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Human Healthcare- Infection Control: Sterinova

 

Quality Assurance
Sterinova can be used with total confidence as it is manufactured in a Good Manufacturing Practice facility in conformance with European standards.

The active ingredient in Sterinova is US EPA registered.

 

Validation of Effectiveness
Having identified the microorganisms of concern, Medentech then evaluated the dosages and effectiveness of Sterinova under 'clean' and 'dirty' conditions. Because hypochlorites are known to be degraded in the presence of milk, Sterinova was evaluated in the presence of milk to simulate 'dirty' conditions.

 

Bacteria
Efficacy tests were undertaken to determine activity against bacteria of the Sterinova solution. The tests were performed by an independent, US FDA registered laboratory at different temperatures and with milk concentrations up to 1% (equivalent to 50mls of milk deposit in a typical 5 litre sterilising unit). In all cases all micro-organisms were dead well within the 30 minute disinfecting period used in the Sterinova method.

 

For further information info@medentech.com


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