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The EV3 SpiderFX is commonly associated with the SpiderFX Embolic Protection Device, which is used in the field of interventional cardiology. The device is designed to capture and remove embolic debris that may be released during certain vascular procedures, particularly during carotid artery stenting.

Key features of the EV3 SpiderFX Embolic Protection Device may include:

Embolic Protection: The primary function of the device is to provide protection against embolic debris dislodged during the intervention. It helps prevent these debris from reaching and potentially blocking smaller blood vessels.

Flexible Design: The SpiderFX typically has a flexible design that allows it to navigate through blood vessels, facilitating the deployment and retrieval process.

Distal Protection: The device is designed to be positioned distal to the treatment site, capturing any embolic debris before it can travel downstream.

Capture Basket: The device often includes a capture basket that traps and retains embolic debris, preventing it from causing harm in the circulation.

Compatibility: The SpiderFX device is designed for compatibility with various catheters and guide wires commonly used in interventional procedures.

Cordis is a well-known medical device company that produces a variety of products, including devices used in interventional cardiology and vascular procedures.

The Cordis Saber PTA balloon is likely designed for use in percutaneous transluminal angioplasty procedures. Angioplasty is a medical procedure used to open narrowed or blocked blood vessels, typically arteries, to improve blood flow. During angioplasty, a balloon catheter is inflated at the site of the blockage to widen the vessel and restore blood flow.

Here are some general features you might expect from a PTA balloon like Cordis Saber:

Balloon Material: The balloon is typically made of materials like polyethylene or polyurethane.

Inflation System: It would likely have an inflation system that allows controlled inflation and deflation of the balloon during the procedure.

Catheter Design: The balloon is mounted on a catheter, which is a flexible tube that allows the device to be threaded through blood vessels to the site of the blockage.

Guidewire Compatibility: PTA balloons are often designed to be used with guide wires for precise placement.

The Terumo Runthrough series refers to a range of guide wires manufactured by Terumo Corporation, a global medical device company. Guide wires are essential tools in interventional procedures, particularly in cardiology and radiology, where they are used to navigate through blood vessels and provide support for the delivery of catheters and other interventional devices.

Key features of the Terumo Runthrough guide wires, which may vary depending on the specific model and application, include:

Hydrophilic Coating: Many Terumo guide wires are known for their hydrophilic coating, which enhances lubricity and facilitates smooth navigation through blood vessels, reducing friction.

Flexible Design: The guide wires are designed to be flexible, allowing them to navigate through tortuous vessels with precision.

Radiopaque Tip: The tips of the guide wires are often radiopaque, making them visible under fluoroscopy or other imaging modalities. This feature aids interventionalists in visualizing the position of the guide wire during the procedure.

Various Tip Configurations: Guide wires may come with different tip configurations, such as soft or floppy tips for ease of navigation or more supportive tips for crossing lesions.

Different Lengths and Diameters: Terumo typically offers guide wires in various lengths and diameters to accommodate different patient anatomies and procedural requirements.

Biosensors is a medical device company known for its innovations in interventional cardiology, particularly in the field of coronary stents. The BioMatrix platform includes a range of drug-eluting stents (DES) designed to be used in the treatment of coronary artery disease.

Key features of the BioMatrix stent platform, which may extend to the NeoFlex model if it's a part of the series, may include:

Drug-Eluting Stent: The stents in the BioMatrix platform are drug-eluting, meaning they are coated with a medication (such as an anti-restenotic drug) designed to inhibit the regrowth of tissue inside the treated blood vessel.

Biodegradable Polymer: Some versions of the BioMatrix stent use a biodegradable polymer to deliver the drug to the target site. The polymer gradually dissolves over time, leaving only the metallic stent behind.

Flexible Design: The stents are designed to be flexible, allowing for easier navigation and deployment in the coronary arteries.

Thin-Strut Technology: Thin struts can contribute to improved deliverability and conformability of the stent to the vessel wall.

Various Sizes: The BioMatrix stent platform typically offers stents in various sizes to accommodate different patient anatomies and lesion characteristics.

Ptca guide wire is a steerable guide wire with a maximum diameter
Of 0.014 inches (0.36mm) and available in 160 cm and 300 cm lengths

Dimensions

Ptca balloon catheter is intended to be used for percutaneous transluminal coronary angioplasty (ptca)

Dimensions