British Two Wheeler Spares Supplies Suppliers and Manufacturers

We are proposing about 1000 1200 Mt/ton monthly of iron slag derived from the desulphurisation skimming process. This material is a iron by- product that is encapsulated in varying levels of contaminants (S,Mg,Si). In order to enhance its usability, the material is processed and screened. We can propose two specifications of Iron Slag : 1. >85% Fe Average 600mm Max Fraction 2. >78% Fe Average 20-300mm Fraction The level of Fe% in the slag has been estimated by water displacement test. For any further information please feel free to contact

We are proposing about 2000tons of iron slag derived from the desulphurisation skimming process. This material is a iron by- product that is encapsulated in varying levels of contaminants (S,Mg,Si). In order to enhance its usability, the material is processed and screened. We can propose two specifications of Iron Slag - European Code: 19.12.01 - Basel Code: B1010 - HS Code: 2619.0020 - Quantity: 2000 tons currently available - Monthly quantity: 500-1000 tons depending on production - Size: 350 1200 mm - Fe content: from 77 to 86% - C content: above 2,5-3% - Bulk density: 2,8-3,4 tons/m3 - Loading type: loose in 20 (26-27 tons on average) The level of Fe% in the slag has been estimated by water displacement test. For any further information please feel free to contact us

The Aluminium Incinerated scrap is the by-product derived from the reprocessing IBA Incinerator bottom ash). It can be classified as follows: Basel code B1010. EW Code: 17 04 02. With a low melting point at 660'C, on visual inspection, aluminium can be found as melted and re-solidified particles or rocks. This happens to aluminium foil that is converted into small droplets during the incineration process. Some larger and thicker aluminium packaging items can still be partially recognised as they retain their shape. The heterogeneous nature of the processed material is due to the diversified conditions present in the combustion chamber, (some relatively cooler regions in the furnace). The stock can contain all kind of aluminium packing. We can currently provide this material in three different fractions and with different aluminium content: 3-8 mm split in two different qualities: 65% ± 3% Al 85% ± 3% Al 8-16 mm: about 70% ± 3% Al 16-60 mm: about 80% ± 3% Al The material contains minor impurities typically stones, ash, glass. Such components are inherent and adhere to the scrap surface. The total impurities can be sorted, but not fully removed. The collected stock is stored in warehouse on cemented flooring. It can be loaded loose in 20' Feet heavy duty container.

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.

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.

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: 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.

For medical gases, Argon is commonly used in various medical applications, including surgical procedures, where it can be employed for tissue coagulation or as a cryogen. The specific details of a product, such as its pressure, purity, and intended use, would be provided by the manufacturer or supplier.

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.

Teleflex is a global provider of medical technologies, offering a wide range of products, including devices for vascular access, anesthesia, respiratory care, and more.

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

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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.

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.