IEEE P11073-10425/D3, Jun 2017
Part 10425: Device Specialization--Continuous Glucose Monitor (CGM)
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- Language: English
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About This Item
P11073-10425/D3, Jun 2017 is a technical standard for the device specialization of a continuous glucose monitor (CGM), placing the document in the context of bioengineering, computing and processing, and communication-enabled medical device systems. It is relevant to how CGM-related data and device behavior are defined, represented, and exchanged in a structured way. For organizations working with P11073-10425/D3, Jun 2017, the value lies in supporting more consistent interoperability and clearer implementation expectations across connected health solutions.
About P11073-10425/D3, Jun 2017
This standard addresses the CGM device specialization within the P11073 family, focusing on the technical description of a continuous glucose monitor in a form that can support interoperable health information exchange. P11073-10425/D3, Jun 2017 is most useful where device data needs to be interpreted consistently across software, monitoring platforms, or related clinical workflows. Its scope is aligned with bioengineering and computing systems that depend on well-defined device semantics rather than informal product-specific conventions.
Where is P11073-10425/D3, Jun 2017 used?
P11073-10425/D3, Jun 2017 is typically used in connected diabetes care environments where CGM devices must communicate with software applications, gateways, or monitoring tools. It may be relevant to device integration, data ingestion, patient-facing health platforms, and clinical review systems that handle continuous glucose readings. The standard is also useful for engineering teams and procurement processes that need a clear technical reference when evaluating CGM interoperability, data handling, and implementation consistency.
Importance in practice
In practice, P11073-10425/D3, Jun 2017 helps reduce ambiguity when CGM data is exchanged or processed across systems. That can improve design control, testing, and compliance efforts by giving teams a common technical basis for implementation and validation. For product development and integration work, the standard supports more consistent device behavior, fewer interpretation errors, and better alignment between hardware, software, and communication interfaces in a medical monitoring setting. Because it is inactive, it may also be relevant for legacy support or reference work.
- Continuous glucose monitor device specialization
- Interoperable health data representation
- Connected diabetes monitoring systems
- Implementation and validation reference
- Legacy technical reference use
- Publication Date: 2017
- 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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