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rapid, validated bio-decontamination for critical environments

The Halton Vita VDU-750 supports contamination control in pharmaceutical manufacturing environments, including sterile and non-sterile manufacturing areas. The validated VH₂O₂ decontamination process helps facilities meet GMP requirements, support Annex 1 compliance and strengthen their Contamination Control Strategy (CCS).

Key performance facts

Effective agains bacteria, viruses, fungi and spores

Penetrates hard-to-reach areas and porous materials

No residue — hydrogen peroxide breaks down into hydrogen and oxygen

Fully automated vaporising, distribution and aeration process

Consistent and validated disinfection results

Safe for sensitive materials, including electronics

Short process time with rapid aeration

Seamless integration with facility automation systems




How it works

The VDU-750 operates as a fully automated system, reducing the risk of human error and ensuring repeatable, validated results. During each cycle, the system continuously monitors critical process parameters, including hydrogen peroxide concentration, relative humidity, air temperature, exposure time and process status.

After the decontamination phase, an integrated catalytic aeration process rapidly removes residual hydrogen peroxide, allowing the space to return to operation with minimal downtime.

Complete and fast process


Application areas



VH₂O₂ Decontamination as a Service

References

Trusted by Hospitals Around the World

Halton is a trusted partner for hospitals worldwide. Our advanced indoor air solutions are installed in hundreds of operating rooms across Europe, Asia, the Middle East and beyond.

Talk to a Operating Room Ventilation Expert

Planning a new operating room, renovating a surgical suite, or addressing airflow, pressure, or comfort challenges? Our team can help you select the right ventilation strategy, optimize clean airflow and pressure control, and evaluate energy-efficient solutions tailored to your clinical environment.

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