Bioquell Clarus L (or L2/L-4/TD0190041) Hydrogen Peroxide Vapour (VHP) Generator

• Surface bio-decontamination of laboratories and cleanrooms.
• Sterilisation of biological safety cabinets, isolators, and pass-through chambers.
• Decontamination of sensitive equipment and instrumentation in pharmaceutical and biotech facilities.
• Use in animal research facilities for pathogen control.
• Terminal sterilisation in hospital pharmacies and sterile compounding areas.

Decontamination Agent

Hydrogen Peroxide Vapour (VHP).

Mobility

Typically a mobile, wheeled unit for ease of relocation between areas.

Decontamination Efficacy

Designed to achieve a 6-log sporicidal reduction for this class of equipment.

Typical Coverage Area

For this class of generator, it can typically decontaminate volumes ranging from small isolators to medium-sized rooms.

Power Supply

Commonly operates on standard single-phase electrical supply, typically 230V, 50Hz for the UK market.

Control System

Units of this type usually feature integrated control panels for cycle programming and monitoring.

• What is Hydrogen Peroxide Vapour (VHP) decontamination?

  VHP decontamination uses gaseous hydrogen peroxide to achieve broad-spectrum bio-decontamination, effectively killing bacteria, viruses, fungi, and spores on exposed surfaces. It is a dry process, making it suitable for sensitive equipment.

• Is this unit suitable for continuous use?

• What kind of maintenance does a VHP generator require?

• Are there any specific facility requirements for operating a VHP generator?

• Can this system be integrated with building management systems (BMS)?

Fumigation systems are valued for their ability to eliminate contaminants and pathogens in controlled environments. Buyers typically prioritise chamber size, gas circulation efficiency, and safety interlocks when selecting used units. Industry sentiment suggests these systems offer strong reliability when maintained properly. Key considerations include previous usage history, seal integrity, and availability of replacement parts. Well-maintained examples deliver consistent performance across pharmaceutical, biotech and laboratory applications. Buyers should verify calibration records and operational logs before purchase to ensure continued effectiveness and regulatory compliance.

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