IEEE P11073-10404/D11, Oct 2008
Part 10404: Device Specialization - Pulse Oximeter
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- Language: English
- License Type: Single User
- Updates: Not Included
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- Language: English
- License Type: Enterprise / Multi User
- Updates: Included
About This Item
P11073-10404/D11, Oct 2008 is a bioengineering standard focused on the device specialization for a pulse oximeter. It addresses the technical context for how this type of physiological monitoring device is defined and handled within a structured standards framework. For manufacturers, engineers, and buyers, the document helps anchor product expectations around pulse oximetry terminology, functional scope, and interoperability considerations that are important when comparing or evaluating medical device documentation.
Overview of P11073-10404/D11, Oct 2008
This technical document forms part of the broader P11073 family and narrows in on pulse oximeter device specialization. In practical terms, P11073-10404/D11, Oct 2008 is relevant to the way pulse oximetry equipment is described, organized, and assessed in bioengineering environments. It is most useful where consistent device definitions and structured information exchange matter, especially in medical device design, integration, or procurement workflows that rely on clear technical alignment.
Typical use cases
P11073-10404/D11, Oct 2008 is typically consulted when working with pulse oximeters used for oxygen saturation and pulse rate monitoring. It may support device specification review, interface mapping, and documentation alignment for clinical monitoring systems. The standard is also relevant in healthcare engineering settings where pulse oximeter data must be handled consistently across equipment, software, or device records. Its scope is especially useful for teams that need a shared technical reference for this device category.
Why it matters
This standard matters because pulse oximetry is often used in safety-critical monitoring, where consistent device definition can reduce ambiguity during design and evaluation. P11073-10404/D11, Oct 2008 can help support compliance-oriented documentation, procurement comparison, and testing against a known technical reference. For bioengineering teams, that consistency may improve traceability and lower the risk of misinterpretation when specifying or validating pulse oximeter-related functionality.
- Device specialization for pulse oximeters
- Bioengineering and medical device context
- Structured reference for technical documentation
- Useful for specification and evaluation workflows
- Inactive standard status
- Publication Date: 2009
- Standard Status: Inactive
- Publisher: IEEE
- Subject: Bioengineering
- Official IEEE: Doi link
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