VENUE FAMILY
Point of care ultrasound for emergency care
Caption Guidance
Scan with confidence: The right tool in the right hands for cardiac ultrasound in critical moments
Find out howFEATURES
Made for your point of care
SHOCK TOOLKIT
Automated shock assessment
REAL-TIME EF
For accurate, instant, and rapidly updating results
EFAST TOOL
A structured approach to trauma assessments
AUTO B-LINES
Highlight and count B-lines, in real time
Nerveblox™
Perform ultrasound-guided peripheral nerve blocks with Nerveblox
VIEWPOINT™ 6
Accelerating and automating ultrasound workflow at point of care
Ready for sudden changes in patient health
From its straightforward design to its AI-enabled Auto Tools, the Venue family of point of care ultrasound systems empower physicians to make fast assessments in tough situations.
AI-enabled Auto Bladder Volume
Automatically recall parameter settings with Follow Up
Remove the clutter with Simple Screen
Built-in teaching assistance with Scribble
Quickly assess kidneys and the bladder with Renal Diagram
Review lung segment images in one view with Lung Diagram
Venue probes
Product tutorial gallery
References
- 1. 2015 WSD Fact Sheet, www.word-sepsis-day.org (2015).
- 2. Venue and Venue Go R3 technical claims document (DOC2391130) Venue Fit technical claims document (DOC2454794)
- 3. Messaging and claims DOC2454794 and DOC2391130.
- 4. Based on internal GE HealthCare study Point of Care Ultrasound – Encounter-based workflow with Venue Family R4 and ViewPoint 6 POC Module improves operational outcomes, June 2022 DOC2757861.
^ Venue family is intended to be used in hospitals and medical clinics. Venue Sprint is intended to be used in home environments and road or air ambulance, in addition.
‡ Available on Venue, Venue Go and Venue Fit. These systems are designed for compatibility with commercially available Ultrasound contrast agents. Because the availability of these agents is subject to government regulation and approval, system features intended for use with these agents may not be commercially marketed nor made available before the contrast agent is cleared for use. Contrast-related system features are enabled only on systems for delivery to an authorized country or region of use.