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Homepage>BS EN 1040:2005 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of basic bactericidal activity of chemical disinfectants and antiseptics. Test method and requirements (phase 1)
sklademVydáno: 2006-01-16
BS EN 1040:2005 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of basic bactericidal activity of chemical disinfectants and antiseptics. Test method and requirements (phase 1)

BS EN 1040:2005

Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of basic bactericidal activity of chemical disinfectants and antiseptics. Test method and requirements (phase 1)

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Označení normy:BS EN 1040:2005
Počet stran:44
Vydáno:2006-01-16
ISBN:0 580 46960 3
Status:Standard
DESCRIPTION

BS EN 1040:2005


This standard BS EN 1040:2005 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of basic bactericidal activity of chemical disinfectants and antiseptics. Test method and requirements (phase 1) is classified in these ICS categories:
  • 71.100.35 Chemicals for industrial and domestic disinfection purposes
  • 11.080.20 Disinfectants and antiseptics

This European Standard specifies a test method and the minimum requirements for basic bactericidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted 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 water.

This European Standard applies to active substances (antibacterial biocides) and to formulations under development that are planned to be used in food, industrial, domestic and institutional, medical and veterinary areas. It applies also to the evaluation of bactericidal activity of chemical antiseptics and disinfectants when appropriate standards are not available.

NOTE 1 This European Standard does not evaluate the activity of a product for an intended use.

NOTE 2 This method corresponds to a phase 1 test (Annex F).