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Cordis
Endovascular catalog

Endovascular catalog

Product catalog summary

About Us
Cordis specializes in cardiology and endovascular platforms, offering high-quality products such as diagnostic and interventional catheters, balloons, self-expanding stents, guide wires, and vascular closure devices. The company leverages its experience in product innovation and Cardinal Health's operational expertise to meet evolving healthcare needs.

Access Portfolio

AVANTI®+ Sheath Introducer: Features a patented SLIX™ Valve for smooth transitions and monitoring capabilities. It offers a hexacuspid design for maneuverability and hemostasis, a rotating suture collar, and a kink-resistant cannula.
BRITE TIP® Catheter Sheath Introducer: Provides flexibility and control with a kink-resistant cannula and a patented SLIX™ Valve. It has a dual-layer cannula for accessing tortuous vessels and a silicone-coated cannula for smooth entry.
Obturators: Designed to prevent kinking and ease insertion with a flexible shaft and atraumatic distal tip.
Vessel Dilators: Facilitate catheter entry with a lubricious coating and optimized tapering to minimize tissue trauma.

Diagnostic Portfolio

EMERALD® Diagnostic Guidewire: Designed for percutaneous entry and guidance of catheters, offering solid tensile strength to minimize stretching or fracturing.
Diagnostic Catheters: Includes SUPER TORQUE®, TEMPO®, TEMPO AQUA®, and NYLEX® catheters, each offering unique features such as high flow rates, pressure limits, and compatibility with micro-catheters.

Interventional Portfolio

Guiding Catheters: VISTA BRITE TIP® series offers excellent visualization and precise placement with a co-extruded kink-resistant cannula.
Steerable Guidewires: Includes AQUATRACK®, STORQ®, JINDO®, and others, providing various features for enhanced maneuverability and support.
PTA Balloons: Available in different sizes (.035”, .018”, .014”) with various models like POWERFLEX®, SABER®, and SLEEK® offering specific features for dilatation procedures.

Stent Systems

S.M.A.R.T.® Vascular Stent System: Offers self-expanding stents for vascular applications.
Biliary Stents: Includes self-expanding and balloon-expandable options like S.M.A.R.T.® and PALMAZ® series for biliary interventions.
Carotid Systems: PRECISE® series provides stent systems for carotid artery procedures.

Closure Portfolio

MYNXGRIP® and MYNX ACE® Vascular Closure Devices: Designed for secure closure of vascular access sites.
EXOSEAL® Vascular Closure Device: Offers a unique closure mechanism for vascular procedures.

General Information
Includes contact details for U.S. and global headquarters, customer service, technical information, and policies on product usage, returns, and complaints.

Guidewires: The catalog lists PTFE-coated guidewires with different diameters, lengths, and flexible ends. These are categorized into J-Curve and Straight Tip types, with specific product codes for each configuration. The guidewires are designed for percutaneous entry and guidance of angiographic catheters, with some models featuring a fixed-core or movable-core design.

Diagnostic Catheters: Various types of diagnostic catheters are described, including SUPER TORQUE®, TEMPO®, and TEMPO AQUA® catheters. These catheters are available in different French sizes and lengths, with specifications on flow rates, inner diameters, and guidewire acceptance. The catalog highlights features such as braided polyurethane or nylon bodies, high flow rates, and pressure limits.

Specialty Catheters: The document also covers specialty catheters like the OUTBACK® Elite Re-Entry Catheter, ELITECROSS™ Support Catheter, and FRONTRUNNER® XP CTO Catheter. These products are designed for specific applications such as re-entry into the true lumen of vessels, providing support and steerability, and facilitating guidewire placement in chronic total occlusions.

Key Features and Benefits: The catalog emphasizes features like ergonomic handles, highly visible markers, and hydrophilic coatings that enhance the usability and effectiveness of the catheters. It also notes the importance of reducing fluoroscopy time and improving torque control for better maneuverability.

Additional Information: The document references specific pages for detailed information on indications, contraindications, warnings, and precautions associated with the use of these medical devices.

Product Overview
The document provides detailed specifications and features of various medical devices used in endovascular procedures, focusing on stents, embolic protection systems, and vascular closure devices.

Stent Systems
The stents described are designed for carotid artery stenting, featuring a micromesh design and multi-segmental construction. They offer high radial resistive force, are crush-recoverable, and have a maximum foreshortening of 8%. The stents are made from nitinol and are compatible with a 135cm delivery system. Various sizes are available, with sheath compatibility ranging from 5F to 8F depending on the stent diameter.

