An emergency should never wait in the pile.
In the ED, the flow never stops. The Milvue Suite triages exams at acquisition and pushes critical cases - displaced fractures, pneumothorax, pleural effusions (Europe) - to the top of the worklist.
The right exam, at the right time, first.
Prioritization sits between the modality and the PACS. No workstation change, no disruption: the worklist reorders itself, the radiologist decides.
- Automatic triage of incoming exams in real time
- Critical cases flagged and pushed to the top of the list
- Up to −1 h on time to treatment
- The radiologist remains the sole decision-maker
Three steps, zero friction.
No break in the chain, no workstation change: the solution slots into your existing flow.
Incoming exam
Every incoming image is analyzed as it arrives.
Flagging
Critical cases are identified with a confidence score.
Prioritized worklist
The list reorders; the emergency goes ahead of routine.
An innovative solution that answers a safety need by augmenting physicians' capabilities.
The facts, no noise.
CE-marked medical device, Class IIa, developed by Milvue. Native integration, protected data.
| Modalities | Standard radiography (CR / DX) |
|---|---|
| Context | ED, trauma, triage |
| Population | Adult and pediatric |
| Output | Priority + pre-filled report |
| Integration | Native RIS / PACS |
| Device | CE marked class IIa · FDA (TechCare Trauma, US) · Health Canada (Smart Trauma) * |
Regulatory detail:
- TechCare Alert is a specific configuration of the SmartUrgences module included in the Milvue Suite, and is available under the names TechCare Trauma (United States) and Smart Trauma (Canada).
- The Milvue Suite software, developed by Milvue, is a Class IIa medical device according to EU MDR Regulation 2017/745 - Notified Body: BSI, CE 2797.
- Smart Trauma is Health Canada licensed and a Class II medical device.
- TechCare Trauma is FDA cleared and a Class II medical device according to US regulations.