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.
I can provide some general information about guiding catheters and Medtronic's involvement in the medical device industry. Guiding Catheter: A guiding catheter is a medical device used in interventional cardiology and radiology procedures. It is designed to guide and support other devices, such as guidewires and balloons, to the target location within the blood vessels. Medtronic: Medtronic is a global healthcare company that produces a wide range of medical devices and technologies. They are involved in various medical specialties, including cardiology, neurology, diabetes, and more.
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.
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.
I can provide some general information: PTFE Guide Wire: PTFE stands for polytetrafluoroethylene, which is a synthetic fluoropolymer of tetrafluoroethylene. It is known for its low friction properties and is often used in medical applications. Medtronic: Medtronic is a global healthcare company that produces a wide range of medical devices and technologies. This includes products used in cardiology, neurology, diabetes, and other medical specialties.
I can provide general information about guide wires used in medical procedures. Guide wires play a crucial role in various interventional procedures, such as angiography and angioplasty, where they are used to navigate through blood vessels and provide a pathway for the delivery of catheters and other medical devices.
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 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 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.