Embolic Protection Systems
The ANGIOGUARD® RX Emboli Capture Guidewire System is highlighted for its ease of use and effectiveness in capturing emboli during carotid artery procedures. It features a rapid exchange system, medium and extra support wires, and a filter with 100μ pore sizes for optimal emboli capture. The system is compatible with an 8F guiding catheter and a 6F sheath.

Vena Cava Filters
The document describes the CORDIS® Vena Cava filters, which use nitinol technology for dual-layer filtration and self-centering design to prevent tilting. The OPTEASE® Retrievable Vena Cava Filter offers the option of retrieval within 23 days, while the TRAPEASE® Permanent Vena Cava Filter is designed for permanent placement.

Vascular Closure Devices
The MYNXGRIP®, MYNX ACE®, and EXOSEAL® Vascular Closure Devices are discussed, each offering unique features for secure closure of femoral arterial and venous access sites. The MYNXGRIP® and MYNX ACE® devices use a GRIP™ sealant that dissolves within 30 days, while the EXOSEAL® device provides a simple 3-step procedure for closure.

Indications and Contraindications
The document includes indications, contraindications, warnings, and precautions for the use of the ANGIOGUARD® RX Emboli Capture Guidewire System and other guidewires. It emphasizes the importance of proper training and adherence to procedural guidelines to ensure patient safety.

Guidewires: Guidewires are delicate instruments requiring careful handling. Inspect for damage before use and avoid using damaged guidewires. Manipulation should be under fluoroscopic guidance, and resistance should be investigated before proceeding to avoid damage or vessel injury. Store in a cool, dry place and avoid exposure to high temperatures or organic solvents.

Complications: Potential complications include air embolism, hematoma, infection, and vessel perforation. Physicians should be familiar with these risks before attempting procedures.

AVANTI®+ Sheath Introducer: Intended for arterial and venous procedures, this device should not be reused or resterilized. Store properly and avoid exposure to high temperatures or organic solvents. Complications may include air embolism and vessel perforation.

AVIATOR® Plus PTA Dilatation Catheter: Used for angioplasty in peripheral vasculature, it is contraindicated for coronary arteries. Store in a cool, dry place and avoid reuse. Ensure balloon size matches vessel diameter to prevent damage. Potential complications include myocardial infarction and thrombosis.

ELITECROSS™ Support Catheter: Facilitates placement of devices beyond stenotic lesions. Not for use in cerebral or coronary vasculature. Avoid reuse and exposure to high temperatures. Complications may include vessel damage and infection.

EMERALD® Diagnostic Guidewire: Used for catheter introduction, it should not be reused. Store properly and avoid exposure to high temperatures or organic solvents. Ensure proper handling to maintain integrity.

EXOSEAL® Vascular Closure Device
Indication for Use: The device is used for femoral artery puncture site closure to reduce hemostasis and ambulation times in patients undergoing catheterization procedures with specific sheath introducers.
Warnings: Do not use if the package is damaged or if the device appears defective. Maintain sterile conditions to prevent infection.
Precautions: Avoid use in unsuitable vessels and ensure proper training in device use.
Special Patient Populations: Safety not established in patients with certain conditions such as recent myocardial infarction, uncontrolled hypertension, or bleeding disorders.

FRONTRUNNER® XP CTO Catheter
Indications: Facilitates guide wire placement beyond stenotic lesions in peripheral vasculature.
Warnings: Single use only. Do not use in cerebral or coronary vasculature.
Precautions: Use by trained physicians only, and avoid excessive bending or kinking.

MAXI LD® PTA Dilatation Catheter
Indications: Intended to dilate stenoses in peripheral arteries below the aortic arch.
Warnings: Single use only. Ensure balloon pressure does not exceed rated burst pressure.
Precautions: Verify catheter functionality and suitability before use.

MYNX ACE® and MYNXGRIP® Vascular Closure Devices
Indications for Use: Used to seal femoral arterial access sites and reduce hemostasis and ambulation times.
Warnings: Single use only. Do not use if packaging is damaged or if puncture site is improperly located.
Precautions: Use by trained professionals only, and verify puncture site location with angiogram.

Overview: This document provides detailed information on various medical devices, including diagnostic catheters, PTA dilatation catheters, and vena cava filters. It outlines their indications, contraindications, warnings, precautions, and potential complications.

