Ureteral Stent Double J Stent Suppliers and Manufacturers

BBRAUN VASCUFLEX MULTI-LOC MULTIPLE STENT DELIVERY SYSTEM

With XIENCE Sierra's new stent design, the XIENCE reputation now extends to offer unmatched deliverability, even with challenging complex lesions. ULTRA LOW STENT CROSSING PROFILE1 OF 0.039â?³ FOR EASIER CROSSING enabled by the new stent design and balloon technology1 XIENCE Sierra's exceptional deliverability also comes from the enhanced stent delivery system featuring a single-piece outer member for added pushability and trackability. Expanded Treatment Optionsâ?¡ With 5.5 mm post-dilatation capability for 3.5 mm and 4.0 mm stents, XIENCE Sierra can treat most large vessels. PROVIDES UNSURPASSED PRECISION IN PLACEMENT AND AVOID GEOGRAPHIC MISS zero shortening even at max expansion of 5.5 mm2 XIENCE SIERRA ENSURES COATING INTEGRITY3 even at max expansion XIENCE Sierra coating remains intact at maximum post-dilatation expansion of 5.5 mm from 3.5 mm XIENCE Sierra (3.5 x 18 mm) 25x magnification at max expansion of 5.5 mm XIENCE Sierra (3.5 x 18 mm) 150x magnification at max expansion of 5.5 mm Synergy coating shows multiple cracks with delamination at its max expansion of 4.25 mm from 3.5 mm Xience Xpedition represents a powerful combination of deliverability, strong clinical data and broad availability of meaningful sizes, three factors that make this product well-suited to treat a wide range of patients, The impact of the changes to the stent delivery system is particularly notable in patients with complex coronary anatomy. For these patients, physicians have a new technology to reach the blockage and restore blood flow with ease and confidence. In order to cater the variegated demands of our beloved clients, we are offering a wide range of Abbott Xience Xpedition Stent

NEW XIENCE SIERRA STENT DESIGN The new XIENCE Sierra Stent Design, with Slim Flex Technology, has a lower crossing profile1 and greater post-dilatation expansion NEW STENT DELIVERY SYSTEM FOR COMPLEX CASES Design innovations built to provide the flexibility, crossability, and pushability needed for even the most complex cases. The XIENCE V®, XIENCE nano®, XIENCE PRIME®, XIENCE PRIME® LL, XIENCE Xpedition®, XIENCE Xpedition® SV and XIENCE Xpedition® LL , XIENCE Alpine®, and XIENCE SierraTM (XIENCE Family) of Everolimus Eluting Coronary Stents on the MULTI-LINK VISION® or MULTI-LINK MINI VISION® Delivery System INDICATIONS The XIENCE Sierra stent system is indicated for improving coronary artery luminal diameter in patients, including those with diabetes mellitus, with symptomatic heart disease due to de novo native coronary artery lesions (length â?¤ 32 mm) with reference vessel diameters of â?¥ 2.25 mm to â?¤ 4.25 mm. In addition, the XIENCE Sierra stent system is indicated for treating de novo chronic total coronary occlusions. CONTRAINDICATIONS The XIENCE Sierra stent system is contraindicated for use in: Patients who cannot tolerate, including allergy or hypersensitivity to, procedural anticoagulation or the post-procedural antiplatelet regimen. Patients with hypersensitivity or contraindication to everolimus or structurally related compounds, or known hypersensitivity to stent components (cobalt, chromium, nickel, tungsten, acrylic, fluoropolymers), or with contrast sensitivity. WARNINGS It is not recommended to treat patients having a lesion that prevent complete inflation of an angioplasty balloon. Judicious patient selection is necessary because the use of this device carries the associated risk of stent thrombosis, vascular complications, and/or bleeding events. This product should not be used in patients who are not likely to comply with the recommended antiplatelet therapy.

The second-generation Xience V everolimus-eluting stent incorporates advanced design features such as a cobalt-chromium stent platform coated with an antirestenotic drug, everolimus, incorporated into a biocompatible polymer with a long history of medical use. The efficacy of the stent has been demonstrated with low rates of angiographic restenosis, whilst randomized trials comparing the Xience V everolimus-eluting stent to the first-generation Taxus paclitaxel-eluting stent have found a reduction in repeat revascularization rates. Further randomized trials, including 'all-comer' patients and registries of unselected patients are currently further evaluating the efficacy and safety of the Xience V stent in high-risk, complex cases.We also offer one of the most primary quality stents in the market, The Xience V Stent Coronary artery stents are devices (small metallic mesh tubes) that are placed over a balloon catheter and delivered to the narrowed portion of the coronary artery. The balloon is used to expand the stent. The stent presses against the narrowed vessel wall, holding the vessel open. This results in a wider artery channel to improve blood flow to the heart muscle. This may be followed by repeat balloon inflations within the stent to achieve the result desired by your doctor. Once the balloon has been deflated and withdrawn, the stent stays in place permanently, holding the coronary artery open. The inner lining of the artery grows over the surface of the stent, making the stent a permanent part of your artery

