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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.20 Transfusion, infusion and injection equipment>BS EN ISO 24072:2023 Aerosol bacterial retention test method for air-inlet on administration devices
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immediate downloadReleased: 2023-07-05
BS EN ISO 24072:2023 Aerosol bacterial retention test method for air-inlet on administration devices

BS EN ISO 24072:2023

Aerosol bacterial retention test method for air-inlet on administration devices

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Standard number:BS EN ISO 24072:2023
Pages:16
Released:2023-07-05
ISBN:978 0 539 04713 4
Status:Standard

BS EN ISO 24072:2023 - Aerosol Bacterial Retention Test Method for Air-Inlet on Administration Devices

Introducing the BS EN ISO 24072:2023, a comprehensive guide to the aerosol bacterial retention test method for air-inlet on administration devices. This standard is a must-have for any organization or individual involved in the manufacturing, testing, or use of administration devices. It provides a detailed and systematic approach to ensuring the highest level of safety and efficiency in your operations.

Key Features

The BS EN ISO 24072:2023 is a 16-page document, packed with valuable information and guidelines. It was released on the 5th of July, 2023, and is the latest version of this standard, ensuring that you have the most up-to-date and relevant information at your fingertips.

The standard is identified by the ISBN number 978 0 539 04713 4, guaranteeing its authenticity and credibility. It is recognized and accepted globally, making it a valuable addition to your library, regardless of your location or the nature of your operations.

What Does It Cover?

The BS EN ISO 24072:2023 provides a detailed description of the aerosol bacterial retention test method for air-inlet on administration devices. This test is crucial in ensuring that administration devices are safe for use and do not pose a risk of bacterial contamination.

The standard provides a step-by-step guide on how to conduct the test, including the necessary equipment, procedures, and safety measures. It also provides guidelines on how to interpret the results and implement necessary corrective actions.

Who Should Use It?

The BS EN ISO 24072:2023 is designed for use by a wide range of individuals and organizations. These include manufacturers of administration devices, testing laboratories, regulatory bodies, and healthcare providers. It is also a valuable resource for researchers and academics in the field of medical device safety and testing.

Why Choose BS EN ISO 24072:2023?

Choosing the BS EN ISO 24072:2023 means choosing a standard that is globally recognized and respected. It is developed by experts in the field and is based on the latest research and best practices. By implementing this standard, you can ensure that your administration devices are safe, efficient, and compliant with international regulations.

Furthermore, the standard is easy to understand and implement, making it a practical choice for organizations of all sizes and levels of expertise. It is also regularly updated to reflect changes in technology and regulations, ensuring that you always have access to the most current information.

Order Your Copy Today

Don't miss out on this essential resource. Order your copy of the BS EN ISO 24072:2023 today and take the first step towards ensuring the safety and efficiency of your administration devices. Remember, a small investment today can save you from significant costs and risks in the future.

With the BS EN ISO 24072:2023, you can be confident that you are following the best practices in the industry and are well-equipped to meet the challenges of the ever-evolving medical device landscape.

DESCRIPTION

BS EN ISO 24072:2023


This standard BS EN ISO 24072:2023 Aerosol bacterial retention test method for air-inlet on administration devices is classified in these ICS categories:
  • 11.040.20 Transfusion, infusion and injection equipment
This document specifies a test method to assess bacterial retention ability of finished stand-alone and integrated air-inlet filters on administration devices for infusion and transfusion applications.