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EN 16616:2015

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

Chemical disinfectants and antiseptics - Chemical-thermal textile disinfection - Test method and requirements (phase 2, step 2)

Withdrawn date

02-29-2016

Published date

08-12-2015

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This European Standard specifies a test method and the minimum requirements for the microbicidal activity of a defined disinfection process for the treatment of contaminated linen. This procedure is carried out by using a washing machine as defined in Chapter 5.3.2.17 and refers to the disinfection step without prewash. This European Standard applies to areas and situations where disinfection is indicated. Such indications occur in patient care, for example:-in hospitals, in community medical facilities and in dental institutions;-in schools, kindergartens and nursing homes;- institutions where patients are accommodated, which could suffer from transmissible diseases;- other applications where hygienic treatment of linen is necessary (e.g. food processing, hotels, workwear e. g. from the pharmaceutical industry, laboratories, foodstuffs area or similar institutions).The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used.NOTE This method corresponds to a phase 2 step 2 test (Annex F).

Committee
CEN/TC 216
DevelopmentNote
Supersedes PREN 16616. (08/2015)
DocumentType
Standard
PublisherName
Comite Europeen de Normalisation
Status
Withdrawn

Standards Relationship
ONORM EN 16616 : 2015 Identical
SN EN 16616 : 2015 Identical
UNE-EN 16616:2015 Identical
NF EN 16616 : 2015 Identical
BS EN 16616:2015 Identical
DIN EN 16616:2015-10 Identical
I.S. EN 16616:2015 Identical
PN EN 16616 : 2015 Identical
NS EN 16616 : 2015 Identical
UNI EN 16616 : 2015 Identical
NEN EN 16616 : 2015 Identical

UNE-EN 14065:2017 Textiles - Laundry processed textiles - Biocontamination control system
I.S. EN 14065:2016 TEXTILES - LAUNDRY PROCESSED TEXTILES - BIOCONTAMINATION CONTROL SYSTEM
BS EN 14065:2016 Textiles. Laundry processed textiles. Biocontamination control system
EN 14065:2016 Textiles - Laundry processed textiles - Biocontamination control system
DIN EN 14065:2016-08 TEXTILES - LAUNDRY PROCESSED TEXTILES - BIOCONTAMINATION CONTROL SYSTEM

EN 13624:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity in the medical area - Test method and requirements (phase 2, step 1)
EN 285:2015 Sterilization - Steam sterilizers - Large sterilizers
EN 14348:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)
EN 12353:2013 Chemical disinfectants and antiseptics - Preservation of test organisms used for the determination of bactericidal (including Legionella), mycobactericidal, sporicidal, fungicidal and virucidal (including bacteriophages) activity
EN 13727:2012+A2:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
EN 14563:2008 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)
EN 14562:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
EN 14561:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)

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