The sterile transfer chamber uses vaporized hydrogen peroxide (VHP) as a biological cleaning agent, which can effectively kill fungi, bacterial reproductive bodies, spores, viruses, mycoplasma and other microorganisms. VHP sterilization is a low-temperature, atmospheric pressure decontamination process that has good material compatibility, broad-spectrum, high efficiency, and environmental friendliness;

The sterile transfer chamber is automatically controlled by a SIEMENS programmable logic controller (PLC) for each operating stage of the equipment, with a simple operating interface that allows for the setting and acquisition of cycle parameters. The system runs accurately, stably, and reliably;

The inlet and outlet are double door structures with pneumatic sealing, pneumatic locking, and dual door interlocking functions for working status;

Throughout the entire cycle, the material remains in a Class 100 (A) environment to prevent contamination, and the clean environment inside the cabin also prevents contamination of the A/B clean areas after opening the cabin door;

The sterile transfer chamber is equipped with a trolley type material support and rail guide system inside, making the entry and exit and loading and unloading of materials more convenient; The system monitors the temperature, humidity, and pressure inside the cabin in real-time, with friendly human-machine interaction functions. The optional VHP concentration, dust particle, and planktonic bacteria detection ports make operation more convenient;

Equipped with a built-in VHP generation system, the cyclic loop technology optimizes sterilization time; The sterilization process can be displayed through charts, with real-time online display of key parameters; Save data for each cycle, allowing real-time querying of data records and output of data parameters and charts.

◆ It has an independent ventilation and exhaust unit, including fans, valves, and exhaust pipelines, which can quickly replace VHP gas in the cabin and prevent it from entering the HVAC system; The residual level of VHP gas shall not exceed the occupational health requirements; Residual VHP concentration ≤ 1ppm.

The design and production specifications of the product comply with the relevant requirements of the Chinese Good Manufacturing Practice (GMP); Easy to verify, with good reproducibility. Having complete DP/IQ/OQ/PQ/FAT documents and implementation.