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.
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
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 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.
Verathon is a medical device company that produces various products, including devices used in airway management and visualization. Here are some general considerations based on the components mentioned: Gliderite Rigid Stylet: A stylet is a rigid or flexible rod-like device that is often used to assist in the placement of various medical instruments, such as endotracheal tubes or other airway devices. Verathon: Verathon's products are often related to airway management and medical imaging, so the Gliderite Rigid Stylet might be used in procedures involving airway management. Applications: Rigid stylets are commonly used in the field of anesthesiology and emergency medicine to aid in the insertion of airway devices, ensuring proper placement and reducing the risk of complications.
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.
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.
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 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.
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 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.
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.