Ethylene Oxide Sterilizer For Infusion Set

Ethylene oxide sterilizer for Infusion Set Product Benefits and Features:

This EtO sterilizer is engineered to deliver maximum sterilization efficiency while maintaining the integrity of delicate medical polymers such as PVC, silicone, and polyurethane. The equipment operates under low-temperature and low-humidity conditions, ensuring that the material's transparency, flexibility, and mechanical performance remain unchanged after sterilization. Its airtight stainless steel pressure chamber provides superior corrosion resistance and long service life, while an intelligent PLC control system ensures precise regulation of temperature, humidity, gas concentration, and exposure time. The system also supports real-time data logging, automatic cycle control, and digital traceability to meet strict EN1422 and ISO 11135 requirements.

Applications:

This sterilizer is widely used in medical device factories, pharmaceutical packaging plants, and hospital central sterile supply departments (CSSDs). It is particularly well-suited for sterilizing infusion sets, blood transfusion sets, catheters, syringe components, breathing tubes, and other polymer-based consumables that cannot withstand high-temperature steam sterilization. The system ensures uniform gas penetration into complex components, including internal tubing and connectors, providing reliable sterilization even for densely packed production batches. For OEM and ODM medical manufacturers, this sterilizer significantly improves production efficiency while ensuring product sterility and regulatory compliance.

 

 

Precautions and Operating Instructions:

Operators must strictly adhere to ethylene oxide sterilization safety procedures to ensure product quality and workplace safety. Adequate ventilation must be performed after each sterilization cycle to remove residual ethylene oxide gas and prevent toxic residues. Proper ventilation and gas monitoring systems should be installed to maintain a safe environment. Regular maintenance, leak checks, and calibration are necessary to ensure long-term stability and compliance with environmental standards. Additionally, operators should receive training in ethylene oxide gas handling, emergency response, and sterilization validation procedures.

About Riches

 

 

 

 

Production Environment

Production Environment

Production Environment

FAQ

Can the EtO sterilizer be customized according to our infusion set production capacity and factory layout?
Yes, absolutely. Hangzhou Riches Engineering Co., Ltd. provides complete customization services based on your factory's production scale, sterilization volume, and available space. We can design different chamber sizes (from small pilot units to large industrial systems) and configure sterilization cycles to match the batch size and packaging type of your infusion sets. Our engineering team also offers layout optimization and utility connection guidance to ensure smooth integration with your existing production environment.

Can Riches adjust the sterilization cycle parameters to match our specific product materials?
Certainly. Different infusion set materials-such as PVC, silicone, or PE-have varying thermal and chemical sensitivities. Riches provides customized sterilization cycle development services, including fine-tuning temperature, humidity, gas concentration, and exposure duration to protect material integrity while achieving complete sterilization. All parameters are validated according to ISO 11135 standards to ensure compliance and repeatability.

Is it possible to integrate our customized sterilizer with automated loading and unloading systems?
Yes. For large-scale B2B manufacturers, Riches offers integrated automation solutions that include conveyor loading, vacuum preconditioning, and post-sterilization aeration systems. These components can be customized and synchronized with your production management software (MES or SCADA) to form a seamless sterilization workflow, improving throughput and reducing manual handling.

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