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.
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.
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.
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.
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.
based on the typical characteristics of safety needles in the medical field, a "GRIPPER PLUS Safety Needle" might be designed to enhance safety during medical procedures involving needle use. Safety needles often incorporate features to minimize the risk of needlestick injuries for healthcare professionals. These features may include mechanisms to retract or shield the needle after use, reducing the potential for accidental exposure to contaminated needles. Additionally, such needles often prioritize ease of use, providing a secure grip for healthcare practitioners.
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.
he Haemonetics Cell Saver 5/5+ FastPack is a component of the Cell Saver autotransfusion system, produced by Haemonetics Corporation. The Cell Saver system is used in the medical field, particularly in surgical procedures, to collect and reinfuse a patient's own blood lost during surgery. This process is known as autologous blood transfusion. Here are some general features and considerations for the Haemonetics Cell Saver 5/5+ FastPack: Autotransfusion System: The Cell Saver system is designed to collect and process blood from the surgical field, filter out unwanted materials, and then return the washed and filtered blood back to the patient. FastPack Technology: The term "FastPack" likely indicates a feature related to the efficiency and speed of the blood processing within the system. Compatibility: The Cell Saver 5/5+ FastPack is typically designed to be compatible with the Cell Saver 5 and Cell Saver 5+ devices, which are part of the Cell Saver system. Safety and Efficiency: Autotransfusion systems aim to provide a safe and efficient means of reducing the need for allogeneic blood transfusions by using the patient's own blood. Usage in Various Surgeries: Cell Saver systems, including the FastPack component, can be used in a variety of surgical procedures where blood loss is expected
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.
The Haemonetics Cell Saver 5/5+ Bowl Kit with the product code 225M004C is a component of the Haemonetics Cell Saver 5 and Cell Saver 5+ autotransfusion systems. These systems are used in medical settings, particularly during surgeries, to collect, process, and reinfuse a patient's own blood that is lost during the procedure. Here are some general features and considerations related to the Haemonetics Cell Saver 5/5+ Bowl Kit: Autotransfusion System: The Haemonetics Cell Saver 5/5+ is an autotransfusion system designed for blood salvage during surgery. It helps minimize the need for allogeneic blood transfusions. Bowl Kit: The Bowl Kit is a critical component of the system, and it typically includes a collection bowl where blood is collected, processed, and washed before being returned to the patient. Compatibility: The Bowl Kit is designed to be compatible with the Cell Saver 5 and Cell Saver 5+ devices. Processing Blood: The autotransfusion system processes shed blood from the surgical field, removes unwanted materials, and returns the washed blood to the patient. 225M004C: The specific product code is used for identification and ordering purposes. It helps in ensuring that the correct component or kit is being used.
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.