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Vasoview Hemopro 2 Endoscopic Vessel Harvesting System

The gold standard for EVH, with insulated jaws and spot cautery feature

Vasoview Hemopro Endoscopic Vessel Harvesting System

High performance in endoscopic vessel harvesting

Vasoview 6 Pro Endoscopic Vessel Harvesting System

Refined design via input from users of previous Vasoview devices

iCast Covered Stent System

Acrobat SUV Vacuum Stabilizer

Local stabilization of a target vessel during off-pump CABG

Acrobat V Vacuum Stabilizer

Local stabilization of a target vessel during off-pump CABG

Acrobat-i Stabilizer

Access and control for hard to reach vessels during CABG

Acrobat-i Positioner

Lifts and holds the heart. Designed for apical or nonapical placement.

Xpose 3 Positioner

Lifts and holds the heart. Designed for apical or nonapical placement.

Axius Blower Mister

Controlled delivery of CO2 and saline during CABG

Axius Coronary Shunts

Myocardial protection during target vessel anastomosis

Heartstring III Proximal Seal System

Clampless hemostasis during proximal anastomosis in CABG
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Getinge / Maquet Cardiopulmonary GmbH Issues Medical Device Removal for Certain Lots of ROTAFLOW Centrifugal Pumps (RF-32 Pumps)

On January 8, 2024, Getinge / Maquet Cardiopulmonary GmbH (MCP) notified affected customers of a nationwide recall (medical device removal) for certain lots of ROTAFLOW Centrifugal Pumps (RF-32 pumps) due to a potentially compromised sterile barrier.  The RF-32 pumps are intended to maintain blood flow during extracorporeal circulation and are packaged in sterile bags supplied to MCP/Getinge from its supplier, Nelipak.

Please download the notice for more comprehensive information and instructions.

Medical Device Removal for Certain Lots of RF-32 ROTAFLOW Centrifugal Pumps Jan 8 2024 Download PDF

Medical Device Removal Notice - Quadrox

Maquet Cardiopulmonary GmbH/Getinge is initiating a voluntary Medical Device Removal for the Cardiotomy Reservoirs (VKMO 10000-USA, VKMO 11000-USA), QUADROX-iD (BEQ-HMOD 30000, HMOD 70000, and BEQ-HMOD 70000), QUADROX-iR (HMO 71100, HMO 70100, BEQ-HMO 71100, HMO 51100, HMO 50100, BEQ-HMO 51100), and QUADROX-, i (HMO 50000, HMO 51000, HMO 70000, HMO 71000, and BEQ_HMO 71000, HMO 10000, HMO 11000, HMO 30000 and HMO 31000) Oxygenators due to a risk of potentially compromised packaging sterility that may result in the risk of infection/harm to the patient. All lots are being removed. 

Please download the notice for more comprehensive information and instructions.

Quadrox Oxygenator Notice 18 May 2023 Download PDF