CerroZone Mini (up to 180 CFM) - CerroZone A Marmon/Berkshire Hathaway Company [REQUEST CUSTOM PRICING]
The CerroZone Mini Operates at the Source of Contamination and Disease Transmission
People are the Source of Contamination
• Humans shed 37 million bacteria per hour
• These pathogens travel through the air on indoor air currents
• These airborne pathogens land on surfaces creating additional
pathways of disease transmission
CerroZone Works at the Source of the Problem
• CerroZone operates and eliminates opportunistic pathogens
at the Source where they are created and spread
• Creating Healthier Environments keeps staff safe and happier
• Reduction of airborne pathogens keeps facilities safer for
patients and visitors
Engineered for Healthcare
FDA 510(k) Class II Medical Device Clearance
UL 2998 “Zero Ozone” Designation
California CARB Standard Compliant
3rd Party Clinical Validation
Made in the USA
A Marmon/Berkshire Hathaway Company
Built to Defend
Air Travels From One Source Through Hundreds of Feet of Duct Work to Reach All Areas of a Building HVAC is Designed to Supply Heated or Cooled Air to an Entire Building
– Not To Protect Human Life
HVAC is Not Designed for Critical Pathogen Control at the Room Level
Continually Defending Against the Transmission of Dangerous Airborne Pathogens and VOCs
SOURCE-CONTROL TECHNOLOGY
• CerroZone Operates At The Room
• Level Where People Are Present
• Whole Building HVAC
• CerroZone Technology Engineered for Healthcare
To achieve this level of ”Clean Airflow” CFM delivery using HVAC only, creates several problems:
• Increase in Electric Usage and Higher Maintenance Costs
• Use of HEPA Filters May ‘Choke’ HVAC Equipment Creating
Unwanted Mechanical Failures
• Restricted Air Flow Caused by HEPA Filters can Lead to Pressure
Changes and Air Balance Problems
Harnessing the Power of HVAC
1. Air from the room is drawn into the unit through a series of fans and proprietary filters.
2. Internal UV-C lamps generate ozone within the sealed mixing chamber.
3. Ozone destroys all microorganisms within the mixing chamber. Viruses, bacteria, mold, fungus and VOCs are eradicated.
4. The air within the chamber passes through the
proprietary catalyst converting the Ozone back to
Oxygen.
5. Clean and Purified Air is Returned to the Room.
Proof of Efficacy – 3rd Party Testing
Bacteriophage MS2 (1/4 the size of SARS-CoV-2) – over 99.998% per pass,
99.9999% removal in a room. Testing conducted at Aerosol Research and
Engineering “ARE” Laboratories (Olathe, KS).
SARS-CoV-2 (original and Delta strains) – over 99.998% per pass, 99.9999% removal
in a room. Testing conducted at the University of Missouri Laboratory for Infectious
Disease Research (Columbia, MO), MRIGlobal (Kansas City, MO), and Innovative
Bioanalysis (Costa Mesa, CA).
Gram-Positive (Staphylococcus) and Gram-Negative (Pseudomonas) bacteria -- over
99% removal per/pass with both. Testing conducted at ARE Labs (Olathe, KS).
Ammonia (NH4 ) – 100% removal (hit limits of detection) per/pass. No by-products
detected. Testing conducted at ARE Labs (Olathe, KS).
Hydrogen Sulfide (H2 S) – 100% removal (hit limits of detection) per/pass. No by-
products detected. Testing conducted at ARE Labs (Olathe, KS).
Ozone (O3 ) – The "Zero Ozone" testing at Intertek has a 5 PPB (parts per billion)
max threshold. The testing on CerroZone units showed less than 1 PPB and went
down to the detection limit of the sensors since the catalyst was removing
background ozone from the room.
FDA – 510(k) Class II device clearance approved on July 1st of 2022.
Proof of Efficacy – 3rd Party Testing
Cerrozone - A Marmon/Berkshire Hathaway Company