IEEE P11073-10425/D2, Dec 2016 PDF | Request Standard
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IEEE P11073-10425/D2, Dec 2016

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

Standard by IEEE, 2017

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About This Item

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P11073-10425/D2, Dec 2016 is a focused technical standard for the Device Specialization—Continuous Glucose Monitor (CGM) within the P11073 framework, addressing how CGM-related device information should be structured and handled. It is relevant to bioengineering applications where device interoperability, data consistency, and clear device specialization matter. For teams working with glucose monitoring systems, this standard helps define a common technical basis for exchange, testing, and implementation. As an inactive document, P11073-10425/D2, Dec 2016 remains useful for reference and historical comparison.

What is P11073-10425/D2, Dec 2016?

P11073-10425/D2, Dec 2016 is a draft-level specification tied to the P11073 family and the continuous glucose monitor specialization. Its purpose is generally to describe the device-specific details needed so CGM equipment can be represented in a consistent way within broader health-device communications. In practical terms, it supports a clearer technical model for CGM behavior, attributes, and data handling. That makes it a useful reference for engineers, integrators, and compliance teams working on medical device interoperability.

Where is P11073-10425/D2, Dec 2016 used?

This standard is typically used in environments that develop or evaluate continuous glucose monitoring devices, related software interfaces, and healthcare data exchange components. It is especially relevant where CGM devices need to connect with monitoring platforms, diagnostic systems, or other bioengineering workflows that depend on structured device information. P11073-10425/D2, Dec 2016 may also be consulted during design reviews, interoperability testing, and documentation work for systems that manage patient glucose data in a controlled technical format.

Why is P11073-10425/D2, Dec 2016 important?

P11073-10425/D2, Dec 2016 matters because CGM systems depend on consistent device representation to reduce integration errors and support reliable data handling. A specialized standard can help improve design control, simplify testing, and support more predictable communication between devices and software. For organizations working with medical monitoring technology, it provides a reference point for technical alignment and risk reduction. It is also valuable when comparing implementations or maintaining compatibility across product revisions and system interfaces.

  • Continuous glucose monitor device specialization
  • Bioengineering and device communication context
  • Structured data and interface consistency
  • Reference material for testing and integration
  • Inactive standard for technical review
SKU: 60547d07683a

  • Publication Date: 2017

  • Standard Status: Inactive

  • Publisher: IEEE

  • Subject: Bioengineering; Components, Circuits, Devices and Systems

  • Official IEEE: Doi link
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