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IEEE P11073-10425-2014/Cor1/D7, Apr 2016

Part 10425: Device Specialization - Continuous Glucose Monitor (CGM) - Corrigendum 1

Standard by IEEE, 2016

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About This Item

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P11073-10425-2014/Cor1/D7, Apr 2016 is a corrigendum for Part 10425 of the device specialization for Continuous Glucose Monitors (CGM). It addresses corrections to the underlying technical requirements used in bioengineering and networked medical-device contexts, helping clarify how CGM-related information and device behavior are specified. For manufacturers, integrators, and compliance teams, this standard supports more consistent interpretation of the documentation and requirements around CGM interoperability and system design.

Overview of P11073-10425-2014/Cor1/D7, Apr 2016

This document belongs to the P11073 family and focuses on the Continuous Glucose Monitor device specialization in Part 10425. As a corrigendum, P11073-10425-2014/Cor1/D7, Apr 2016 is intended to correct or refine published text rather than introduce a completely new technical scope. It is relevant where CGM devices must be described, exchanged, or evaluated within a structured communications framework, particularly in environments that depend on precise device data definitions and consistent implementation.

Typical use cases

P11073-10425-2014/Cor1/D7, Apr 2016 is typically used when reviewing or implementing CGM-related device profiles, data exchange behavior, or interface requirements within healthcare technology systems. It may be consulted by teams working on glucose monitoring equipment, connected medical-device platforms, or software that handles CGM data in a standardized way. The document is also useful during specification review, interoperability testing, and procurement checks where a corrected reference for the CGM specialization is needed.

Why it matters

For CGM-related products, accurate specification is important because even small wording changes can affect implementation, testing, and interoperability. P11073-10425-2014/Cor1/D7, Apr 2016 helps reduce ambiguity in a technical area where device communication and data consistency are closely tied to clinical reliability. Using the corrected text can support better design control, clearer compliance review, and more dependable comparisons between equipment, especially when teams need a stable reference for development or verification work.

  • Continuous Glucose Monitor device specialization
  • Corrigendum for Part 10425 corrections
  • Medical device data and communication context
  • Useful for interoperability and compliance review
SKU: fadb60c0d178

  • 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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