UNE-EN 13624:2014
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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)
Hardcopy , PDF
Spanish, Castilian, English
02-04-2014
27-07-2022
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
5 Test methods
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 fungicidal 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) Neutralizer and Rinsing liquids
B.1 Neutralizers
B.2 Rinsing liquids
B.3 Neutralizer added to the agar for counting
Annex C (informative) Flow diagrams
C.1 Dilution neutralization method
C.2 Membrane filtration 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
E.1 Introduction
E.2 General guidelines for the application and
interpretation of test methods in accordance
with European Standards for chemical disinfectants
and antiseptics
E.3 Guide to the interpretation of tests for chemical
disinfectants and antiseptics
Annex ZA (informative) Clauses of this European
Standard addressing essential requirements or
other provisions of EU Directives
Bibliography
This European Standard specifies a test method and the minimum requirements for fungicidal or yeasticidal activity of chemical disinfectant and antiseptic product that form a homogeneus, physically stable preparation when diluted with hard water or-in case of ready- to- use products- with water. Products can only be tested at concentration of 80% or les (97% with a modified method for special cases) as some dilution is always produced by adding the test organisms and interfering subtance.This European Standard applies to areas and situations where disinfection or antisepsis 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.
| Committee |
CTN 111
|
| DocumentType |
Standard
|
| Pages |
58
|
| PublisherName |
Asociación Española de Normalización
|
| Status |
Superseded
|
| Standards | Relationship |
| NBN EN 13624 : 2013 | Identical |
| ONORM EN 13624 : 2013 | Identical |
| NEN EN 13624 : 2013 | Identical |
| EN 13624:2013 | Identical |
| I.S. EN 13624:2013 | Identical |
| NF EN 13624 : 2013 | Identical |
| DIN EN 13624:2013-12 | Identical |
| BS EN 13624:2013 | Identical |
| NS EN 13624 : 2013 | Identical |
| ISO 4793:1980 | Laboratory sintered (fritted) filters — Porosity grading, classification and designation |
| 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 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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