China Hangzhou Bocon company profile

Welcome to Hangzhou Bocon Mechanical& Electrical Equipment Co., Ltd(HZBOCON). The HZBOCON is an advanced global EO-sterilizer supplier. We not only provide safe and stable sterilizers but also provide associated equipment, such as preconditioning room and aeration room. Thoroughly technology consulting, site planning, and after-sale service help you to solve all of the technical problems.

Hangzhou Bocon Mechanical And Electrical Equipments Co., Ltd, was established in 2006. Our company is a high-tech enterprise that multifunctionally and comprehensively comprises research, development, production, sales, and international patent certification. Our company insists on innovation, emphasis on service, and concentrates on quality. Customer primary, quality utmost, and credit paramount are our longtime insistent policy.

Quality Goal : the acceptance rate of 100% !

Seriously treat every customer, every order is our duty, to meet customer requirements is our aim: from the procurement semi-finished production, welding, assembly, testing and experiment monitoring the whole process, step by step of control, strictly follow the ISO 13485:2016 quality management system control program to control.

Quality Policy: reputation from lasting quality!

Performance from the constant pursuit. In 2010, we developed a preheating cabinet, and put it into the market, in succession, we developed the preheating, sterilization, and aeration one-body cabinet and applied for a patent. At the same time we also developed the manufacture preheating room, aeration room, automatic transmission system of EO sterilizer, EO tail gas treatment system, and all of these had been sold and used. We got a good impression from our customers.

URS (User Requirement Specifications)

Definition of requirements to fulfill the demands of the process. Generally, URS is required for eto sterilizer machine before making the design.
In order to meet the user requirement, we pay special attention to the URS (User Requirement Specifications) (such as chamber size, product, package, EO percentage, etc.)
Issued by: User

FDS (Functional Design Specifications)

Specification in which the demands of the buyer are transferred into a technical solution (from the manufacturer's point of view)
Issued by: Manufacturer

DESIGN SPECIFICATION (DS)

Specification of the technical basis and specification of the limiting factors that are to be considered during development, construction and assembly. DS ensures that all customer requirements and current valid standards from CGMP, EU, EN ISO and the FDA are satisfied.

FAT / SAT (Factory Acceptance Test /Site Acceptance Test)

Documented acceptance tests at the supplier/customer with test log, test summary, list of open issues, and release certificates.
In BOCON, before the sale, the factory provides customers with the design and consultation on the overall equipment and facilities of the ETO workshop and assists in the formulation of the overall planning and layout of the ETO workshop. According to the characteristics of the customer site and product, material, packaging, transportation, and future development, we choose the material, configuration, control mode, volume, and quantity for the sterilizer. To assist in the preparation of the ethylene oxide sterilization process, verification scheme, ETO workshop management rules and regulations, equipment use and maintenance, etc. At the same time to provides relevant standards, preheating, residual analysis, processing technology consultation, and cooperation.

DQ, IQ, OQ, PQ

DQ(Design Qualification)
IQ (Installation Qualification)
OQ(Operational Qualification)
PQ(Performance Qualification)
From product and requirements specifications, to risk analyses, to planning and execution of the individual qualification steps, we takes care of everything implementation requires.

Validation: BOCON would provide software validation. IQ, OQ report, and support of PQ after installation.

This future plan aims to drive the ETO sterilizer factory(hzbocon) towards enhanced operational efficiency, environmental responsibility, and technological advancement while prioritizing safety and quality assurance.

Technological Upgrades

Automation: Implement advanced automation in the sterilization process to improve efficiency and reduce human intervention.

IoT Integration: Incorporate Internet of Things (IoT) devices for real-time monitoring and maintenance of ETO sterilization equipment.

Environmental Impact Emission Control:

Invest in emission control technologies to minimize the release of ethylene oxide into the environment.

Safety Measures Employee Training:

Provide comprehensive training programs to ensure that employees are well-versed in handling ETO safely and effectively. Safety Protocols: Review and update safety protocols to meet or exceed industry standards, prioritizing worker safety.

Regulatory Compliance Adherence to Standards:

Stay updated with the latest regulatory requirements related to ETO sterilization and ensure full compliance in all operations.

Quality Assurance Process Optimization:

Continuously improve sterilization processes to enhance product quality while maintaining efficiency. Quality Control Systems: Implement robust quality control systems to ensure consistent and reliable sterilization outcomes.