1. Diagnostic Catheters:

Indications: Designed to deliver radiopaque contrast medium to selected sites in the vascular system.
Contraindications: None known.
Complications: Possible complications include air embolism, hematoma, infection, and vessel wall perforation.

2. OPTA® Pro PTA Dilatation Catheter:

Indications: Used to dilate stenoses in various arteries and treat obstructive lesions in dialysis fistulae.
Contraindications: Not for use in coronary arteries.
Warnings: Single-use only, do not exceed rated burst pressure, and use under fluoroscopic observation.
Precautions: Verify catheter functionality before use, and ensure proper training for operators.
Adverse Effects: Include air embolism, aneurysm, and vessel wall perforation.

3. OPTEASE® Retrievable Vena Cava Filter:

Indications: Prevents recurrent pulmonary embolism in specific situations where anticoagulants are contraindicated or have failed.
Contraindications: Not for patients with septic embolism risk, uncontrolled infections, or large IVC diameter.
Warnings: Single-use components, proper orientation during implantation, and potential for filter fracture.
Precautions: Store properly, do not reuse, and ensure fluoroscopic control during procedures.

Conclusion: The document emphasizes the importance of adhering to specified guidelines for the safe and effective use of these medical devices, highlighting the need for proper training and awareness of potential risks.

OPTEASE® Filter
Indications: Used for preventing recurrent pulmonary embolism (PE) when anticoagulants are contraindicated, have failed, or in emergency situations.
Contraindications: Not for patients with septic embolism risk, uncontrolled infections, or IVC diameter >30mm.
Warnings: Retrieval only via femoral vein; single-use components; do not exceed 800 psi when injecting contrast medium.
Precautions: Store properly; do not reuse; use under fluoroscopic control.

OUTBACK® Elite Re-Entry Catheter
Indications: Facilitates guidewire and catheter placement in peripheral vasculature.
Contraindications: Not for coronary or cerebral vasculature.
Warnings: Single-use only; avoid organic solvents; do not use if package is damaged.
Precautions: Store properly; use by trained physicians; confirm vessel visualization before use.

PALMAZ® Balloon-Expandable Stent
Indications: Palliation of malignant neoplasms in the biliary tree.
Contraindications: Not for perforated ducts or patients with bleeding disorders.
Warnings: Single-use only; store properly; use only recommended balloon catheters.
Potential Complications: Include cholangitis, stent migration, and pancreatitis.

PALMAZ BLUE® Transhepatic Biliary Stent
Indications: Similar to PALMAZ® Stent for biliary tree neoplasms.
Contraindications: Same as PALMAZ® Stent.
Warnings: Single-use only; avoid high inflation rates; do not use certain contrast media.
Precautions: Use by trained physicians; verify device integrity before use.

Overview: This document provides detailed information on the use, indications, contraindications, warnings, precautions, and potential complications associated with various medical devices, specifically focusing on transhepatic biliary stents and PTA (Percutaneous Transluminal Angioplasty) catheters.

1. PALMAZ GENESIS® Transhepatic Biliary Stent:

Indications: Used for palliation of malignant neoplasms in the biliary tree.
Contraindications: Not suitable for perforated ducts, patients with uncorrected bleeding disorders, or severe ascites.
Warnings: Not for vascular use, single-use only, avoid high inflation rates, and store properly. Allergic reactions possible for those sensitive to cobalt-chromium alloy.
Precautions: Use by trained physicians only, verify device integrity before use, and avoid dissimilar metal corrosion.
Potential Complications: Include sepsis, stent migration, obstruction, pancreatitis, and more.

2. PALMAZ® XL Transhepatic Biliary Stent:

Indications: Similar to the PALMAZ GENESIS®, for malignant neoplasms in the biliary tree.
Contraindications: Same as above, with additional caution for patients allergic to stainless steel.
Warnings and Precautions: Similar to PALMAZ GENESIS®, emphasizing single-use and proper handling.
Potential Complications: Similar to those listed for PALMAZ GENESIS®.

3. POWERFLEX® Extreme PTA Dilatation Catheter:

Indications: Treatment of obstructive lesions in various arteries and dialysis fistulae.
Contraindications: Not for coronary arteries.
Warnings: Single-use only, avoid over-pressurization, and use recommended inflation medium.
Precautions: Ensure device suitability and use by trained professionals.
Adverse Effects: Include air embolism, aneurysm, and vessel perforation.

