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ASTM E 3151 : 2018

Current

Current

The latest, up-to-date edition.

Standard Test Method for Determining Antimicrobial Activity and Biofilm Resistance Properties of Tube, Yarn, or Fiber Specimens

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

01-02-2018

€56.53
Excluding VAT

CONTAINED IN VOL. 11.08, 2018 Provides an in vitro, quantitative assay to evaluate the antimicrobial activity of specimens with tubular geometries or small segments of yarn or fibers that have been treated with an antimicrobial agent.

Committee
E 35
DocumentType
Test Method
Pages
9
PublisherName
American Society for Testing and Materials
Status
Current

1.1This test method is designed as an in vitro, quantitative assay to evaluate the antimicrobial activity of specimens with tubular geometries or small segments of yarn or fibers that have been treated with an antimicrobial agent. Further, the method was designed to provide a quantitative assessment of a specimen’s ability to resist microbial colonization and subsequent biofilm formation relative to an untreated control specimen.

1.1.1The difference in number between the planktonic microbial population recovered from the treated test specimen and the population recovered from the control test specimen is the measure of the antimicrobial activity.

1.1.2The measure of the ability of the treated test specimen to resist biofilm development is the difference between the adherent microbial population recovered from the treated test specimen and the adherent microbial population recovered from the control test specimen.

1.2Testing is to be performed by individuals trained in microbiological techniques under appropriately controlled conditions to ensure the integrity of results and personnel safety.

1.3The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

1.4This standard may involve hazardous materials, operations, and equipment. This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.

1.5This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM E 2756 : 2024 : REV A : EDT 1 Standard Terminology Relating to Antimicrobial and Antiviral Agents
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ASTM E 691 : 2020 Standard Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method
ASTM E 2756 : 2019 Standard Terminology Relating to Antimicrobial and Antiviral Agents
ASTM E 691 : 2019 : EDT 1 Standard Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method
ASTM E 691 : 2023 Standard Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method
ASTM E 2756 : 2010 Standard Terminology Relating to Antimicrobial and Antiviral Agents
ASTM E 691 : 2022 Standard Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method
ASTM E 1054 : 2021 Standard Test Practices for Evaluation of Inactivators of Antimicrobial Agents
ASTM E 691 : 2009 Standard Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method
ASTM E 691 : 2021 Standard Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method
ASTM E 2756 : 2018 Standard Terminology Relating to Antimicrobial and Antiviral Agents
ASTM E 1054 : 2008 Standard Test Methods for Evaluation of Inactivators of Antimicrobial Agents

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