BS EN 14561:2006
Current
The latest, up-to-date edition.
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)
Hardcopy , PDF
English
30-06-2006
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
5 Test method
5.1 Principle
5.2 Materials and reagents
5.3 Apparatus and glassware
5.4 Preparation of test organism suspensions and product
test solutions
5.5 Procedure for assessing the bactericidal activity of
the product
5.6 Experimental data and calculation
5.7 Verification of methodology
5.8 Expression of results and precision
5.9 Interpretation of results - conclusion
5.10 Test report
Annex A (informative) Referenced strains in national collections
Annex B (informative) Suitable neutralizers
Annex C (informative) Graphical representations of the test method
Annex D (informative) Example of a typical test report
Annex E (informative) Information on the application and interpretation
of European Standards on chemical disinfectants
and antiseptics
Annex ZA (informative) Relationship between this European Standard
and the Essential Requirements of EU Directive
93/42/EEC
Bibliography
Defines a test method and the minimum requirements for bactericidal 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.
Committee |
CH/216
|
DevelopmentNote |
Supersedes 02/564186 DC (06/2006)
|
DocumentType |
Standard
|
Pages |
40
|
PublisherName |
British Standards Institution
|
Status |
Current
|
Supersedes |
This European Standard specifies a test method and the minimum requirements for bactericidal 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 — even if they are not covered by the EEC/93/42 Directive on Medical Devices.
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 kindergardens 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 This method corresponds to a phase 2, step2 test (see AnnexE).
Standards | Relationship |
NBN EN 14561 : 2006 | Identical |
SN EN 14561 : 2006 | Identical |
NF EN 14561 : 2007 | Identical |
UNI EN 14561 : 2006 | Identical |
NS EN 14561 : 1ED 2006 | Identical |
I.S. EN 14561:2006 | Identical |
EN 14561:2006 | Identical |
NEN EN 14561 : 2006 | Identical |
UNE-EN 14561:2007 | Identical |
DIN EN 14561:2006-08 | Identical |
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 14820:2004 | Single-use containers for human venous blood specimen collection |
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