4. POWERFLEX® P3 and PRO PTA Catheters:

Indications: Similar to POWERFLEX® Extreme, with additional indication for post-dilation of stents.
Contraindications: Not for coronary arteries.
Warnings and Precautions: Emphasize single-use, proper handling, and use by trained professionals.
Adverse Effects: Similar to those listed for POWERFLEX® Extreme.

Adverse Effects: The document lists potential adverse effects of using the PTA catheter, including air embolism, aneurysm, hematoma, vessel wall perforation, vascular complications, embolism, allergic reactions, pyrogenic reactions, hemorrhage, hypotension/hypertension, ischemia, necrosis, and thrombosis.

PRECISE PRO RX® Carotid Stent Indications: This stent system is indicated for patients at high risk for adverse events from carotid endarterectomy, requiring carotid revascularization with specific criteria regarding stenosis and vessel diameter.

Contraindications: Contraindications include patients who cannot undergo antiplatelet or anticoagulation therapy, those with uncorrected bleeding disorders, allergies to nitinol, and specific lesion characteristics.

Warnings: Only trained physicians should use the device. The safety and efficacy with other embolic protection systems are not established. Long-term performance is unknown, and infection can lead to serious complications. Proper stent sizing is crucial to prevent migration.

Precautions: Venous access should be available during procedures, and catheters should be manipulated under fluoroscopy. The delivery system is not for power injection, and resistance during introduction should prompt withdrawal and replacement.

Potential Adverse Events: These include air embolism, allergic reactions, aneurysm, angina, arrhythmia, arterial occlusion, bacteremia, cerebral edema, device damage, death, and embolization.

PRECISE® Transhepatic Biliary Stent Indications: This system is for palliation of malignant neoplasms in the biliary tree.

Contraindications: Include stenting of perforated ducts, patients with bleeding disorders, and severe ascites.

Warnings: The device is for single use only, and reuse may compromise structural integrity. It should not be used with certain contrast media or exposed to organic solvents.

Precautions: The device should be used by trained physicians, and manipulation should be under fluoroscopy. Fractures may occur, especially with overlapping stents.

Potential Complications: Include sepsis, stent misplacement, migration, obstruction, pancreatitis, bile duct perforation, and liver abscess.

S.M.A.R.T.® Flex Biliary Stent Indication: This stent system is for palliation of malignant strictures in the biliary tree.

Contraindications: Include total biliary occlusion, perforated ducts, bleeding disorders, and severe ascites.

General Warnings/Precautions: The device is for single use, and resistance during insertion should prompt withdrawal. It should not be exposed to organic solvents, and use in patients with contrast sensitivity is not recommended.

Potential Adverse Events: Include infection, pancreatitis, duct rupture, allergic reactions, drug reactions, and tumor overgrowth.

Indications: The S.M.A.R.T. CONTROL® and S.M.A.R.T.® Vascular Stent Systems are designed to improve luminal diameter in patients with specific arterial lesions. The SABER® and SAVVY® PTA Dilatation Catheters are intended for dilating stenoses in various peripheral arteries and for post-dilation of stents.

Contraindications: The stent systems are contraindicated for patients with nickel titanium hypersensitivity or those unable to undergo antiplatelet therapy. The PTA catheters are contraindicated for use in coronary arteries.

Warnings: Stents should not be used in patients with contrast media allergies or certain medical conditions. The PTA catheters are for single use only and should not be exposed to high temperatures or organic solvents. Proper handling and storage are crucial to maintain device integrity.

Stent Placement and Handling: Careful manipulation under fluoroscopy is required. Resistance during insertion or deployment should not be forced. Stents should not be lengthened or shortened beyond their nominal length.

Complications: Potential complications include stent migration, thrombosis, embolization, and various vascular and systemic reactions.

Adverse Events: Possible adverse events from catheter use include vessel perforation, hemorrhage, infection, and thrombosis.

SLALOM® PTA Dilatation Catheter
Indications: Used for dilating stenoses in various arteries and treating obstructive lesions in dialysis fistulae.
Contraindications: Not for coronary arteries.
Warnings: Single use only, do not exceed burst pressure, use under fluoroscopic observation.
Precautions: Verify catheter functionality, use by trained physicians, consider heparinization.
Adverse Events: Includes air embolism, aneurysm, and perforation.

SLEEK® OTW PTA Dilatation Catheter
Indications: Balloon dilatation of femoral and popliteal arteries.
Warnings: Sterile, single use, do not exceed burst pressure.
Precautions: Use under fluoroscopic guidance, inspect catheter before use.
Adverse Events: Includes vessel perforation, hemorrhage, and infection.

