upnmed compatible Goldway Toco fetal probe
Product Description
Goldway Toco fetal probe
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.
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.
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 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.
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.
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.
As the world's largest condom maker, we also manufacture personal lubricants. We manufacture latex condoms that are made from premium quality natural rubber latex. Our condoms are designed with total reliability whereby each condom is electronically tested to provide maximum protection and safety. Every design is carefully engineered by our Research and Development team which comprises of industry experts and each variant is developed to create the ultimate pleasure and safety for consumers. All our lubricants are Class IIa medical devices which comply with the new EU MDR regulations in force since May 2021. Medical Device ingredients are pharmaceutical grade, whereas non-medical / cosmetic lubricants have no restrictions. All our lubricants are compatible with latex condoms and are all 100% paraben free. Our personal lubricants can be used up to 6 months after opening. Our personal lubricants also meet the stringent harmonized standards such as ASTM D7661, NF97-034 and the WHO guidelines. *MOQ Condoms from 3000 gross * MOQ Lubes from 10000 Tubes/bottles
Principal The manual steering system is the device that a helm pump driven by the rotation of the steering wheel supplies oil to the cylinder and pushes the piston of the cylinder to have the rudder shaft move. It is a simple system consisting of a helm pump and a cylinder. Cylinder has 4 types of single, rotary, twin, and two rudder. D-I offers the best options to combine kinds of help pumps and cylinders. Our choice mostly satisfies customers, but in case of your special needs, you have many optional ways. The number of rotation wheels is defined by the capacity of the cylinder and the helm pump (cc/rev). You can select the specification you want. Key features Simple system 2 helm pumpsâ??below 50cc, above 50cc Compatible with commercial handles in the range of 300 mm to 1,500 mm Dual handle installation is possible. The lock valve is supplied as default, which can fix the rudder where the handle stops. Structure that the rudder does not rotate even when the tide powers the rudder Rudder angle indicator attachable Application Suitable for vessels below 500 HP A range of vessels from leisure ships, fishing boats, commercial boats, and passenger boats
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