An endobronchial tube is a medical device designed for use in the respiratory system, specifically within the bronchial tubes. These tubes are used in various medical procedures, such as bronchoscopy, endobronchial intubation, and lung surgery. The primary purpose of an endobronchial tube is to maintain an open airway and facilitate the delivery of oxygen or anesthesia to the patient's lungs during surgical or diagnostic procedures. Key features and uses of endobronchial tubes include: Bronchoscopy: Endobronchial tubes are often used in bronchoscopy procedures, allowing physicians to visually examine the bronchial tree and perform diagnostic or therapeutic interventions. Lung Surgery: During certain lung surgeries, endobronchial tubes may be employed to isolate and collapse one lung, providing a clear field of view for the surgeon. Ventilation: Endobronchial tubes can be used for selective lung ventilation. They can be positioned to direct ventilation to a specific lung, allowing the other lung to be collapsed or isolated. Anesthesia: In some cases, endobronchial tubes are used for delivering anesthesia during thoracic surgeries or procedures.
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 some general information: CORDIS: CORDIS is a brand known for producing medical devices, particularly in the field of cardiology. CORDIS is a part of Cardinal Health. Product Code 534518T: The product code suggests that it's associated with a specific medical device or product, likely in the field of cardiology or vascular interventions.
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.
I can provide some general information based on the terms used: Asahi: Asahi Intecc Co., Ltd. is a company known for producing medical devices, particularly guidewires and microcatheters for interventional procedures in cardiology and radiology. Sion Blue: The term "Sion Blue" could refer to a specific type or model of guidewire produced by Asahi Intecc. Guidewires are thin, flexible wires used to navigate through blood vessels during various medical procedures.
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 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.
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.
8410-0254 HyperSoft 3D Advanced, 2.5mm Large Loop Dia, 4cm INDICATIONS FOR USE: The MicroPlex�® Coil System (MCS) is intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae. The MCS is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature
Covidien EGIA60AMT - Endo GIA Reload -Articulating, Medium/Thick -Cartridge Color: Purple -Staple Size (Inner to Outer): 3mm, 3.5mm, 4mm
The Hem-o-lok Ligating Clip System, produced by Teleflex under the Weck brand, is a medical device used in surgical procedures for the ligation (closing off) of vessels or tissue structures. The Hem-o-lok clips are commonly utilized in laparoscopic and robotic surgeries. Key features and aspects of the Teleflex Weck Hem-o-lok Ligating Clip System include: Material: The clips are typically made from a polymer material, providing a secure and reliable closure when applied to vessels or tissues. Design: Hem-o-lok clips are designed to be easy to use, with a simple mechanism for application. They are available in various sizes to accommodate different surgical needs. Application: Surgeons use Hem-o-lok clips to occlude or ligate blood vessels or other structures during surgery. These clips are widely used in minimally invasive procedures, such as laparoscopic and robotic surgeries. Secure Closure: The design of the clips aims to provide a secure closure, preventing bleeding or leakage from the ligated structures. Color Coding: The clips are often color-coded according to size for easy identification during surgery, allowing surgeons to choose the appropriate clip for the vessel or tissue being ligated.
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.
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.
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.
Surgicel is a brand of absorbable hemostats used in surgical procedures to control bleeding. Surgicel Absorbable Hemostat is often employed in various surgical specialties, including general surgery, cardiovascular surgery, neurosurgery, and orthopedic surgery. These products are designed to help surgeons achieve hemostasis (control bleeding) in various situations. Here are some key features of Surgicel Absorbable Hemostat: Material: Surgicel is often made from oxidized regenerated cellulose. Absorption: Surgicel is absorbable and eventually breaks down within the body. Application: It is typically applied directly to the bleeding site and conforms to the tissue to provide a physical barrier and help control bleeding. Varieties: Surgicel is available in different forms, including sheets, patches, and powder, to suit various surgical needs. Biocompatibility: Surgicel is designed to be biocompatible, meaning it is generally well-tolerated by the body.
Guide wires are commonly used in medical procedures, particularly in cardiology and radiology, to guide catheters and other devices through blood vessels or other anatomical structures. The Terumo Radifocus Guide Wire M is likely designed for use in vascular interventions. Here are some general characteristics you might find in Terumo guide wires: Material: Guide wires are typically made of materials such as stainless steel or nitinol. Coating: Some guide wires may have hydrophilic or hydrophobic coatings to enhance their performance during navigation through blood vessels. Tip Design: The tip design may vary based on the intended application, with options like floppy or stiff tips. Diameter and Length: Guide wires come in various diameters and lengths to suit different procedures and anatomies. Radiopaque Markers: Radiopaque markers help visualize the position of the guide wire under fluoroscopy.
If "NOVOSYN VIOLETT" is a product or medical device, it may be associated with a manufacturer, such as a pharmaceutical or medical equipment company. To obtain the most accurate and up-to-date information, I recommend the following steps: Contact the Manufacturer: Try reaching out to the manufacturer associated with the product. They should be able to provide details about the product, its use, and any relevant specifications. Medical Professionals or Institutions: If you are a healthcare professional or associated with a medical institution, you may inquire within your organization for information about the specific product. Product Catalogs or Documentation: Check medical product catalogs, manuals, or documentation from relevant manufacturers or suppliers. This information is often available through official channels. Online Resources: Search online medical databases, catalogs, or supplier websites for the specific product code or name. Sometimes, product details are available on official websites or medical supply platforms.
Smith & Nephew is a global medical technology company that manufactures a wide range of medical devices, including those used in orthopedics, sports medicine, wound management, and advanced surgical procedures. To obtain accurate and up-to-date information about the product with the code "ASC4250-01," I recommend the following steps: Official Smith & Nephew Channels: Check the official Smith & Nephew website or contact their customer support directly. The company's official channels are likely to provide the most accurate and current information about their products. Product Documentation: If you have access to the product documentation or packaging, it should contain detailed information about the product, its specifications, and its intended use. Medical Professionals or Facilities: If you are associated with a medical institution or healthcare facility, inquire within your organization. Medical professionals and facilities often have direct access to product information. Authorized Distributors or Suppliers: Reach out to authorized distributors or suppliers of Smith & Nephew products. They may be able to provide information about the product code in question. Online Medical Product Databases: Some online medical product databases or catalogs may provide information about specific medical devices. Check reputable medical supply platforms for details.
The Bard PerFix Light Plug is a medical device used in hernia repair. Bard is a well-known manufacturer of medical devices, and their hernia repair products include mesh implants designed to reinforce and support weakened or damaged tissue in the abdominal wall. Key features and considerations for the Bard PerFix Light Plug may include: Hernia Repair: The PerFix Light Plug is specifically designed for use in hernia repair procedures. Hernias occur when organs or tissues protrude through a weak spot in the surrounding muscle or connective tissue. Mesh Material: The product is likely made of a mesh material. Meshes used in hernia repair are often constructed from synthetic materials, such as polypropylene. Plug Design: The term "plug" suggests that the device is designed to fill or cover a defect in the abdominal wall associated with a hernia. Lightweight Design: The inclusion of "Light" in the product name may indicate that the mesh is designed to be lightweight while still providing effective support. Surgical Technique: The PerFix Light Plug is used by surgeons during hernia repair procedures to reinforce the tissue and reduce the risk of hernia recurrence.
