Atherectomy Catheter, Tip Diameter 3.0 - 2.1 Mm, 3.4-2.4 Mm, Catheter Diameter 7 F (2.47 Mm), Catheter Length: 120 Cm, 135 Cm., The Device Is Intended For Use As An Embolic Protection System To Contain And Remove Embolic Material (Thrombus/Debris) During Angioplasty, Stenting, Or Thrombectomy Procedures In The Coronary, Peripheral, And Carotid Arteries. Features A Braided Nitinol Filter With Heparin Coating. Compatible With 0.014-0.018 Micro Conductor. Filter Diameters Ranging From 3 To 7 Mm In 9 Different Models (Including Half Models) Provide Less Vascular Irritation And Improved Capture Efficiency. Gradual Change In Hole Size, Well Balanced Density. Using A Unique Weaving Technology, The Mesh Naturally Adheres To The Vessel Wall. Minimum Compatibility With 6F Catheter., • Reinforced Catheter, Consisting Of 7 Segments • Atraumatically Polished Distal Part Of The Catheter • 2 Platinum Markers, Allowing You To Disconnect The Coils In The Desired Part • External Diameter 2.4F, Internal 1.7F, Internal Diameter 0.017; Diameter 2.5/2.0F - Internal Diameter 0.021; Diameter 3.1/2.6 F - Internal Diameter 0.027; • Available In Lengths 150 Cm, 156 Cm, 167 Cm. • Available In Two Types: “Regular” And “Extra Support”., • Balloons: - Compliant - Extra Compliant - For Vessel Bifurcation Balloon Shaft: Proximal Od - 2.8F, Distal Od - 2.1F • Dual Lumen Shaft (Coaxial System) - One For Balloon Inflation And Deflation, The Other Is Compatible With Dmso, Adhesive And Coils • Variable Shape Balloon • Available Dimensions:4Mm/10Mm; 4Mm/15Mm; 4Mm/20Mm; 4 Mm/11Mm, Distal Tip – 5 Mm, Intended To Restore Blood Flow In Patients Who Have Suffered An Ischemic Stroke Due To Occlusion Of A Large Intracranial Vessel. It Is A Non-Detachable Stent-Retriever With A Parametric Design (Snail-Shaped In Cross Section). The Length Of The Pusher Is 200 Cm. The Length Of The Working Part Of The Stent Retriever For A Diameter Of 4 Mm Is 20, 40 Mm; For A Diameter Of 6 Mm - 20, 24, 40 Mm. Radiopaque Markers On The Working Part Of The Stent-Retriever: 5 And 10 (For Ø 4 Mm), 6 And 10 (For Ø 6 Mm). Possibility Of Using A Device With A Diameter Of 4 Mm In Vessels Of 2-4 Mm, With A Diameter Of 6 Mm In Vessels Of 2-5.5 Mm. Compatible With 0.021 And 0.027 Id Microcatheters, Self-Expanding Intracranial Stent With Fibrin-Gerapin Coating. Drug Coating Significantly Reduces The Risk Of Developing Restenosis Or Thrombosis Of The Stent, And Also Leads To Faster Formation Of Neointima And Accelerated Closure Of The Aneurysm. X-Ray Visualization Of The Stent Contour Along The Entire Length, Which Provides Better Control Of Wall Application And Stent Opening Behavior During The Procedure. The Presence Of Three Distal And Three Proximal Markers, As Well As An Additional Midline Marker, Facilitating Positioning In The Neck Of The Aneurysm. Possibility Of Re-Closure And Stent Placement Even At 95% Dilation. Protective Titanium Oxide/Oxynitride Coating To Reduce Platelet Adhesion And Promote Vascular Endothelialization. The Range Of Stent Diameters Is From 2.5Mm To 4.5Mm. Available Lengths From 10Mm To 25Mm. Compatibility Of All Sizes Of Stent With Microcatheter 0.0165-0.017. Possibility Of Use In Vessels Ranging In Size From 1.5 Mm To 4.5 Mm., Introducer For Transradial Access Complete With Hemostasis Cuff, Description: Acrylic Aspherical Folding Single-Component Posterior Chamber Intraocular Lenses With An Ultra Violet Filter And A Blue Part Of The Spectrum Filter, Should Be Intended To Replace The Human Lens When Correcting Aphakia In Adult Patients. The Lens Must Consist Of Aspherical Optics With A Diameter Of At Least 6.0 Mm, Made Of Soft Acrylic Material With A High Refractive