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>UNE EN 1657:2025 - Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
sklademVydáno: 2025-07-30
UNE EN 1657:2025 - Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)

UNE EN 1657:2025

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)

Antisépticos y desinfectantes químicos. Ensayo cuantitativo de suspensión para la evaluación de la actividad fungicida o levuricida de los antisépticos y desinfectantes químicos utilizados en el área veterinaria. Método de ensayo y requisitos (fase 2, etapa 1).

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Označení normy:UNE EN 1657:2025
Počet stran:51
Vydáno:2025-07-30
Status:Norma
Počet stran (Španělsky):54
DESCRIPTION

UNE EN 1657:2025

This document specifies a test method and the minimum requirements for fungicidal or yeasticidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted with hard water or in the case of ready-to-use-products with water. Products can only be tested at a concentration of 80 % or less, as some dilution is always produced by adding the test organisms and interfering substance. This document applies to products that are used in the veterinary area i.e. in the breeding, husbandry, production, transport and disposal of all animals except when in the food chain following death and entry to the processing industry. EN 14885 specifies in detail the relationship of the various tests to one another and to use recommendations . 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 1 test.

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