IEEE P11073-10425-2014/Cor1/D3, Jan 2016
Part 10425: Device Specialization - Continuous Glucose Monitor (CGM) - Corrigendum 1
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About This Item
P11073-10425-2014/Cor1/D3, Jan 2016 is a corrigendum for Part 10425, covering device specialization for a Continuous Glucose Monitor (CGM). It addresses corrections to the underlying technical specification used in bioengineering and connected device environments, where consistent data handling, communication, and device behavior are important. For manufacturers, integrators, and testers working with CGM systems, this document helps support clearer implementation and more reliable interoperability.
P11073-10425-2014/Cor1/D3, Jan 2016 overview
This standard applies to the CGM device specialization within the broader P11073 framework, which is commonly associated with personal health device communication. As a corrigendum, P11073-10425-2014/Cor1/D3, Jan 2016 is intended to correct or refine the published requirements rather than define an entirely new scope. It is relevant to engineering teams that need accurate protocol behavior, data representation, and implementation guidance for continuous glucose monitoring equipment and related communication interfaces.
Typical use cases
This document is typically used when designing or validating CGM devices that exchange measurement data with monitoring platforms, gateways, or clinical data systems. It may also support conformance work, interface testing, and product integration in diabetes management workflows. In practice, P11073-10425-2014/Cor1/D3, Jan 2016 can be useful for teams coordinating sensor data communication, device specialization logic, and system compatibility across personal health technologies and connected biomedical equipment.
Why this standard matters
For CGM-related products, small specification errors can affect interoperability, implementation consistency, and test results. P11073-10425-2014/Cor1/D3, Jan 2016 matters because it helps align device behavior with the corrected technical text, reducing ambiguity for development and compliance activities. That can improve procurement confidence, support more repeatable verification, and lower the risk of mismatched data interpretation between devices and receiving systems in healthcare and personal monitoring applications.
- Continuous glucose monitor specialization
- Corrigendum corrections and clarifications
- Device communication and data exchange
- Implementation and conformance support
- Personal health device interoperability
- Publication Date: 2016
- Standard Status: Active
- Publisher: IEEE
- Subject: Bioengineering; Communication, Networking and Broadcast Technologies; Components, Circuits, Devices and Systems; Computing and Processing
- Official IEEE: Doi link
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