Covidien ABSTACK30 Absorbatack Fixation Device Part # ABSTACK30 Exp 3/19 Covidien ABSTACK30 Absorbatack Fixation Device is an absorbable tack fixation device, for use in laparoscopic hernia repair. The NEW AbsorbaTack (ABSTACK30X) fixation device for laparoscopic hernia repair continues to deploy tacks when the shaft is flexed over 3 cm. Covidien ABSTACK30 Absorbatack Fixation Device Features Designed with patient comfort in mind No metal required for fixation Supports a minimally invasive approach through 5 mm shaft and easy-to-use design Fixation strength Provides strong temporary mesh fixation, with retention strength comparable to the â??gold standardâ?? ProTackâ?¢ fixation device at 1 week and 2 months in an animal model1 Peace of mind Reduces the likelihood of inadvertent needle sticks in the OR, since no sharp piloting needles are required for deployment Potentially fewer visceral attachments than permanent tack fixation1 Violet tack with black-dot visualization feature to optimize visibility In Perfect sealed condition but past expiration date. Not for human use in the US. Expiration dates have mostly to do with sterilization and not the integrity of the product. The manufacturers sterilize the products after they are packaged and it lasts so many years. The only products we caution customers about are ones that are absorbable or drug coated.
Material Number: M0031681890 Description: Straight, 2-tip marker Total / Distal Length: 150cm/6.0cm The Excelsior SL-10 Microcatheter with Thin Wall Technology and Lubricious Hydrolene�® Outer Surface is designed to provide outstanding performance 1.7F (0.56mm) Low Profile Distal Shaft, Excelsior SL-10 Microcatheter is designed with a low profile tip to enhance access to distal vasculature and ease of passage of the catheter trip through stent interstices. Atraumatic Distal Tip, Specifically engineered for atraumatic access, the rounded, low-durometer, unbraided tip offers exceptional softness and flexibility. Variety of Tip Shapes, Offered in six clinically relevant shapes to improve access and navigability.
8410-0254 HyperSoft 3D Advanced, 2.5mm Large Loop Dia, 4cm INDICATIONS FOR USE: The MicroPlex�® Coil System (MCS) is intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae. The MCS is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature
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
Echelon Endopath Staplers with gray, white, blue, gold, and green reloads deliver six staggered rows of staples with a single cut line in-between. A safety lock-out feature in the Ethicon reloads is designed to prevent a used reload from being re-fired. A staple retaining cap on the Echelon reload, protects the staple leg points during shipping and transportation. All Echelon Endopath Cartridges are compatible only within the Echelon Endopath Family of Staplers. Wide range of cartridges: Accommodates various tissue thicknesses, all with 6-row stapling capability. All cartridges fit through a 12mm trocar. Endoscopic Linear Cutter Reloads
The Ethicon 8702H is a specific type of suture produced by Ethicon, a subsidiary of Johnson & Johnson and a leading manufacturer of surgical sutures and other medical devices. The product you mentioned, "7-0 Prolene Suture," refers to a specific size and type of suture. Here are some key details about the Ethicon 8702H 7-0 Prolene Suture: Suture Material: Prolene is the brand name for a synthetic, non-absorbable monofilament suture material made of polypropylene. Monofilament sutures like Prolene are smooth and reduce tissue drag, making them suitable for various surgical applications. Size: The "7-0" designation indicates the size of the suture. In this case, it is a very fine suture. Suture sizes are denoted numerically, with smaller numbers indicating larger sizes. Color: The "blue" in "blue monofilament" indicates the color of the suture. Suture colors are used to enhance visibility during surgery. Non-Absorbable: Prolene sutures are non-absorbable, meaning they do not break down or dissolve over time. This characteristic makes them suitable for applications where long-term tissue support is required. Indications: Prolene sutures are commonly used in various surgical procedures, including cardiovascular, ophthalmic, and plastic surgery. The choice of suture material and size depends on the specific requirements of the surgical procedure.
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.
I can provide general information about guide wires used in medical procedures. Guide wires play a crucial role in various interventional procedures, such as angiography and angioplasty, where they are used to navigate through blood vessels and provide a pathway for the delivery of catheters and other medical devices.
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 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.