You just clicked a link to go to another website. If you continue, you may go to a site run by someone else.
We do not review or control the content on non-Medtronic sites, and we are not responsible for any business dealings or transactions you have there. Your use of the other site is subject to the terms of use and privacy statement on that site.
It is possible that some of the products on the other site are not approved in your region or country.
Your browser is out of date
With an updated browser, you will have a better Medtronic website experience. Update my browser now.
The content of this website is exclusively reserved for Healthcare Professionals in countries with applicable health authority product registrations, except those practicing in France as some of the content is not in compliance with the French Advertising law N°2011-2012 dated 29th December 2011, article 34.
Click “OK” to confirm you are a Healthcare Professional.
The Crescent™ RA jugular dual lumen catheter offers a right atrial design and includes both an introducer for a percutaneous technique and a blunt-tip obturator for a surgical cut-down technique.
Download Brochure
Right atrial placement
The jugular dual lumen catheter is a single-use dual lumen catheter that provides both venous drainage and reinfusion of blood via the jugular vein. It is indicated for use in pediatric patients with acute respiratory failure requiring veno-venous extracorporeal membrane oxygenation where other available treatment options have failed and continued clinical deterioration is expected, or the risk of death is imminent.
Radiopaque markers identify drainage sites, reinfusion port, catheter tip, and axial orientation.
Crescent-shaped lumen and large reinfusion port help optimize pressure flow performance.
Multiple suture points provide additional stability, reducing the chance of twisting or migration when the patient moves.
Crescent™ RA Jugular Right Atrial Dual Lumen Catheter
One unit per carton
| Code | French size | Insertion length | Connector |
|---|---|---|---|
| 70413 | 13 Fr | 8.9 cm | 1/4 in |
| 70415 | 15 Fr | 9.7 cm | 1/4 in |
| 70419 | 19 Fr | 14.5 cm | 1/4 in |
Find additional feature information along with a variety of educational resources and tools.
REFERENCES
1. Bench testing data on file at Medtronic.
2. Compared to products without radiopaque markers. Design verification and validation data on file. These tests may not be indicative of clinical performance.
3. Design verification and validation data on file. These tests may not be indicative of clinical performance.
DISCLAIMER
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.
© 2025 Medtronic. All rights reserved, Medtronic, Medtronic logo and Engineering the extraordinary are trademarks of Medtronic. All other brands are trademarks of a Medtronic company.
