BS EN 17387:2021
Chemical disinfectants and antiseptics. Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action. Test method and requirements (phase 2, step 2)
| Standard number: | BS EN 17387:2021 |
| Pages: | 42 |
| Released: | 2021-08-18 |
| ISBN: | 978 0 539 04131 6 |
| Status: | Standard |
BS EN 17387:2021 - Chemical Disinfectants and Antiseptics
Standard Number: BS EN 17387:2021
Pages: 42
Released: 2021-08-18
ISBN: 978 0 539 04131 6
Status: Standard
Overview
The BS EN 17387:2021 standard is an essential document for professionals in the medical and healthcare sectors, providing a comprehensive quantitative test method for evaluating the bactericidal, yeasticidal, and/or fungicidal activity of chemical disinfectants. This standard is specifically designed for use on non-porous surfaces without mechanical action, ensuring that the disinfectants are effective in real-world medical environments.
Key Features
- Comprehensive Testing: The standard outlines a detailed test method and requirements for assessing the efficacy of chemical disinfectants against bacteria, yeast, and fungi.
- Medical Area Focus: Tailored for use in medical settings, ensuring that disinfectants meet the stringent hygiene standards required in healthcare environments.
- Non-Porous Surfaces: Specifically designed for testing on non-porous surfaces, which are common in medical facilities.
- No Mechanical Action: The test method evaluates the disinfectants' effectiveness without the need for mechanical action, providing a realistic assessment of their performance.
Why Choose BS EN 17387:2021?
In the medical field, maintaining a sterile environment is crucial to prevent the spread of infections. The BS EN 17387:2021 standard provides a reliable and scientifically validated method for testing the effectiveness of chemical disinfectants. By adhering to this standard, healthcare facilities can ensure that their disinfectants are capable of eliminating harmful microorganisms, thereby safeguarding patient health and safety.
Detailed Test Method
The standard includes a phase 2, step 2 test method, which is a rigorous and detailed procedure for evaluating the disinfectants' activity. This method involves:
- Preparation of test organisms and test surfaces.
- Application of the disinfectant to the test surfaces.
- Incubation and assessment of microbial reduction.
- Detailed criteria for interpreting the results.
This structured approach ensures that the test results are accurate and reproducible, providing confidence in the disinfectants' performance.
Compliance and Certification
Adopting the BS EN 17387:2021 standard helps healthcare facilities comply with national and international regulations regarding hygiene and infection control. Certification to this standard demonstrates a commitment to maintaining high standards of cleanliness and patient safety.
Who Should Use This Standard?
The BS EN 17387:2021 standard is invaluable for a wide range of professionals, including:
- Healthcare facility managers and administrators.
- Infection control specialists.
- Quality assurance and compliance officers.
- Manufacturers of chemical disinfectants.
- Laboratories conducting disinfectant efficacy testing.
Conclusion
The BS EN 17387:2021 standard is a critical resource for ensuring the effectiveness of chemical disinfectants in medical settings. By providing a detailed and scientifically validated test method, this standard helps healthcare facilities maintain high levels of hygiene and protect patient health. Whether you are a healthcare professional, a manufacturer, or a laboratory technician, this standard is an essential tool for ensuring the safety and efficacy of disinfectants.
BS EN 17387:2021
This standard BS EN 17387:2021 Chemical disinfectants and antiseptics. Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action. Test method and requirements (phase 2, step 2) is classified in these ICS categories:
- 11.080.20 Disinfectants and antiseptics
- 71.100.35 Chemicals for industrial and domestic disinfection purposes
This document specifies a test method and the minimum requirements for bactericidal and yeasticidal and additionally fungicidal 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.
Dilutions are necessary as three concentrations in the active to non-active range are tested.
This document applies to products that are used in the medical area for disinfecting non-porous surfaces without mechanical action.
This document applies to areas and situations where disinfection or antisepsis is medically indicated. Such indications occur in patient care, for example:
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in hospitals, in community medical facilities and in dental institutions;
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in clinics of schools, of kindergartens and of nursing homes; and can occur in the workplace and in the home. It can also include services such as laundries and kitchens supplying products directly for the patients.
EN 14885 specifies in detail the relationship of the various tests to one another and to use recommendations.
Using this document, it is possible to determine the activity of products like commercial formulations or active substances on bacteria and/or fungi in the conditions in which they are used and therefore it corresponds to a phase 2, step 2 test.
This method excludes the evaluation of the activity of products against mycobacteria and bacterial spores.
Dentistry. Materials used for dental equipment surfaces. Determination of resistance to chemical disinfectants
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