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Join us at

EuroELSO

23 - 26 April 2025
Booth A.1

Allianz MiCo,
Milan, Italy

Medtronic Symposia

From Innovation to Impact – Dual Lumen Cannulation in VV ECMO

Thursday, 24 April 2024
12:45 - 13:45 
Room: Sky 1

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Speakers EuroElso2025

Easier, smarter ECMO1: Nautilus™ evidence and Vitalflow™† first experiences

Friday, April 25, 2025
12:45 - 13:45 
Room: Sky 1

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Speakers EuroElso2025

Medtronic ECLS Training Center

ect-training-education

Join our Extracorporeal Life Support workshops

April 24 - 25, 2025
Medtronic booth A.1

Date  Time  Workshop Trainers 
Thursday,
24 April 		 15:00-16:30
Precision in practice; dual lumen in VV ECMO.
 Cannulation simulation for adult respiratory ECMO cases with our dual lumen catheter Crescent™
Dawid Staudacher,
Chris Harvey   
Thursday,
25 April 		 11:15-12:45  Expert hands for tiny hearts.
Cannulation simulation of pediatric VV ECMO cases using our
Crescent™ RA dual lumen catheter.		 Brian W. Gray,
Mirjana Cvetkovic
Friday,
25 April		 14:00-15:15  Master the future of ECMO today with VitalFlow™†.
Experience different hands-on scenarios with VitalFlow™† ECMO		 Medtronic trainers 
Friday,
25 April		 15:30-16:45  Master the future of ECMO today with VitalFlow™†.
Experience different hands-on scenarios with VitalFlow™† ECMO		 Medtronic trainers 
Product image

Crescent™ RA Jugular Dual Lumen Catheter

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Crescent™ Jugular Dual Lumen Catheter

ect-crescent

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Nautilus™ Smart ECMO Module

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Discover our educational offer

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1

Medtronic usability data and design verification on file. Compared to Nautilus™ Smart technology.

† Vitalflow™ ECMO system is not CE marked and is not commercially available on the European market.

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.