Medtronic Acute Care & Monitoring at Euroanaesthesia 2026
Medtronic is bringing 3 product launches.
This year, the Medtronic booth is built around how care actually happens.
Not in silos. But across a continuous journey.
† See Argos™ cardiac output monitor Instructions for Use (IFU).
‡ Compared to the McGRATH™ MAC video laryngoscope.
§ Vased 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.
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