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.
ACIST Medical Systems is known for its innovations in contrast delivery systems for medical imaging, particularly in the field of cardiology. The "ACIST NAVVUS RX MICROCATHETER" suggests a microcatheter associated with contrast delivery or imaging guidance. Here are some general considerations for components like microcatheters used in imaging procedures: Contrast Delivery: Microcatheters are often used in conjunction with contrast media to enhance visibility during medical imaging procedures, such as angiography. Navigation: The term "NAV" in "NAVUS" suggests navigation, which could indicate that the microcatheter is designed for precise and controlled navigation within blood vessels or specific anatomical structures. RX: The "RX" designation often denotes a product intended for diagnostic or therapeutic interventions. Imaging Modalities: Microcatheters are commonly used in procedures like angiography, where detailed imaging of blood vessels is required.
Teleflex: Teleflex is a global provider of medical technologies, including products for vascular access, anesthesia, respiratory care, surgical care, and more. They offer a range of vascular products, and the Arrow brand is associated with vascular access and intervention. Rediguard IAB (Intra-Aortic Balloon): Intra-aortic balloon pumps are medical devices used to temporarily support the heart's pumping function and improve coronary artery blood flow. The term "Rediguard" suggests that it may have features related to safety or guarding.
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.