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>UNE standards>UNE EN 17111:2019 - Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
in stockReleased: 2019-07-29
UNE EN 17111:2019 - Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)

UNE EN 17111:2019

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)

Antisépticos y desinfectantes químicos. Ensayo cuantitativo de portadores para la evaluación de la actividad virucida de los instrumentos utilizados en el área médica. Método y requisitos de ensayo (fase 2, etapa 2).

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Standard number:UNE EN 17111:2019
Pages:43
Released:2019-07-29
Status:Standard
Pages (Spanish):46
DESCRIPTION

UNE EN 17111:2019

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. This European Standard applies to areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example: in hospitals, in community medical facilities and in dental institutions; in clinics of schools, of kindergartens and of nursing homes; 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 .

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