The CentriMag™ Acute Circulatory Support System is a blood pumping system used to support patients with acute heart and lung failure.
The CentriMag™ Device is the ONLY acute circulatory support system approved for 30-day VAD use* and cleared for ECMO** allowing escalation and de-escalation of therapy.1-3,*
The CentriMag motor has been updated with streamlined lock design for a simple locking process. Two spring-loaded levers automatically lock the CentriMag™ or PediMag™ blood pumps into the motor for effortless insertion. Multiple points of contact provide a strong hold to keep the pump in place, providing confidence in insertion stability.
The CentriMag blood pump functions as:
Driven by Full MagLev™ Flow Technology, the CentriMag and PediMag Pumps include a free-floating magnetically levitated rotor for a contact-free environment. This innovative technology results in excellent hemodynamics, which can lead to minimized blood stagnation, friction and shear stress.6,7
Full MagLev Flow Technology provides a contact-free environment that features:
The CentriMag System includes both pediatric and adult pump options, producing flows up to 1.5 LPM for pediatric, and 10 LPM for adult.
*PMA approval for 30-day use of CentriMag System components include: CentriMag™ Pump, CentriMag™ Console, CentriMag™ Motor, Mag Monitor, Flow Probe, and CentriMag™ Drainage Cannula and CentriMag™ Return Cannula. Optional accessories include: CentriMag™ System Cart, CentriMag™ System Transporter and Pressure Transducer. PMA approval for 30-day use of CentriMag™ System excludes: PediMag™ Blood Pump and any other pediatric components or accessories.
**ECMO clearance for >6-hour use is indicated for the CentriMag™ Blood Pump to be used with: CentriMag™ Console, CentriMag™ Motor, Mag Monitor, and Flow Probe. Optional accessories include: CentriMag™ System Cart, CentriMag™ System Transporter and Pressure Transducer. ECMO clearance for the CentriMag™ Blood Pump is for adult use only.
† Approved for 30-day use
†† COVID-19 Temporary Expanded Indication under US FDA enforcement policy guidance
MAT-2012990 v4.0
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