Ultrasound voice control: demonstration and workflow record
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Yenra | Prepared September 19, 2026
Companion guide: https://yenra.com/voice-activated-ultrasound/

Use in an approved nonclinical demonstration with the ultrasound service and vendor. Test only documented commands. Record expected action, observed action, visible confirmation and recovery; do not test unapproved controls during patient care.

Keep the completed record privately. This file has no form submission or data collection.

1. System model, software release, enabled feature and country:
   ____________________________________________________________

2. Clinical task being considered for voice input:
   ____________________________________________________________

3. Supported language, activation method and microphone requirements:
   ____________________________________________________________

4. Exact supported command from the current manual:
   ____________________________________________________________

5. Expected action and how the operator confirms it:
   ____________________________________________________________

6. Observed action, missed commands and unintended activations:
   ____________________________________________________________

7. Representative room conditions and participating staff:
   ____________________________________________________________

8. Manual fallback, cancel behavior and training needs:
   ____________________________________________________________

9. Where speech is processed; recording, retention and network requirements:
   ____________________________________________________________

10. Comparison with the normal workflow including corrections:
   ____________________________________________________________

11. Agreed acceptance criteria, owner and unresolved questions:
   ____________________________________________________________

12. Review after software, microphone or workflow changes:
   ____________________________________________________________

Source context: use the companion guide and the following primary references to clarify terminology. The responsible team must check current instructions and evidence for the exact equipment or treatment.
https://investor.gehealthcare.com/news-releases/news-release-details/ge-healthcare-introduces-ai-enhanced-voluson-signature-20-and-18
https://www.accessdata.fda.gov/cdrh_docs/pdf23/K233692.pdf