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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.10 Anaesthetic, respiratory and reanimation equipment>BS EN ISO 27427:2023 Anaesthetic and respiratory equipment. Nebulizing systems and components
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immediate downloadReleased: 2023-07-27
BS EN ISO 27427:2023 Anaesthetic and respiratory equipment. Nebulizing systems and components

BS EN ISO 27427:2023

Anaesthetic and respiratory equipment. Nebulizing systems and components

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Standard number:BS EN ISO 27427:2023
Pages:42
Released:2023-07-27
ISBN:978 0 539 05171 1
Status:Standard

BS EN ISO 27427:2023 Anaesthetic and Respiratory Equipment - Nebulizing Systems and Components

Introducing the BS EN ISO 27427:2023, the latest standard for anaesthetic and respiratory equipment, specifically focusing on nebulizing systems and components. This comprehensive guide is an essential resource for healthcare professionals, equipment manufacturers, and anyone involved in the design, production, and application of anaesthetic and respiratory equipment.

Released on 27th July 2023, this standard is the most up-to-date and relevant guide in the industry. It is meticulously designed to ensure the highest level of safety and efficiency in the use of nebulizing systems and components.

Key Features

The BS EN ISO 27427:2023 standard spans a total of 42 pages, each packed with crucial information and guidelines. It covers a wide range of topics, from the basic principles of operation to the intricate details of equipment design and maintenance. This standard is a comprehensive guide that leaves no stone unturned when it comes to anaesthetic and respiratory equipment.

With its unique ISBN number 978 0 539 05171 1, this standard is easily identifiable and accessible for reference. It is a valuable addition to any medical library, serving as a reliable source of information for both professionals and students in the field.

Importance of the Standard

The BS EN ISO 27427:2023 standard is more than just a guide; it is a benchmark for quality and safety in the field of anaesthetic and respiratory equipment. It sets the bar for what is expected of nebulizing systems and components, ensuring that they meet the highest standards of performance and reliability.

By adhering to this standard, manufacturers can ensure that their products are not only safe and effective but also competitive in the market. For healthcare professionals, this standard provides assurance that the equipment they use is of the highest quality, capable of delivering the best possible care to their patients.

Current Status

The BS EN ISO 27427:2023 is currently a standard, meaning it is recognized and accepted by the industry. It is the definitive guide for anaesthetic and respiratory equipment, setting the standard for excellence in the field.

Whether you are a manufacturer looking to improve your products, a healthcare professional seeking to enhance your practice, or a student aiming to broaden your knowledge, the BS EN ISO 27427:2023 standard is an invaluable resource. Don't miss out on this opportunity to stay ahead in the field of anaesthetic and respiratory equipment. Get your copy of the BS EN ISO 27427:2023 standard today!

DESCRIPTION

BS EN ISO 27427:2023


This standard BS EN ISO 27427:2023 Anaesthetic and respiratory equipment. Nebulizing systems and components is classified in these ICS categories:
  • 11.040.10 Anaesthetic, respiratory and reanimation equipment
This document specifies requirements for the safety and performance testing of general-purpose nebulizing systems intended for continuous or breath-actuated delivery of liquids, in aerosol form, to humans through the respiratory system. This document includes gas-powered nebulizers (which can be powered by, e.g., compressors, pipeline systems, cylinders, etc.) and electrically powered nebulizers [e.g. spinning disc, ultrasonic, vibrating mesh (active and passive), and capillary devices] or manually powered nebulizers. This document does not specify the electrical requirements of electrically powered nebulizers. This document does not specify the minimum performance of nebulizing systems. This document does not apply to: a)       devices intended for nasal deposition; b)       devices intended solely to provide humidification or hydration by providing water in aerosol form. NOTE 1        ISO 80601-2-74 and ISO 20789 cover these devices. c)        drug-specific nebulizers or their components (e.g. metered dose inhalers, metered liquid inhalers, dry powder inhalers). NOTE 2        ISO 20072 covers these devices. NOTE 3        See Annex A for rationale.