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IEEE P11073-10425-2014/Cor1/D8, May 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/D8, May 2016 is a corrigendum for Part 10425, covering Device Specialization for a Continuous Glucose Monitor (CGM). It addresses technical corrections to the underlying specification used in bioengineering and connected device systems, helping maintain clearer requirements for CGM-related interoperability and data handling. For teams working with medical sensing and communication technologies, this document matters because even small editorial or technical fixes can affect implementation consistency, validation, and compliance checks.

About P11073-10425-2014/Cor1/D8, May 2016

This document serves as a corrective update to the Part 10425 specialization for continuous glucose monitoring within the P11073 family. Its role is typically to refine or amend the technical wording of the original specification so that device behavior, terminology, or interface expectations are interpreted more consistently. In a CGM context, that can be important for aligning sensor output, communication structures, and related processing requirements across implementations that rely on a stable technical reference.

Where is P11073-10425-2014/Cor1/D8, May 2016 used?

P11073-10425-2014/Cor1/D8, May 2016 is most relevant in environments that develop or integrate continuous glucose monitoring systems. That includes medical device engineering, communication protocol work, and software or hardware integration for glucose sensing equipment. It may also be consulted during specification review, test planning, or procurement of CGM-compatible components where the correct interpretation of the technical document is important. Its focus supports controlled exchange of data within connected healthcare device workflows.

Importance in practice

In practice, this standard helps reduce ambiguity in a CGM-related technical specification. Corrigenda are important because they can clarify requirements that affect implementation, verification, and documentation. For developers and test teams, using the correct version supports more consistent design decisions and helps avoid errors in conformance work. For buyers and compliance teams, it provides a more reliable reference when checking whether a device or system aligns with the expected specialization and related communication behavior.

  • Corrigendum to Part 10425
  • Continuous glucose monitor specialization
  • CGM device communication context
  • Technical correction for implementation review
SKU: 08f63ccd8305

  • Publication Date: 2016
  • Standard Status: Inactive
  • 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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