ČSN EN ISO/IEEE 11073-10421 (980014)

Health informatics - Device interoperability - Part 10421: Personal health device communication - Device specialization - Peak expiratory flow monitor (peak flow)

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STANDARD published on 1.6.2026


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The information about the standard:

Designation standards: ČSN EN ISO/IEEE 11073-10421
Classification mark: 980014
Catalog number: 523501
Publication date standards: 1.6.2026
SKU: NS-1271271
The number of pages: 84
Approximate weight : 283 g (0.62 lbs)
Country: Czech technical standard
Category: Technical standards ČSN

The category - similar standards:

IT applications in health care technology

Annotation of standard text ČSN EN ISO/IEEE 11073-10421 (980014):

This document establishes a normative definition of communication between personal telehealth peak flow mo-nitoring 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

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