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EtO Sterilization Cabinet For PVC/PE/TPU Medical Items

EtO Sterilization Cabinet For PVC/PE/TPU Medical Items

The EtO Sterilization Cabinet for PVC, PE, and TPU medical items is a professional low-temperature sterilization solution specifically engineered for heat- and moisture-sensitive polymer-based medical devices. Designed to meet the strict requirements of medical device manufacturers, this system utilizes ethylene oxide gas to achieve deep and reliable sterilization without damaging delicate plastic materials. It is widely applied in the sterilization of disposable and reusable medical products where conventional high-temperature steam sterilization is not suitable.

Features

EtO sterilization cabinet for PVC/PE/TPU medical items Advantages and Key Features:
 

This EtO sterilization cabinet offers exceptional compatibility with polymer materials such as PVC, PE, and TPU, ensuring that medical items maintain their physical integrity, transparency, flexibility, and mechanical strength after sterilization. The system operates at low temperatures, typically between 25°C and 65°C, preventing thermal deformation, brittleness, or discoloration of plastic products. Advanced gas concentration control and precise humidity regulation ensure uniform EtO penetration, enabling thorough microbial inactivation even within complex structures such as long tubing, multilayer packaging, and narrow lumens.

The cabinet is equipped with an intelligent PLC control system and automated sterilization programs, providing accurate management of temperature, humidity, pressure, gas dosage, and aeration cycles. This ensures stable and repeatable sterilization performance across different batches. Integrated safety systems, including leak detection, negative pressure protection, and multi-stage exhaust gas treatment, guarantee safe operation and environmental compliance. Energy-efficient aeration modules also help reduce residual EtO levels quickly, improving production turnover efficiency.

EtO sterilization cabinet for PVC/PE/TPU medical items
 
EtO sterilization cabinet for PVC/PE/TPU medical items
Application:

The EtO sterilization cabinet is widely used for sterilizing PVC, PE, and TPU medical products such as infusion sets, catheters, drainage tubes, breathing circuits, oxygen masks, blood bags, medical connectors, and various disposable surgical accessories. It is suitable for medical device factories, contract sterilization centers, and hospital supply centers that require high reliability and regulatory compliance. The system is ideal for high-volume production environments where consistent sterilization quality is critical for global market approval.

 

 

 

FAQ

Can the EtO sterilization cabinet be customized for different sizes of PVC, PE, and TPU medical products?
Yes. The EtO sterilization cabinet can be fully customized in chamber volume, rack configuration, and loading system to match different product dimensions and batch capacities. Whether you are sterilizing small disposable connectors or large-volume breathing circuits and tubing sets, the internal layout can be engineered to optimize gas circulation and loading efficiency. This ensures uniform sterilization results while maximizing throughput for your specific production scale.

 

Can sterilization parameters be customized for different polymer materials?
Absolutely. Different plastic materials such as PVC, PE, and TPU have varying tolerance levels to temperature, humidity, and gas concentration. Our EtO sterilization system supports customized sterilization recipes, allowing precise adjustment of temperature range, humidity level, EtO dosage, exposure time, and aeration cycle. This ensures effective microbial inactivation while protecting material properties such as flexibility, transparency, and mechanical strength.

 

Can the EtO sterilization cabinet be customized to meet international regulatory standards?
Yes. The system can be tailored to comply with major international standards such as ISO 11135, GMP, and CE requirements. Customization options include validation-ready software, data recording and traceability functions, safety interlock systems, and exhaust gas treatment modules. This enables medical device manufacturers to meet regulatory audit requirements in different global markets while maintaining stable and compliant sterilization performance.

 

 

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