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for extracorporeal membrane oxygenation (ECMO) and extracorporeal life support (ECLS)
Bio-Medicus Life Support™ catheters, intended for ECLS or CPB, are available in sizes appropriate for adult and pediatric patients.
The Bio-Medicus Life Support™ catheter helps address the challenges for the range of patients you treat.
Watch this video to learn how the Bio-Medicus Life Support™ catheter helps address the challenges for a wide range of patients.
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Bio-Medicus Life Support™ offers catheter options so that you have the flexibility to uniquely treat each patient — smallest to largest, young to old — with varying extracorporeal support needs.
Used for VA or VV configurations. Designed for drainage or return at different insertion lengths, with side holes only near the tip.
Up to 18 cm insertion length.
50 and 55 cm lengths to assist in targeted vascular locations.
Designed for efficient drainage and optimized flow dynamics.1
38 cm length for drainage from inferior vena cava.
55 and 61 cm lengths; longer insertion length allows various tip placements to support drainage flow.
For catheter placement configurations that require smaller sizes and shorter insertable lengths.
10–11.5 cm for return.
10–11.5 cm for drainage.
Developed with extensive user input.
The thin, kink-resistant wall design promotes optimized flow rates.2
Features such as fingerlet tip supports create a no-step transition, allowing for smooth insertion.3
Bio-Medicus Life Support™ cannulae are made with Elast-Eon™*, a biocompatible and biostable polyurethane/silicone copolymer.‡ Elast-Eon™* is commonly used in prolonged use and implantable medical devices, including ECLS dual lumen catheters.
We developed the Bio-Medicus Life Support™ catheter by listening to the needs of ECLS physicians regarding technique and configurations.
Femoral arterial access to perfuse the leg.
Return/drainage catheters LS96550-, LS96555-2
Pressure loss (mmHg) |
Flow rate (L/min of water) |
|||||
---|---|---|---|---|---|---|
550-015 |
550-017 |
555-019 |
555-021 |
555-023 |
555-025 |
|
100 |
2.0 |
2.8 |
3.7 |
4.7 |
> 6.0 |
> 6.0 |
-40 |
1.2 |
1.7 |
2.2 |
2.9 |
3.7 |
4.5 |
Drainage catheters LS96438-, LS96355-, LS96360-2
Pressure loss (mmHg) |
Flow rate (L/min of water) | |||||||
---|---|---|---|---|---|---|---|---|
355-021 |
438-021 |
360-023 |
438-023 |
360-025 |
438-025 |
360-027 |
360-029 |
|
-40 |
3.4 |
3.7 |
4.1 |
4.6 |
5.1 |
5.5 |
> 6.0 |
> 6.0 |
Return/drainage catheters LS96010- (mini), LS96110- (mini), LS96218- (flex)2
Pressure loss (mmHg) |
Flow rate (L/min of water) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
010-009 |
010-011 |
010-013 |
010-015 |
218-015 |
218-017 |
218-019 |
218-021 |
218-023 |
218-025 |
|
100 | 0.6 |
1.2 |
2.0 |
2.8 |
3.0 |
4.1 |
5.5 |
> 6.0 |
> 6.0 |
> 6.0 |
-40 | 0.4 |
0.8 |
1.3 |
1.8 |
1.9 |
2.4 |
3.5 |
4.0 |
4.9 |
5.9 |
Find available training resources for extracorporeal life support products.
Nautilus™* ECMO, Nautilus™* Smart ECMO module, Crescent™* jugular dual lumen catheter, and Crescent™* RA are manufactured by MC3, Inc. and exclusively distributed by Medtronic.
Important safety information
Only physicians trained and experienced in using percutaneous catheterization techniques (such as the Seldinger technique), ECMO, and ECLS should use this device.
Note: The benefits of catheterization for extracorporeal circulation must be weighed against the risk of systemic anticoagulation and subsequent propensity for hemorrhage.
Caution: Ensure that the catheter size selected is of adequate size for the vessel to allow distal perfusion of the limb when the catheter is in place. Improper catheter size may be difficult to advance. The vessel must be large enough to ensure perfusion and venous return.
Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgery procedures. For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the Instructions for Use.
Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.
*™ Third-party brands are trademarks of their respective owners.
† 21CFR870.4100.
‡ Elast-Eon™* is a siloxane urethane copolymer.
1. Medtronic data on file: design validation. These tests may not be indicative of clinical performance.
2. Based on Medtronic flow rate/pressure loss data on file. Clinical results will vary due to the patient’s condition and blood composition.
3. Medtronic data on file. Design validation and verification report. These tests may not be indicative of clinical performance.