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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.
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.
Penumbra is a medical device company known for developing and manufacturing products used in neurovascular and peripheral vascular interventions.
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.
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: 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 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.
STERRAD Cassette features proprietary technology utilizing low-temperature hydrogen peroxide gas plasma for terminal sterilization of medical devices. Their sterilant comes in an easily loaded cassette format that delivers a predefined quantity of hydrogen peroxide per cycle to achieve sterilization both conveniently and effectively. Best of all, each cassette is a closed system, sealed for the operator's safety, and has a chemical indicator on the packaging in order to detect any leakage of sterilant during transportation. Finally, unlike some sterilization modalities, ASP's uniquely bar-coded STERRAD System cassettes can be transported via ground or air shipment. Product Features: STERRAD system sterilant cassettes made by ASP The pre-loaded cassette provides an easy and highly effective way to sterilize Each STERRAD sterilant cassette is a closed system and sealed for the operator's safety Each STERRAD sterilant cassette is individually wrapped with an external leak monitor to detect any leakage during transportation
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.
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.
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.
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.
Stryker is a well-known company that specializes in medical technologies, including surgical equipment and devices. Suction systems are commonly used in medical settings to remove fluids, blood, or debris during surgical procedures. Here are some general considerations: StrykeFlow II: This could be a specific model or version of a suction system provided by Stryker. Suction System: Suction systems are essential in medical procedures to maintain a clear surgical field by removing unwanted fluids and materials. Applications: Suction devices are used in a variety of medical settings, including surgery, endoscopy, and other procedures where maintaining a clear visual field is crucial.
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.
Bard is a well-known manufacturer of medical devices, including products for hernia repair. Meshes are commonly used in hernia repair procedures to provide support and reinforcement to weakened or damaged tissue in the abdominal wall. Here are some general considerations: Anatomical Design: The term "ANATOMICAL MESH" suggests that the mesh is designed to fit anatomical contours, potentially allowing for better conformity to the patient's anatomy during hernia repair. 3DMAX MID: This part of the name may refer to specific design features or characteristics of the mesh. For example, "3DMAX" might imply a three-dimensional design for optimal support. Mesh Material: Hernia repair meshes are typically made of synthetic materials, such as polypropylene, which is known for its durability and biocompatibility. Surgical Technique: The mesh is used by surgeons during hernia repair procedures to reinforce and support the abdominal wall, reducing the risk of hernia recurrence.