Index And An A Constant Of At Least 118.7 And Supporting Haptics. Lens Material: Hydrophobic Acrylate/Methacrylate Copolymer Should Be Used, Absorbing Ultra Violet And Blue Parts Of The Spectrum, The Configuration Should Be Anteriorly Asymmetrical Biconvex. The Lens Must Have A Chromophore Filter That Blocks The Blue Part Of The Spectrum Like A Natural Human Lens. The Intraocular Lens Should Reduce The Penetration Of Blue Waves From 62% At 400Nm To 23% At 475Nm. The Lens Must Be Folded Before Implantation Due To The Properties Of The Optics Material. Once Implanted, It Should Gently Unfold To Its Full Size. The Configuration Should Be Anteriorly Asymmetrical Biconvex. The Size Of The Optics Should Be No More Than 6 Mm. The Total Length Of The Lens Should Be No More Than 13 Mm. The Refractive Index Must Be At Least 1.55. Diopter Should Be From +6.0 To +14.0 In 1 D Steps, From +15.0 To +26.0 In 0.5 D Steps, From +26.0 To 30.0 In 1.0 D Steps, Catheters For Radiofrequency Coagulation Are Intended For The Procedure Of Endovasal Radiofrequency Obliteration Of The Veins Of The Lower Extremities. Used In The Treatment Of Varicose Veins And Chronic Venous Insufficiency Of The Lower Extremities., A Drug-Eluting Coronary Stent Containing A Polymer-Based Drug (D, L-Lactide-Co-Caprolactone), The Absorption Time Of Which Is Synchronous With The Release Of The Drug (3-4 Months), Which Leads To A Reduced Risk Of Restenosis And Thrombosis, As Well As Sirolimus (The Active Substance). Basic Functional Requirements, Technical Characteristics: Presence Of A Stent Diameter Of 2.00 Mm; 2.25 Mm; 2.50 Mm; 2.75 Mm; 3.00 Mm; 3.50 Mm 4.00 Mm; 4.50 Mm., Intracranial Stent For The Treatment Of Stenoses With Fibrin-Gerapin Coating. Drug Coating Significantly Reduces The Risk Of Developing Restenosis Or Thrombosis Of The Stent, And Also Leads To Faster Formation Of Neointima And Accelerated Closure Of The Aneurysm. The Diameter Of The Stents Is From 3.0 Mm To 5.0 Mm. Stent Length Is From 15 Mm To 30 Mm. Recommended Vessel Diameter Is From 2.0Mm To 4.5Mm. Due To Its Low Profile, The Stent Can Be Delivered Through A 0.0165-Inch Catheter, Resulting In No Microcatheter Exchange Required For Stent Delivery, Minimizing Procedure Time And Procedural Risks. The Presence Of Three Distal And Three Proximal Markers, As Well As Two Gold Markers On The Delivery Guide, Greatly Facilitates Positioning. Possibility Of Stent Repositioning In Case Of Its Deployment Up To 90%., Self-Expanding Nitinol Stent On A Delivery System With An Rx Port At A Distance Of 28 Cm From The Tip Of The Catheter. Tantalum Markers On Each End Of The Stent, Fibrin-Gerapin Coated Nitinol Flow Redirection Stent. Drug Coating Significantly Reduces The Risk Of Developing Restenosis Or Thrombosis Of The Stent, And Also Leads To Faster Formation Of Neointima And Accelerated Closure Of The Aneurysm. Stent Diameter Is From 2.5 To 8.0 Mm. Can Be Used In Vessels With A Diameter From 1.5 Mm To 8.0 Mm. Stent Length From 10 Mm To 50 Mm. Self-Expanding Intracranial Stent. The Device Must Have High Coverage Of The Vessel Walls And The Ability To Change Hemodynamic Forces And Vectors In The Segment Bearing The Aneurysm. Nitinol Composite Wire With A Platinum-Iridium Core Provides 100% Visualization Along The Entire Length Of The Stent. The Stents Are Compatible With A Guidewire Of 0.017, 0.027, 0.039. Possibility Of Repositioning The Stent If It Is Expanded Up To 90%. Possibility Of 3D Modeling Of Dimensions., Device For Neurovascular Embolization Of Cerebral Vessels Spiral Wallaby Avenir™ Coil System, Cardiac Diagnostic Catheters For Transradial, Femoral Approaches And Catheterization Of Cardiac Cavities
