Linkage multi-stage locking sterile connection device, docking device, system and connection method

CN117537199BActive Publication Date: 2026-10-16JUYI TECH SHANGHAI CO LTD
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Patent Information

Application Number
CN202311282831.8
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2023-09-28
Publication Date
2026-10-16
Estimated Expiration
2043-09-28

AI Technical Summary

Technical Problem

这个压力会导致隔离膜与连接件之间的摩擦力过大,隔离膜抽离时,两连接件容易出现位移,影响无菌流体通路的密闭性,使得无菌耦合连接器的可靠性变差

Benefits of technology

[0028] 1. This invention does not distinguish between male and female, so users do not have to waste time and effort distinguishing between male and female when constructing sterile fluid channels, thus improving the efficiency of sterile connection.

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Abstract

The application discloses a connecting device, a docking device, a system and a connecting method, and relates to the technical field of sterile connectors. The technical scheme points of the application include a main body, a connecting rod, a locking component, an isolation film and a sealing ring; a pipe head is arranged on the main body, and the sealing ring is in communication with the pipe head in the main body; the isolation film is arranged on the side, away from the pipe head, of the sealing ring; the connecting rod is hingedly connected to the main body; a butt wall is arranged on the main body, and the connecting rod and the butt wall are symmetrically arranged on the two sides of the pipe head axis; the locking component is connected to the connecting rod, and the locking component is used for applying different sizes of pressure to the butt wall, and part or all of the pressure is used for converting into axial extrusion force on the sealing ring. In the application, the construction of the sterile fluid passage is realized by applying different sizes of axial extrusion force on the sealing ring, the possibility of displacement of the two sealing rings when the isolation film is pulled away is effectively reduced, and the reliability of the sterile fluid passage is ensured.
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