Ureteral Stent Double J Stent Suppliers and Manufacturers

The EverFlex stent is designed for use in the treatment of peripheral arterial disease (PAD), specifically in the iliac arteries. Key features of the EverFlex Protege stent may include: Self-Expanding Design: The stent is self-expanding, meaning it can open and conform to the shape of the artery without the need for balloon inflation. Nitinol Construction: The stent is typically made of nitinol, a nickel-titanium alloy known for its flexibility and ability to maintain shape memory. Longitudinal Flexibility: The stent is designed to provide longitudinal flexibility, allowing it to adapt to the natural movement of the vessel. Iliac Artery Treatment: The EverFlex Protege stent is specifically indicated for use in the iliac arteries, which are located in the pelvis.

Terumo is a well-known medical device company, and Ultimaster is a brand associated with their drug-eluting stent (DES) products. Drug-eluting stents are devices used in interventional cardiology to treat coronary artery disease.

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.

the Boston Scientific Promus Elite is a coronary drug-eluting stent system. It is designed for use in patients undergoing percutaneous coronary intervention (PCI) procedures to treat coronary artery disease. Here are some key features and points related to the Boston Scientific Promus Elite coronary stent: Drug-Eluting Stent: The Promus Elite is a drug-eluting stent (DES), meaning it is coated with medication to help prevent the re-narrowing (restenosis) of the treated coronary artery. Drug Coating: The stent typically features a polymer coating containing an anti-proliferative drug. This drug is slowly released over time to inhibit the growth of tissue inside the stent, reducing the risk of restenosis. Cobalt Chromium Alloy: The stent is often made of a cobalt chromium alloy, known for its strength and flexibility. This material allows for a thin stent strut design, which can be beneficial in terms of deliverability and conformability. Delivery System: The stent is delivered to the target area using a catheter-based delivery system. The catheter is guided through the blood vessels to the site of the coronary artery lesion. Radiopaque Markers: Radiopaque markers on the stent aid in proper placement and visualization under X-ray guidance during the procedure.

The "SpiderFX" may refer to a specific type of embolic protection device used during carotid artery stenting procedures. Embolic protection devices are designed to capture and remove debris released during the stenting process to prevent it from traveling to the brain, reducing the risk of stroke.

it's common for medical device companies like Medtronic to manufacture guiding catheters used in various interventional procedures, including cardiovascular interventions. Guiding catheters are medical devices used to guide and support the delivery of other interventional devices, such as angioplasty balloons, stents, or embolic protection devices, during procedures like angiography and angioplasty.

Material Number: M0031681890 Description: Straight, 2-tip marker Total / Distal Length: 150cm/6.0cm The Excelsior SL-10 Microcatheter with Thin Wall Technology and Lubricious Hydrolene�® Outer Surface is designed to provide outstanding performance 1.7F (0.56mm) Low Profile Distal Shaft, Excelsior SL-10 Microcatheter is designed with a low profile tip to enhance access to distal vasculature and ease of passage of the catheter trip through stent interstices. Atraumatic Distal Tip, Specifically engineered for atraumatic access, the rounded, low-durometer, unbraided tip offers exceptional softness and flexibility. Variety of Tip Shapes, Offered in six clinically relevant shapes to improve access and navigability.

Terumo Runthrough NS PTCA is a medical device designed for use in percutaneous transluminal coronary angioplasty (PTCA) procedures. PTCA is a minimally invasive procedure used to treat coronary artery disease by widening narrowed or blocked coronary arteries. Here are some key points about the Terumo Runthrough NS PTCA: Manufacturer: Terumo Corporation is a Japanese company known for its medical devices and healthcare products. Type: The Runthrough NS PTCA is a guide wire used in PTCA procedures. Guide wires are essential tools that help navigate catheters and other interventional devices through blood vessels during angioplasty. Function: The guide wire assists in guiding and positioning the catheter within the coronary arteries. It helps the interventional cardiologist navigate through the blood vessels and reach the site of the blockage or narrowing. Features: The "NS" in Runthrough NS may refer to "non-support" or "normal support," indicating the level of support provided by the guide wire. The choice of guide wire depends on factors such as the location and severity of the arterial blockage. Usage: The Terumo Runthrough NS PTCA guide wire is specifically designed for use in PTCA procedures to help facilitate the placement of angioplasty balloons and stents.

he Terumo Runthrough NS PTCA (Percutaneous Transluminal Coronary Angioplasty) guide wire is a product manufactured by Terumo Corporation, a global medical device company. Guide wires are essential tools used in cardiovascular procedures, particularly in angioplasty and stenting, to navigate through blood vessels and provide support for the delivery of catheters and other interventional devices. Key features and characteristics of the Terumo Runthrough NS PTCA guide wire may include: Hydrophilic Coating: Many Terumo guide wires, including the Runthrough NS, are known for their hydrophilic coating. This coating facilitates smoother navigation through blood vessels, reducing friction and enhancing steerability. Flexible Design: The guide wire is designed to be flexible, allowing it to navigate tortuous vessels and reach target locations with precision. Radiopaque Tip: The tip of the guide wire is often radiopaque, making it visible under fluoroscopy or other imaging modalities. This feature helps interventional cardiologists visualize the position of the guide wire during the procedure. Different 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. Various Lengths and Diameters: Terumo typically offers guide wires in various lengths and diameters to accommodate different patient anatomies and procedural requirements.

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.