SLEEK® RX PTA Dilatation Catheter
Indications: Balloon dilatation of femoral and popliteal arteries.
Contraindications: Not for coronary arteries.
Warnings: Single use only, do not exceed burst pressure.
Precautions: Use under fluoroscopic guidance, ensure tight connections to avoid air introduction.
Adverse Events: Includes vessel perforation, thrombosis, and allergic reactions.

STORQ® Steerable Guidewire
Indications: Used in angiographic procedures to position catheters.
Warnings: Single use, do not reuse or resterilize.
Precautions: Store properly, do not use if damaged, avoid organic solvents.
Complications: Includes air embolism and infection.

SUPER TORQUE® Diagnostic Catheter
Indications: Provides angiographic visualization and measurement.
Warnings: Single use, avoid excessive friction, do not exceed pressure rating.
Precautions: Store properly, avoid entrapment, do not use if damaged.
Complications: Includes air embolism and thrombosis.

TRAPEASE® Permanent Vena Cava Filter
Indications: Prevents recurrent pulmonary embolism in specific situations.
Contraindications: Not for patients with septic embolism risk or large IVC diameter.
Warnings: Single use, do not exceed pressure rating, post-implantation catheterization may be impeded.

TRAPEASE® Filter Specifications and Precautions:
The TRAPEASE® Filter is designed for use by trained physicians in diagnostic and percutaneous interventional techniques. It should be stored in a cool, dark, dry place and not exposed to temperatures above 54°C. The filter is MRI safe at field strengths of 3.0 Tesla or less. Potential complications include filter fracture, air embolism, and thrombus formation. Allergic reactions may occur in individuals sensitive to nickel titanium (Nitinol).

VISTA BRITE TIP® Guiding Catheter Specifications and Precautions:
This catheter is intended for intravascular introduction of devices into the coronary or peripheral vascular systems. It is for single use only and should not be reused or resterilized. Store in a cool, dark, dry place and inspect before use. Complications may include air embolism, vessel damage, and infection.

General Product Usage and Storage:
Most products are supplied sterile and should not be reused or reshaped. Store in a cool, dark, dry place and use before the "Use By" date. Federal law restricts these devices to sale by or on the order of a physician.

Return Policy:
Products can be returned within 180 days for full credit, with a 10% restocking charge applied after this period. Returns must be accompanied by a Return Authorization Number and sent to the specified address.

Trademarks:
The document lists various trademarks owned by Cardinal Health, including TRAPEASE®, VISTA BRITE TIP®, and others, which are part of the Cordis portfolio.

Catalog excerpts

Endovascular Catalog

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About Us 4 Access Portfolio 5 • • • • AVANTI®+ Sheath Introducer 6 BRITE TIP® Catheter Sheath Introducer 7 Obturators 8 Vessel Dilators 9 Diagnostic Portfolio 10 Diagnostic Guidewires 11 • EMERALD® Diagnostic Guidewire 11 Crossing Portfolio 25 • OUTBACK Elite Re-Entry Catheter 26 • ELITECROSS™ Support Catheter 27 • FRONTRUNNER® XP CTO Catheter 28 ® Interventional Portfolio 29 Guiding Catheters 32 • VISTA BRITE TIP® Guiding Catheter 32 • VISTA BRITE TIP® IG Guiding Catheter 32 AQUATRACK® Hydrophilic Nitinol Guidewire 37 STORQ® Steerable Guidewire 38 JINDO® Steerable Guidewire ...

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MAXI LD® PTA Dilatation Catheter 92 MYNX ACE® Vascular Closure Device 93 MYNXGRIP® Vascular Closure Device 93 NYLEX® Diagnostic Catheter, TEMPO® Diagnostic Catheter , TEMPO AQUA® Diagnostic Catheter 94 OPTA® Pro PTA Dilatation Catheter 94 OPTEASE® Retrievable Vena Cava Filter 95 OUTBACK® Elite Re-Entry Catheter 98 PALMAZ® Balloon-Expandable Stent 99 PALMAZ BLUE® Transhepatic Biliary Stent 100 PALMAZ GENESIS® Transhepatic Biliary Stent 101 PALMAZ® XL Transhepatic Biliary Stent 102 POWERFLEX® Extreme PTA Dilatation Catheter 103 POWERFLEX® P3 PTA Dilatation Catheter 104 POWERFLEX®...

