BS EN ISO/IEEE 11073-10421:2026 - Health Informatics Standard for Peak Expiratory Flow Monitors

Introducing the BS EN ISO/IEEE 11073-10421:2026, a comprehensive standard that sets the benchmark for device interoperability in personal health device communication, specifically focusing on the specialization of peak expiratory flow monitors. This standard is an essential resource for manufacturers, healthcare providers, and technology developers who are committed to enhancing the quality and reliability of health informatics systems.

Key Features and Benefits

• Standard Number: BS EN ISO/IEEE 11073-10421:2026
• Pages: 78
• Release Date: January 16, 2026
• ISBN: 978 0 539 30816 7
• Status: Standard

Comprehensive Coverage

This standard provides a detailed framework for the interoperability of personal health devices, with a specific focus on peak expiratory flow monitors. It ensures that devices can communicate effectively, providing accurate and reliable data that is crucial for patient monitoring and management.

Enhancing Device Communication

The BS EN ISO/IEEE 11073-10421:2026 standard is designed to facilitate seamless communication between personal health devices and healthcare systems. By adhering to this standard, manufacturers can ensure that their devices are compatible with a wide range of health informatics systems, enhancing the overall efficiency and effectiveness of healthcare delivery.

Focus on Peak Expiratory Flow Monitors

Peak expiratory flow monitors are critical tools in the management of respiratory conditions such as asthma. This standard provides specific guidelines for the design and functionality of these devices, ensuring that they deliver precise measurements that healthcare professionals can rely on for accurate diagnosis and treatment planning.

Global Recognition and Compliance

As a globally recognized standard, the BS EN ISO/IEEE 11073-10421:2026 is a testament to the commitment to quality and interoperability in health informatics. Compliance with this standard not only enhances the credibility of manufacturers but also assures healthcare providers and patients of the reliability and accuracy of the devices they use.

Why Choose This Standard?

Choosing the BS EN ISO/IEEE 11073-10421:2026 standard means choosing a future-proof solution that aligns with the latest advancements in health informatics. It is an investment in quality, reliability, and interoperability, ensuring that your devices meet the highest standards of performance and safety.

Who Should Use This Standard?

This standard is ideal for:

• Medical device manufacturers looking to ensure their products meet international interoperability standards.
• Healthcare providers seeking reliable and accurate devices for patient monitoring.
• Technology developers focused on creating innovative health informatics solutions.

Conclusion

The BS EN ISO/IEEE 11073-10421:2026 standard is an indispensable resource for anyone involved in the development, manufacturing, or use of peak expiratory flow monitors. By adhering to this standard, you are ensuring that your devices are at the forefront of health informatics technology, providing the highest level of care and accuracy for patients worldwide.

Embrace the future of health informatics with the BS EN ISO/IEEE 11073-10421:2026 standard and ensure your devices are equipped to meet the demands of modern healthcare environments.

BS EN ISO/IEEE 11073-10421:2026

This standard BS EN ISO/IEEE 11073-10421:2026 Health informatics. Device interoperability is classified in these ICS categories:

• 35.240.80 IT applications in health care technology

This document establishes a normative definition of communication between personal telehealth peak flow monitoring devices (agents) and managers (e.g., cell phones, personal computers, personal health appliances, and set top boxes) in a manner that enables plug-and-play interoperability. It leverages work done in other ISO/IEEE 11073 standards including existing terminology, information profiles, application profile standards. It specifies the use of specific term codes, formats, and behaviors in telehealth environments restricting optionality in base frameworks in favor of interoperability. This document defines a common core of functionality of a peak-flow monitoring device. The use case is restricted to personal respiratory monitoring and therefore does not include hospital-based spirometry. Continuous and high-acuity monitoring (e.g., for emergency response) are outside the scope of the use case. In the context of personal health devices, a peak flow meter is a device is used to measure the respiratory function of those managing respiratory conditions such as asthma and chronic obstructive pulmonary disease. The ability to identify declining respiratory status prior to the need for acute intervention improves the quality of life for the individual while reducing the overall costs of care. Respiratory status data are collected by a personal respiratory monitoring device and forwarded to a central data repository for review and action by a health care provider. The data are episodic in nature and are forwarded at designated intervals or when the person is symptomatic.