Dry Fog Sterilization Service

The Sterile Science Dry Fog system provides a high technology solution to disinfect pharmaceutical suites, cleanrooms, healthcare facilities, critical production and laboratory areas.

Facility, safety and infection control managers trust Sterile Science to rapidly and effectively provide a six log kill (99.9999%) of microbial, bacterial and fungal contamination.

Superior Performance

The Dry Fog system uses a combination of industry leading cold sterilant and our state of the art Dry Fog delivery system to rapidly and safely deliver vapor to even the most complex areas. The multi-port dry fogging head allows for rapid vapor dispersion that ensures that the most distant areas are reached effectively

  • Controlled and consistently accurate droplet size (Sauter Mean Droplet diameter of 5.9 microns)
    • Minimizes risk of condensation
    • Does not wet surfaces
    • Ensures penetration into inaccessible areas
  • Dry Fog system can decontaminate multiple linked rooms simultaneously

Short Process Time

Typically, the entire sterilization process can be completed in less than 3 hours, depending upon room size and ventilation system efficiency, compared to up to 3-5 days with some conventional systems

  • No pre-conditioning of the room is required
  • No need for additional fans for coverage
  • No long aeration process

The Sterile Science Dry Fog system results in substantially lower clean room downtime.

Enivonrmentally Friendly, EPA Registered Chemistry

The Dry Fog System utilizes Minncare® a peracetic acid and hydrogen peroxide based proprietary chemistry developed by Mar Cor for optimized biocidal efficacy. It is a fully biodegradable sporicide that will leave no measurable air residuals. Minncare is registered by the EPA for use as a fog to enhance existing cleaning and disinfection process.

  • Contains only pharmaceutical quality raw materials
  • No toxic aldehyde vapors
  • Fully biodegradable
  • EPA Registration Number 52252-4

Fully Validated and Widely Used

  • The Dry Fog System has been validated by hundreds of FDA audited pharmaceutical production facilities worldwide
  • A valid and reproducible procedure according to international Pharma Standards
  • Efficacy results can be verified using biological and chemical indicators
  • Chemistry has passed AFNOR Norm NF T 72-281, showing a 6.9 log reduction of bacteria spores

For a partial list of facilities using the Dry Fog system, review our Reference List or contact a Sterile Science specialist

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