Propokan Pro doo, the market leader in the Republic of Serbia in ultraviolet systems for disinfection of HVAC systems, has successfully completed the 1st phase of testing its products for residential, commercial and health facilities for the efficiency of destruction of all viruses and bacteria, including SARS-CoV-2 (the virus that causes COVID-19 disease). The test report entitled "Neutralization of viruses and bacteria by the microbiological system of UVC radiation" states that the projected radiation dose HVAC UVC Sterilization Duct, by exposure to UVC rays with a wavelength of 253.7 nm, destroys all viruses and bacteria with an efficiency greater than 99,00%.
The testing was performed in an accredited testing laboratory, which is both a certification and a control body. The test is designed to model the exposure time in parallel with the inactivation of all viruses and bacteria, including the virus SARS-CoV-2 in air moving in the HVAC system or ventilation. The product has been tested HVAC UVC Sterilization Duct, intended for both residential and commercial and health facilities. Phase 2 testing is currently underway.
Propokan Pro d.o.o. now, as a reliable supplier of microbiological systems, it has a certificate for air and surface disinfection. Propokan Pro d.o.o. is recognized worldwide in the areas of UVC disinfection and indoor air quality. Our product reduces indoor air pollution, sterilizes viruses, bacteria and mold, neutralizes odors and provides disinfection of air and chemical-free surfaces. Propokan Pro d.o.o. is recognizable for its innovations, numerous patents and awards.
HVAC UVC Sterilization Duct it is not intended to diagnose, treat, prevent or cure any disease.
The Agency for Medicines and Medical Devices of the Republic of Serbia, with its expert opinion no. 515-00-02055-2020-7 dated 6 November 2020, confirmed that HVAC UVC Sterilization Channel is not considered a medical device, ie. that it does not comply with the EU Directive 93/42 / EEC (Directive on General Medical Devices), or the EU Directive 98/79 / EC in vitro diagnostic medical devices), so that for its placing on the market of the Republic of Serbia, it is not necessary to obtain a Decision on registration of a medical device.