BS EN ISO 19223:2021 - Lung Ventilators and Related Equipment: Vocabulary and Semantics

In the ever-evolving field of medical technology, precision and clarity are paramount. The BS EN ISO 19223:2021 standard is an essential resource for professionals involved in the design, development, and application of lung ventilators and related equipment. Released on April 30, 2021, this comprehensive document provides a detailed vocabulary and semantics framework that ensures consistency and understanding across the industry.

Comprehensive Coverage

Spanning 150 pages, this standard is meticulously crafted to cover a wide array of terminologies and concepts associated with lung ventilators. It serves as a critical reference point for manufacturers, healthcare providers, and regulatory bodies, ensuring that all parties are aligned in their understanding and communication regarding these vital medical devices.

Key Features

• Standard Number: BS EN ISO 19223:2021
• Release Date: April 30, 2021
• ISBN: 978 0 539 15017 9
• Status: Standard

Why This Standard Matters

The importance of standardized vocabulary in the medical field cannot be overstated. With the BS EN ISO 19223:2021, professionals are equipped with a unified language that facilitates clear communication, reduces misunderstandings, and enhances the safety and efficacy of lung ventilators. This is particularly crucial in critical care settings where precision can significantly impact patient outcomes.

Enhancing Communication

By establishing a common set of terms and definitions, this standard helps bridge the gap between different stakeholders in the healthcare industry. Whether you are a clinician, engineer, or regulatory official, having a shared vocabulary ensures that everyone is on the same page, thereby streamlining processes and improving collaboration.

Supporting Innovation

Innovation in medical technology is driven by a deep understanding of existing systems and terminologies. The BS EN ISO 19223:2021 provides the foundational knowledge necessary for innovators to develop new solutions that are compatible with current standards. This not only accelerates the development process but also ensures that new products meet the rigorous demands of the healthcare industry.

Who Should Use This Standard?

This standard is indispensable for a wide range of professionals, including:

• Medical Device Manufacturers: Ensure that your products meet international standards and are easily understood by healthcare providers worldwide.
• Healthcare Providers: Gain a deeper understanding of the equipment you use daily, enhancing your ability to provide top-notch care.
• Regulatory Bodies: Utilize a standardized framework to evaluate and approve new medical devices, ensuring they meet safety and efficacy requirements.
• Researchers and Academics: Access a comprehensive resource that supports your studies and innovations in the field of respiratory care.

Conclusion

The BS EN ISO 19223:2021 standard is more than just a document; it is a vital tool that supports the advancement of medical technology and the improvement of patient care. By providing a clear and consistent vocabulary, it empowers professionals across the healthcare industry to communicate effectively, innovate confidently, and deliver exceptional care to those who need it most.

Invest in this standard to ensure that you are at the forefront of medical technology and patient care. With its comprehensive coverage and authoritative guidance, the BS EN ISO 19223:2021 is an invaluable asset for anyone involved in the field of lung ventilators and related equipment.

BS EN ISO 19223:2021

This standard BS EN ISO 19223:2021 Lung ventilators and related equipment. Vocabulary and semantics is classified in these ICS categories:

• 01.040.11 Health care technology (Vocabularies)
• 11.040.10 Anaesthetic, respiratory and reanimation equipment

This document establishes a vocabulary of terms and semantics for all fields of respiratory care involving mechanical ventilation, such as intensive-care ventilation, anaesthesia ventilation, emergency and transport ventilation and home-care ventilation, including sleep-apnoea breathing-therapy equipment. It is applicable

• in lung ventilator and breathing-therapy device standards,

• in health informatics standards,

• for labelling on medical electrical equipment and medical electrical systems,

• in medical electrical equipment and medical electrical system instructions for use and accompanying documents,

• for medical electrical equipment and medical electrical systems interoperability, and

• in electronic health records.

This document is also applicable to those accessories intended by their manufacturer to be connected to a ventilator breathing system or to a ventilator, where the characteristics of those accessories can affect the basic safety or essential performance of the ventilator and ventilator breathing system.

NOTE This document can also be used for other applications relating to lung ventilation, including non-electrical devices and equipment, research, description of critical events, forensic analysis and adverse event (vigilance) reporting systems.

This document does not specify terms specific to breathing-therapy equipment, or to physiologic closed-loop ventilation, high-frequency ventilation or negative-pressure ventilation; nor to respiratory support using liquid ventilation or extra-corporeal gas exchange, or oxygen, except where it has been considered necessary to establish boundaries between bordering concepts.