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Cordis is a worldwide leader in the development and manufacture of interventional vascular technology with a more than 50-year history of delivering pioneering products to treat millions of patients. US Headquarters Our focus is in cardiology and endovascular platforms, with high-quality products such as diagnostic and interventional catheters, balloons, self-expanding stents, guide wires, and vascular closure devices. Working with our customers, we identify solutions that provide the best possible results for both physicians and patients. 1820 McCarthy Blvd Milpitas, CA 95035 P: 408.273.3700...

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AVANTI®+ Sheath Introducer The Cordis AVANTI®+ Sheath Introducer is the pioneer of catheter sheath introducer technology. Featuring a patented SLIX™ Valve, the AVANTI®+ Sheath Introducer provides smooth transitions, monitoring capabilities and exceptional performance for your procedural success, as well as: • A hexacuspid design that provides a balance between catheter maneuverability and hemostasis. • A rotating suture collar that facilitates procedural flexibility. It stays in place and allows patient movement. • A kink-resistant cannula design integrating a soft, flexible inner layer with...

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Cordis A Cardinal Health company AVANTI®+ Sheath Introducer The Cordis AVANTI®+ Sheath Introducer is the pioneer of catheter sheath introducer technology. Featuring a patented SLIX™ Valve, the AVANTI®+ introducer provides smooth transitions, monitoring capabilities and exceptional performance for your procedural success Vessel Dilator Key Features • .035" guidewire compatible • Unique SLIX™ valve for uncompromised valve hemostasis • Flexible and kink resistant • Excellent OD/ID ratio • Smooth insertion • Units per package: 5 For information on indications, contraindications, warnings, and...

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Cordis A Cardinal Health company BRITE TIP® Catheter Sheath Introducer Provides excellent visualization of the tungsten-filled radiopaque tip, which facilitates exact location of the sheath's distal tip for accurate positioning. Longer lengths are available for a wide variety of interventional procedures. vessel dilator Key Features • Co-extruded kink resistant cannula • Unique SLIX™ valve for excellent valve hemostasis • 3mm atraumatic, and radiopaque distal tip for precise placement • Smooth transition between cannula and dilator • Excellent kink resistance and back up support • 5 units per...

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Cordis A Cardinal Health company Accessories Portfolio Key Features • Flexible shaft helps prevent kinking of the sheath when the sheath is used in a patient for a long period of time without a product in place • Easy French size identification provided by a color coding system and the number on the hub • Easy to store boxes with small dimensions • Ease of insertion through the sheath and minimal vessel damage thanks to the rounded atraumatic distal tip • No "backing out" of the obturator by the secure snap fit between obturator and sheath • Low profile hub to ease placement and manipulation •...

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Cordis. A Cardinal Health company Vessel Dilators Key Features • Facilitate the percutaneous entry of angiographic catheters • With Luer hubs • Units per package: 10 Color Code Guidewire compatibility (inch) .021" .035" .021" .035" .038" .021" .035" .038" .035" .038" .035" .038" .035" .038" Endovascular Catalog Page 9 ► cordis.com

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Diagnostic Guidewires EMERALD® Diagnostic Guidewire Intended for percutaneous entry and guidance of catheters, the Cordis EMERALD® Diagnostic Guidewire complements our diagnostic catheter and catheter sheath introducer lines. Performance, endurance and safety are built into each EMERALD® Guidewire with solid tensile strength to minimize the likelihood of stretching or fracturing. Learn more on page 11. Diagnostic Catheters SUPER TORQUE® Diagnostic Catheter Used in coronary angioplasty. Constructed from polyurethane to deliver exceptional responsiveness and flow rates, optimal torque, and shape...

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Cordis. A Cardinal Health company Diagnostic Guidewires EMERALD® Diagnostic Guidewire Intended for percutaneous entry and guidance of catheters, the Cordis EMERALD® Diagnostic Guidewire complements our diagnostic catheter and catheter sheath introducer lines. Performance, endurance and safety are built into each EMERALD® Guidewire with solid tensile strength to minimize the likelihood of stretching or fracturing. Diameter (inch) Length (cm) PTFE-Coated Straight Tip Diameter (inch) .035 .035 PTFE-Coated J-Curve PTFE-Coated J-Curve Diameter (inch) Length (cm) J-Radius (mm) Product Code...

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Endovascular catalog

Endovascular catalog

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