PREN 17111 : DRAFT 2017
Current
The latest, up-to-date edition.
CHEMICAL DISINFECTANTS AND ANTISEPTICS - QUANTITATIVE CARRIER TEST FOR THE EVALUATION OF VIRUCIDAL ACTIVITY FOR INSTRUMENTS USED IN THE MEDICAL AREA - TEST METHOD AND REQUIREMENTS (PHASE 2, STEP 2)
10-04-2017
European foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
5 Test method
Annex A (informative) - Example of a typical
test report
Annex B (informative) - Examples of viruses sorted
according to their presence in the human body in
case of virus infection
Annex C (normative) - Detoxification of test mixtures
by molecular sieving
Annex D (informative) - Calculation of the viral infectivity
titre
Bibliography
Describes a test method and the minimum requirements for virucidal 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
|
DocumentType |
Draft
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Current
|
Standards | Relationship |
17/30354236 DC : 0 | Identical |
DIN EN 17111:2017-05 (Draft) | Identical |
17/30354236 DC : DRAFT MAR 2017 | Identical |
DIN EN 17111:2018-12 | 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 14476:2013+A1:2015 | Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal 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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