DANSK DSF/FPREN 17111 PDF

This European Standard specifies a test method and the minimum requirements for virucidal activity of chemical disinfectant products that form a homogeneous, physically stable preparation when diluted with hard water – or in the case of ready-to-use products – with water. This European Standard applies to products that are used in the medical area for disinfecting instruments by immersion – even if they are not covered by the EEC/93/42 Directive on Medical Devices. This European Standard applies to areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example: a) in hospitals, in community medical facilities and in dental institutions; b) in clinics of schools, of kindergartens and of nursing homes; c) and may occur in the workplace and in the home. It may also include services such as laundries and kitchens supplying products directly for the patients. NOTE 1 – the method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used. NOTE 2 – This method corresponds to a phase 2, step 2 test. EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations".