70124

Description

The Crescent™ catheter is the first FDA-cleared jugular dual-lumen long-term ECMO catheter, offering:

More accurate placement with radiopaque markers for improved visualization¹
Optimal flow efficiency with enhancements in port placement, lumen design, and tip geometry.²
Maintenance of desired blood flow with features that help keep the catheter securely in place during patient ambulation.

Potential complications related to the use of ECMO devices include, but are not limited to, heart, vessel, or lung damage, hypoxia, anemia, irritation, toxic reaction, infection, hemorrhage, liver or kidney failure, stroke, and death. The benefits of extracorporeal support must be weighed against the risk of systemic anticoagulation and must be assessed by the prescribing physician..

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