View the Liberant™ thrombectomy system blood conservation unit.

LMT-CT12

Liberant™ Thrombectomy System Blood Conservation Unit Closed

The Liberant™ device is an ultrasonic-controlled thrombectomy system for use in the peripheral arterial and venous vessels.

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Indications, Safety, and WarningsIndications for Use: The Liberant thrombectomy system is indicated for the removal of fresh, soft emboli or thrombi from the vessels of the peripheral arterial and venous systems.Contraindications: Do not use the Liberant thrombectomy system in the coronary vasculature or neurovasculature. Do not use in patients for whom anticoagulant or antiplatelet therapy is contraindicated.Potential Adverse Effects of the Device on Health: The potential complications include, but are not limited to the following: allergic reaction to device materials; anemia; death; embolization; hemorrhage; hypotension; infection; ischemia or infarction; pain; thrombosis; total occlusion of treated vessel; venous valvular damage; vessel damage, including arteriovenous fistula, dissection, perforation, pseudoaneurysm, or vascular aneurysm; adverse events associated with endovascular procedures, including acute renal impairment, allergic reaction to contrast medium, cerebrovascular accident, hemorrhage or hematoma at access site, hypertension.Indications, contraindications, warnings and instructions for use can be found in the product labeling supplied with each device, or contact a Medtronic representative.CAUTION: Federal law (USA) restricts this device to sale by or on the order of a physician.UC202600649 EN

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LMT-CT12

Liberant™ Thrombectomy System Blood Conservation Unit Closed

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United States

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LMT-CT12 Liberant™ Thrombectomy System Blood Conservation Unit Closed

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United States

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LMT-CT12

Liberant™ Thrombectomy System Blood Conservation Unit Closed