IEEE 11073-10472-2010
Part 10472: Device specialization--Medication monitor
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About This Item
11073-10472-2010 is a technical standard for a medication monitor within the IEEE 11073 device specialization family. It addresses how this kind of biomedical device is described and integrated in communication-oriented health technology environments, helping support consistent interpretation of medication monitoring data. For manufacturers, integrators, and procurement teams, the standard matters because it provides a clearer basis for compatibility, design alignment, and product evaluation in systems where medication-related monitoring information must be handled reliably.
Overview of 11073-10472-2010
This standard belongs to the IEEE 11073 framework and focuses on a specific device specialization: the medication monitor. In practical terms, 11073-10472-2010 defines a structured technical context for representing and communicating information associated with medication monitoring equipment. That makes it relevant to bioengineering and communication systems where device data needs to be exchanged in a consistent way. It is especially useful when aligning product behavior, interface expectations, and system integration requirements across related healthcare technologies.
Typical use cases
Typical use cases include medical device implementations that monitor medication-related events or status and need to communicate those results within a larger health information system. The standard may be applied during device design, interface specification, interoperability planning, or conformance testing for equipment used in clinical environments. It is also relevant when engineering teams and system integrators need a shared reference for handling medication monitor data in networked healthcare workflows, particularly where consistent device communication is important.
Why it matters
Standards such as 11073-10472-2010 help reduce ambiguity in how device behavior and communication are defined for specialized medical equipment. That can support more consistent product development, clearer supplier requirements, and better testing outcomes. In regulated or safety-sensitive environments, a stable technical reference can also reduce integration risk and improve confidence that a medication monitor will fit expected workflows. For buyers and engineers, it offers a practical benchmark when evaluating compatibility and design suitability.
- IEEE 11073 device specialization
- Medication monitor context
- Biomedical communication alignment
- Interoperability and testing reference
- Inactive English-language standard
- Publication Date: 2010
- Standard Status: Inactive
- Publisher: IEEE
- Subject: Bioengineering; Communication, Networking and Broadcast Technologies
- Official IEEE: Doi link
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