“The RDS Becomes Mainstream in Healthcare IFU’s” See news section.

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Certified for Performance & Efficacy

TMG Health Technologies products have been independently certified for performance and efficacy in the deactivation of pathogens including Endospores.

The RDS Product Series has the distinction of achieving pathogen deactivation up to 99.9999% or a 6 LOG₁₀ in a single 30 Second cycle. ¹ 


EPA Test Standards: ASTM 3135, ASTM E1153, ATCC-BAA1556, ATCC-3513563, ATCC-4255595, ATCC-3279148.


EPA Certified Lab Testing: NG 3513563, NG 4255595, NG 3279148, NG 33592, NG 43598, NG 6538, NG 8769, NG 16022, NG 15597-81.


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All TMG Health products are manufactured and assembled under the same roof, in a 70,000 square foot UL, TUV, ISO 9000:2015, EPA Registered USA facility that meets or exceeds the quality assurance standards as outlined by International Organization of Standards

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Copyright © 2024 TMG Health Technologies | Terms of Use | Privacy | Web Design by Once Interactive
TMG Health Technologies is a biosafety company focused on the rapid decontamination of major pathogens in the workspace. We are a team of experienced technology Executive’s integral to the development of advanced technologies in Healthcare, UVC, Communications, Optics and Wireless. Collectively, we bring a entrepreneurial spirit and outside-the-box thinking to the “HAI” marketplace by concentrating on the people, the process and the technological aspects associated with this major health concern. The Model RDS-32a Rapid Decontamination System is the first of many products. Our goal is to leverage state-of-art technologies that elevate product functionality and performance, are easy to use and offer a real ROI to the customer.
¹ Independently Lab Certified, March 2021. Deactivation efficacy is a factor of the Pathogens resistance, System Intensity, Cycle Time and Distance. Always follow CDC Guidelines prior to the use and operation of all UVC systems.
Advisory
All information, without limitation, on this website is not intended to be used for medical diagnosis or treatment. The information provided is specific to the products represented and is validated by independent certified laboratories to confirm system performance and efficacy.
The RDS systems meet the requirements of UL Intertek 60601-1 for Safety, the FCC for communications EPA registration and the FDA Guidelines for UVC disinfection systems. All systems are made in the USA under strict ISO9001:2015 standards
TMG Health Technologies advises all Users and Operators to follow the national guidelines for operations, safety and disinfection protocols as outlined by the CDC and OSHA
References to disinfection, decontamination, termination and Log reduction are referring generally to the deactivation of pathogens and are not intended to refer to any specific definition of the term as may be used for other purposes by the FDA or the EPA.
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