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IEEE P11073-10425-2014/Cor1/D4, Jan 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/D4, Jan 2016 is a corrigendum focused on Part 10425: Device Specialization - Continuous Glucose Monitor (CGM), updating the technical record for bioengineering and networked device communication. It is relevant where CGM systems exchange data through standardized interfaces and need consistent interpretation of device behavior, messaging, and related requirements. For engineers, integrators, and procurement teams, this document helps clarify the intended specification baseline and supports more reliable implementation and review.

What is P11073-10425-2014/Cor1/D4, Jan 2016?

This technical document is a corrigendum to the Part 10425 device specialization for continuous glucose monitor systems. P11073-10425-2014/Cor1/D4, Jan 2016 is used to refine or correct the published requirements so the CGM specialization remains aligned with the intended communication and device model. In practice, it supports clearer reading of the standard by addressing points that affect interoperability, data exchange, and conformance interpretation within a medical device communications framework.

Where is P11073-10425-2014/Cor1/D4, Jan 2016 used?

P11073-10425-2014/Cor1/D4, Jan 2016 is mainly used in environments involving continuous glucose monitoring equipment and the systems that receive or process CGM data. That can include medical device development, interface design, software integration, and conformity review for healthcare monitoring workflows. It is most relevant when a CGM device must communicate reliably with companion systems, gateways, or clinical data handling tools that depend on a shared technical specification.

Why is P11073-10425-2014/Cor1/D4, Jan 2016 important?

This corrigendum matters because even small corrections can affect how a CGM specialization is implemented, tested, or interpreted. P11073-10425-2014/Cor1/D4, Jan 2016 helps reduce ambiguity in compliance work, supports consistent engineering decisions, and can lower the risk of mismatched expectations between device suppliers and system integrators. For standards-based procurement and verification, it provides a more dependable reference point for reviewing communication behavior and specialized requirements.

  • Continuous glucose monitor device specialization
  • Corrigendum for technical clarification
  • Medical device communication context
  • Interoperability and conformance review
  • English-language standards reference
SKU: ccfdf145025c

  • Publication Date: 2016

  • Standard Status: Inactive

  • Publisher: IEEE

  • Subject: Bioengineering; Communication, Networking and Broadcast Technologies; Components, Circuits, Devices and Systems

  • Official IEEE: Doi link
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