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PREN 17111 : DRAFT 2017

Current

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)

Published date

10-04-2017

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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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