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Client Success Stories and Solutions for our Customers

Welcome to Junmu’ Client Success Stories section, where we proudly showcase our completed orders and solutions spanning medical and laboratory equipment. Here, you’ll gain valuable insights into our diverse product range, satisfied customers, and the regions we serve. We believe transparency builds trust—and these case studies reflect our commitment to excellence in both medical and laboratory fields.

cSSD

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The Disinfection Supply Center Management Traceability System is a series of software products developed by Junmu Medical based on years of experience in hospital infection control and combined with digital information technology, which not only meets the urgent need for improving CSSD management in Chinese hospitals but is also tailor-made for China’s Ministry of Health’s latest standards. It focuses on providing a comprehensive management solution for sterile supply in hospitals and is committed to promoting the development of hospital infection prevention and control, thereby minimizing the risk of infections.

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Design Basis

1. CSSD(Central Sterile Supply Department) Management Standard WS 310.1-2016
2. CSSD (Central Sterile Supply Department) Cleaning, Disinfection, and Sterilization Technical Operation Code WS 310.2-2016
3. CSSD(Central Sterile Supply Department) Cleaning Disinfection and Sterilization Result Test Code WS 310.3-2016
4. The Central Air Conditioning Ventilation System of Public Places Meets the Cleanliness Standard WS 394-2012
5. Technical Standard for Disinfection of Medical Institutions (2023 edition)
6. Disinfection Management Measures (Issued on December 26, 2017)
7. General Hospital building design standard 51039-2014
8. Standard Design Code of Clean Workshop GB 50073-2013
9. China Hospital Construction Guidelines (2018 Edition)
10. Standard for Architectural Lighting Design (GB 50034-2013)

Design Principle

1. The whole process from a contaminated area to a clean area, without any cross or reverse.
2. Physical barriers are placed between the decontamination area, package inspection and sterilization area, and sterile area.
3. Delivery paths are established between the decontamination area and the package inspection &sterilization area; the buffer rooms should be placed separately for people to enter.
4. The handwashing facility in the buffer room should be inductive.
5. A sealing-type sanitary ware room should be included in the package inspection &sterilization area.

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