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Stingray Catheter
The Stingray Catheter includes a small balloon for fluoroscopic positioning at the distal tip of the shaft. The distal end of the catheter is coated with a hydrophilic layer, compatible with a 6F guiding catheter with a minimum inner diameter of 0.070 inches (1.7 mm). It can be used with guidewires with an inner diameter of ≤0.014 inches (0.36 mm). The product is sterilized with ethylene oxide and is intended for single use.
Product English Name:
Stingray Catheter
Alias:
CTO Re-Entry Balloon Catheter,Stingray Balloon
Intended Use:
The Stingray CTO Re-Entry Balloon Catheter is designed to guide, manipulate, control, and support guidewires to access discrete areas of the coronary and peripheral vascular systems. When used as part of a system that includes the Crossboss CTO Penetration Microcatheter, Stingray CTO Re-Entry Balloon Catheter, and Stingray CTO Penetration Guidewire, it is suitable for placing conventional guidewires into stenotic coronary lesions (including chronic total occlusions [CTOs]) distally via an intraluminal approach before PTCA or stent intervention procedures.
Product Introduction

The Stingray Catheter is a specialized medical device designed for re-entry into the true lumen during chronic total occlusion (CTO) procedures. It features a unique balloon design that aids in fluoroscopic positioning, ensuring precise navigation through complex vascular structures. The catheter's hydrophilic coating enhances maneuverability, making it compatible with standard guidewires and guiding catheters. Its single-use, sterilized design ensures safety and reliability in clinical settings.

1. The Stingray Catheter is characterized by its small balloon at the distal tip, which allows for accurate fluoroscopic positioning. This feature is crucial for navigating through challenging vascular pathways, especially in CTO cases.
2. The catheter's structure includes a hydrophilic coating on the distal end, which reduces friction and improves the ease of movement through blood vessels. It is compatible with 6F guiding catheters and guidewires with an inner diameter of ≤0.014 inches, ensuring versatility in various clinical scenarios.
3. The primary use of the Stingray Catheter is to facilitate the placement of guidewires into stenotic coronary lesions, particularly in CTOs. It is often used in conjunction with other specialized devices like the Crossboss Microcatheter and Stingray Guidewire to achieve successful re-entry into the true lumen before PTCA or stent placement.

The Stingray Catheter, also known as the CTO Re-Entry Balloon Catheter, is a vital tool in interventional cardiology. Its design, featuring a small balloon and hydrophilic coating, ensures precise navigation and ease of use. When paired with other specialized devices, it becomes an indispensable part of the toolkit for treating complex coronary lesions, particularly in chronic total occlusions.

Main Features

The Stingray Catheter is designed to provide precise re-entry into the true lumen during CTO procedures. Its key features include a small balloon for fluoroscopic positioning, a hydrophilic coating for smooth navigation, and compatibility with standard guidewires and guiding catheters.

1. The small balloon at the distal tip of the Stingray Catheter allows for accurate fluoroscopic positioning, which is essential for navigating through complex vascular structures.
2. The hydrophilic coating on the distal end of the catheter reduces friction, making it easier to maneuver through blood vessels and reducing the risk of vessel trauma.
3. The catheter is compatible with 6F guiding catheters and guidewires with an inner diameter of ≤0.014 inches, ensuring it can be used in a wide range of clinical scenarios.
4. The Stingray Catheter is designed for single use and is sterilized with ethylene oxide, ensuring patient safety and reducing the risk of infection.
5. When used as part of a system with the Crossboss Microcatheter and Stingray Guidewire, the Stingray Catheter enhances the success rate of re-entry into the true lumen in CTO procedures.

The Stingray Catheter's main features, including its small balloon, hydrophilic coating, and compatibility with standard devices, make it a reliable tool for re-entry in CTO procedures. Its single-use, sterilized design ensures safety, while its integration with other specialized devices enhances its effectiveness in complex cases.

Clinical Applications

The Stingray Catheter is primarily used in interventional cardiology for re-entry into the true lumen during chronic total occlusion (CTO) procedures. It is often used in conjunction with other devices to facilitate guidewire placement in stenotic coronary lesions.

1. The Stingray Catheter is used in the treatment of chronic total occlusions (CTOs) in coronary arteries, where it aids in re-entry into the true lumen.
2. It is often used in conjunction with the Crossboss Microcatheter and Stingray Guidewire to enhance the success rate of guidewire placement in complex lesions.
3. The catheter is particularly useful in cases where traditional guidewire techniques have failed, providing a reliable alternative for re-entry.
4. The Stingray Catheter is also used in peripheral vascular interventions, where it aids in navigating through challenging vascular structures.
5. Its compatibility with standard guidewires and guiding catheters makes it a versatile tool in various clinical scenarios, including PTCA and stent placement procedures.

The Stingray Catheter is a key tool in the treatment of chronic total occlusions, offering a reliable method for re-entry into the true lumen. Its use in conjunction with other specialized devices enhances its effectiveness, making it a valuable asset in both coronary and peripheral vascular interventions.

Purchasing Guide

When purchasing the Stingray Catheter, it is important to consider product specifications, compatibility with other devices, budget, and intended clinical use. This guide provides key considerations for procurement.

1. Product specifications: Ensure the Stingray Catheter is compatible with 6F guiding catheters and guidewires with an inner diameter of ≤0.014 inches. Verify the presence of a hydrophilic coating and a small balloon for fluoroscopic positioning.
2. Product type: The Stingray Catheter is a single-use, sterilized device designed for re-entry in CTO procedures. Confirm that the product meets your clinical needs and is compatible with other devices like the Crossboss Microcatheter and Stingray Guidewire.
3. Budget: Consider the cost of the Stingray Catheter in relation to its clinical benefits. Evaluate the cost-effectiveness of using this device in conjunction with other specialized tools.
4. Usage scenarios: The Stingray Catheter is primarily used in interventional cardiology for CTO procedures. Ensure that your facility has the necessary infrastructure and expertise to utilize this device effectively.

Purchasing the Stingray Catheter requires careful consideration of product specifications, compatibility, budget, and clinical use. Its integration with other specialized devices enhances its effectiveness, making it a valuable addition to any interventional cardiology toolkit.

 Precautions

When using the Stingray Catheter, it is important to follow proper handling and usage guidelines to ensure patient safety and device effectiveness. This section outlines key precautions.

1. Ensure the Stingray Catheter is used only once and is properly disposed of after use to prevent contamination and infection.
2. Verify compatibility with 6F guiding catheters and guidewires with an inner diameter of ≤0.014 inches before use.
3. Handle the catheter with care to avoid damaging the hydrophilic coating or the small balloon at the distal tip.
4. Follow proper fluoroscopic positioning techniques to ensure accurate placement of the catheter during the procedure.
5. Monitor the patient closely for any signs of complications, such as vessel trauma or contrast media reactions, during and after the procedure.

Using the Stingray Catheter requires adherence to strict handling and usage guidelines to ensure patient safety and device effectiveness. Proper disposal, compatibility verification, and careful handling are essential to minimize risks and achieve optimal outcomes.

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