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 Accu-Chek Performa Test Strips are used in conjunction with Accu-Chek Performa blood glucose meters. These test strips are an essential component for monitoring blood glucose levels in individuals with diabetes. Here are some key points about Accu-Chek Performa Test Strips: Compatibility: Accu-Chek Performa Test Strips are specifically designed to work with Accu-Chek Performa blood glucose meters. Blood Glucose Monitoring: These test strips are used to measure the concentration of glucose in a small blood sample. This helps individuals with diabetes manage their blood sugar levels. Quick Results: The test strips provide rapid and accurate results, allowing individuals to monitor their blood glucose levels conveniently at home. Capillary Action Technology: The strips often use capillary action technology, which helps to draw in a precise amount of blood for the test. Coding: Some blood glucose test strips require manual coding to match the code on the test strip vial with the code on the meter. It's important to follow the specific instructions provided by the manufacturer regarding coding. Storage: Proper storage of test strips is essential for accurate results. Test strips are typically stored in a cool, dry place, and users should check the expiration date before use.
the Cordis Emerald Guidewire is a product developed by Cordis Corporation, a subsidiary of Cardinal Health. Guidewires are medical devices used in various interventional procedures to navigate through blood vessels, providing access for other devices and treatments. Key features of the Cordis Emerald Guidewire may include: Material: The guidewire is typically made from materials like stainless steel or nitinol, which offer flexibility and support for navigating through the vascular system. Coating: Guidewires may have hydrophilic or hydrophobic coatings to enhance their lubricity, making it easier for them to pass through blood vessels. Tip Design: The tip of the guidewire is often designed to be atraumatic, reducing the risk of vessel injury during navigation. Radiopacity: The guidewire is often designed with radiopaque markers to aid in fluoroscopic visualization during procedures. Length and Diameter: Guidewires come in various lengths and diameters to suit different procedures and anatomies.
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 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.
Key features and characteristics of the Bard Denali DL950F Vena Cava Filter may include: Retrievable Design: The Bard Denali DL950F is often designed to be retrievable, allowing for potential removal when the risk of pulmonary embolism has decreased. Cone Design: Vena cava filters typically have a cone-shaped design that helps to trap and prevent blood clots from traveling to the pulmonary arteries. Biocompatible Materials: The filter is typically made of biocompatible materials suitable for long-term implantation. Ease of Deployment: The deployment mechanism is designed for ease of use during the implantation procedure. Radiopaque Markers: Radiopaque markers are often incorporated into the design to aid in accurate placement under fluoroscopy or other imaging modalities. Compatibility with Imaging: The device is designed to be compatible with various imaging technologies, allowing healthcare professionals to monitor its position and effectiveness.
Zimmer Biomet's Biomend Collagen Patch is a medical device commonly used in various surgical procedures, particularly in the field of oral and maxillofacial surgery, periodontics, and other specialties. Please note that product details and availability may change over time. Here are some general features and considerations associated with the Biomend Collagen Patch: Material: Biomend Collagen Patches are typically made from collagen, a protein naturally found in the body. Collagen patches are used for their biocompatibility and ability to promote tissue healing. Biocompatibility: Collagen is known for its biocompatibility, meaning it is generally well-tolerated by the body. Biomend Collagen Patches may be used to support and enhance the healing process. Resorbable: Collagen patches are often designed to be resorbable, meaning they gradually break down over time as the body's natural healing processes take place. Applications: Biomend Collagen Patches are commonly used in various surgical procedures, including dental and oral surgeries, to help manage soft tissue and promote healing.
The description "BARD PTFE FELT PLEDGETS 9.5MM X 4.8MM RECTANGLE" indicates a product manufactured by Bard that consists of PTFE (polytetrafluoroethylene) felt material formed into pledgets with specific dimensions. PTFE is a synthetic polymer known for its nonstick properties, chemical resistance, and durability. Here are some general considerations based on the description: Material: PTFE is a high-performance polymer with excellent chemical resistance and low friction properties. The use of PTFE in pledgets suggests applications in surgery or medical procedures where such properties are advantageous. Pledgets: Pledgets are small pieces of material, often used in surgical procedures to reinforce sutures or provide additional support. Dimensions: The specified dimensions are 9.5mm by 4.8mm, indicating the length and width of the rectangular PTFE felt pledgets. BARD: Bard is a well-known medical device company that produces a range of healthcare products, including materials used in surgical and medical applications.