IEEE P11073-10424-2014/Cor1/D3, Feb 2016
Part 10424: Device Specialization -Sleep Apnoea Breathing Therapy Equipment (SABTE) - Corrigendum 1
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About This Item
P11073-10424-2014/Cor1/D3, Feb 2016 is a corrigendum to Part 10424 for device specialization in Sleep Apnoea Breathing Therapy Equipment (SABTE). It is relevant to bioengineering and connected device design, where accurate terminology and requirements help support consistent engineering, interoperability, and compliance work. For manufacturers, specifiers, and test teams, this document helps clarify the technical baseline for equipment used in sleep apnoea breathing therapy applications.
P11073-10424-2014/Cor1/D3, Feb 2016 overview
This technical document is part of the P11073 series and addresses the specialization of devices used in sleep apnoea breathing therapy. P11073-10424-2014/Cor1/D3, Feb 2016 serves as Corrigendum 1, so its role is to refine or correct the underlying Part 10424 text rather than introduce a separate device profile. In practice, it supports clearer interpretation of device terms, data exchange expectations, and implementation details for SABTE-related systems within a broader health technology context.
Typical use cases
P11073-10424-2014/Cor1/D3, Feb 2016 is most relevant where sleep apnoea breathing therapy equipment needs a shared technical reference for device behavior or information exchange. That can include product development, verification planning, clinical integration, and documentation for therapy systems used in respiratory care. It may also be useful when aligning connected device functions with related communication or processing requirements in engineering workflows, especially where precise device specialization supports consistent implementation across teams.
Why this standard matters
For organizations working with SABTE, this standard matters because small wording or requirement corrections can affect design control, testing, and compliance interpretation. Using P11073-10424-2014/Cor1/D3, Feb 2016 helps reduce ambiguity when comparing product behavior against a recognized technical reference. That can improve consistency between suppliers, engineering groups, and validation teams, while also lowering the risk of mismatched requirements in procurement or integration projects involving sleep apnoea breathing therapy equipment.
- Corrigendum to Part 10424
- Sleep apnoea breathing therapy equipment specialization
- Device terminology and requirement clarification
- Support for testing and compliance review
- Relevant to connected health device engineering
- Publication Date: 2016
- 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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