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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.080 Sterilization and disinfection>11.080.20 Disinfectants and antiseptics>BS EN 17111:2018 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)
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BS EN 17111:2018 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)

BS EN 17111:2018

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)

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Standard number:BS EN 17111:2018
Pages:44
Released:2018-10-31
ISBN:978 0 580 97011 5
Status:Standard
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BS EN 17111:2018


This standard BS EN 17111:2018 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) is classified in these ICS categories:
  • 11.080.20 Disinfectants and antiseptics
This document 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 document applies to products that are used in the medical area for disinfecting instruments by immersion. This document 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".