VHP™ DC-A
Decontamination Chamber Atmospheric
Ensure reliable, high-level surface biodecontamination of pre-sterilized material packages to support contamination control in cleanroom material transfer.
Product Benefits
The VHP™ DC-A Biodecontamination Chamber Atmospheric is designed to facilitate aseptic material transfer from lower to higher classification areas, such as cleanrooms. Ideal for surface biodecontamination of pre-sterilized material packages–including vial stopper bags, wrapped components and syringes–it delivers efficient, short cycle times with consistent, reliable results. This biodecontamination system complies with pharmaceutical manufacturing guidelines, including cGMP, cGAMP, EU Annex 1 and ISO 14644 standards. Our comprehensive functionality services ensure reliable, consistent equipment performance through feasibility studies and cycle development testing.
- Effective Biodecontamination: Non-condensing VHP process achieves a 6-log reduction of bioburden, ensuring thorough biodecontamination.
- Enhanced Efficiency: Short cycle times with proven biodecontamination results throughout the chamber enhance productivity and reliability.
- Simple Integration: Easily install and validate this system in the facility without the impact to the facility’s HVAC system, the stand-alone system includes all the required processes for thorough and effective biodecontamination.

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Safety Data Sheets (SDS)
Safety Data Sheets (SDS) provide information on STERIS products for purposes of health, safety and environmental requirements.
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