Material: nitinol(nickel+titanium), shape memory property. Anti-migration shape Flexible construction to conform to anatomy Dynamic radial force for maximum lumen size Retrievable Each of two radiopaque markers at both ends of stent Ce Varieties

Used :- For temporary internal drainage from the ureteropelvic junction to the bladder. Caution:- Periodic evaluation is advised. Polyurethane T-Flex / soft-Flex . Intended for one time use. This Device is Supplied sterile in peel-open packages.

The EvroPlus Evrolimus eluting stent system is a combination product comprised of two regulated components : a device (a coronary stent system) and a drug product (a formulation of Everolimus contained in a polymer coating) pre mounted a balloon catheter between two GOLD radio opaque marker bands. Strut Thickness (m) : 60±5

Sirolimus Eluting Coronary Stent System A Value - Added DES...... Production Description: +100% biodegradable PLGA Coating +Controlled drug release for continuous effect

Cardiac stent

Drug eluting stent

We can supply you good price & quantity.

Endopyelotomy Stent

Different ranges of Stent such as Everoplus, Kotonar, Coherent & Insistent.

The Medtronic Resolute Integrity Zotarolimus-Eluting Coronary Stent System (Resolute Integrity System) is a device/drug combination product comprised of the following device components: the Integrity Coronary Stent and MicroTrac delivery systems and a drug component (a formulation of zotarolimus in a polymer coating).

Endeavor Resolute uses a proprietary new biocompatible polymer called BioLinx. ... Developed by Medtronic scientists, BioLinx is the first polymer created specifically for use on a drug-eluting stent. The BioLinx polymer features a unique blend of hydrophilic and hydrophobic elements for optimal performance.

Product description New design solar mounting solutions 1) living house and home building. 2) commercial building, factory, shopping mall, school, stadium etc. 3) power station, field operation and some huge engineer construction. Roof solar mounting system 1. Unmatched durability---10 year warranty. 2. Easy to install---the simple design and pre-assembled components ensure a quick and easy installation. 3. All weather

Sirolimus-eluting coronary stent system plga coating Properties: Intervention equipments Type: Embolization equipments Brand name: Codura Model number: 2.5mm - 4.0mm Place of origin: Guangdong, china (mainland) Licence number: Iso13485 Material: L605 cobalt-chromium Stent location: Blood stent

PLS Medical is a leading manufacturer in China with rich experience and know-how in the fields of designing, manufacturing and marketing for various medical guidewires and medical catheters. Our guidewire have been succeeded to got patent in China in 2008, by far it is one of the 3 patents to manufacturing the J-tip guidewire in the world, and all the equipments of the whole production line to manufacturing guidewire and catheters are creating, developing and assembling by PLS people ourselves. The guidewire we are running now included PTFE Coated guidewire;Hydrophilic guidewire, Neurological Micro-guidewire; Zebra guidewire; Steerable Guidewire or movable guidewire etc., it is widely used in the clinics application of cardiology, urology, neurology, tumour, gastroenterology etc.; The catheter series included central venous cahteter, introducer sheath, pressure transducer, ureteral stents or urology pigtail catheter, hemostasis valve kits, Ileus catheter,biopsy forceps etc. PLS Medical provides OEM manufacturing various of guidewires and catheters, also we provide and sell the CHINA MADE EQUIPMENTS and Tenology for the whole production line of central venous catheter,seldinger guidewire, PTFE coated guidewire, Ureteral Stents.For further information, please log on our website www.plsmedical.com, or You can contact our sales for the further the information.

PLS Medical is a leading manufacturer in China with rich experience and know-how in the fields of designing, manufacturing and marketing for various medical guidewires and medical catheters. Our guidewire have been succeeded to got patent in China in 2008, by far it is one of the 3 patents to manufacturing the J-tip guidewire in the world, and all the equipments of the whole production line to manufacturing guidewire and catheters are creating, developing and assembling by PLS people ourselves. The guidewire we are running now included PTFE Coated guidewire;Hydrophilic guidewire, Neurological Micro-guidewire; Zebra guidewire; Steerable Guidewire or movable guidewire etc., it is widely used in the clinics application of cardiology, urology, neurology, tumour, gastroenterology etc.; The catheter series included central venous cahteter, introducer sheath, pressure transducer, ureteral stents or urology pigtail catheter, hemostasis valve kits, Ileus catheter,biopsy forceps etc.