Cotton Face Mask
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N95 Face Mask
PPE Kit
Latex Surgical Gloves
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Vinyl Gloves Contact me for more details .
ASTM F2100-19 Level 2 approved The full-width nosepiece guarantees a proper fit Secured with ear loops to be placed behind the ears Features soft, fluid resistant, polypropylene inner and outer facing assuring comfort on the inside and protection on the outside. BFE�¢?�¥98% PFE 98% Splash resistance 120mmHg Non-Sterile
CIF : 3 Ply Mask -FDA L1 50/Box Color : Blue, pink, white $1.5 including $0.2 commission $1.60 Inclusive $0.2 Commission for Black Timeï¼?Fast Boat 10-18Days MOQ: 50M-5B SOP: 1. NCNDA, LOI 2 DRAFT SBLC/LC or TT 3 Seller offer life Video 3. IMFPA, Spa SBLC/LC or TT 4. CIF PORT, Buyer INSPECTION 5.Seller Release SGS &Buyer release FUND 6 Buyer Customs clearance
CIF : 3Ply Mask -FDA L1 50/Box Color : Blue, pink, white $1.5 including $0.2 commission $1.60 Inclusive $0.2 Commission for Black Time - Fast Boat 10-18Days MOQ: 50M-5B SOP: 1. NCNDA, LOI 2 DRAFT SBLC/LC or TT 3 Seller offer life Video 3. IMFPA, Spa SBLC/LC or TT 4. CIF PORT, Buyer INSPECTION 5. Seller Release SGS &Buyer release FUND 6 Buyer Customs clearance
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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
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.
Terumo is a well-known medical device company, and Ultimaster is a brand associated with their drug-eluting stent (DES) products. Drug-eluting stents are devices used in interventional cardiology to treat coronary artery disease.
Surgicel is a brand of absorbable hemostats used in surgical procedures to control bleeding. Surgicel Absorbable Hemostat is often employed in various surgical specialties, including general surgery, cardiovascular surgery, neurosurgery, and orthopedic surgery. These products are designed to help surgeons achieve hemostasis (control bleeding) in various situations. Here are some key features of Surgicel Absorbable Hemostat: Material: Surgicel is often made from oxidized regenerated cellulose. Absorption: Surgicel is absorbable and eventually breaks down within the body. Application: It is typically applied directly to the bleeding site and conforms to the tissue to provide a physical barrier and help control bleeding. Varieties: Surgicel is available in different forms, including sheets, patches, and powder, to suit various surgical needs. Biocompatibility: Surgicel is designed to be biocompatible, meaning it is generally well-tolerated by the body.
Guide wires are commonly used in medical procedures, particularly in cardiology and radiology, to guide catheters and other devices through blood vessels or other anatomical structures. The Terumo Radifocus Guide Wire M is likely designed for use in vascular interventions. Here are some general characteristics you might find in Terumo guide wires: Material: Guide wires are typically made of materials such as stainless steel or nitinol. Coating: Some guide wires may have hydrophilic or hydrophobic coatings to enhance their performance during navigation through blood vessels. Tip Design: The tip design may vary based on the intended application, with options like floppy or stiff tips. Diameter and Length: Guide wires come in various diameters and lengths to suit different procedures and anatomies. Radiopaque Markers: Radiopaque markers help visualize the position of the guide wire under fluoroscopy.
If "NOVOSYN VIOLETT" is a product or medical device, it may be associated with a manufacturer, such as a pharmaceutical or medical equipment company. To obtain the most accurate and up-to-date information, I recommend the following steps: Contact the Manufacturer: Try reaching out to the manufacturer associated with the product. They should be able to provide details about the product, its use, and any relevant specifications. Medical Professionals or Institutions: If you are a healthcare professional or associated with a medical institution, you may inquire within your organization for information about the specific product. Product Catalogs or Documentation: Check medical product catalogs, manuals, or documentation from relevant manufacturers or suppliers. This information is often available through official channels. Online Resources: Search online medical databases, catalogs, or supplier websites for the specific product code or name. Sometimes, product details are available on official websites or medical supply platforms.
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 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.