Euroanesthesia 2026

Medtronic Acute Care & Monitoring at Euroanaesthesia 2026

Medtronic is bringing 3 product launches.

Medtronic is bringing 3 product launches.
One connected patient pathway.

Experience how monitoring supports decisions
From procedural sedation to OR to the ICU to care at home after discharge.

Where to find us?
Booth 5.111
ACM2U truck outside the main entrance

Stronger together. Individually unique.

Argos™* cardiac output monitor

Advanced hemodynamic insights from a single arterial line

Reliable trending¹
Easy-to-use²
No disposables^†

McGRATH™ MAC+ video laryngoscope

Designed for better visualization^‡

The 45% larger, 4.5x higher resolution screen^‡ gives a clear, unobstructed view of the airway, helping to improve first- pass success^§,3,4

Corsano™* multi-parameter wearable with AF screening

Continuous monitoring beyond the hospital

Clinical-grade accuracy, provides real-time monitoring of multiple vital signs and AF screening^◊,5,6

MEDICAL EDUCATION

Science at sundown

Join us for an evening of scientific exchange and networking to discuss the latest advancement in anesthesia.

From the evidence to action - How to make an impact to advance patient safety.

Refine, redefine, reimagine healthcare

Illuminating the patient pathway:
Science, signals and impact

Expert faculty:

Prof. Anil Hormis

Rotherham General Hospital, UK

Prof. Osama Abou Arab

University hospital of Amiens, France

Prof. Patrick Schoettker

CHUV University Hospital, Switzerland

Jake Dove

Distinguished Scientist, Medtronic

Download the agenda (open in new window)

Our booth story is more than products: it’s a connected patient pathway.

This year, the Medtronic booth is built around how care actually happens.
Not in silos. But across a continuous journey.

Live events at the booth

Why routine use: Make your first attempt your best attempt with McGRATH™ MAC+
Dr. Patrick Schoettker, MD
Professor and Head of Anesthesiology, CHUV | Lausanne University Hospital
Sat 6 June | 15:30–16:00
Sun 7 June | 15:00–15:30

**Advanced hemodynamic insights with Argos™*: Minimally invasive cardiac monitoring**
Paula Smith, Sr.
Global Marketing Program Manager | INVOS™ regional oximetry & Argos™* cardiac output monitor
Sun 7 June | 12:30–13:00

Step inside the ACM2U truck
Outside the main entrance

The ACM2U is Medtronic’s mobile education and demonstration truck, bringing the full Acute Care & Monitoring portfolio directly to you.

After visiting 40 hospitals across Europe and engaging over 4,000 healthcare professionals, ACM2U is now at Euroanaesthesia 2026.

Available Sunday 7 June and Monday 8 June.

Visit us for the full experience

Booth 5.111
ACM2U truck outside the main entrance

For a personalized demo, contact us (open in new window)

^† See Argos™ cardiac output monitor Instructions for Use (IFU).

^‡ Compared to the McGRATH™ MAC video laryngoscope.

^{§ V}ased on evidence comparing the McGRATH™ MAC video laryngoscope with direct laryngoscope and other video laryngoscopes.

^◊The CardioWatch 287-2 is intended for atrial fibrillation screening.

^*Third-party brands are trademarks of their respective owners. All other brands are trademarks of a Medtronic company.

Argos™* cardiac output monitor is manufactured by Retia Medical Systems, Inc. and distributed by Medtronic.

The Corsano™* multi-parameter wearable is manufactured by Corsano Health B.V. and distributed by Medtronic.

The Corsano™* multi-parameter wearable is not intended for use in high-acuity environments.

Patient monitoring products should not be used as the sole basis for diagnosis or therapy and are intended only as an adjunct in patient assessment.

For trained personnel only. For specific indications and instructions for use, please refer to the product manual.

The material on this website should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s). Please note that the intended use of a product may vary depending on geographical approvals.

See the device manual(s) for detailed information regarding the intended use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events. For a MRI compatible device(s), consult the MRI information in the device manual(s) before performing a MRI. If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com. Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.

Medtronic products placed on European markets bear the CE mark and the UKCA mark (if applicable). For any further information, contact your local Medtronic representative.