
Automated Laboratory Diagnostic & Cold Plasma Decontamination Systems

Diagnostic & Research Laboratories
Designed for central sterile supply departments (CSSD) and biomedical testing laboratories, this integrated system delivers rapid, low-temperature decontamination for delicate optical endoscopes, robotic instruments, and diagnostic fluidic assemblies. Operating without high heat or toxic chemical aeration, it protects capital equipment while ensuring stringent SAL 10^-6 sterility assurance.
Advanced low-temperature sterilization workstations combined with automated fluidic handling, digital traceability, and clinical validation logging for high-volume healthcare departments.
Vaporized hydrogen peroxide followed by radio-frequency gas plasma eliminates spores at 45°C–55°C.
Integrated barcode tracking logs every instrument set, operator ID, and physical cycle parameter for compliance audits.

Coordinated hardware, optical routing, and nurse station displays.
Modular components engineered to function harmoniously within high-acuity clinical environments.
Vaporized hydrogen peroxide followed by radio-frequency gas plasma eliminates spores at 45°C–55°C.
Integrated barcode tracking logs every instrument set, operator ID, and physical cycle parameter for compliance audits.
Residual sterilant is broken down into water vapor and atmospheric oxygen, requiring zero external ventilation ducts.
Ergonomic sliding racks maximize chamber capacity to handle high daily surgical turnover volumes.
How our integrated architecture accelerates preparation, execution, and patient handoff.
Instruments placed in cassettes; barcode scan links set ID with surgical theater schedule.
Deep vacuum diffusion of VH2O2 followed by RF plasma glow discharge achieving SAL 10^-6.
Validated sterile release with printed batch certificate, ready for immediate operating room delivery.
Measurable benefits for surgical teams, intensive care nurses, and hospital administration.
Protects delicate micro-optical coatings and electronic robotic joints from heat degradation and moisture corrosion.
Automated digital cycle verification certificates with cryptographic timestamps for regulatory records.
Instruments are immediately dry, cool, and ready for immediate clinical redeployment upon cycle completion.
Low power consumption and non-toxic byproducts eliminate hazardous waste disposal protocols.
Connect with our solutions engineering team in Richmond, BC to arrange a facility review, room planning consultation, and system deployment timeline.