Tso3 Inc.

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Contact: Charles Hancock
Web: http://www.tso3.com
E-Mail:
Address: 2505, Dalton Avenue, Québec, Quebec G1P 3S5, Canada
Phone: +1-(418)-651-0003/866-715-0003 | Fax: +1-(418)-653-5726 | Map/Directions >>

Profile: Tso3 Inc.specializes in offering sterilization solutions. Our Sterizone® is a 125 l and low-temperature sterilizer, which is designed for the rapid sterilization of heat and moisture-sensitive medical devices. It generates ozone which is a sterilant through an integrated generator. Ozone is an environmental friendly microbiocide which rapidly kills the hardiest microorganisms. Our system uses only water, oxygen and electricity. Its by-products are water vapor and oxygen. There are no toxic wastes produced by the system, which requires special handling, storage and disposal.

FDA Registration Number: 3004148947
US Agent: Alexandre Jokic / Tso3 Corp.
Phone: +1-(844)-833-0003 E-Mail:

4 Products/Services (Click for related suppliers)

• Biological Sterilization Process Indicator (FDA Code: FRC / 880.2800)

A biological sterilization process indicator is a device intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor adequacy of sterilization. The device consists of a known number of microorganisms, of known resistance to the mode of sterilization, in or on a carrier and enclosed in a protective package. Subsequent growth or failure of the microorganisms to grow under suitable conditions indicates the adequacy of sterilization.

• Ethylene-Oxide Gas Sterilizer (FDA Code: FLF / 880.6860)

An ethylene gas sterilizer is a nonportable device intended for use by a health care provider that uses ethylene oxide (ETO) to sterilize medical products.

• Physical/Chemical Sterilization Process Indicator (FDA Code: JOJ / 880.2800)

• Sterilization Wrap (FDA Code: FRG / 880.6850)

A sterilization wrap (pack, sterilization wrapper, bag, or accessories, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used.