ： Recommended Product Information Registration Form: The recommending manufacturer needs to accurately fill in the product registration form of the recommended equipment (Attachment 1).

3. Product Structure Composition ： Recommended Product Technical Parameters and Configuration Details Table: The recommending manufacturer needs to accurately fill in the product technical parameters and configuration details table of the recommended equipment (Attachment 2).

4. Qualification and Qualification Documents: Medical Device Production License, Medical Device Registration Certificate, Medical Device Registration Inspection Report, product brochures (original) and instructions of the recommended model, etc.

5. Product Comparison : What are the brands and models of similar and same-level products on the market, and what are the technical and characteristic differences of this equipment from similar and same-level products.

6. Installation Conditions : Detail the environment, conditions, auxiliary supporting facilities, water and electricity pipelines, etc. required for equipment installation and operation, and whether there are any special installation site requirements.

7. Main Users : Specify the main user list of this recommended model in China (Grade-A hospitals), focusing on providing Changsha City's Grade-A hospitals' bidding notices or contracts, and provide configuration lists and warranty period descriptions. 市内三甲医院的中标通知书或合同，同时要提供配置清单及质保年限说明。