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SteriTech

SteriTech is a South African company, established in 1996, with the aim of providing specialist Residual Infection Control products, along with the technical support necessary for their successful use.

SteriTech's holistic range of Infection Control products range from instrument reprocessing products, to surface disinfectants, to detergent-disinfectants, hand hygiene products, airborne microbial control products and other disinfectant-based niche products.

All of these products are based on SteriTech concentrate, SteriTech's active ingredient complex, (a Quaternary Ammonium Compound / Tributyl Tin Oxide Blend) which is used in all SteriTech products, just at differing levels depending on the purpose for which the product is intended to be used.

To this day SteriTech has not split its focus and is still 100% dedicated to supplying strictly Infection Control related products. With 15 years of experience in many different industries, SteriTech endeavour to provide Infection Control Solutions which are tailor-made to practical in-use situations, rather than just the theory governing Infection Control.

We, at SteriTech, firmly believe in traceable and accredited Quality Control Systems to ensure that the Quality of our products is always maintained at the very highest levels. This is intended to not only comply with the moral & ethical standards we set ourselves, but also to give our customers the ultimate peace of mind. As such SteriTech, in terms of its administrative and manufacturing divisions, carries the following accreditation certifications:
SABS 636:2009 (Permit number 7333/10881): Disinfectants based on Quaternary Ammonium Compounds

SABS 490:2009 (Permit number 7333/14207): Disinfectants Alcohol-based Handrub
ISO 9001:2008 (Registration number LS 4531): Quality Management Systems in respect of the Developing, Marketing and Registering of Holistic Residual Infection Protection Products for the Medical, Dental, Veterinary, Beauty, Culinary, Agriculture, Education and Aviation Industries.

ISO 13485:2004 (Registration number MDS 0006): Medical Devices - Quality Management Systems - Requirements for Registration Purposes in respect of the Developing, Marketing and Registering of Holistic Residual Infection Protection Products for the Medical, Dental and Veterinary Industry.

In addition to the above-mentioned accreditations, all required products are registered in terms of the government-mandated Compulsory Specification regulations of the country in which they are sold.