Healthcare Professionals

React 68 Catheter

Aspiration Catheter for
Acute Ischemic Stroke

OVERVIEW

The React™ 68 Catheter features a coil and braid design along with end-to-end Nitinol construction — easing navigation to the M1 and M2 segments. This catheter combined with the Riptide™ Aspiration System is designed to revascularize patients experiencing acute ischemic stroke.

At Medtronic, we’re constantly innovating to expand options for treatment in the fight against acute ischemic stroke (AIS). We provide solutions like the React 68 Catheter to empower the expertise of our physician partners, and enable them to treat their AIS patients.


REACT WITH SPEED.
REACT WITH AGILITY.
REACT WITH CONFIDENCE.

React 68 Catheter Video

Discover the React™ 68 Catheter was built to help treat Acute Ischemic Stroke patients with speed, agility, and confidence by watching its durable, end-to-end flat Nitonol construction and combined COil + BRAid design in action.
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PRODUCT DETAILS

Picture showing React coil

Navigability of a Coil

Picture showing React braid

Pushability of a Braid

Picture showing React Nitinol construction

Durability of Nitinol

React™ COBRA Technology

Picture showing React coil and braid

Overlapping combination of a Nitinol COil+ BRAid to deliver flexibility and pushability.


MANUALS AND TECHNICAL GUIDES

React 68 Catheter Instructions for Use

This technical manual includes indications, warnings, precautions, product specifications, instructions, and clinical study summary. Find in the product labeling supplied with each device or call Medtronic at 800-961-9055.


MODEL SPECIFICATIONS

Download the model specifications sheet to use as a quick reference guide for the React 68 Catheter and the Riptide Aspiration System.

pdf React 68 Catheter (.pdf)

Model specs and ordering information for React 68 Catheter

191KB

pdf Riptide Aspiration System (.pdf)

Model specs and ordering information for Riptide Aspiration System

337KB


INDICATIONS

The Riptide Aspiration System is intended for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral M1 and M2 segments, basilar, and vertebral arteries) within 8 hours of symptom onset. Patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment.


All claims have been substantiated and data is on file TR-NV15399 Rev A.