Medtronic Resolute Integrity DES Drug-eluting Stent (SD 2.75)

Medtronic Resolute Integrity DES Drug-eluting Stent (SD 2.75)

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Product Details:

Usage Type Professional Interventional Cardiology
Instruments Type Single-use Cardiovascular Implant
Features Continuous Sinusoidal Design, Enhanced Flexibility, Superior Deliverability, Zotarolimus Coating for Controlled Drug Release, Integrity Platform
Measurement Range Diameter: 2.75 mm, Length: 838 mm
Storage Instructions Store in original packaging, keep dry, avoid extreme temperatures
Shelf Life Up to 2 years (see packaging)
Function Drug-eluting coronary stent for maintaining vessel patency and reducing restenosis
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Medtronic Resolute Integrity DES Drug-eluting Stent (SD 2.75) Price And Quantity

Catheter Compatibility 6F guide catheter compatible
Balloon Compatibility Compatible with standard balloon angioplasty catheters
Stent Design Continuous sinusoid single wire construction
Indication Coronary artery disease, treatment of de novo lesions
Drug Coating Zotarolimus controlled-release pharmaceutical agent
Packaging Sterile, single-use packaging with clear labeling
Expiration Date Printed on packaging
Sterility Assurance Gamma irradiated, sterile upon delivery
Delivery System Rapid-exchange system
Latex Content Latex-free
Radiopacity Excellent, for fluoroscopic visualization
Market Authorization CE Marked, FDA Approved
Stent Surface Finish Smooth electro-polished

Medtronic Resolute Integrity DES Drug-eluting Stent (SD 2.75) Product Specifications

Instruments Type Single-use Cardiovascular Implant
Dimension (L*W*H) Stent Diameter: 2.75 mm, Stent Length: Variety of options (e.g., 8, 12, 15, 18, 24, 30, 38 mm)
Use Percutaneous Coronary Intervention (PCI)
Operating Type Manual (Interventional Procedure)
Weight Minimal (single-use, implantable)
Usage Type Professional Interventional Cardiology
Portable Yes (single-use, disposable)
Equipment Type Drug-eluting Coronary Stent
Function Drug-eluting coronary stent for maintaining vessel patency and reducing restenosis
Condition Sterile, New
Measurement Range Diameter: 2.75 mm, Length: 838 mm
Storage Instructions Store in original packaging, keep dry, avoid extreme temperatures
Shelf Life Up to 2 years (see packaging)
Material Cobalt-Chromium Alloy
Features Continuous Sinusoidal Design, Enhanced Flexibility, Superior Deliverability, Zotarolimus Coating for Controlled Drug Release, Integrity Platform
Technology Zotarolimus-Eluting (DES) Resolute Integrity Platform
Wall Mounted No
Color Metallic (Stent), Transparent tube packaging

Catheter Compatibility 6F guide catheter compatible
Balloon Compatibility Compatible with standard balloon angioplasty catheters
Stent Design Continuous sinusoid single wire construction
Indication Coronary artery disease, treatment of de novo lesions
Drug Coating Zotarolimus controlled-release pharmaceutical agent
Packaging Sterile, single-use packaging with clear labeling
Expiration Date Printed on packaging
Sterility Assurance Gamma irradiated, sterile upon delivery
Delivery System Rapid-exchange system
Latex Content Latex-free
Radiopacity Excellent, for fluoroscopic visualization
Market Authorization CE Marked, FDA Approved
Stent Surface Finish Smooth electro-polished

Product Description

Brand	Medtronic
Stent Diameter (mm)	2.75
Stent Length (mm)	08, 14, 22, 26 & 30
CAT No	RSINT27508X, RSINT27514X, RSINT27522X, RSINT27526X & RSINT27530X
Catheter Length	300 cm

Resolute Integrity is a drug-eluting stent (DES) and balloon catheter that offers excellent deliverability and flexibility for percutaneous coronary interventions.

Continuous Sinusoidal Design for Flexibility and Deliverability

The unique continuous sinusoidal, single-wire construction of the Resolute Integrity stent enhances its flexibility and conformability, allowing for precise navigation and placement even in complex coronary anatomies. This innovative design reduces the risk of vessel trauma during percutaneous coronary intervention (PCI) and improves deliverability through tortuous vessels, ensuring effective treatment of de novo lesions.

Controlled Zotarolimus Drug Elution Reduces Restenosis

With advanced zotarolimus drug coating, the stent delivers a controlled and sustained release of the pharmaceutical agent directly to the vessel wall. This targeted approach minimizes the potential for restenosis, a common post-angioplasty complication, and supports long-term vessel patency. The technology is specifically developed for optimal drug diffusion and patient outcomes.

Superior Visualization and Professional Compatibility

Radiopacity is a standout feature of the Resolute Integrity DES, ensuring that clinicians have excellent fluoroscopic visibility during navigation and deployment. Compatibility with standard balloon angioplasty catheters and 6F guide catheters facilitates integration with existing procedural workflows, while its rapid-exchange delivery system streamlines use in interventional cardiology settings.

FAQ's of Medtronic Resolute Integrity DES Drug-eluting Stent (SD 2.75):

Q: How is the Medtronic Resolute Integrity DES implanted during a coronary intervention?

A: The stent is delivered via a rapid-exchange system compatible with standard balloon angioplasty catheters. Once positioned at the site of the de novo coronary lesion, the stent is expanded and deployed using the balloon, maintaining vessel patency while releasing zotarolimus to limit restenosis.

Q: What are the primary clinical benefits of using the Resolute Integrity DES?

A: The use of zotarolimus-eluting technology reduces restenosis by delivering a controlled dose of medication directly to the vessel wall. The continuous sinusoidal design enhances flexibility and deliverability, lowering the risk of vessel trauma and enabling successful treatment of complex vascular anatomies.

Q: When should the Resolute Integrity DES be considered for patient treatment?

A: This drug-eluting stent is indicated for the treatment of de novo lesions in patients with coronary artery disease undergoing percutaneous coronary intervention (PCI). It should be used when maintaining vessel patency and minimizing restenosis risk are critical goals.

Q: Where is the expiration date for the stent found, and how should it be stored?

A: The expiration date is clearly printed on the packaging. The stent should be stored in its original, sterile packaging, kept dry, and protected from extreme temperatures to maintain sterility and product integrity.

Q: What stent lengths are available and what is the measurement range for this device?

A: The Resolute Integrity DES is available in a range of lengths-such as 8, 12, 15, 18, 24, 30, and 38 mm-with a fixed stent diameter of 2.75 mm. This allows for precise matching to lesion length during coronary procedures.

Q: How does the stent's radiopacity enhance procedural outcomes?

A: Its excellent radiopacity provides clear fluoroscopic visualization, allowing clinicians to accurately track, position, and deploy the stent, which is particularly valuable during challenging or complex interventions.

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