Rotational Excisional Atherectomy
Continuous Active Aspiration
Rotating helix creates continuous negative pressure at tip; actively aspirating and transporting material into a collecting bag.
Rotating Abrading Vortex
Additional luminal gain is achieved by a vortex created around the rotating cylinder. Large side windows further break down and effi ciently remove detached material.
Modifying Beveled Tip
Rotating atraumatic catheter head with blunt facets modifi es and detaches mixed morphology lesions.
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Please consult product labels and package inserts for indications, contraindications, hazards, warnings, precautions, and instructions for use. BD, the BD Logo, and Rotarex are trademarks of Becton, Dickinson and Company or its affiliates. © 2021 BD. Illustrations by Mike Austin © 2021. All Rights Reserved. BD-32064
Rotarex™ Rotational Excisional Atherectomy System Safety and Risk Information: The Straub Endovascular System is herein referred to as the BD Rotarex™ Indication For Use: When operated with a Rotarex™
vasculature · In instances of persistent vasospasm · In patients not suitable for atherectomy/thrombectomy · In patients with known or suspected allergies to any component of the Straub Endovascular System · In patients with hemodynamic instability, shock or severe coagulatory disorders · In patients where it is impossible to achieve suffi cient anticoagulation and platelet aggregation inhibition · In areas of known or suspected infection, especially at the puncture site or target vessel segment · In vessels which are oversized or undersized for the particular Rotarex™
extremity peripheral arteries. It is not intended for use in coronary, carotid, pulmonary, iliac or renal vasculature. Contraindications: Use of the Rotarex™
use of a Straub provided guidewire · When the Straub provided guidewire cannot completely cross the target lesion · Where the Straub provided guidewire is in a subintimal position of any length ·Where the Straub provided guidewire has become threaded or entangled in the wire mesh of a stent, stent graft or the lining of a stent graft · Where the target lesion is located in a region of marked vessel tortuosity (has a radius of curvature ≤2 cm) or is heavily calcifi ed.
catheter used · In stents, stent grafts or bypass grafts ·Without the
single use catheter, the Straub Endovascular System is intended for use as an atherectomy device and to break up and remove thrombus from upper and lower family of catheters is contraindicated in the following situations and locations: · In the cardiopulmonary, coronary, cerebral, iliac and renal vasculature · In the venous
Rotational Excisional Atherectomy System
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