Cordis

Product Details:

Cordis VISTA BRITE TIP® - Cardinal Health Englishh

PDF... BRITE TIP®. Guiding Catheter – Designed for support and performance ... SM7752*. XB 3.5 LBT. Long VISTA BRITE TIP®, 120 cm. SM7400*. XB 3.5. 125 cm.

PDFGuiding catheter compatibility: 5F (min ID 0,056”) ... The ADROIT™ Guiding Catheter 5F is also available with a .058” inner diameter ... XB 3.5 LBT. Extra Back ...
ADROIT Guiding Catheter Brochure - Cardinal HealtPDFMedtronic. Launcher®. % Whip. 32.03. 5F. 6F. Cordis ADROIT™. Guiding Catheter ... 672-054-0E. XB 3.5 LBT. Long BRITE TIP®. 672-054-0L. XB 4. 672-056-00.
Cordis Radial Solutions - Cardinal

PDF4F, 5F, 6F. Length (cm). 6.5, 10, 20. Mini Guidewire. 0.014" polymer-coated ... the guiding catheter version of the popular diagnostic catheter, designed for ... XB 3.5. 90 cm. 670-054-90. XB 3.5 LBT. Long VISTA BRITE TIP®. 556-054-0l.
Product Catalog - AWSPDFVISTA BRITE TIP® Guiding Catheters. Catheter Shapes. Extra Support. XB 3. XB 3.5. XB 4. XB 4.5 ... XB 4 LBT. 556-056-0L. 100. XBLAD 3.5 LBT. 556-060-0L. 100. Hockey Stick. H-STICK LBT ... 5F INFINITI® Diagnostic Catheters. E-10.

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Owing to our immense market knowledge, we are able to offer excellent quality Avanti Surgical Catheter.

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The Cordis INFINITI® 4F, 5F and 6F line of diagnostic catheters is ideal for coronary angioplasty. These catheters incorporate proprietary Vestan Nylon to deliver ...
The Cordis INFINITI™ 4F, 5F and 6F line of diagnostic catheters is ideal for coronary angioplasty.The Cordis INFINITI® 4F, 5F and 6F line of diagnostic catheters is ideal for ... These catheters incorporate proprietary Vestan Nylon to deliver exceptional ...

Additional Information:

• Production Capacity: long term
• Delivery Time: 3--4 working days
• Packaging Details: 5pcs in (1-BOX)

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Indications

The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.

Contraindications

None known for guiding catheters.

Warnings

Risk of reuse: This product is designed and intended for single use. It is not designed to undergo reprocessing and resterilization after initial use. Reuse of this product, including after reprocessing and/or re-sterilization, may cause a loss of structural integrity which could lead to a failure of the device to perform as intended and may lead to a loss of critical labeling/use information all of which present a potential risk to patient safety. Do not use with Ethiodol™ or Lipiodol™ contrast media, or other such contrast media which incorporates the components of these agents.

Precautions

• Store in a cool, dark, dry place.
• Do not use open or damaged packages.
• Use prior to the “Use By” date.
• Do not resterilize.
• Do not expose to organic solvents.
• Inspect the guiding catheter before use to verify that its size, shape and condition are suitable for the specific procedure.
• If strong resistance is met during manipulation, discontinue the procedure and determine the cause of the resistance before proceeding. If the cause of the resistance can not be determined, withdraw the catheter.
• Torquing the guiding catheter excessively while kinked may cause damage which could result in possible separation along the catheter shaft. Should the guiding catheter shaft become severely kinked, withdraw the entire system (guiding catheter, guidewire and catheter sheath introducer).
• Advancement, manipulation and withdrawal of the guiding catheter should always be performed under fluoroscopic guidance.
• Extreme care must be taken to avoid damage to the vasculature through which the guiding catheter passes. The guiding catheter may occlude smaller vessels. Care must be taken to avoid complete blood flow blockage.
• Large internal lumen guiding catheters require less force on the syringe during injection.

Complications

Procedures requiring percutaneous catheter introduction should not be attempted by physicians unfamiliar with the possible complications. Complications may occur at anytime during or after the procedure. Possible complications include, but are not limited to the following:

• air embolism
• hematoma at the puncture site
• infection
• perforation of the heart
• vessel damage, dissection or perforation
• vasospasm
• ischemia
• hemorrhage
• arrhythmia
• reaction to contrast media
• death

Product Details:

The femoral sheath is a structure within bilateral femoral triangles. The femoral sheath contains the femoral vein, artery, and lymphatics.
The Cordis sheath portfolio is comprised of the AVANTI™+ Sheath Introducer and the BRITE TIP™ Interventional Sheath Introducer.

Additional Information:

• Production Capacity: LONG TERM
• Delivery Time: 3-4 WORKING DAYS
• Packaging Details: 5PCS IN (1-BOX)

Product Details:

EMPIRA™ PTCA Balloons - CordisEMPIRA™ Pre Dilatation and Post Dilatation PTCA Balloons catheters helps you reach and treat a wide range of lesions with exceptional crossability 
EMPIRA™ NC Balloon Catheter delivers crossability & best-in-class controlled growth to a wide range of lesions. EMPIRA™ NC RX PTCA
The Cordis PTCA Balloon Portfolio includes the EMPIRA™ Balloon, which helps to treat a wide range of lesions with exceptional crossability and recrossability.

Additional Information:

• Production Capacity: EMPIRA PTCA Balloons Cordis
• Delivery Time: 3-4 DAYS
• Packaging Details: 1PCS

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EMERALD Guidewire - CordisThe Cordis EMERALD Guidewire complements our diagnostic catheter and catheter sheath introducer
502521 Cordis EMERALD Guidewire 0.035 x 150cm, 3mm J tip

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